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Black Pepper, the "King of Spices": Chemical composition to applications

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Arabian Journal of Chemical and Environmental Research

Vol. 06 Issue 1 (2019) 12–56

Black Pepper, the “King of Spices”: Chemical composition to


applications

B. Hammouti 1*, M. Dahmani 1, A. Yahyi1, A. Ettouhami1, M. Messali 2,


A. Asehraou3, A. Bouyanzer 1, I. Warad4 and R. Touzani1
1
Laboratory of Applied Chemistry and Environment (LCAE), Department of Chemistry, Faculty of Science. Mohammed
Premier University, BP717, 60000 Oujda, Morocco.
e-mails: e-mail: [email protected]; [email protected]; [email protected];
[email protected] ; [email protected]
2
Department of Chemistry, Taibah University, 30002, Al-Madina Al-Mounawara, Saudi Arabia
e-mail: [email protected]
3
Laboratory of Biochemistry and Biotechnology (LBB), Faculty of Sciences, University Mohammed Premier, Oujda,
Morocco; e-mail: [email protected]
4
Department of Chemistry and Earth Sciences, PO Box 2713, Qatar University, Doha, Qatar ;
e-mail: [email protected]

Received 04 March 2019, Revised 30 April 2019, Accepted 03 May 2019

Abstract
This article brings together an overview of the historical and scientific works on black pepper (BP). It’s well
known as the king of spices, and literature which is very rich showing that it was well cultivated tens of
centuries ago before the birth of Christ. It was known first in India but its economic importance as well as
medical uses extended to several countries. The ancient books illustrated the displacements of caravans of
merchants known as route of Silks and Spices. Actually, the countries of India, Brazil, and Indonesia are the
greatest commercial exporters. The major compound of black pepper is piperine that imparts pungency and
biting taste to it. Hundreds of millions of results on black pepper on Google reflects the importance of this
naturally occurring alkaloid. The numerous health effects and beneficial therapeutic properties have been
largely demonstrated. The chemical composition of BP is so various to find heterocyclic components, and
mineral ions as potassium, calcium, magnesium, iron … Advanced extraction and quick characterization yield
these numerous alkaloids based on piperine. Also, the development of new formulations improves its in vivo
bioavailability and explains the multiple uses of this “King” of spices in the medicinal applications. Black
pepper and its isolated compounds served also as efficient corrosion of mild steel in acidic media

Keywords: Black Pepper, Piperine, Alkaloid; Medical uses.


*Corresponding author. E-mail address: [email protected]

ISSN : 2458-6544 © 2019 mocedes.org. All rights reserved.


B. Hammouti et al. / Arab. J. Chem. Environ. Res. 06 (2019) 12-56 13

Content

1. Introduction 13
2. History 14
3. The World's Top Black Pepper Producing Countries 14
4. Chemical Composition of Black Pepper 18
4.1. Major compounds 20
4.2. Essential oil of Black Pepper 26
4.3. Aroma Substances 27
4.4 Substances with Pungent Taste 28
5. Medical uses of Black Pepper 29
5.1. Antioxidant active chemicals, 30
5.2. Cholesterol Lowering and Immune Enhancer, 31
5.3. Anticancer 32
6. Biotechnology of Pepper 33
6.1. Black pepper production and protection 33
6.2. Black pepper processing 33
6.3. Quality control of black pepper 34
7. Pepper : diseases and Managements 35
8. Other applications 36
8.1. Anticorrosion 36
8.2. Organotin (IV) derivative of Piperic acid 37
9. Conclusion 38
10. References 38

1. Introduction
Piper nigrum, is called as black pepper and known as the “King” of spices, is a member of the family
piperaceae. The fruit of Piper nigrum, also called as pepper is an ancient and famous spice throughout
the world. Piper nigrum is a native of Malabar seashore of India and has its utility as a redolent
stimulant in cholera, flatulence, arthritis disease, gastrointestinal disorders in livestock, dyspepsia and
anti-periodic in malarial fever. Piper nigrum is the familiar species of genus piper because of its high
economic, commercial and medicinal values. The genus piper is having a rich phytochemistry and
researchers showed the ample presence of alkaloids, amides and terpenoids [1-10]. The various
pharmacological activities of Piper nigrum are radical scavenging, antioxidant, anti-insecticidal,
allelopathy, anticonvulsant, anti-inflammatory, anti-tubercular, antibacterial, antipyretic,
exterofective and antioxidant. This large climbing liana (up to 20 m in length) of evergreen forests in
southwest India, black pepper (Piper nigrum), a perennial crop of the tropics belongs to Piperaceae
family [3-7] as grouped below :

Kingdom Division Class Order Family Genus Species


Plantae Manoliophyta Magnoliopsida Piperales Piperaceae Piper nigram

Literature reported the genus Piper contains more than 1000 species [8-12]. P. nigrum has different
common names according to its location and languages. Its common name in English is pepper, in

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Urdu (kali mirch), in Indonesian (Lada Hitam), in Vietnamese (Tiêu đen), in Greek (pipe´ri), in
Chinese (hujiao), in French (poivre commun), filfil (‫ )فلفل أسود‬in Arabic, pfeffer in German and
pimienta in Spanish. Figure 1 shows the Evolution of BP from tree to be collected and dried. We
cannot imagine houses and restaurants without black pepper; consequently, high demand for nutrients
and medical uses was imposed during centuries. As a conclusive remark, P. nigrum should not only
be regarded as “King of spices” but can also be considered as part of the kingdom of medicinal agents,
comprising a panoply of bioactive compounds with potential nutraceutical and pharmaceutical
applications.

Figure 1: Black Pepper : from tree to collect


2. History
Researchers pointed out that black pepper marked the history of humankind that the mummy of
Ramesses II of ancient Egypt, dating back at least as early as 13th century BCE, contained black
pepper [13-17]. Moreover, Ahmad in his book, advanced that nearly 3000 years before the birth of
Christ, both Babylonians and Assyrians were trading in spices, primarily black pepper, with the
people of the Malabar coast in the state of Kerala on the Indian subcontinent [18].
P. nigrum, native to India, requires high temperatures with heavy and frequent rainfalls and well-
draining soil for optimum growth [14, 19-21]. These plants cannot tolerate frost. These conditions
are usually met in the countries of India, Brazil, and Indonesia, so these are the greatest commercial
exporters of peppercorns [21, 22].

3. The World's Top Black Pepper Producing Countries


There is hardly any city or village in India devoid of a market for the sale of spices, which are
considered one of the most prevalent foodstuffs in the country, and it is even said that the name spice
in Arabic Bharat (‫ )بهارات‬is derived from the ancient name of India Bharat. Also, the prices and

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amount of spices were considered in the past, an indication of the growth or decline of the economy
in the country. Near silks and spices demand by various populations in continents, West and east Asia
was connected to middle east, Africa and Europe via the known silk and spices Road [23]. Several
ways were cited in literature as China to Rome road along with horses in exchange for wool, gold,
and silver coming in from the Europe via the Mediterranean Sea [24] or via Tombouctou (or
Timbuktu) as well as the South Africa [25, 26]. This route, illustrated in Figure 2, was mainly
maritime or camel route used by many countries to trade spices [26, 27]. The availability of spices
like cinnamon, cassia, cardamom, ginger, pepper, nutmeg, cloves was rare in the west. These
commodities were highly sought after. Before the 15th century, the whole market of spices was
controlled by the Arabs and the North African men which made them extremely costly. With the
advent of the Age of Exploration sailing, long distances became possible and Europeans used this
opportunity to forge economic relations with the east. This made the middlemen useless and the
availability of spices easy and cheap [28]. The main mode of transportation used was the camel.
Camel was domesticated (Figure 3) around 1000 BCE [29]. This allowed the Arabs to export
frankincense and myrrh. These became the most valued commodity for the Romans, the Greeks, and
the Egyptians. The trade flourished and at its height, the route saw 3000 tons of incense trading. The
root cause of the decline of the route was the discovery of shorter and cheaper sea routes that made
trading more efficient.

Figure 2: Silks and Spices Route [28]

The analyses of Frankopan [31] and Hansen [32] show that the history of the 7000-km long trade route,
known as the Silk Road dated around 1500-year-old trade corridor. Currently, its leading producer is
Vietnam, which produces 34% of the world-wide production of 470,000 metric ton [30,33]. Vietnam
is the world leader in the production of black pepper, producing 163,000 tons which are about 34%

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of the world’s production. The plant is a traditional cash crop in the country, and 95% of the black
pepper produced is for export primarily to the US, India, the Netherlands, and Germany. Indonesia is
the second largest producer at 89,000 tons while India produces 53,000 tons. Top black pepper-
producing regions in India are Kerala, Karnataka, Konkan and Tamil Nadu. Other countries on the
list are Brazil (42,000 tons) and China (31,000) [34]. Distribution of BP production is presented in
Figure 4.

Figure 3: Relief with camel, Persepolis, Iran. Image courtesy Wikimedia Commons [28, 30]

Figure 4: The World's Top Black Pepper Producing Countries by Benjamin Elisha Sawe on June 7
2019 in Economics [35]

The "King" of spices, black pepper (Piper nigrum L.) and the "Queen" of spices, cardamom (Elettaria
cardamomum M.), both perennial crops of the tropics, are the most important and most widely sought-
after spice crops of the world (Figure 5). Black pepper was once one of the most traded spices

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worldwide, often referred to as “black gold” because it was used as currency throughout the
commercial routes between Europe and India [36].
We have shown that the production of different spices during time created spontaneously an economic
business between productive and imported countries. The Global Market increased significantly, as
we observe with Coffee, rice, exotic fruits etc… (Figure 6). Whether organic agriculture combined
with fair trade marketing systems can mutually strengthen and benefit smallholder farmers in
emerging economies have significant income gains they were able to add to their wealth [36-40].

Black pepper (Piper nigrum L.) Cardamom (Elettaria cardamomum M.)


Figure 5: The King and Queen of Spices

Figure 6: Global Market of agriculture [33].

CATR (Center of Advance Trade Research) [36], reported that India, stays the home of spices since a
long trading history with ancient and medieval civilizations of the world. Ancient trade routes connected
India with Europe, Middle East and the rest of the world exists as a testimony to world’s preference for

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Indian spices since ancient times. Indian spices are known for its exquisite aroma and medicinal
properties. Moreover, India has the world’s largest domestic market for spices. Presently, India is the
world’s largest producer, consumer and exporter of spices. It produces about 75 of the 109 varieties of
spices listed by the International Organization for Standardization (ISO) and accounts for half of the
global trading in spices. Top spices produced in India include pepper, cardamom, chilli, ginger, turmeric,
coriander, cumin and others. Kerala is the topmost spice producing state in India and is also the largest
producer of Pepper and Cardamom. The top importers of Indian spices in 2017 were: Vietnam, USA,
Malaysia, Thailand, Sri Lanka, UAE and UK. India has remained the topmost world exporter of spices
throughout, followed by Vietnam and China. The top imported spices in the world in 2017 were Whole
Pepper (USD 2.2 billion) and Capsicum (USD 1 billion). India was the fifth largest exporter of Whole
Pepper in 2017 [36].

4. Chemical composition of Black Pepper


Since black pepper has been used in both cooking and traditional medicine to cure constipation,
toothaches, oral abscesses, and sunburn, among others [40], it is evident that it receives more attention
to researchers and herbal users. Studies show that these properties of BP are mainly due to this
pungent alkaloid called piperine and its structural analogues [41-63]. Piperine (Figure 7) isolated
firstly from the extract of pepper by Hans Christian Ørsted in 1819 [64]. It was extracted as a yellow
crystalline compound with a melting point of 128 to 130 °C. The study of degradation of piperine,
flavour of BP was widely studied for various applications in medical uses [65-78].

Figure 7: Piperine issued from black pepper

Near piperine, the volatile (essential) oil for odor and flavor as well as for massage [79] contribute to
its value. Black pepper contains also (11–14%) protein, (47–53%) fiber, and (10–13.5%) starch [80].

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The content of piperine, volatile oil, starch, and fiber can vary markedly in different pepper varieties
and is indicative of the quality of black pepper [81]. Black pepper contains about 5–9% of the
alkaloids piperine and piperettine and about 1.2– 5% of volatile oil [82]. Essential oil is a small
portion of a plant material, which consists mainly of terpenes, sequiterpenes, and their derivatives
that are responsible for the characteristic aroma, and imparts the identifying flavor and odor most
closely associated with the plant itself [83]. Phytochemical studies as well as progresses in extraction
methods and techniques have shown that plants in genus Piper contain a variety of chemical
constituents, such as piperolides, propenylphenols, amides, neolignans, lignans, flavonoids, terpenes,
and steroids [84,85], that demonstrate cytotoxic, anti-inflammatory, antimycobacterial, insecticidal,
antiprotozoal, analgesic, anxiolytic, and antidepressant activities11. Black pepper (Piper nigrum L.),
which is well known regarded as the king of spices, is also widely used in the traditional medicine in
many countries. Piperine is the main chemical constituent of this plant, which has diverse activities,
such as central nervous system depression, cytotoxic, anti-inflammatory, and hepatoprotective
effects, as well as the ability to enhance bioavailability.
Nakatani et al., in 1986, identified five phenolic amides from Piper nigrum, seven compounds from
P. retrofractum, and two compounds from P. baccatum. All the phenolic amides possess significant
antioxidant activities that are more effective than the naturally occurring antioxidant, alpha-
tocopherol. One amide, feruperine, has antioxidant activity as high as the synthetic antioxidants,
butylated hydroxyanisole (BHA) and butylated hydroxytoluene (BHT) [86].
Black pepper contains 47%-53% fiber, 11%-14% protein, and 10%-13.5% starch [87,88]. It is also a
source of potassium, calcium, manganese, iron, and minute amounts of vitamins K and C. Essential
oil is present in a small portion of pepper plant material, which consists of terpenes, sesquiterpenes,
and their derivatives, which are the reason for the aroma and flavor of pepper plant [87,88]. Essential
oils of black pepper are extracted from seeds and leaves. More than 250 volatiles have been reported
to be present in this valuable spice. The main compounds detected are germacrene D, limonene, b-
pinene, a-phellandrene, b-caryophyllene, a-pinene, and cis-b-ocimene.
Ravindran and Peter, [89,90], demonstrated that piperine exists as 4 isomeric structures: piperine
(trans-trans isomer), isopiperine (cis-trans isomer), chavicine (cis-cis isomer), and isochavicine
(trans-cis isomer); however, the 3 geometric isomers of piperine have almost no pungency [68]. Later
investigations have demonstrated the presence of other alkaloids, including piperanine, piperettine,
piperylin A, piperolein B, and pipericine, all possessing some degree of pungency in the pepper
extract. Nevertheless, the overall contribution of these alkaloids to pungency of pepper was found to
be small.

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4.1. Major compounds


The major components of black pepper “piperine” and nearest ones are classified as bioactive
molecules as shown later [91]. Structures of compounds 1−55 isolated from Piper nigrum found in
the literature (Table 1):

Table 1: Structures of compounds 1−55 isolated from Piper nigrum.


Structure Name Ref

Achilleamide (1) [92]

2,4-(E,E)-dodecadienyl [93]
piperidide (2)

Pipernigramide A (3) [94]

1-cinnamoylpiperidine (4) [95]

N-trans-feruloyl piperidine (5) [96]

Coumaperine (6) [97]

Piperanine (7) [98]

Piperoleine A (8) [99]

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Piperoleine B (9) [100]

Pipernigramide B (10) [94]

Piperine (11) [100]

Pipernonaline (12) [101]

piperchabamide B (13) [102]

Piperchabamide C (14) [99]

Piperettine (15) [100]

Dehydropipernonaline (16) [101]

(2E,4E,12E)-13-(3,4-
methylenedioxyphenyl)-1-(1-
piperidinyl)-2,4,12-tridecatrien- [103]
1-one (17)

[99]
Tricholeine (18)

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Piperyline (19) [100]

Brachyamide B (20) [102]

1-[(2E,10E)-11-(3,4- [13]
methylenedioxyphenyl)-2,10-
undecenoyl]pyrrolidine (21)

Piperettyline (22) [99]

6,7-dehydrobrachyamide B [99]
(23)

1-[(2E,4E,10E)-11-(3,4-
methylenedioxyphenyl)-2,4,10- [105]
undecatrienoyl] pyrrolidine
(24)

Brachyamide A (25) [100]

Pellitorine (26) [101]

Kalecide (27) [99]

N-isobutyl-(2E,4E)- [102]
hexadecadienamide (28)

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N-isobutyl-(2E,4E)- [102]
octadecadienamide (29)

N-isobutyl-(2E,4E,12Z)- [100]
octadeca-2,4,12-trienamide
(30)

N-isobutyl-(2E,4E,14Z)-eicosa-
2,4,14-trienamide (31) [100]

Piperlonguminine (32) [100]

Piperchabamide D (33) [101]

Retrofractamide A (34) [100]

Retrofractamide B (35) [102]

Guineensine (36) [10]

Brachystamide B (37) [99]

Pipernigramide C (38) [94]

Ferulyltyramine (39) [99]

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N-trans-feruloyldopamine (40)
[106]

Pipernigramide D (41) [94]

Pipernigramide E (42) [94]

Pipernigramide F (43) [94]

Pipernigramide G (44) [94]

(2E,4E)-5-(3,4-
methylenedioxyphenyl)-2,4- [107]
Pentadienal (45)

Piperic acid (46) [108]

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Methyl piperate (47) [108]

Pipernigrester A (48) [94]

(+)-Bornyl piperate (49) [109]

(6E)-7-(3,4-
Methylenedioxyphenyl)- [104]
heptenoic acid (50)

(8E)-9-(3,4-
Methylenedioxyphenyl)- [104]
nonenoic acid (51)

Cubebinol (52) [110]

(-)-Dehydrodiconiferyl alcohol [111]


(53)

(-)-Secoisolariciresinol (54) [112]

2R,3R)-2-[(3,4-
Dimethoxyphenyl)methyl]-3-
[(3,4,5- [113]
trimethoxyphenyl)methyl]-1,4-
butanediol (55)

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4.2. Essential oil of Black Pepper


Although some studies have been carried out to determine the ingredients of black pepper Essential
Oil (EO) cultivated in various regions of the world, but there is little data about some physicochemical
characteristics of EO of black pepper cultivated in Chittagong, Bangladesh. The major components
of black pepper EO were caryophyllene (19.12%), limonene (9.74%), and camphene (8.44%) (Table
2). The contents of moisture, dry matter, protein, fatty oil, ash, carbohydrate, and crude fiber in black
pepper samples were determined as 2.20, 96.12, 12.66, 14.41, 12.49, 42.56, and 5.55%, respectively
[114].
Table 2: some components of essential oil of BP [114]

Caryophyllene (sesquiterpene, (R) and (S) Limonene Camphene (monoterpene,


bicyclic) (19.12%) (Monoterpene) (9.74%) bicyclic) (8.44%)

The chemical composition of essential oils obtained by three techniques: classical hydrodistillation
(CHD) and by microwave hydrodistillation on low and high microwave power was given in Table 3.
Results showed that in the CHD extraction oil, β-caryophyllene as sesquiterpene hydrocarbon was
the major compound present with 49.80%. MWHP extraction oil realized at a high microwave power
(700W) was also rich in β-caryophyllene with relatively the same amount 52.67%.
Table 3: some components of essential oil of BP [115]

Relative amount (%)


Microwave extraction (%) Classical
MWLP MWHP extraction (CHD)
Compounds RT(a) 280w 700w
Sabinene 9.11 - 3.01
-Copaene 22.92 5.95 8.86 5.76
Germancene-D 23.39 1.13 1.83 1.68
Caryophyllene 24.32 8.25 52.67 49.80
-Humulene 25.30 0.72 4.00 3.86
Cubenol 27.20 3.85 5.10 5.20
Caryophyllene oxide 29.08 63.13 4.79 2.46
(a) Retention time in GC analysis
(b) Microwave power used in microwave hydrodistllation of essential oils

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However, at low power 280W, the oxygenated compound caryophyllene oxide was selectively
extracted with a high amount 63.13% because of his strongly microwave absorption [16]. In the case,
β-caryophyllene as non-polar compound presented a lower percentage 8.25% [115]. In comparison
of the essential oil of Piper majusculum from Piperaceae family was obtained by hydrodistillation
technique, twelve components accounting were identified for 93.79% of the total oil. The major
components were β-caryophyllene (17.27%), caryophyllene oxide (14.26%), α-selinene (14.21%)
and cis-calamenene (9.62%) [116].

4.3. Aroma Substances


In some spice plants, the odour corresponds with that of the main components of the volatile fraction.
Aroma compounds produced by plants, mainly attract pollinators as bees, seed dispersers and provide
defence against pests or pathogens. However, in humans, about 300 active olfactory receptor genes
are involved to detect thousands of different aroma compounds and modulates expression of different
metabolic genes regulating human psychophysiological activity, brain function, pharmacological
signalling, and therapeutic potential [117]. Belitz et al. [118] in their book “Food Chemistry”
summarized the important odorants of black pepper usually in lower concentrations. The aroma of
ground pepper is not stable due to losses of important aroma substances with time. The most known
aroma are (−)-Sabinene, (+)-Sabinene, (−)-α-Pinene, (−)-β-Pinene, (S)-Limonene, (+)-β-Pinene, (R)-
Limonene, Myrcene … (Table 4).

Table 4: Major aroma components of essential oil of BP [118]

Sabinene Pinene

Limonene Myrcene

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4.4. Substances with Pungent Taste


The hot burning pungent taste of black pepper is caused by the non-volatile compounds: piperine as
the most important pungent substance, piperanine and Piperylin as shown above in Table 1. Pepper
is sensitive to light since the trans,trans-diene system of piperine isomerizes to the cis,trans-diene
system of the almost tasteless isochavicin on exposure to light [119]. As shown in Table 5.

Table 5: piperine molecule at four isomeres

piperine = E,E-(trans-trans)-piperine isopiperine = Z,E-(cis-trans)-piperine

Chavicine = Z,Z-(cis-cis)-piperine Isochavicine = E,Z-(tans-cis)-piperine

Srinvisan [41] concluded that piperine has been experimentally demonstrated by a number of
independent investigators to possess diverse physiological effects. It has been evidenced to protect
against oxidative damage by inhibiting or quenching free radicals and lower lipid peroxidation and
beneficially influence cellular thiols, antioxidant molecules and antioxidant enzymes in different
situations of oxidative stress. The most far-reaching attribute of piperine has been its inhibitory
influence on hepatic, pulmonary, and intestinal drug metabolizing system. It strongly inhibits a
particular cytochrome. Both black pepper and piperine have been evidenced to have a definite effect
on intestinal motility, the antidiarrhoral property, and on the ultrastructure of intestinal microvilli
improving the absorbability of nutrients. Among other physiological effects piperine exerts, its
potential antifertililty influence on the reproductive system has been clearly established in in vitro
and animal systems.

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5. Medical uses of Black Pepper


Its distinctive pungent flavor due to the presence of an alkaloid piperine, make black pepper the most
utilised both in cooking and medicinal treatments. Databases are very rich offer infinite documents
on the use of piperine in traditional therapies of Chinese as well as in Indian medicine. The chemical
structural of piperine containing three parts : aliphatic chain headed by both amide and aromatic
moieties offers this wide applications (Figure 8).

Figure 8: Synergistic oft he three parts of piperine molecule

Survey of literature show the various biological activities such as anti-infective, antimicrobial,
insecticidal, anti-inflammatory, antiamoebic, antiulcer, and antidepressant of piperine [120-129].
Piperine can be also used widely in pain management, chills, rheumatism arthritis, influenza, and
fever as well as hypotension, vascular cell modulation, and anti-cancer activity. It also acts on many
enzyme systems (including p-glycoproteins) [130-136]. Piperine has been shown to help digestion of
food i.e. stimulation of appetite, the enhancement of blood circulation, salivation, to have antioxidant
activity, and to enhance drug bioavailability [137-139].
Piperine, a pungent alkaloid found in pepper, helps increase the absorption of selenium, B-group
vitamins, and beta-carotene, among other nutrients. It also helps stimulate saliva secretion, which
increases the production of digestive juices, responsible for breaking down proteins, increasing
digestibility and reducing the possibility of heartburn and other gastrointestinal issues. Piperine also
increases the bioavailability of certain compounds. This is especially true when it comes to curcumin,
the active compound of turmeric that helps fight inflammation. In a study published in Planta Medica
(1998), it was found that piperine enhanced the extent of absorption (bioavailability) and serum
concentration of curcumin in both rats and humans with no unfavorable side effects. Piperine also

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interferes with inflammatory signaling mechanisms and inhibits pro-inflammatory cytokines, which
are small proteins secreted by some cells and linked with a number of degenerative diseases.
Moreover, black pepper's antioxidant content helps the body to fight and repair the free radicals'
damage that contribute to cardiovascular diseases, inflammation, and more [140].

5.1. Antioxidant active chemicals


Black pepper contains an important source of natural antioxidant. The main role of antoxidant protect
cells against free radicals, which may play a role in heart disease, cancer and other diseases. Free
radicals are molecules produced when your body breaks down food or when you're exposed to
tobacco smoke or radiation [141]. The importance of antioxidants for maintaining the physiological
functions of liver, kidney, digestive system, and prevention of cardiovascular diseases and cancer has
also been highlighted [142]. They have beneficial influence on lipid metabolism efficacy as anti-
diabetics. They have ability to stimulate digestion and; have antioxidant; Meghwal and Goswami
collected the Antioxidant active chemicals isolated from black pepper : Ascorbic-acid, -carotene,
Camphene, Carvacrol, Eugenol, -terpinene, Lauric-acid, Linalyl-acetate, methyl-eugenol, myrcene,
myristic-acid, myristicin, palmitic-acid, piperine, terpinen-4-ol, ubiquinone [136].
Significant correlation between EPR and thiobarbituric acid methods was assessed by study of
antioxidant activity changes in relation to irradiation doses and also in the case of spice storage,
between EPR and reducing power methods [143]. Peppercorns especially black pepper, which
constitutes an important component in the diet of many sub-Saharan and oriental countries, can
therefore be promoted for their nutritional importance as antioxidants and radical scavengers [144].
The physico-chemical properties and bio-efficacies, antioxidant activities, of the encapsulated black
pepper essential oil in hydroxypropyl-β-cyclodextrin (HPβCD), in comparison with the major
ingredient in the oil, β-caryophyllene was improved by 4 times [145]. The biological control of root-
knot nematode (Meloidogyne incognita) by aqueous leaf extracts of black pepper was
investigated and could be a possible replacement for synthetic nematicides with fewer side effects in
the soil and on crops [146]. Nanoliposomes of piperine-rich extract of black pepper holds promise as
nutraceuticals in designer food applications [147]. Also, Vidangadi churna is a traditional polyherbal
ayurvedic formulation used in conditions like antifertility, antibacterial, antiprotozoal properties,
abdominal disorders, lung diseases and antiinflamatory. It's composed of Embelia ribes (false black
pepper fruit), Hordeum vulgare, Mallotus philippinensis, Terminalia chebula and rock salt. It showed
significant antioxidant activity [148]. Black pepper (Piper nigrum L.) which is a very widely used
spice, known for its pungent constituent piperine. However, in addition to its culinary uses, pepper

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has important medicinal and preservative properties, and, more recently, piperine has been shown to
have fundamental effects on p-glycoprotein and many enzyme systems, leading to biotransformative
effects including chemoprevention, detoxification, and enhancement of the absorption and
bioavailability of herbal and conventional drugs. Based on modern cell, animal, and human studies,
piperine has been found to have immunomodulatory, anti-oxidant, anti-asthmatic, anti-carcinogenic,
anti-inflammatory, anti-ulcer, and antiamoebic properties [149]. Excessive free radical generation
overbalancing the rate of their removal leads to oxidative stress. Oxidative stress has been implicated
in cardiovascular disease, inflammatory diseases, cancer, and other chronic diseases. The
antioxidative effects of turmeric/curcumin, clove/eugenol, red pepper/capsaicin, black
pepper/piperine, ginger/gingerol, garlic, onion, and fenugreek, which have been extensively studied
and evidenced as potential antioxidants [150].

5.2. Cholesterol Lowering and Immune Enhancer


Black pepper and piperine reduce cholesterol uptake and enhance translocation of cholesterol
transporter proteins. It enhances digestion process by helping faster break down of larger fat
molecules into easily digestible simple molecules and prevents the accumulation of fat in body. Black
pepper exhibits immunomodulatory effect on human body [69,77,151,152].
Black and red pepper has been used for centuries as spice or food with healthful applications and
suggest that dietary inclusion of peppers may attenuate some cardiometabolic risk markers associated
to Western-style diet [153]. Piperaceae, a Latin name derived from Greek, which in turn originates
from the Arabic word babary-black pepper, is considered one of the largest families of basal dicots,
found in tropical and subtropical regions of both hemispheres. They are also used in folk medicine
for treatment of many diseases in several countries including Brazil, China, India, Jamaica and
Mexico. Pharmacol. studies of Piper species point toward the vast potential of these plants to treat
various diseases. Many of these species are biol. active and have shown antitumor, antimicrobial,
antioxidant, insecticidal, anti-inflammatory, antinociceptive, enzyme inhibitor, antiparasitic,
antiplatelet, piscicide, allelopathic, antiophidic, anxiolytic, antidepressant, antidiabetic,
hepatoprotective, amebicide and diuretic possibilities [154]. Comprehensive assessment effectiveness
and food products quality forecast was substantiated using organoleptic profiles construction and
usage of differential equations. The pastas with spices based on soft diet cottage cheese produced of
variable recipes quality was selected as an object of the study. In the pastas compounds such spices
as allspice, black pepper, ginger, cinnamon, anise, cloves, cardamom, fenugreek and nutmeg were
used in amt. of 0.27...1.1%. The analytical research results on product quality were obtained from

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organoleptic parameters and content of biological active substances (tannin, catechin, and rutin) with
usage of symbolic computer mathematics and graphic images methods [155]. Diabetes mellitus is a
metabolic disorder and emerging pandemic of the 21st century. Piperine, the chief alkaloid present in
Piper nigrum (black pepper), has a wide array of uses in alternative and complementary therapies.
The effect of piperine on blood glucose level was studied in streptozotocin induced diabetic rats in
subacute study models. The results suggest that piperine (50mg/kg) showed antidiabetic activity in
streptozotocin induced diabetic rats [156]. Black pepper oil and its major components were
investigated for the biological activities related to the prevention of Alzheimer’s Disease via AChE
inhibition and anti-inflammatory activity via COX-2 inhibition [157]. An improved method of sample
preparation was used in a microplate assay to evaluate the bactericidal activity levels of 96 essential
oils including Black pepper oil against Campylobacter jejuni, Escherichia coli, there are possible
significance of these results with regard to food microbiological is discussed [158].

5.3. Anticancer
The cancer is the disease of today or of the century and cancer research is the subject of trillions of
papers and research into new drugs has become an economic issue bringing in trillions of dollars.
Natural products have been used for the treatment of various diseases and are becoming an important
research area for drug discovery [159]. Amaral et al resumed that Since the 1980s, a total of 174 new
compounds with indications for cancer treatment have been approved for commercialization, of
which a total of 93 (53%) were natural products or derived directly or based on them. Due to the
relative ease of access to the plants, most of the discoveries of anticancer compounds were derived
from plants, among these discoveries the drug obtained from the bark of Taxus brevifolia (paclitaxel)
presents one of the most successful stories in plant-based research [160]. Piperine exerts antitumor
activities in a variety of cancers [132,161-164]. Literature pointed on the characteristic pungency and
biting taste of pepper is due high content of piperine in it. Piperine has been exploited for many
therapeutic purposes in the past and is anticipated to remain so in the future. Piperine is an important
dietary phytochemical due to its presence in spicy foods as well as its pharamacological activities
(antiinflammatory, antimetastatic, anti-cancer, larvicidal, leishmanicidal, immunosuppressive,
antimycobacterial, and antiparasitic activities) [132,165-172].
Different studies have shown that the regular consumption of certain vegetables and fruits can reduce
disease risks. Piperine, which give chilli peppers and black pepper and its analogues have a favourable
toxicity profile, but are cytotoxic towards a range of cancer cell lines including blood cancer and lung
cancer [173]. Both PI3K/AKT/mTOR/S6K1 and mitogen activated protein kinase (MAPK) signaling
cascades play an important role in cell proliferation, survival, angiogenesis, and metastasis of tumor

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cells. The black pepper (Piper nigrum L.) is very active against human prostate and breast cancer
cells. these findings suggest that CPO can interfere with multiple signaling cascades involved in
tumorigenesis and used as a potential therapeutic candidate for both the prevention and treatment of
cancer [174].

6. Biotechnology of Black Pepper

6. 1. Black pepper production and protection


Black pepper is one of the worldwide most used spices. It’s is obtained from unripe fruits, called
peppercorns, of the plant species Piper nigrum L, of the Piperaceae family. The productivity of black
pepper (Pipper nigrum) in mainly linked to (1) genetic potential of the plant, (2) biotic and abiotic
stress factors, and (3) level of adoption of good agricultural practices [175]. The lack of control of
these factors can compromise the productivity and/or the quality of the final product. Some standards
to be implemented in crop production (vegetative production, irrigation, nutrients, etc…) and crop
protection from insects and diseases are reported by [175-177]. The major diseases affecting pepper
plantations are caused by nematodes and fungus (Phytophthora capsici) on foot, while leaf spots are
caused by fungus (Colletotrichum gloeosporioides) and bacteria (Xanthomonas campestris pv.
beticola) diseases [175,176]. Biotechnology approaches are considered as promising tools to control
of pathogens via development of plant resistance and biopesticides [176]. Among bacteria, strains of
Pseudomonas fluorescens, Bacillus pumilis, B. macerans and B. circulans demonstrated efficiency in
nematode control when used as biocontrol agent, and strains of Trichoderma sp showed their
protective effect against nematodes and Phytophthora capsici [178]. Among some black pepper
cultivars, one hybrid and two wild germplasms, showed promising result in resistance to
Phytophthora capsici [179].

6. 2. Black pepper processing


The black pepper processing includes the post-harvest operations of the fruits. The main unit
operations, mostly practiced, are reported in Figure 9. Black pepper is obtained from dried immature
berries, harvested when one or more berries turn to orange or red color on a spike [175]. During
maturation of fruits, the piperine and starch contents increase, while the volatile oils and non-volatile
resins decrease [180]. Therefore, the fruits should be harvested at the same and carefully chosen stage
of maturity, to ensure a low crop loss during processing and a uniform final product with high quality.
The spikes were then subject of threshing operation, which consists of harvesting berries from spikes,
mostly done by hand or using mechanical machine. The fruits are then washed in running tap water,

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then blanched in boiling water, for one to five minutes, and then let to sun drying for 2 to 5 days
[181].
Harvesting

Threshing

Washing

Blanching

Drying

Winnowing and Grading

Grinding

Packaging

Storage
Figure 9. Flow diagram of black pepper processing [182].

Blanching allows the oxidation of phenols by phenolase enzymes, leading to the development of a
brown color in fruits [183,184], and permits also the decontamination of fruits by reducing their
microbial load. However, the blanching period should be lower as far as possible to avoid enzyme
denaturation and loss of volatile flavor compounds. The dried fruits are then subject of winnowing to
remove extraneous materials (vegetable seeds, leaves, sand, dust, small stones and light foreign
matter, etc.). The dried and destoned pepper fruits are then graded, then grinded and packed.

6. 3. Quality control of black pepper


During processing, black pepper is subject to various physical, chemical and microbiological defects.
High concentrations of toxic elements [185] and pathogenic microorganisms [186] were detected in
processed peppers. The quality control of the product along the processing chain is mandatory to
avoid risks associated with these defects (FAO/WHO, 1995) [187]. The effectiveness of some
treatments in pathogens and spoilage microorganisms’ decontamination of black pepper was

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demonstrated, such as sterilization and microwave treatments [188] and gaseous acetic acid treatment
[189]. In addition, the standards adopted by FAO/WHO (CXS-326-2017) [190] for black pepper
commercialization, include color, odor and flavor characteristics, as well as physical (size, shape,
extraneous matter, etc.) and chemical (moisture, piperine, volatile oil, non-volatile ether extract, ash,
etc.) properties (FAO/WHO, 2017). The sun drying between polythene sheets for 2-3 hours, followed
by direct sun drying for 3-4 days produced dried berries with good color, higher aroma, better
oleoresin and piperine contents and high market price [190].
The quality of black pepper is related mainly to the piperine, which is the most abundant alkaloid
responsible of pungent taste of black peppers [191]. The content of piperine in black pepper is of 2%
to 9% of the product, depending on the growing conditions [192, 193], and maturity stage of fruits
[166].

7. Pepper : diseases and Managements


Despite its very diverse chemical composition, pepper is attacked by pests and diseases and
consequently influence its production. Biotic agents of disease of pepper include fungi, bacteria,
nematodes, and viruses. Abiotic disorders include a number of unfavorable cultural or climatic
conditions, such as sunlight, nutrient deficiency, and temperature excesses [194-199]. Diseases affect
all parts of the pepper plant including the foliage, stems, roots, fruit, and young seedlings. Fungi and
bacteria cause a variety of symptoms such as leaf and fruit spotting, wilting and plant death. Typical
symptoms of viral infections are stunting, mottling of foliage and fruit, and small, misshapen fruit.
Abiotic disorders such as sunscalding or blossom end rot greatly interfere with the fruit quality and
reduces yield [200-203]. Management of diseases begins prior to planting of the crop and many
techniques are used to minimize losses due to disease problems [204]. Control methods include, but
are not limited to, the use of cultivars with resistance to diseases, pathogen-free seeds, sterilized
equipment for transplant production, rouging and eradication of diseased plants and alternative hosts,
field sites that are pathogen-free and isolated from other solanaceous crops, soil fumigation, and
application of pesticides and other disease-suppression compounds [205]. It was also confirmed that
residues of imidacloprid and abamactine remain in vegetables: tomatoes, cucumbers and peppers,
especially after a few days of spraying of pesticides and the amounts of imidacloprid and abamactine
residues were very high after the first day of spraying. Until the fifth day of spraying, the amounts of
residues of the two pesticides remained high (due to high concentrations used by farmers) and this
may pose a serious risk to human health via food consumption. However, photodegradation caused a
decrease of the pesticide residues in the plant parts [206].

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8. Other applications
8.1. Anticorrosion
Their wide uses in different medical fields incited researchers to test extract, oil and isolated
compounds of black pepper as Corrosion inhibitor of metallic materials in aggressive media [114,
207-215]. The molecular structures of various components of black pepper having aromatic rings,
double bonds as well as heteroatoms facilitating their reactivity at the metal surface by adsorption to
form coordination with metallic atoms. Black pepper created a barrier film at the metal surface leading
to its protection against corrosion process. Effect of black pepper (BP) extract and its piperine,
piperanine and piperic acid isolated from BP on corrosion of C38 steel in 1 M HCl solution was
investigated by weight loss method. Piperine and piperanine were isolated by ethanol in yield 6 from
ground BP [215]. Results obtained from weight loss measurements indicate that the natural
compounds tested exhibit higher efficiency exceeding 95% at 2g/L. The presence of piperine
decreases hugely the corrosion rate and its inhibition efficiency (E%) increases with concentration to
attain 99 % at 10-3M. Piperine adsorbs on the steel surface according Langmuir isotherm. Adsorption
enthalpy were determined and discussed. Effect of temperature was also investigated and activation
parameters were evaluated (Table 6) [212-214]. The lower values of free enthalpy, Gads
ο
< -40
kJ/mol, indicated that piperine and piperanine acted via chemisorption on the iron surface. Also, the
activation energy (Ea) revealed that corrosion process is blocked in the presence of piperine and
piperanine accompanied by an increase of Ea.

Table 6. Corrosion data of steel in 1M HCl without and with 2g/L BP extract or 10-3 mol L-1 of piperine, in
the temperature range 40–70 °C at 1 h [211].

Temperature °(C) Wcorr(mg.cm2.h-1) Ew (%)


40 2.604 -
1M HCl 50 4.834 -
60 9.781 -
70 13.235 -
40 0.143 94.5
Black Pepper 50 0.277 94.2
extract 60 0.536 93.1
70 3.257 75.3
40 0.150 94.2
Piperine 50 0.280 94.1
60 0.480 93.7
70 3.890 70.6

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8.2. Organotin (IV) derivative of Piperic acid


Two organotin (IV) derivatives have been prepared from piperic acid, the former is obtained by
hydrolysis of piperine, which is extracted from black pepper. The two complexes {[n-Bu2SnO2C-
(CH=CH)2-C7H5O2]2O}2 1, and [Ph3SnO2C-(CH=CH)2-C7H5O2]n 2, have been characterized by IR,
1H and 13 C NMR spectroscopic techniques. Single crystal diffraction studies were made to
determine the structures of the two compounds 1 and 2. Compound 1 crystallizes in the triclinic
system (P\-1) and Compound 2 crystallizes in the monoclinic system (P21/c) (Figure 10) [213].

Figure 10: organotin (IV) carboxylates of natural origin pepiric acid (black pepper) [213].

The title compounds were evaluated for their biological activities against a range of cancer cell
lines (BT-474, MDA-MB-231, AU565), Chronic myeloid leukemia cell line (K562), Lung cancer
cell line (H460) and normal cell line 3T3 mouse fibroblast (Table 7).

Table 7: IC50 Value of compounds 1 and 2 against BT-474, H-460, K562, MDA-MB-231 et AU565 [215].

Cytotoxicity and anti-cancer assay : IC50 [µM], NA : Not Active


Comp BT-474 H-460 K562 MDA- AU565 Cytotoxicity assay
MB231 against 3T3 cell line

(1) 6.50 ± 0.80 0.10 ± 0.03 2.60 ± 0.15 6.50 ± 0.80 3.73 ± 0.65 10,70 ± 0,05

(2) 0.17 ± 0.05 NA 0.14 ± 0.00 0.17 ± 0.05 0.12 ± 0.01 10,10 ±0,005
Standard Doxorubicine Doxorubicine Imatinib Doxorubicine Doxorubicine Cycloexamide
Drug 2.10 ± 0.01 0.20 ± 0.03 1.72 ± 0.29 0.57 ± 0.07 0.08 ± 0.003 0,8 ± 0,10

Especially complexes 1 and 2 (derivatives of the piperic acid), i.e. Pipericcarboxylate triphenyltin
[Ph3SnO2C-(CH=CH)2-C7H5O2]n and {[n-Bu2SnO2C-(CH=CH)2-C7H5O2]2O}2 were most active
against all cancer cell lines. These compounds were also active against 3T3 normal cell line, but the
IC50 values were high as compared to cancer cell lines [215].

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10. Conclusions
In this review, We show among the millions of servey research studies that black pepper possesses
a potential in both traditionnal and modern medicine as well as in food. The black pepper is
miraculously really the King of species due to very rich source of a wide variety of chemical
constituents, most of which are biologically active. The long practice of using pepper in different
traditional systems of medicine made its scope from the kitchen, to drugs, to cosmetics, merited at
early time to impose attention in agriculture and economy. Modern experimental research discovered
numerous components : aromatics, aroms, pungents … volatile constituents, monoterpenes,
sesquiterpenes, and specially piperin on the different biological activities reveals the significance of
its use in traditional systems of medicine. The pepper’s use in treating cancer, obesity, hypertension,
diabetes, diarrhea, and its bioavailability signifies its attraction in the future. Biotechnology approach
is one of the most promising technologies to be used to improve black pepper production and
protection. Selected varieties and good agricultural practices should be implemented to improve the
productivity of black pepper. The most common pathogens of black pepper are fungus (Phytophthora
capsici, Colletotrichum gloeosporioides), bacteria (Xanthomonas campestris pv. eticola) and
nematodes. Selected strains of bacteria (Pseudomonas sp., Bacillus sp.) and fungus (Trichoderma sp)
demonstrated their effectiveness as biopesticides in this field. During black pepper processing, good
manufacturing practices (GMP) should be implemented, according to international standards of
FAO/WHO, to control physical, chemical (toxic elements) and microbiological (pathogens) hazards,
and to assure high nutritional value of end product.

11. References

[1] V. S. Parmar, S. C. Jain, K. S. Bisht, R. Jain, P. Taneja, A. Jha, O. D. Tyagi, A. K. Prasad, J.


Wengel, C.E. Olsen, P. M. Boll, Phytochemistry of the genus Piper, Phytochemistry, 46, 4: 597-
673 (1997).
[2] S. A. Norton, Useful plants of dermatology. V. Capsicum and capsaicin, Journal of the American
Academy of Dermatology, 39: 626-628 (1998).
[3] V. Badmaev, M. Majeed, E. P. Norkus, Piperine, an alkaloid derived from black pepper increases
serum response of beta-carotene during 14-days of oral beta-carotene supplementation. Nutrition
Research. 19: 381-388 (1999).
[4] S. Jensen, J. Hansen, P. M. Boll, Lignans and neolignans from piperaceae. Phytochemistry. 33
(318): 523-530 (1993).

AJCER
B. Hammouti et al. / Arab. J. Chem. Environ. Res. 06 (2019) 12-56 39

[5] G. M. Strunz, Unsaturated Amides from Piper Species (Piperaceae). Studies in Natural Products
Chemistry. 24(Part E): 683-738 (2000).
[6] L. Jirovetz, G. Buchbauer, M. B. Ngassoum, M. Geissler, Aroma compound analysis of Piper
nigrum and Piper guineense essential oils from Cameroon using solid-phase microextraction–gas
chromatography, solid-phase microextraction–gas chromatography–mass spectrometry and
olfactometry. Journal of Chromatography A. 976: 265-275 (2002).
[7] D. G. Barceloux, Pepper and Capsaicin (Capsicum and Piper Species) Disease-a-Month. 55: 380-
390 (2009).
[8] G.A. Agbor, J.A. Vinson, J. Sortino, R. Johnson, Antioxidant and anti-atherogenic activities of
three Piper species on atherogenic diet fed hamsters. Experimental & Toxicologic Pathology. 64:
387-391 (2012).
[9] B. Prakash, P. Singh, P. K. Mishra, N. K. Dubey, Safety assessment of Zanthoxylum alatum Roxb.
essential oil, its antifungal, antiaflatoxin, antioxidant activity and efficacy as antimicrobial in
preservation of Piper nigrum L. fruits. International Journal of Food Microbiology. 153: 183-
191 (2012).
[10] N. Ahmad, H. Fazal, B. H. Abbasi, S. Farooq, M. Ali, M. A. Khan, Biological role of Piper
nigrum L. (Black pepper): A review. Asian Pacific Journal of Tropical Biomedicine. 2: S1945-
S1953 (2012).
[11] I.M. Scott, N. Gagnon, L. Lesage, B.J. Philogene, J.T. Arnason, Efficacy of botanical insecticides
from Piper species (Piperaceae) extracts for control of European chafer (Coleoptera:
Scarabaeidae). J. Econ. Entomol. 98: 845-855 (2005).
[12] Heerasing Takooree, Muhammad Z. Aumeeruddy, Kannan R.R. Rengasamy, Katharigatta N.
Venugopala, Rajesh Jeewon, Gokhan Zengin, Mohamad F. Mahomoodally, A systematic review
on black pepper (Piper nigrum L.): from folk uses to pharmacological applications, Journal
Critical Reviews in Food Science and Nutrition,- Issue sup1: 3rd International Symposium on
Phytochemicals in Medicine and Food (3-ISPMF, August 25-29 2018, Kunming, China); Guest
editors: Jianbo Xiao and Weibin Bai, 59: S210-S243 (2019)
[13] S. Fitzgerald, Ramses II, Egyptian Pharaoh, Warrior, and Builder, Compass Point Books,
Minneapolis, MN, pp. 88–90 (2008).
[14] Prabhakaran Nair, Agronomy and Economy of Black Pepper and Cardamom, The “King” and
“Queen” of Spices K.P. Ed. Elsevier ISBN: 978-0-12-391865-9, (2011)
[15] S. Fitzgerald, Ramses II, Egyptian Pharaoh, Warrior, and Builder, Compass Point Books,
Minneapolis, MN, pp. 88–90 (2008).

AJCER
B. Hammouti et al. / Arab. J. Chem. Environ. Res. 06 (2019) 12-56 40

[16] D. Eichholz, Jones WHS, and H. Rackham (1949-1954), Pliny the Elder, Natural History XII,
Harvard University Press, Cambridge, MA, pp. 310–313 (1979).
[17] Nedspice, Pepper Crop Report 2015, (2015) http://www.nedspice.com, Accessed date: 16
August 2017.
[18] Text book for Environmental science and Ecology, Dr. Shaikh Ahmad, Sk. Ismail, Sankalp
Publication, ISBN: 978-93-88660-00-6 (2019) pp504,
[19] K. N. Babu, M. Divakaran, P. N. Ravindran, K. V. Peter, 25: Long pepper Handbook of Herbs
and Spices Pages. 420-437 (2006).
[20] K. P. Prabhakaran Nair, The Agronomy and Economy of Black Pepper (Piper nigrum L.)-The
“King of Spices”. Advances in Agronomy. 82: 271-389 (2004)
[21] RAC Georges, Vegetable Seed Production, ISBN 10: 0851993362 ISBN 13: 9780851993362
Publisher: CABI Publishing, 1999.
[22] Analysis of cinnamon, pepper and cardamom value chains in Sri Lanka March 2017, Institute of
Policy Studies of Sri Lanka, Designed by Haritha Dahanayak, Printed by OLEECO Solutions
(Pvt) Ltd. (2017).
[23] E. M. Loewe, Spices and Silk: Aspects of World Trade in the First Seven Centuries of the
Christian, The Journal of the Royal Asiatic Society of Great Britain and Ireland No. 2: 166-179
(1971).
[24] Jeong Su-Il, The silk road encyclopedia, Ed. Irvine, CA : Seoul Selection, ISBN: 1624120768
9781624120763 (2016).
[25] C. Defremery and D.R. Sanguitti, Voyages d’Ibn Battuta, Collection d’Ouvrages Orientaux
publiée par la Société Asiatique, T.4, Paris (1879).
[26] J F. Ade Ajayi, Histoire de l’Afrique, VI. L’Afrique au XIX siecle jusque vers les années 1880.
Udicef. ISBN (UNESCO): 92-3-202498-5 (1997)
[27] B. Fowlkes-Childs, M. Seymour, The World between Empires: Art and Identity in the Ancient
Middle East, N.Y.: The Metropolitan Museum of Art, New Haven, ISBN: 9781588396839
(2019)
[28] https://www.khanacademy.org/humanities/world-history/ancient-medieval/silk-road/a/the-silk-
road
[29] I. Usa, Yemen Country Study Guide Volume 1 Strategic Information and Developments,
Publisher: Int'l Business Publications, USA Language: English ASIN: B00928ODN6
(September 1, 2012).
[30] http://blog.goodsonmove.com/2017/03/top-5-ancient-trade-routes.html

AJCER
B. Hammouti et al. / Arab. J. Chem. Environ. Res. 06 (2019) 12-56 41

[31] P. Frankopan, P., 2015. The silk roads: a new history of the world. Bloomsbury Publishing Plc,
London, UK (2015).
[32] V. Hansen, The Silk Road: A New History. Oxford University Press, Oxford, UK (2012).
Levinson, M., 2006. The Box: How the Shipping Container Made the World Smaller and the
World Economy Bigger. Princeton University Press, Princeton, NJ., ISBN-10: 0190218428
(2010)
[33] Julia Lernoud, Jason Potts, Gregory Sampson, Bernhard Schlatter, Gabriel Huppe, Vivek Voora,
Helga Willer, Joseph Wozniak, and Duc Dang, The State of Sustainable Markets – Statistics and
Emerging Trends 2018. ITC, ISBN: 978-92-9137-408-3, Geneva (2018).
[34] Nedspice, Pepper Crop Report 2015, (2015) http://www.nedspice.com, Accessed date: 16
August 2017.
[35] The World's Top Black Pepper Producing Countries By Benjamin Elisha Sawe on June 7 2019
in Economics
[36] Product Profile: Spices By CATR, (Centre for Advance Trade Research) | January 17, 2019
[37] Priyanka Parvathi, Hermann Waibel, Organic Agriculture and Fair Trade: A Happy Marriage?
A Case Study of Certified Smallholder Black Pepper Farmers in India. World Development. 77:
206-220 (2016).
[38] M. Hema, R. Kumar, N.P. Singh, Volatile price and declining profitability of black pepper in
India. Disquieting future Agricultural Economics Research Review. 20,1: 61-76 (2007).
[39] D. Pimentel, P. Hepperly, J. Hanson, D. Douds, R. Seidel, Environmental, energetic, and
economic comparisons of organic and conventional farming systems. BioScience. 55,7: 573-582
(2005).
[40] B.L. Barham, J.G. Weber The economic sustainability of certified coffee: Recent evidence from
Mexico and Peru. World Development. 40, 6: 1269-1279 (2012).
[41] K. Srinivasan, Black pepper and its pungent principle-piperine: a review of diverse physiological
effects. Crit. Rev. Food Sci. 47: 735–748 (2007).
[42] F.M. Rauscher, R.A. Sanders, J.B. Watkins, Effects of piperine on antioxidant pathways in
tissues from normal and streptozotocin-induced diabetic rats. J. Biochem. Mol. Toxic. 14: 329–
334 (2000).
[43] J.D. Lambert, J. Hong, D.H. Kim, V.M. Mishin, C.S. Yang, Piperine enhances the bioavailability
of the tea polyphenol (−)-epigallocatechin-3-gallate in mice. J. Nutr. 134: 1948–1952 (2004).
[44] C.D. Doucette, A.L. Hilchie, R. Liwski, D.W. Hoskin, Piperine, a dietary phytochemical, inhibits
angiogenesis. Journal of Nutritional Biochemistry 24: 231-239 (2013).

AJCER
B. Hammouti et al. / Arab. J. Chem. Environ. Res. 06 (2019) 12-56 42

[45] S.H. Kim, Y.C. Lee, Piperine inhibits eosinophil infiltration and airway hyperresponsiveness by
suppressing T cell activity and Th2 cytokine production in the ovalbumininduced asthma model.
Journal of Pharmacy and Pharmacology 61: 353-359 (2009).
[46] B. Krishnamoorthy, V. Parthasarathy, Improvement of black pepper. Plant Sciences Reviews,
37, 2010 (2011).
[47] S.W. Lee, Y.K. Kim, K. Kim, H.S. Lee, J.H. Choi, W.S. Lee, C.-D. Jun, J.H. Park, J.M. Lee,
M.-C. Rho, Alkamides from the fruits of Piper longum and Piper nigrum displaying potent cell
adhesion inhibition. Bioorganic & Medicinal Chemistry Letters. 18: 4544-4546 (2008).
[48] S.W. Lee, M.-C. Rho, Park, H.R., Choi, J.-H., Kang, J.Y., Lee, J.W., Kim, K., Lee, H.S., Kim,
Y.K., Inhibition of diacylglycerol acyltransferase by alkamides isolated from the fruits of Piper
longum and Piper nigrum. Journal of Agricultural and Food Chemistry. 54: 9759-9763 (2006).
[49] W. Lee, K.-Y. Kim, S.-N. Yu, S.-H. Kim, Chun, S.-S., Ji, J.-H., Yu, H.-S., S.-C. Ahn,
Pipernonaline from Piper longum Linn. induces ROS-mediated apoptosis in human prostate
cancer PC-3 cells. Biochemical and Biophysical Research Communications. 430: 406-412
(2013).
[50] M. Mueller, S. Hobiger, A. Jungbauer, Anti-inflammatory activity of extracts from fruits, herbs
and spices. Food Chemistry. 122, 987-996 (2010).
[51] S. Panda, A. Kar, Piperine lowers the serum concentrations of thyroid hormones, glucose and
hepatic 50 D activity in adult male mice. Hormone and Metabolic Research. 35: 523-526 (2003).
[52] I.-K. Park, S.-G. Lee, S.-C. Shin, J.-D. Park, Y.-J. Ahn, Larvicidal activity of isobutylamides
identified in Piper nigrum fruits against three mosquito species. Journal of Agricultural and Food
Chemistry. 50: 1866-1870 (2002).
[53] V.S. Parmar, S.C. Jain, K.S. Bisht, R. Jain, P. Taneja, A. Jha, O.D. Tyagi, A.K. Prasad, J.
Wengel, C.E. Olsen, Phytochemistry of the genus piper. Phytochemistry. 46: 597-673 (1997).
[54] C. Pradeep, G. Kuttan, Effect of piperine on the inhibition of lung metastasis induced B16F-10
melanoma cells in mice. Clinical & Experimental Metastasis. 19: 703-708 (2002).
[55] S. V. Reddy, P. V. Srinivas, , B. Praveen, , K. H. Kishore, , B. C. Raju, , U. S. Murthy, J. M.
Rao, Antibacterial constituents from the berries of Piper nigrum. Phytomedicine. 11, 7-8: 697-
700 (2004).
[56] J.C. Reed, M. Pellecchia, Methods and Compounds Useful to Induce Apoptosis in Cancer Cells.
Google Patents. I. Sasidharan, A.N. Menon, Comparative chemical composition and
antimicrobial activity of berry and leaf essential oils of piper nigrum l. International Journal of
Biological & Medical Research. 1: 215-218 (2010).

AJCER
B. Hammouti et al. / Arab. J. Chem. Environ. Res. 06 (2019) 12-56 43

[57] K. Selvendiran, S.M. Banu, D. Sakthisekaran, Protective effect of piperine on benzo (a) pyrene-
induced lung carcinogenesis in Swiss albino mice. Clinica Chimica Acta. 350: 73-78 (2004).
[58] G. Singh, P. Marimuthu, C. Catalan, M. Delampasona, Chemical, antioxidant and antifungal
activities of volatile oil of black pepper and its acetone extract. Journal of the Science of Food
and Agriculture. 84: 1878-1884 (2004).
[59] S.I.H. Taqvi, A.J. Shah, A.H. Gilani, Blood pressure lowering and vasomodulator effects of
piperine. Journal of Cardiovascular Pharmacology. 52: 452-458 (2008).
[60] F. Tasleem, I. Azhar, S.N. Ali, S. Perveen, Z.A. Mahmood, Analgesic and antiinflammatory
activities of Piper nigrum L. Asian Pacific journal of tropical medicine. 7: S461-S468 (2014).
[61] M.N. Thakare, Pharmacological screening of some medicinal plants as antimicrobial and feed
additive. Masters’ Thesis. Department of Animal and Poultry Science, Virginia Polytechnic
Institute and State University, Blackburg, Virginia, USA (2004).
[62] N. Ujam, P. Eze, B. Umeokoli, C. Abbah, F. Okoye, C. Esimone, Evaluation of antiplasmodial
and immunomodulatory activities of extracts of endophytic fungi isolated from four Nigerian
medicinal plants. Planta Medica International Open 4: Tu-PO-80 (2017).
[63] Z. Zarai, E. Boujelbene, N.B. Salem, Y. Gargouri, A. Sayari, Antioxidant and antimicrobial
activities of various solvent extracts, piperine and piperic acid from Piper nigrum. Lwt-Food
Science and Technology. 50: 634-641 (2013).
[63bis] F.A. Fluckiger, D. Hanbury, Pharmacographia: A History of the Principal Drugs of Vegetable
Origin, Met with in Great Britain and British India. London: Macmillan. p. 584. ASIN
B00432KEP2, (1879).
[64] P. Nisha, Rekha S. Singhal, Aniruddha B. Pandit, The degradation kinetics of flavor in black
pepper (Piper nigrum L.). Journal of Food Engineering. 92: 44–49 (2009).
[65] A. Szallasi, Piperine: researchers discover new flavor in an ancient spice. Trends in
Pharmacological Sciences. 26, 9: 437-439 (2005).
[66] S.C.B. Kotte, P.K. Dubey, P.M. Murali, Identification and characterization of stress degradation
products of piperine and profiling of a black pepper (Piper nigrum L.) extract using LC/Q-TOF-
dual ESI-MS. Analytical Methods. 6, 19: 8022-8029 (2014).
[67] L. Gorgani, M. Moham G. D. Najafpour, M. Nikzad, Piperine—The Bioactive Compound of
Black Pepper: From Isolation to Medicinal Formulations. comprehensive Review. 16, 1: 124-140
(2017).
[68] F. Namjoyan, H. Hejazi, Z. Ramezani, Evaluation of Drying Process on the Composition of
Black Pepper Ethanolic Extract by High Performance Liquid Chromatography With Diode Array

AJCER
B. Hammouti et al. / Arab. J. Chem. Environ. Res. 06 (2019) 12-56 44

Detector, Jundishapur J Nat Pharm Prod. 7, 4: 163–167 (2012).


[69] L. Wang, V. Palme, S. Rotter, N. Schilcher, M. Cukaj, D. Wang, A. Ladurner, E. H. Heiss, H.
Stangl, V. M. Dirsch, A. G. Atanasov, Piperine inhibits ABCA1 degradation and promotes
cholesterol efflux from THP‐1‐derived macrophages. Mol Nutr Food Res. 61, 4: 1500960
(2017).
[70] Ui-Hyun Park 1, Hong-Suk Jeong, Eun-Young Jo, Taesun Park, Seung Kew Yoon, Eun-Joo
Kim, Ji-Cheon Jeong, Soo-Jong Um, Piperine, a component of black pepper, inhibits
adipogenesis by antagonizing PPAR gamma activity in 3T3‐L1 cells. J. Agric. Food Chem., 60:
3853-3860 (2012). https://doi.org/10.1021/jf204514a
[71] H. Jwa, Y. Choi, U.H. Park, S.J. Um, S. K. Yoon, T. Park, Piperine, an LXR alpha antagonist,
protects against hepatic steatosis and improves insulin signaling in mice fed a high‐fat diet.
Biochem. Pharmacol., 84: 1501-1510 (2012). https://doi.org/10.1016/j.bcp.2012.09.009
[72] S. Choi, Y. Choi, S. Kim, J. Jang, T. Park, Piperine reverses high fat diet‐induced hepatic
steatosis and insulin resistance in mice. Food Chem., 141: 3627-3635 (2013).
https://doi.org/10.1016/j.foodchem.2013.06.028
[73] M. Meghwal, T.K. Goswami, Piper nigrum and piperine: an update. Phytother. Res. 27: 1121-
1130 (2013).
[74] Ajazuddin, A. Alexander, A. Qureshi, L. Kumari, P. Vaishnav, M. Sharma, S. Saraf, S. Saraf,
Role of herbal bioactives as a potential bioavailability enhancer for active pharmaceutical
ingredients. Fitoterapia, 97: 1-14 (2014). https://doi.org/10.1016/j.fitote.2014.05.005
[75] H.K. Han, The effects of black pepper on the intestinal absorption and hepatic metabolism of
drugs. Expert Opin. Drug Metab. Toxicol., 7: 721-729 (2011).
[76] T. Velpandian, R. Jasuja, R.K. Bhardwaj, J. Jaiswal, S. K. Gupta, Piperine in food: interference
in the pharmacokinetics of phenytoin. Eur. J. Drug Metab. Pharmacokinet., 26: 241-247
(2001). https://doi.org/10.1007/bf03226378
[77] A. Duangjai, K. Ingkaninan, S. Praputbut, N. Limpeanchob, Black pepper and piperine reduce
cholesterol uptake and enhance translocation of cholesterol transporter proteins. J. Nat. Med., 67:
303-310 (2013).
[78] J.R. Piggot, Z. Othman, Effect of irradiation on volatile oils of black pepper. Food Chemistry.
46(2): 115-119 (1993).
[79] E. Jayashree, J.T. Zachariah, P. Gobinath, Physicochemical properties of black pepper from
selected varieties in relation to market grades. Journal of Food Science and Technology, 46, 3:
263-265 (2009).

AJCER
B. Hammouti et al. / Arab. J. Chem. Environ. Res. 06 (2019) 12-56 45

[80] V. S. Govindarajan, Pepper chemistry, technology, and quality evaluation. CRC Critical Reviews
in Food Science and Nutrition, 9 (2): 115-225 (1977).
[81] S. Tewtrakul, K. Hase, S. Kadota, T. Namba, K. Komatsu, K. Tanaka, Fruit oil composition of
Piper chaba Hunt., P. longum L. and P. nigrum L. Journal of Essential Oil Research, 12(5): 603-
608 (2000).
[82] A.C. Kimoro, M. Hasan, H. Singh, Extraction Of sarawak black pepper essential oil using
supercritical carbon dioxide. Arabian Journal for Science and Engineering, 35(2): 7-16 (2010).
[83] R.M. Gutierrez, A.M. Gonzalez, C. Hoyo-Vadillo, Alkaloids from piper: a review of its
phytochemistry and pharmacology. Mini. Rev. Med. Chem., 13, 2: 163-93 (2013).
[84] G.H. Tang, D.M. Chen, B.Y. Qiu, L. Sheng, Y.H. Wang, G.W. Hu, F.W. Zhao, L.J. Ma, H.
Wang, Q.Q. Huang, J.J. Xu, C.L. Long, J. Li, Cytotoxic amide alkaloids from Piper
boehmeriaefolium. J. Nat. Prod. 74, 1: 45-9 (2011).
[85] N. Nakatani, R. Inatani, H. Ohta, A. Nishioka, Chemical constituents of peppers (Piper spp.) and
application to food preservation: naturally occurring antioxidative compounds. Environ. Health
Perspect. 67: 135–142 (1986).
[86] F.M. Al-Jasass, M.S. Al-Jasser, Chemical composition and fatty acid content of some spices and
herbs under Saudi Arabia conditions. Science World Journal. (859892): 1-5 (2012).
[87] a) E. Jayashree, T. Zachariah, P. Gobinath, Physico-chemical properties of black pepper from
selected varieties in relation to market grades. Journal of Food Science & Technology. 46: 263-
265 (2009) ; b) A. Nirmala Menon, K. P. Padmakumari &A. J. Jayalekshmy, Essential Oil
Composition of Four Major Cultivars of Black Pepper (Piper nigrum L.) Journal of Essential Oil
Research, 14(2): 84-86 (2002).
[88] P. Ravindran, Black pepper: Piper nigrum. Boca Raton, Fla.: CRC Press. Reverchon E, De Marco
I. 2006. Supercritical fluid extraction and fractionation of natural matter. J. Supercrit. Fluids. 38:
146-66 (2003).
[89] K.V. Peter, Handbook of herbs and spices. Sawston, UK: Woodhead Publishing, eBook ISBN:
9780857095671 (2012).
[90] A. Samykutty, A.V. Shetty, G. Dakshinamoorthy, M.M. Bartik, G.L. Johnson, B. Webb, G.
Zheng, A. Chen, R. Kalyanasundaram, G. Munirathinam, Piperine, a bioactive component of
pepper spice exerts therapeutic effects on androgen-dependent and androgen-independent
prostate cancer cells. Planta Med. 8: 65889 (2013).
[91] H. Greger, O. Hofer, Polyenoic acid piperideides and other alkamides from Achillea
millefolium. Phytochemistry. 28, 9: 2363-2368 (1989). https://doi.org/10.1016/S0031-

AJCER
B. Hammouti et al. / Arab. J. Chem. Environ. Res. 06 (2019) 12-56 46

9422(00)97985-8
[92] R.N. Shakhmaev, A.U. Ishbaeva, V.V. Zorin, Stereoselective synthesis of natural (2E,4E)-
dienamides and their synthetic analogs. Russ. J. Org. Chem. 48,7: 908-913 (2012).
[93] H. Pei, L. Xue, M. Tang, H. Tang, S. Kuang, L. Wang, , Xu Ma, X. Cai, Y. Li, M. Zhao, A.
Peng, H. Ye, L. Chen, Alkaloids from Black Pepper (Piper nigrum L.) Exhibit Anti-
Inflammatory Activity in Murine Macrophages by Inhibiting Activation of NF-κB Pathway.
Journal of Agricultural and Food Chemistry, 68,8: 2406-2417 (2020).
https://doi.org/10.1021/acs.jafc.9b07754
[94] T. S. Usia, S. Kadota, Y. Tezuka, Alkamides from Piper nigrum L. and their inhibitory activity
against human liver microsomal cytochrome P450 2D6 (CYP2D6). Nat Prod Commun. 1, 1: 1-
7 (2006).
[95] R. Inatani, N. Nakatani, H. Fuwa, Structure and Synthesis of New Phenolic Amides from Piper
nigrum L., Agric Boil Chem. 45, 3: 667-673 (1981).
[96] N. Nakatani, R. Inatani, H. Fuwa, Structures and Syntheses of Two Phenolic Amides from Piper
nigrum L. Agric. Biol. Chem., 44, 12: 2831-2836 (1980).
[97] Q. M. Ngo, P. T. Tran, M. H. Tran, J. A. Kim, S. S. Rho, C. H. Lim, J. C. Kim, M. H. Woo, J.
S. Choi, J. H. Lee, B. S. Min, Alkaloids from Piper nigrum Exhibit Antiinflammatory Activity
via Activating the Nrf2/HO-1 Pathway. Phytother Res. 31, 4: 663-670 (2017).
[98] Y. Tu, Y. Zhong, H. Du, W. Luo, Y. Wen, Q. Li, C. Zhu, Y. Li, Anticholinesterases and
antioxidant alkamides from Piper nigrum fruits. Nat. Prod. Res. 30, 17: 1945-9 (2016).
[99] C. Dawid, A. Henze, O. Frank, A. Glabasnia, M. Rupp, K. Buning, D. Orlikowski, M. Bader, ;
T. Hofmann, Structural and sensory characterization of key pungent and tingling compounds
from black pepper (Piper nigrum L.). J. Agric. Food Chem. 60, 11: 2884-95 (2012).
[100] S. W. Lee, Y. K. Kim, K. Kim, H. S. Lee, J. H. Choi, W. S. Lee, C. D. Jun, J. H. Park, J. M.
Lee, M. C. Rho, Alkamides from the fruits of Piper longum and Piper nigrum displaying potent
cell adhesion inhibition. Bioorg. Med. Chem. Lett. 18, 16: 4544-6 (2008).
[101] K. Li, W. Zhu, Q. Fu, Y. Ke, Y. Jin, X. Liang, Purification of amide alkaloids from Piper
longum L. Using preparative two-dimensional normal-phase liquid chromatography x reversed-
phase liquid chromatography. Analyst. 138, 11: 3313-20 (2013).
[102] C. Sun, S. Pei, Y. Pan, Z. Shen, Rapid structural determination of amides in Piper longum by
high-performance liquid chromatography combined with ion trap mass spectrometry. Rapid
Commun. Mass Spectrom. 21, 9: 1497-503 (2007).
[103] F. Kiuchi, N. Nakamura, M. Saitoh, K. Komagome, H. Hiramatsu, N. Takimoto, Y. Tsuda,

AJCER
B. Hammouti et al. / Arab. J. Chem. Environ. Res. 06 (2019) 12-56 47

Synthesis and nematocidal activity of aralkyl-and aralkenylamides related to piperamide on


second-stage larvae of Toxocara canis. Chemical and pharmaceutical bulletin. 45, 4: 685-696
(1997).
[104] G.H. Tang, D.M. Chen, B.Y. Qiu, L. Sheng, Y.H. Wang, G.W. Hu, F.W. Zhao, L. J. Ma, H.
Wang, Q.Q. Huang, J.J. Xu, C.L. Long, J. Li, Cytotoxic amide alkaloids from Piper boehmeriae
folium. J. Nat. Prod., 74, 1: 45-9 (2011).
[105] H. A. Pedersen, S. K. Steffensen, C. Christophersen, Cinnamoylphenethylamine 1H-NMR
Chemical Shifts: A Concise Reference for Ubiquitous Compounds. Nat. Prod. Commun. 5, 8:
1259-1262 (2010).
[106] B. G. Pring, Isolation and identification of amides from Piper callosum. Synthesis of
pipercallosine and pipercallosidine. J. Chem. Soc. Perk. T1. 7:1493-1498 (1982).
[107] P. Choochana, J. Moungjaroen, N. Jongkon, W. Gritsanapan, P. Tangyuenyongwatana,
Development of piperic acid derivatives from Piper nigrum as UV protection agents. Pharm.
Biol. 53, 4: 477-82 (2015).
[108] T. Rukachaisirikul, S. Prabpai, P. Kongsaeree, A. Suksamrarn, (+)-Bornyl Piperate, a New
Monoterpene Ester from Piper aff. pedicellatum Roots. Chem. Pharm. Bull. 52, 6: 760-761
(2004).
[109] J. E. Batterbee, R. S. Burden, L. Crombie, D. A. Whiting, Chemistry and synthesis of the lignan
(–)-cubebin. J. Chem. Soc. C. 18, 19: 2470-2477 (1969).
[110] G, M. D.; M, A.; M, P.; P, L., Dihydrobenzofuran Neolignans from Arum italicum.
Heterocycles, 38, 5: 1099-1102 (1994).
[111] T. Umezawa, L. B. Davin, N. G. Lewis, Formation of the lignan, (−) secoisolariciresinol, by
cell free extracts of Forsythia intermedia. Biochem Bioph Res Co. 171, 3: 1008-1014 (1990).
[112] S. Nishibe, K. Okabe, S. Hisada, Isolation of phenolic compounds and spectroscopic analysis
of a new lignan from Trachelospermum asiaticum var. intermedium. Chem Pharm Bull. 29, 7:
2078-2082 (1981).
[113] S. Morshed, M.D. Hossain, M. Ahmad, M. Junayed, Physicochemical Characteristics of
Essential Oil of Black Pepper (Piper nigrum) Cultivated in Chittagong, Bangladesh, Journal of
Food Quality and Hazards Control 466-69 (2017).
[114] R. Rmili, H. Elmsellem, M. Ramdani, B. El Mahi, Z. Ghazi, A. Chetouani, A. Aouniti, B.
Hammouti, Composition of Piper Nigrum L. Essential Oils Extracted by Classical
Hydrodistillation and Microwave-assisted Hydrodistillation and Inhibitory Effect on the
Corrosion of mild steel in hydrochloric acid, J. Mater. Environ. Sci. 7 (7): 2646-2657 (2016)

AJCER
B. Hammouti et al. / Arab. J. Chem. Environ. Res. 06 (2019) 12-56 48

[115] W.M.N.H.W. Salleh, E. Rajudin, F. Ahmad, H.M. Sirat, D. Arbain, Essential oil composition
of Piper majusculum Ridl. from Indonesia, J. Mater. Environ. Sci. 7 (6): 1921-1924 (2016)
[116] Yogesh Kumar, Om Prakash, Himanshu Tripathi, Sudeep Tandon, Madan M. Gupta, Laiq-Ur
Rahman, Raj K. Lal,5 Manoj Semwal, Mahendra Pandurang Darokar, and Feroz Khan,
AromaDb: A Database of Medicinal and Aromatic Plant’s Aroma Molecules With
Phytochemistry and Therapeutic Potentials, Front Plant Sci. 9: 1081 (2018). doi:
10.3389/fpls.2018.01081
[117] H.-D. Belitz · W. Grosch · P. Schieberle Food Chemistry, Springer 4th revised and extended
ed. ISBN 978-3-540-69933-0 e-ISBN 978-3-540-69934-7 DOI 10.1007/978-3-540-69934-7
(2009)
[118] T. Ezawa, Y. Inoue, S. Tunvichien, R. Suzuki, I. Kanamoto, Changes in the Physicochemical
Properties of Piperine/β-Cyclodextrin due to the Formation of Inclusion Complexes,
International Journal of Medicinal Chemistry, ID 8723139: 9 pages (2016),
https://doi.org/10.1155/2016/8723139
[119] K. Hashimoto, T. Yaoi, H. Koshiba, T. Yoshida, T. Maoka, Y. Fujiwara, Y. Yamamoto, K.
mori, Photochemical isomerization of piperine, a pungent constituent in pepper. Food Science
and Technology International, 2(1) 24-29 (1996).
[120] N.S. Jeganathan, K. Kannan, Quantitative Estimation of Piperine in Trikatuku Curanam, Asian
Journal of Chemistry, 20, No. 2 1621-1626 (2008).
[121] R. De Cleyn, M. Verzele, Constituents of Peppers Part VII. Spectroscopic Structure Elucidation
of Piperine and its Isomers, Bulletin des Sociétés Chimiques Belges 84(5): 435-438 (1975).
[122] H.C.F. Su, Insecticidal properties of black pepper to rice weevils and cowpea weevils, J. Econ.
Entomol. 70: 18-21 (1977).
[123] M. Miyakado, I. Nakayama, H. Yoshioka, N. Nakatani The Piperaceae amides I: Structure of
pipercide, a new insecticidal amide from Piper nigrum L. Agric Biol Chem. 43: 1609-1611
(1979).
[124] A.M. Mujumdar, J.N. Dhuley, V.K. Deshmukh, P.H. Raman, S.R. Naik, Anti-inflammatory
activity of piperine. Japanese J. Med. Sci. Biol. 43: 95-100 (1990).
[125] S. Ghoshal, B.N.K. Prasad, V. Lakshmi, Antiamoebic activity of Piper longum fruits against
Entamoeba histolytica in vitro and in vivo. J. Ethnopharmacol. 50: 167-170 (1996).
[126] Z. Zarai, E. Boujelbene, Salem N. Ben, Y. Gargouri, A. Sayari, Antioxidant and antimicrobial
activities of various solvent extracts, piperine and piperic acid from Piper nigrum. LWT-Food
Sci Technol. 50: 634-641 (2013).

AJCER
B. Hammouti et al. / Arab. J. Chem. Environ. Res. 06 (2019) 12-56 49

[127] W.S. Tavares, I. Cruz, F. Petacci, S.S. Freitas, J.E. Serratilde, J.C. Zanuncio, Insecticide activity
of piperine: Toxicity to eggs of Spodoptera frugiperda (Lepidoptera: Noctuidae) and Diatraea
saccharalis (Lepidoptera: Pyralidae) and phytotoxicity on several vegetables. J Med Plants Res.
5: 5301-5306 (2011).
[128] P. Storz, Reactive oxygen species in tumor progression. Front. Biosci., 10: 1881-1896 (2005).
[129] J.S. Bang, H.M. Choi, B.-J. Sur, S.-J. Lim, J.Y. Kim, H.-I. Yang, et al., Anti-inflammatory and
antiarthritic effects of piperine in human interleukin 1β-stimulated fibroblast-like synoviocytes
and in rat arthritis models. Arthritis Res. Ther. 11: R49 (2009).
[130] M.H. Mehmood, A.H. Gilani, Pharmacological basis for the medicinal use of black pepper and
piperine in gastrointestinal disorders. J Med Food. 13: 1086-1096 (2010).
[131] S.A. Lee, S.S. Hong, X.H. Han, J.S. Hwang, G.J. Oh, K.S. Lee, et al., Piperine from the fruits
of Piper longum with inhibitory effect on monoamine oxidase and antidepressant-like activity.
Chem Pharm Bull. 53: 832-835 (2005).
[132] E.A. Correa, E.D. Högestätt, O. Sterner, F. Echeverri, P.M. ZygmuntIn vitro TRPV1 activity
of piperine derived amides. Bioorg Med Chem. 18: 3299-3306 (2010).
[133] L. Hlavačková, A. Janegová, O. Uličná, P. Janega, A. Černá, P. Babál, Spice up the
hypertension diet-curcumin and piperine prevent remodeling of aorta in experimental L-NAME
induced hypertension. Nutr Metab (Lond). 8: 72 (2011).
[134] J. Zheng, Y. Zhou, Y. Li, D.P. Xu, S. Li, H.B. Li, Spices for Prevention and Treatment of
Cancers, Nutrients, 8(8): 495 (2016), https://dx.doi.org/10.3390%2Fnu8080495
[135] S. Li, Y. Lei, Y. Jia, N. Li, M. Wink, Y. Ma, Piperine, a piperidine alkaloid from Piper nigrum
re-sensitizes P-gp, MRP1 and BCRP dependent multidrug resistant cancer cells. Phytomedicine,
19: 83-87 (2011).
[136] M. Meghwal, T. K. Goswami, Piper nigrum and piperine: an update. Phytotherapy Research.
27, 8: 1121-1130 (2013).
[137] T.J. Zachariah, V.A. Parthasarathy, Black pepper. Chem. spices 196, p. 21; ISBN-13: 9781
845934057 (2008).
[138] S. Li, Y. Lei, Y. Jia, N. Li, M. Wink, Y. Ma, Piperine, a pip aeridinelkaloid from Piper nigrum
re-sensitizes P-gp, MRP1 and BCRP dependent multidrug resistant cancer cells. Phytomedicine.
19: 83-87 (2011).
[139] J.S. Pruthi, Major spices of India: crop management and post-harvest technology, Major Spices
India Crop Manag Post-Harvest Technol (1993).
www.cabdirect.org/cabdirect/abstract/20043186295

AJCER
B. Hammouti et al. / Arab. J. Chem. Environ. Res. 06 (2019) 12-56 50

[140] E.A. Correa, E.D. Högestätt, O. Sterner, F. Echeverri, P.M. ZygmuntIn vitro TRPV1 activity
of piperine derived amides, Bioorg Med Chem, 18: 3299-3306 (2010).
[141] L. Hlavackova, A. Janegova, O. Ulicna, P. Janega, A. Cerna, P. Babal, Spice up the
hypertension diet-curcumin and piperine prevent remodeling of aorta in experimental L-NAME
induced hypertension. Nutr Metab (Lond). 8: 72 (2011).
[142] G. Shoba, D. Joy, T. Joseph, M. Majeed, R. Rajendran, P.S. Srinivas, Influence of piperine on
the pharmacokinetics of curcumin in animals and human volunteers. Planta Med., 64(4):353-6
(1998).
[143] Murlidhar Meghwal and TK Goswami, Chemical Composition, Nutritional, Medicinal And
Functional Properties of Black Pepper: A Review, Scientific Reports, 1(2): 172 (2012).
http://dx.doi.org/10.4172/scientificreports.172
[144] Douglas W. Wilson, Paul Nash, Harpal Singh Buttar, Keith Griffiths, Ram Singh, Fabien De
Meester, Rie Horiuchi, Toru Takahashi, The Role of Food Antioxidants, Benefits of Functional
Foods, and Influence of Feeding Habits on the Health of the Older Person: An Overview,
Antioxidants (Basel). 6(4): 81 (2017). https://dx.doi.org/10.3390%2Fantiox6040081
[145] M. Suhaj, J. Rácová, M. Polovka, V. Brezová, Effect of γ-irradiation on antioxidant activity
of black pepper (Piper nigrum L.), Food Chem., 97 (4) 696-704 (2006).
[146] G. A. Agbor, J. A. Vinson, J. E. Oben, J. Y. Ngogang, Comparative analysis of the in
vitro antioxidant activity of white and black pepper, Nutrition Research, 26 (12) 659-663 (2006).
[147] J. Rakmai, B. Cheirsilp, J. C. Mejuto, A. Torrado-Agrasar, J. Simal-Gándara, Physico-chemical
characterization and evaluation of bio-efficacies of black pepper essential oil encapsulated in
hydroxypropyl-beta-cyclodextrin, Food Hydrocolloids, 65, 157-164 (2017).
[148] S. H. Nile, A. S. Nile, Y. S. Keum, V. Baskar, S. Ramalingam, In vitro and in
planta nematicidal activity of black pepper (Piper nigrum L.) leaf extracts, Crop Protection
100,1-7 (2017).
[149] S. Dutta, .P. Bhattacharjee, Nanoliposomal encapsulates of piperine-rich black pepper extract
obtained by enzyme-assisted supercritical carbon dioxide extraction, J. Food Engin., 201, 49-56
(2017).
[150] S. Mohandas, I. Khalid, C. Shalin, V. Ramesh, Vandana Evaluation of in-vitro antioxidant
activity of Vidangadi churna, World Journal of Pharmacy and Pharmaceutical Sciences 6(11),
963-970 (2017).
[151] M. Meghwal, T.K. Goswami, Piper nigrum and Piperine: An Update, Phytotherapy Research,
27(8) 1121-1130 (2013).

AJCER
B. Hammouti et al. / Arab. J. Chem. Environ. Res. 06 (2019) 12-56 51

[152] K. Srinivasan, Antioxidant Potential of Spices and Their Active Constituents, Critical Reviews
in Food Science and Nutrition, 54(3) 352-372(2014).
[153] Y. Tu, D. Sun, X. Zeng, N. Yao, X. Huang, D. Huang, Y. Chen, Piperine potentiates the hypo-
cholesterolemic effect of curcumin in rats fed on a high fat diet, Experimental and Therapeutic
Medicine, 8,260-266 (2014).
[154]Y. Yanga, D. Kanev, R. Nedeva, A. Jozwik, J. M. Rollinger, W. Grzybek, B. Pyzel, A. W. K.
Yeung, P. Uhrin, J. M. Breuss, J. O. Horbanczuk, C. Malainerg, T. Xu, D. Wang, A. G. Atanasov,
Black pepper dietary supplementation increases high-density lipoprotein (HDL) levels in pigs,
Current Research in Biotechnology, 1: 28-33 (2019)
[155] Z. Sina, J. Nasrollahzadeh, S. Shokraei, M. Rismanchi, F.Foroughi, Black and red peppers
attenuates plasma and lipopolysaccharide-induced splenocytes production of tumor necrosis
factor-α in mice fed a high-fat, high-sucrose diet, J. Func. Foods, 50, 158-163 (2018).
[156] R. Takeara, R. Goncalves, V. Farias dos Santos Ayres, A. C. Guimaraes, H. El-Shemy,
Biological properties of essential oils from the Piper species of Brazil: a review, Aromatic and
Medicinal Plants, 81-93(2017).
[157] V. Goots, N. Yushchenko, U. Kuzmyk, Development of mathematic model of spiced sour-milk
pastas quality, Food and Environment Safety, 17(2) 224-232 (2018).
[158] P. Bandigari, A. Mohammed, S. Arikilla, B. Chanduri, S. Yemba, K. Chinnala, M. Krishna,
Evaluation of anti diabetic activity of seeds of black pepper in streptozotocin induced diabetic
rats, European Journal of Biomedical and Pharmaceutical Sciences, 5(5) 1-6 (2018).
[159] P. Lomarat, K. Sripha, P. Phanthong, W. Kitphati, K. Thirapanmethee, N. Bunyapraphatsara,
In vitro biological activities of black pepper essential oil and its major components relevant to
the prevention of Alzheimer's disease, Thai J. Pharmaceutical Sci.,39(3) 94-101(2015).
[160] M. Friedman, P.R. Henika, R.E. Mandrell, Bactericidal activities of plant essential oils and
some of their isolated constituents against Campylobacter jejuni, Escherichia coli, Listeria
monocytogenes, and Salmonella enterica, J. Food Protection, 65(10) 1545-1560 (2002).
[161] E. Rajesh, Leena S. Sankari, L. Malathi, and Jayasri R. Krupaa, Naturally occurring products
in cancer therapy, J Pharm Bioallied Sci. 7(Suppl 1): S181–S183 (2015). doi: 10.4103/0975-
7406.155895
[162] R. G. Amaral, S. A. dos Santos, L. N. Andrade, P. Severino and A. A. Carvalho, Natural
Products as Treatment against Cancer: A Historical and Current Vision, Clinics in Oncology, 4:
1562 (2019)
[163] A. Samykutty, A.V. Shetty, G. Dakshinamoorthy, M.M. Bartik, G.L. Johnson, B. Webb, G.

AJCER
B. Hammouti et al. / Arab. J. Chem. Environ. Res. 06 (2019) 12-56 52

Zheng, A. X. Chen, R.S. Kalyanasundaram, G. Munirathinam, Piperine, a bioactive component


of pepper spice exerts therapeutic effects on androgen dependent and androgen independent
prostate cancer cells. PLoS ONE. 8:495 (2013). doi: 10.1371/journal.pone.0065889
[164] R. A. Rather and M. Bhagat, Cancer Chemoprevention and Piperine: Molecular Mechanisms
and Therapeutic Opportunities, Front Cell Dev Biol. 6: 10 (2018). doi: 10.3389/fcell.2018.00010
[165] P.B. Yaffe, M. Coombs, C.D. Doucette, M. Walsh, D.W. Hoskin, Piperine, an alkaloid from
black pepper, inhibits growth of human colon cancer cells via g1 arrest and apoptosis triggered
by endoplasmic reticulum stress, Mol. Carcinogen. 54: 1070–1085 (2015). doi:
10.1002/mc.22176.
[166] I. Alam, H. Imam, Z. Riaz, Cancer preventing spices, J. Cancer Metastasis Treat, 1:41-42
(2015). 10.4103/2394-4722.154131
[167] I. Philipova, V. Valcheva, R. Mihaylova, M. Mateeva, I. Doytchinova, G. Stavrakov, Synthetic
piperine amide analogs with antimycobacterial activity. Chem. Biol. Drug Des. [Epub ahead of
print], 91: 763-768 (2018). 10.1111/cbdd.13140
[168] L. Freire-de-Lima, T. S. Ribeiro, G. M. Rocha, B. A. Brandão, A. Romeiro, L. Mendonça-
Previato, et al., The toxic effects of piperine against Trypanosoma cruzi: ultrastructural
alterations and reversible blockage of cytokinesis in epimastigote forms. Parasitol. Res. 102 :
1059–1067 (2008). 10.1007/s00436-008-0876-9
[169] R. A. Rafiq, B. A. Ganai, S. A. Tasduq, Piperine promotes ultraviolet (UV)-B-induced cell
death in B16F10 mouse melanoma cells through modulation of major regulators of cell
survival. RSC Adv. 5, 11884–11894 (2015). 10.1039/C4RA12860E
[170] G. Rodgers, C.D. Doucette, D. Soutar, R. S. Liwski, D. W. Hoskin, Piperine impairs the
migration and T cell-activating function of dendritic cells. Toxicol. Lett. 242, 23–33 (2016).
10.1016/j.toxlet.2015.11.025
[171] J. J. Lu, Bao J. L., X. P. Chen, M. Huang Y. T., Wang, Alkaloids isolated from natural herbs
as the anticancer agents. Evid. Based Compl. Alternat. Med. 2012: 485042 (2012).
10.1155/2012/485042
[172] S. Sahi, P. Tewatia, S. Ghosal, Leishmania donovani pteridine reductase 1: comparative protein
modeling and protein-ligand interaction studies of the leishmanicidal constituents isolated from
the fruits of Piper longum.; J. Mol. Model. 18, 5065–5073 (2012). 10.1007/s00894-012-1508-y
[173] D. A. Soutar, C. D. Doucette, R. S. Liwski, D. W. Hoskin Piperine, A pungent alkaloid from
black pepper, inhibits B lymphocyte activation and effector functions. Phytother Res. 31, 466–
474 (2017). 10.1002/ptr.5772

AJCER
B. Hammouti et al. / Arab. J. Chem. Environ. Res. 06 (2019) 12-56 53

[174] M. Samuel, S. V. Oliver, M. Coetzee, B. D. Brooke, The larvicidal effects of black pepper
(Piper nigrum L.) and piperine against insecticide resistant and susceptible strains of Anopheles
malaria vector mosquitoes. Parasit Vectors 9:238 (2016). 10.1186/s13071-016-1521-6
[175] C. Samuel, J.P. Elijah, D. O. Ayodeji, N.A. Ngozi, A.J. Nnedimkpa, D.C. Maryann, E.C. Kayla,
O.P. Tobechukwu, Lowering the blood brain barrier permeation property of 6-gingerol through
a structural monosubstitution modification approach for the prevention of psychotropic side
effects: an in-silico pharmacokinetics study, Pharmacologyonline, 1, 1-9(2019).
[176] K.-R. Park, D. Nam, H.-M. Yun, S.-G. Lee, H.-J. Jang, G. Sethi, S. K. Cho, K. S. Ahn, β-
Caryophyllene oxide inhibits growth and induces apoptosis through the suppression of
PI3K/AKT/mTOR/S6K1 pathways and ROS-mediated MAPKs activation, Cancer Letters (New
York, NY, United States), 312(2) 178-188 (2011).
[177] T. Thangaselvabal, C.G. Leo Justin, M. Leelamathi, Black pepper (Piper nigrum L.) “the king
of spices” – a review. Agric. Rev., 29 (2), 89-98 (2008).
[178] P.N. Ravindran, K. Nirmal Babu, B. Sasikumar, K.S. Krishnamurthy, Botany and crop
improvement of black pepper. Chapter 5.2, in Black Pepper (Piper nigrum), edited by P.N.
Ravindran, Overseas Publishers Association N.V., published by license under the Harwood
Academic Publishers imprint (2000).
[179] K.P. Ee, C.Y. Shang, Novel Farming Innovation for High Production of Black Pepper (Piper
nigrum L.) Planting Materials. Journal of Agricultural Science and Technology B, 7: 301-308
(2017). doi: 10.17265/2161-6264/2017.05.001
[180] K.V. Ramana, S.J. Eapen, Nematode induced diseases of black pepper. Chapter 2, in Black
Pepper (Piper nigrum), edited by P.N. Ravindran, Overseas Publishers Association N.V.,
published by license under the Harwood Academic Publishers imprint (2000).
[181] R. Suseela Bhai, M. Anandaraj, Y.R. Sarma, S.S. Veena, K.V. Saji, Screening of black pepper
(Piper nigrum L.) germplasm for resistance to foot rot disease caused by Phytophthora capsici
Leonian. Journal of Spices and Aromatic Crops, 16 (2): 115-117 (2007).
[182] T.J. Zachariah, On farm processing of black pepper. Chapter 7.1., in in Black Pepper (Piper
nigrum), edited by P.N. Ravindran, Overseas Publishers Association N.V., published by license
under the Harwood Academic Publishers imprint (2000).
[183] M. Weil, F. Descroix, A.S. Cheong Sing, R. Boulanger, M. Hoarau, A. Levesque and P.
Bohuon, Postharvest treatments of wild pepper (Piper spp.) in Madagascar. Fruits, 68: 371-380
(2014). DOI: 10.1051/fruits/2014025
[184] C.K. Mangalakumari, V.P. Sreedharan, A.G. Mathew, Studies on blackening of pepper (Piper

AJCER
B. Hammouti et al. / Arab. J. Chem. Environ. Res. 06 (2019) 12-56 54

nigrum Linn.) during dehydratation, J. Food Sci. 48 (2): 604-606 (1983).


[185] I. Reinholds, V. Bartkevics, I.C.J. Silvis, S.M. van Ruth, S. Esslinger, Analytical techniques
combined with chemometrics for authentication and determination of contaminants in
condiments: A review. Journal of Food Composition and Analysis, 44: 56-72 (2015). DOI:
10.1016/j.jfca.2015.05.004
[186] S.E. Keller, J.M. VanDoren, E.M. Grasso and L.A. Halik, Growth and survival of Salmonella
in ground black pepper (Piper nigrum), Food Microbiology, 34: 182-188 (2013).
[187] FAO/WHO, Code of hygienic practice for spices and dried aromatic herbs. Codex Alimentarius,
CAC/RCP 42-1995, adopted 1995, Revision 2014 (1995).
[188] M. Djordjevic, M. Sternisa, S.S. Mozina, S. Beszedes, D.S. Simovic, C. Hodur, A. Jokic, Z.
Seres, Z. Black pepper (Piper nigrum L.) bacterial decontamination by sterilization and
microwave treatments. Analecta Technica Szegedinensia, 13(2): 1-5 (2019). DOI:
10.14232/analecta.2019.2.1-5
[189] D. Nei, K. Enomoto and N. Nakamura, A gaseous acetic acid treatment to disinfect fenugreek
seeds and black pepper inoculated with pathogenic and spoilage bacteria. Food Microbiology,
49: 226-230 (2015). http://dx.doi.org/10.1016/j.fm.2015.02.011
[190] FAO/WHO, Standard for black, white and green peppers. Codex Alimentarius, CXS 326-2017,
adopted in 2017 (2017).
[191] T. Ganapathi, S.V. Patil, G.R. Rajakumar, Processing of black pepper (Piper nigrum L.)
through solarization, Internat. J. Agric. Sci., 14: 211-214 (2018),
doi:10.15740/HAS/IJAS/14.1/211-214
[192] B. Chopra, A.K. Dhingra, R.P. Kapoor, D.N. Prasad, Piperine and its various physicochemical
and biological aspects: A review. Open Chem. J., 3: 75-96 (2017).
[193] Z. Stojanovic-Radic, M. Pejcic, M. Dimitrijevic, A. Aleksic, N. V. Anil Kumar, B. Salehi, W.
C. Cho, J. Sharifi-Rad, Piperine-A Major Principle of Black Pepper: A Review of Its Bioactivity
and Studies, Appl. Sci., 9: 4270 (2009), doi:10.3390/app9204270
[194] M.S. Butt, I. Pasha, M. Tauseef Sultan, M. Atif Randhawa, F. Saeed, A. Waqas, Black Pepper
and Health Claims: A Comprehensive Treatise, Crit. Rev. Food Sci. Nutr. 53(9): 875-886 (2013).
doi:10.1080/10408398.2011.571799.
[195] P.D. Roberts, S. Adkins, K. Pernezny, J.B. Jones, Diseases of Pepper and their Management.
In: Naqvi S.A.M.H. (eds) Diseases of Fruits and Vegetables: Volume II. Springer, Dordrecht,
Online ISBN 978-1-4020-2607-2 (2004) https://doi.org/10.1007/1-4020-2607-2_10.
[196] L.K. Chai, F. Elie, A rapid multi-residue method for pesticide residues determination in white

AJCER
B. Hammouti et al. / Arab. J. Chem. Environ. Res. 06 (2019) 12-56 55

and black pepper (Piper nigrum L.), Food Control, 32: 322-326 (2013).
[197] A. Dogan, N. Selcuk, M. Erkan, Comparison of pesticide-free and conventional production
systems on postharvest quality and nutritional parameters of peppers in different storage
conditions, Scientia Horticulturae, 2075: 104-116 (2016).
[198] S.H. Nile, A.S. Nile, Y.S. Keum, V. Baskar, S. Ramalingam, In vitro and in planta nematicidal
activity of black pepper (Piper nigrum L.) leaf extracts, Crop Protection, 100: 1-7 (2017)
[199] R. Aravind, S.J. Eapen, A. Kumar, A. Dinu, K.V. Ramana, Screening of endophytic bacteria
and evaluation of selected isolates for suppression of burrowing nematode (Radopholus similis
Thorne) using three varieties of black pepper (Piper nigrum L.), Crop Protection, 29: 318-324
(2010).
[200] A Pest Management Strategic Plan for Pepper Production in California, The California Pepper
Commission Dec(2004), https://ipmdata.ipmcenters.org/documents/pmsps/CAPepper.pdf
[201] H. Aktas, L. Karni, B. Aloni, A. Bar-Tal, Physiological and biochemical mechanisms leading
to blossom-end rot in greenhouse-grown peppers, irrigated with saline solution. Acta
Horticulturae, 609: 81-88 (2003).
[202] S. Dutta, E. Woo, S.M. Yu, R. Nagendran, B.S. Yun, Y.H. Lee, Control of Anthracnose and
Gray Mold in Pepper Plants Using Culture Extract of White-Rot Fungus and Active Compound
Schizostatin, Journal Mycobiology, 47(1): 87-96 (2019).
[203] J.K. Hong, H.J. Yang, H. Jung, D. J. Yoon, M. K. Sang, Y-C. Jeun, Application of volatile
antifungal plant essential oils for controlling pepper fruit anthracnose by Colletotrichum
gloeosporioides; Plant Pathol. J., 31: 269-277 (2015). 10.5423%2FPPJ.OA.03.2015.0027
[204] Compendium of Pepper Diseases, Ed. K. Pernezny, P. D. Roberts, J. F. Murphy, and N. P.
Goldberg. APS Press, St. Paul, MN. 63pp (2003).
[205] S.L.F. Meyer, D.P. Roberts, D.J. Chitwood, L.K. Carta, R.D. Lumsden, W. Mao, Application
of Burkholderia cepacia and Trichoderma virens, alone and in combination, against Meloidogyne
incognita on bell pepper, Nematropica, 31: 75-86 (2001).
[206] S. Jodeh, S. Al Masri, M. Haddad, O. Hamed, D. Jodeh, R. Salghi, S. Radi, J. Amarah, F. El-
Hajjaji, I. Warad, Evaluation of potential Residue of Imidacloprid and Abamectin in Tomato,
Cucumber and Pepper Plants after Spraying using High Performance Liquid Chromatography
(HPLC), J. Mater. Environ. Sci. 7 (3): 1037-1047 (2016)
[207] K. Srivastava, P. Srivastava, Studies-on plant materials as corrosion inhibitors, British
Corrosion Journal, 16(4): 221-231 (1981).
[208] K. Srivastava, P. Srivastava, Synergistic effect of castor seed and black pepper on the

AJCER
B. Hammouti et al. / Arab. J. Chem. Environ. Res. 06 (2019) 12-56 56

dissolution of mild steel in sulphuric acid. Corros. Prev. Control, 29(3): 18-20 (1980).
[209] P.B. Raja, M.G. Sethuraman, Inhibitive effect of black pepper extract on the sulphuric acid
corrosion of mild steel, Materials Letters, 62(17-18): 2977-2979 (2008).
[210] D. Ladha, N. Shah, S. Thakur, M. Lone, P. Jha, Corrosion inhibition and adsorption behaviour
of black pepper extract on pure aluminum in hydrochloric acid medium: A combined
experimental and computational study, Pigment and Resin Technology 45(2): 106-118 (2016).
[211] F. Kurniawan, K. A. Madurani, Electrochemical and optical microscopy study of red pepper
seed oil corrosion inhibition by self-assembled monolayers (SAM) on 304 SS, Progress in
Organic Coatings, 88: 256-262 (2015).
[212] M. Dahmani, A. Et-Touhami, S. S. Al-Deyab, B. Hammouti, A. Bouyanzer, Corrosion
inhibition of C38 steel in 1 M HCl: A comparative study of black pepper extract and its isolated
piperine. Int. J. Electrochem. Sci., 5 (8): 1060-1069 (2010).
[213] M. Dahmani, S. S. Al-Deyab, A. Et-Touhami, B. Hammouti, A. Bouyanzer, R. Salghi, A. El
Mejdoubi, Investigation of piperanine as HCl ecofriendly corrosion inhibitors for C38 steel. Int.
J. Electrochem. Sci., 7: 2513-2522 (2012).
[214] M.E.A. Belghiti, M. Dahmani, M. Messali, Y. Karzazi, A. Et-Touhami, A. Yahyi, B.
Hammouti, Inhibitive action of piperic acid on C38 steel corrosion in HCl solution, Der Pharma
Chemica, 7(6): 116-125 (2015).
[215] M. Dahmani, A. Ettouhami, B. El Bali, A. Yahyi, C. Wilson, K. Ullah, H. Elmsellem, Organotin
(IV) derivative of Piperic acid and Phenylthioacetic acid: Synthesis, Crystal structure,
Spectroscopic characterizations and Biological activities. Moroccan Journal of Chemistry, 8(1):
8-1 (2019).

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