phenylacetic acid (Q410842)

DrugBank

17 November 2015

Phenylessigsäure.svg
255 × 116; 7 KB

1 reference

German Wikipedia

mass

136.052 dalton

1 reference

PHENYLACETIC ACID (English)

19 October 2016

chemical formula

C₈H₈O₂

1 reference

PHENYLACETIC ACID (English)

19 November 2016

canonical SMILES

C1=CC=C(C=C1)CC(=O)O

1 reference

PHENYLACETIC ACID (English)

19 November 2016

density

1.228 gram per cubic centimetre

1 reference

https://ru.wikipedia.org/?oldid=100126866

Russian Wikipedia

Wikimedia import URL

melting point

77.8±0.8 degree Celsius

1 reference

https://ru.wikipedia.org/?oldid=100617659

Russian Wikipedia

Wikimedia import URL

77.5 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

77 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

found in taxon

Osmorhiza aristata

1 reference

Studies on the Constituents of Osmorhiza aristata (THUNB.) MAKINO et YABE

Pinus edulis

1 reference

Comparative GLC-MS Analysis of Phenolic Acids of Selected Tree Nuts

Juglans cinerea

1 reference

Comparative GLC-MS Analysis of Phenolic Acids of Selected Tree Nuts

Carya ovata

1 reference

Comparative GLC-MS Analysis of Phenolic Acids of Selected Tree Nuts

Juglans nigra

1 reference

Comparative GLC-MS Analysis of Phenolic Acids of Selected Tree Nuts

Castanea mollissima

1 reference

Comparative GLC-MS Analysis of Phenolic Acids of Selected Tree Nuts

Castanea dentata

1 reference

Comparative GLC-MS Analysis of Phenolic Acids of Selected Tree Nuts

Biscogniauxia mediterranea

1 reference

Biscopyran, a phytotoxic hexasubstituted pyranopyran produced by Biscogniauxia mediterranea, a fungus pathogen of cork oak.

Escherichia coli

2 references

Expression of the Arthrobacter viscosus penicillin G acylase gene in Escherichia coli and Bacillus subtilis

A comprehensive genome-scale reconstruction of Escherichia coli metabolism--2011.

Artemisia judaica

1 reference

The Essential Oil of Artemisia judaica L. from the Sinai and Negev Deserts. Aromatic Plants of the Holy Land and the Sinai, Part II

Aspergillus niger

1 reference

A new fatty acid methyl ester and other biologically active compounds from Aspergillus niger

Jeotgalibacillus marinus

1 reference

Chemical constituents of halophilic facultatively anaerobic bacteria, 1.

Bellis perennis

1 reference

Acetylenes and terpenoids of Bellis perennis

Calyx podatypa

1 reference

New and known diketopiperazines from the Caribbean sponge, Calyx cf. podatypa.

Duboisia leichhardtii

1 reference

Phenyllactic acid in Duboisia leichhardtii root cultures B feeding of phenyl[1-14C]alanine

Fragaria

1 reference

Organic acids from fresh California strawberries

Colletotrichum gloeosporioides

1 reference

Isolation of Phenylacetic Acid and Indoleacetic Acid from a Phytopathogenic Fungus,Glomerella cingulata

Lupinus angustifolius

1 reference

Phenolic compounds isolated from bitter lupine seeds and their inhibitory effects on germination and seedling growth of lettuce

Nicotiana tabacum

1 reference

Two new acidic constituents of flue-cured Virginia tobacco

Pelargonium graveolens

1 reference

Analysis of the acid fraction of reunion geranium oil (Pelargonium graveolens L'Her. ex Ait)

Penicillium herquei

1 reference

Hualyzin, a symmetrical urea derivative isolated from Penicillium herquei isolate GA4.

Phycopsis

1 reference

Phycopsisenone, a New Phenolic Secondary Metabolite from the Sponge Phycopsis sp.

Seuratia

1 reference

Phycopsisenone, a New Phenolic Secondary Metabolite from the Sponge Phycopsis sp.

Piper nigrum

1 reference

Pepper Analysis, Composition of Volatile Oil of Black Pepper, Piper nigrum

Plumeria rubra

1 reference

Volatile components of plumeria flowers. Part 2.1 Plumeria rubra L. cv. ‘Irma Bryan’

Pogonomyrmex rugosus

1 reference

Phenylalkenals in ponerine(Leptogenys sp.) and myrmicine (Pogonomyrmex sp.) ants

Tropaeolum majus

1 reference

Identification and quantification of three active auxins in different tissues of Tropaeolum majus

maize

1 reference

Phenylacetic acid as a phytotoxic compound of corn pollen

Jacaranda glabra

1 reference

Jacaranone-derived glucosidic esters from Jacaranda glabra and their activity against Plasmodium falciparum

Stachylidium

1 reference

Stachylines A-D from the sponge-derived fungus Stachylidium sp.

Ceratocystis ips

1 reference

The chemistry of the blue stain fungi. Part 1. Some metabolites of Ceratocystis species associated with mountain pine beetle infected lodgepole pine

Gryllotalpa orientalis

1 reference

In vitro cytotoxic potential on human cancer cells and chemical constituents of Gryllotalpa orientalis

Peltostigma guatemalense

1 reference

Biological activity of secondary metabolites from Peltostigma guatemalense.

Penicillium digitatum

1 reference

Penicillium digitatum metabolites on synthetic media and citrus fruits.

Penicillium oxalicum

1 reference

A new xanthone from Penicillium oxalicum

Phallus impudicus

1 reference

[Odorous substances of Phallus impudicus L 18. Report on fungi contents]

Saussurea superba

1 reference

Chemical constituents of Saussurea superba

Homo sapiens

2 references

Recon 2.2: from reconstruction to model of human metabolism

A community-driven global reconstruction of human metabolism.

Anthyllis subsimplex

1 reference

Waxes, triterpenes and free acids in Anthyllis sericea

Houttuynia cordata

1 reference

An Effective Quality Control of Pharmacologically Active Volatiles of Houttuynia cordata Thunb by Fast Gas Chromatography-Surface Acoustic Wave Sensor.

Streptomyces malachitofuscus

10 references

Identification, isolation and optimization of antifungal metabolites from the Streptomyces Malachitofuscus ctf9.

Identification, isolation and optimization of antifungal metabolites from the Streptomyces Malachitofuscus ctf9.

Identification, isolation and optimization of antifungal metabolites from the Streptomyces Malachitofuscus ctf9.

Identification, isolation and optimization of antifungal metabolites from the Streptomyces Malachitofuscus ctf9.

Identification, isolation and optimization of antifungal metabolites from the Streptomyces Malachitofuscus ctf9.

Identification, isolation and optimization of antifungal metabolites from the Streptomyces Malachitofuscus ctf9.

Identification, isolation and optimization of antifungal metabolites from the Streptomyces Malachitofuscus ctf9.

Identification, isolation and optimization of antifungal metabolites from the Streptomyces Malachitofuscus ctf9.

Identification, isolation and optimization of antifungal metabolites from the Streptomyces Malachitofuscus ctf9.

Identification, isolation and optimization of antifungal metabolites from the Streptomyces Malachitofuscus ctf9.

Streptomyces chrestomyceticus

1 reference

Inhibition of Biofilm and Virulence Factors of Candida albicans by Partially Purified Secondary Metabolites of Streptomyces chrestomyceticus Strain ADP4

Streptomyces xiamenensis

1 reference

Chemical constituents from the deep sea-derived Streptomyces xiamenensis MCCC 1A01570 and their effects on RXRα transcriptional regulation

Streptomyces humidus

1 reference

Isolation and in vivo and in vitro antifungal activity of phenylacetic acid and sodium phenylacetate from Streptomyces humidus

Caenorhabditis elegans

1 reference

Modeling Meets Metabolomics-The WormJam Consensus Model as Basis for Metabolic Studies in the Model Organism

Carica papaya

1 reference

Volatile components of papaya (Carica papaya L., Solo variety)

Eucalyptus leucoxylon

1 reference

Composition of Australian Honey Extractives. 1. Norisoprenoids, Monoterpenes, and Other Natural Volatiles from Blue Gum (Eucalyptus leucoxylon) and Yellow Box (Eucalyptus melliodora) Honeys

Eucalyptus melliodora

1 reference

Composition of Australian Honey Extractives. 1. Norisoprenoids, Monoterpenes, and Other Natural Volatiles from Blue Gum (Eucalyptus leucoxylon) and Yellow Box (Eucalyptus melliodora) Honeys

subject has role

antineoplastic antimetabolite

1 reference

Medical Subject Headings

15 March 2018

0 references

0 references

0 references

Phenylacetic acid

0 references

Identifiers

GND ID

4174235-7

1 reference

InChI=1S/C8H8O2/c9-8(10)6-7-4-2-1-3-5-7/h1-5H,6H2,(H,9,10)

German Wikipedia

InChI

1 reference

PHENYLACETIC ACID (English)

19 November 2016

2 references

PHENYLACETIC ACID (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

103-82-2

2 references

phenylacetic acid (English)

19 November 2016

https://commonchemistry.cas.org/detail?cas_rn=103-82-2

8 April 2021

1 reference

Phenylacetic acid (English)

19 November 2016

2 references

PHENYLACETIC ACID (English)

19 November 2016

Reaxys registry number

1099647

1 reference

phenylacetic acid (English)

19 October 2016

Gmelin number

68976

0 references

ChEBI ID

30745

mapping relation type

2 references

PHENYLACETIC ACID (English)

19 November 2016

International Chemical Identifier

InChI

InChI=1S/C8H8O2/c9-8(10)6-7-4-2-1-3-5-7/h1-5H,6H2,(H,9,10)

1 reference

PHENYLACETIC ACID (English)

19 November 2016

2 references

inferred from InChIKey

MSBNK-Fac_Eng_Univ_Tokyo-JP009209

1 reference

MassBank accession ID

0 references

MSBNK-Metabolon-MT000056

0 references

SPLASH

splash10-0006-9000000000-6ca33b098558bf13801c

0 references

splash10-000i-0900000000-f898aafe4cecc87d26f1

0 references

splash10-0006-9700000000-43e86e45beae2fa6704f

0 references

splash10-0006-9700000000-c07461cdad68959aa53f

0 references

splash10-0006-9100000000-1e23fd8e6ce900cd8e4c

0 references

NMRShiftDB structure ID

10005843

1 reference

Hazardous Substances Data Bank

0 references

0 references

1 reference

28 October 2019

Phenylacetic acid (English)

10 May 2021

2 references

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

0 references

0 references

1 reference

phenylacetic acid (English)

ECHA Substance Infocard ID

19 November 2016

100.002.862

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.002.862

27 December 2018

Phenylacetic acid (English)

quotation

CAS no.: 103-82-2 (English)

FL number

08.038

1 reference

quotation

CAS no.: 103-82-2 (English)

23 January 2021

08.038

1 reference

28 December 2019

PHENYLACETIC ACID (English)

quotation

CAS no.: 103-82-2 (English)

1 reference

0 references

1 reference

Medical Subject Headings

14 March 2018

1 reference

phenylacetic acid (English)

19 November 2016

DrugBank ID

DB09269

1 reference

Human Metabolome Database ID

HMDB0000209

2 references

based on heuristic

inferred from InChIKey

3 references

phenylacetic acid (English)

19 October 2016

based on heuristic

inferred from InChIKey

2 references

phenylacetic acid (English)

19 November 2016

0 references

1 reference

1 reference

Immune Epitope Database and Analysis Resource

Phenylacetic acid (English)

19 January 2016

1 reference

1 March 2022

0 references

1 reference

6 April 2020

Encyclopædia Britannica Online ID

science/phenylacetic-acid

subject named as

phenylacetic acid

0 references

1 reference

28 October 2013

Great Russian Encyclopedia portal ID

feniluksusnaia-kislota-c6b42a

0 references

JECFA number

1007

1 reference

Evaluations of the Joint FAO/WHO Expert Committee on Food Additives (JECFA)

JSTOR topic ID (archived)

13 May 2021

phenylacetates

0 references

Microsoft Academic ID

0 references

1 reference

26 January 2022

https://docs.openalex.org/download-snapshot/snapshot-data-format

1 reference

1FXH (English)

19 October 2016

1 reference

2INE (English)

19 October 2016

1 reference

1K5Q (English)

19 October 2016

1 reference

2ISF (English)

19 October 2016

1 reference

1PNL (English)

19 October 2016

1 reference

2Y4N (English)

19 October 2016

1 reference

3IXL (English)

19 October 2016

1 reference

4YFB (English)

19 October 2016

1 reference