Towards understanding the phenytoin-like antiepileptic effect of cannabidiol

and related phytocannabinoid metabolites

Insights from molecular modeling *

István Ujváry,1, Antal Lopata2

1
iKem BT, Búza u. 32, 1033 Budapest, Hungary
2
CheMicro Ltd, Budapest, Hungary


Corresponding author: István Ujváry, PhD
iKem BT, Búza u. 32, H-1033 Budapest, Hungary
E-mail: [email protected]

Abstract
In June 2018, the US FDA approved cannabidiol (CBD), a non-psychotropic constituent of Cannabis
sativa, for the treatment of certain forms of pediatric epilepsy. The mechanism by which CBD exerts its
antiepileptic effects is not known and there is also a paucity of data on the fate and biological activity of
human metabolites of CBD. However, similarities have been noted between the anticonvulsant properties
of the antiepileptic drug phenytoin (PHT) and CBD. Herein we describe the results of molecular modeling
studies comparing the stereoelectronic properties of PHT with those of CBD and its carboxylic acid
metabolite (7-COOH-CBD), and of 7-hydroxycannabidivarin (4-OH-CBDV). The similar electrostatic
potential maps of PHT and the cannabinoid metabolites suggest analogous hydrogen bonding interactions
at a potential common target site which involve the hydantoin moiety of PHT on the one hand and the
polar functionalities of the metabolites on the other. Superposition of PHT and 7-COOH-CBD reveals
similarities in the spatial arrangement of their respective polar and hydrophobic moieties. Furthermore, as
shown by their perfect overlay, the 1-cyclohexenecarboxylic acid core of 7-COOH-CBD mimics ∆2(E)-
valproic acid, a non-teratogenic bioactive metabolite of the commonly used antiepileptic valproic acid. We
thus propose that C–7 oxidized phytocannabinoid metabolites are involved in the observed phenytoin-like
anticonvulsant effects of the parent phytocannabinoid drugs.

Keywords: anticonvulsant, cannabidiol, cannabidivarin, epilepsy, hydantoin, oxidative metabolites,

molecular modeling, phenytoin, valproic acid

*
Presented in part as a poster at the 28th Annual Symposium of the International Cannabinoid Research Society, 30 June – 6 July
2018, Leiden, The Netherlands
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INTRODUCTION
Epilepsy is one of the world’s oldest recognized diseases. It is a life-shortening, chronic
neurological disorder globally affecting over 50 million people, of which over 8 million are
below the age of 19 years.1,2 Epilepsy is characterized by partial or generalized spontaneous
seizures which sometimes are accompanied by loss of consciousness, and control of bowel and
bladder functions. Seizure episodes are repetitive and are a result of abnormal neuronal
discharges in a group of brain cells.
Since the landmark discovery by Merritt and Putnam of the anticonvulsant effect of
phenytoin (PHT; Fig. 1) 80 years ago,3 more than two dozen of clinically approved antiepileptic
drugs (AEDs) have become available and several others are under development yet definitive
treatment for epilepsy is still lacking. The currently used AEDs are known to act at one or more
targets, which include voltage- and ligand-gated ion channels, GABA or glutamate transporters or
receptors, and certain enzymes such as carbonic anhydrase.4–8 While epileptic seizures can often
be treated or prevented satisfactorily – and often affordably – by an appropriately selected AED
alone or in combination, a significant number of patients are resistant to current pharmaco-
therapies; side effects from AEDs are also common. This is the case for valproic acid (VPA; Fig.
1) which is a frequently prescribed, broad-spectrum AED but may cause serious side effects
including hepatotoxicity and teratogenicity; one of its bioactive metabolites, ∆2(E)-valproic acid
(∆2(E)-VPA; Fig. 1), however, appears to be safer.9–11 Therefore, there is an urgent need for the
development of new AEDs which are not only effective but also devoid of side effects especially
upon chronic treatment.

Figure 1. Structures of antiepileptic drugs discussed. ∆2(E)-Valproic acid is a bioactive metabolite of valproic acid.

One of the promising new antiepileptic drugs is cannabidiol (CBD, Fig. 2A), a non-
intoxicating constituent of Cannabis sativa L. CBD was first isolated in 1940,12,13 and its
structure determined in 1963.14 Being relatively safe CBD offers a wide range of therapeutic
applications.15–18 Following human clinical trials,19–21 CBD (Epidiolex®) was approved on 25
June 2018 by the US FDA for the treatment of seizures associated with Lennox-Gastaut
syndrome and Dravet syndrome in children.22 Recently, another phytocannabinoid,
cannabidivarin (CBDV; Fig. 2A), the n-propyl homologue of CBD, has also been investigated in
clinical trials.7,23
The exact mechanism of anticonvulsant action of CBD is not known. Prompted by the
pharmacological and certain structural similarities between PHT, ∆2(E)-VPA, and primary
oxidative metabolites of CBD and CBDV, we have compared by molecular modeling key
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stereoelectronic features of these substances. In this communication we survey relevant literature

and report the results of our studies.

Figure 2. Structures of phytocannabinoids (A) and some of their main metabolites (B).

Methods and materials

In brief, for calculations structural input for PHT, ∆2(E)-VPA, and CBD relied on data from earlier
crystallographic and NMR experiments as well as molecular modeling studies. Electrostatic
potential maps (EPMs) were projected onto the electron density surface of the energy minimized
molecules. The surfaces were color-coded according to the potential with electron rich regions
colored red and electron poor regions colored blue. For superpositions, alignments of the energy
minimized structures were done either by balanced steric + electrostatic fields overlays or by 3–5
atom–atom tethers. For details of methodology and additional references on previous structural
and/or molecular modeling studies with PHT and VPA and their analogues as well as on CBD,
see Supplementary material.

Phytocannabinoids as anticonvulsant agents

Preparations of various parts of hemp, C. sativa, have been used for religious, medicinal and
recreational purposes for centuries. The first methodical studies on the therapeutic properties,
including anti-seizure effects, of hemp preparations, in the form of tinctures, were carried out by
O’Shaughnessy in the late 1830s.24 By now, over 140 cannabinoids have been isolated from C.
sativa.25 Recent research has mainly focused on ∆9-tetrahydrocannabinol (THC; Fig. 2A), the
main psychoactive principle of cannabis.26,27 However, THC appears to have paradoxical pro-
and anticonvulsant effects which, along with its psychotropic properties, render this phyto-
cannabinoid unsuitable as an AED.28–30 Interestingly, 11-hydroxy-∆9-THC, which is a short-lived
psychotropic Phase I metabolite of THC, was more active with an earlier peak-effect than the
 4

parent drug as an anticonvulsant in mice suggesting its involvement in the anticonvulsant action
of THC.31
While the endocannabinoid system is known to be involved in the regulation of neuronal
network excitability,32 the multimodal anticonvulsant effects of CBD are not directly mediated by
cannabinoid receptors. In preclinical studies CBD has been shown to reduce neuronal
hyperexcitability through modulation of voltage- or ligand-gated ion channels, by blocking
orphan GPR55, by inhibiting certain enzymes, and through modulation of adenosine mediated
signalling, cytokine expression and TNFα release.15,33–36 Nevertheless, the precise mechanisms of
action(s) of CBD are yet to be elucidated. In several animal models of epilepsy, the anti-
convulsant properties of PHT and CBD have shown similarities in many, though not all,
respects.15 However, while both PHT and VPA affect voltage-gated sodium ion channels, the
action of CBD at this latter target is equivocal.36–38
Many drugs used in therapy are metabolically converted into active metabolites and
interindividual variations in the formation and fate of such active metabolites may cause
variability in the response to treatment of different individuals.39–41 Information on the human
metabolism of CBD is limited42–44 and data on its pharmacokinetics have only been recently
emerging.44–47 CBD appears to have poor bioavailability: in general, therapeutic efficacy could
only be reached with relatively high daily doses (25-50 mg per body kg for pediatric epilepsy, for
example). A large portion of administered CBD is excreted intact or as its glucuronide. Phase I
metabolism of CBD involves CYP450 isoenzymes: sequential oxidation of CBD at the 7-C atom
affords 7-hydroxy-CBD (7-OH-CBD) and 7-nor-1-carboxy-CBD (7-COOH-CBD) (Fig. 2B) as
primary human metabolites; additional biotransformations, including oxidations at multiple sites
and truncation of the n-pentyl side chain, result in >30 oxidative metabolites.42–-44 Little attention
has been paid to the biological activity of CBD metabolites.44 Anticonvulsant effects of 7-OH-
CBD and 7-hydroxycannabidivarin (7-OH-CBDV; Fig. 2B) against PTZ-induced acute seizures
in mice were claimed in a recent patent,48 while 7-OH-CBD was reported to be more effective
than CBD or 7-COOH-CBD in preventing MES-induced generalized seizures in the mouse.49

Results and discussion

Despite their apparent structural differences, certain similarity between the stereoelectronic
properties of CBD and PHT has been noted:50 each drug contains two similarly oriented
hydrophobic rings and, according to this proposal, two similarly positioned electron-donating
functionalities, that is two phenolic hydroxyls in CBD and two carbonyl groups of the hydantoin
ring in PHT. Phenytoin contains two geminal phenyl rings attached to a hydantoin core, which is
capable of both accepting (C=O) and donating (NH) hydrogen bonds at the target site. PHT is
semi-rigid and, in fact, is perfectly superimposable with the three-ring system-containing
carbamazepine, an AED also targeting the sodium ion channel.51–53
We have recently suggested that metabolites of CBD may contribute to or even responsible
for some of the pharmacological properties of the parent phytocannabinoid in vivo.44 We now
have tested by molecular modeling the hypothesis that C–7-oxidized metabolites of CBD are
 5

involved in its observed phenytoin-like effects. This hypothesis has been inspired by the reported
bioisosterism54–56 of the hydantoin ring, present in PHT, and the carboxylic acid functionality,
present in dominant human metabolites of CBD. Herein we report the results of molecular
modeling studies comparing the electrostatic and conformational features of CBD and main
phytocannabinoid metabolites with those of PHT. We also demonstrate the recently noted44
structural similarity of the branched 2-alkenecarboxylic acid ∆2(E)-VPA (Fig. 1) and the 1-cyclo-
hexenecarboxylic acid moiety of 7-COOH-CBD.
There have been several computational approaches to understand the mechanism of
antiepileptic action of PHT and VPA and their analogues but none for CBD. For PHT, CoMFA
studies have revealed that one of the hydantoin-attached phenyl rings can be replaced by alkyl
groups with a 6–7 carbon chain length being optimal for binding to voltage-gated sodium ion
channels in vitro and for anticonvulsant activity in a mouse model of epilepsy.57,58 For example,
replacement of one of the phenyl groups by a cyclohexyl ring provided a sodium ion channel
blocker with respectable activity: IC50 = 58 µM for the racemic cyclohexyl analogue versus IC50
= 40 µM for phenytoin.57 Relevant bioactivity data for the known59 5-cyclohexen-1-yl PHT
analogue, which may be considered a simplified CBD-type compound, are lacking. Interestingly,
5-(o-hydroxyphenyl)hydantoin PHT analogues were reported to have anticonvulsant activity in
the mouse.60 Pharmacophore studies on the flexible VPA and its amides acting as PHT-like anti-
convulsants though scarce established the importance of electrostatic interactions involving their
polar head-group and the requirement of at least one lipophilic moiety attached to it.51,52,61
We have hypothesized that the 7-OH- or 7-COOH moieties of primary CBD metabolites
mimic the hydantoin ring of PHT. Though the electrostatic properties of these functionalities
differ in terms of acidity, there is similarity in terms of hydrogen bonding ability: both the PHT-
hydantoin moiety (pKa = 8.3162,63), either as a lactam or as its lactim tautomer,64 and the
carboxylic acid of the CBD metabolite are capable of forming multiple hydrogen bonds. The
electrostatic similarity of ∆2(E)-VPA and of the polar head group of 7-COOH-CBD is obvious.
The pKa values for VPA and its α,β-unsaturated metabolite are 4.95 and 4.36, respectively;65
relevant data are not available for the phytocannabinoid metabolites, however, the unsubstituted
α,β-unsaturated cyclohexenecarboxylic acid, present as a core fragment in 7-COOH-CBD, has a
pKa of 3.8866 The non-acidic 7-hydroxylated metabolites may also participate in hydrogen
bonding interactions.
To shed light on the structural relatedness of PHT and the cannabinoids, various alignments
have been explored in silico. Based on the known pharmacological and the observed spatial
similarities between PHT and CBD on one hand, and on the reported hydantoin–carboxylic acid
bioisosterism on the other, we compared by molecular modeling the stereoelectronic properties of
PHT, CBD and related cannabinoid metabolites. It must be noted that the energy-minimized
structures of the molecules could not be perfectly overlaid but the relatively low rotational barrier
about the respective C(sp2)–C(sp3) pivot bonds connecting the two phenyl groups and the
hydantoin ring of PHT,53,67,68 and the resorcinol and cyclohexenyl moieties of the
cannabinoids50,69,70 render the conformation of each drug relatively flexible. First, we examined
 6

the spatial relation of PHT and CBD as proposed earlier.50 The original study pointed out the
presence of two freely rotatable hydrophobic rings in both PHT and CBD as well as the “similar
orientations and positions of the[ir] two electron-rich groups”; no superposition was, however,
attempted. In our hand, examining various overlays of the two drugs according to this proposal
satisfactory alignment was obtained only by tethering: (1) the two carbonyl oxygens of PHT and
the two resorcinol oxygens of CBD, and (2) the hydantoin C-5 atom and the cyclohexenyl C-3
atom of PHT and CBD, respectively; this alignment positioned both phenyl rings of PHT over the
limonenyl moiety of CBD (Fig. 3A). However, as seen in Fig. 3B, much better overall alignment
was obtained by tethering the respective carbonyl groups of the isosteric hydantoin and
carboxylic moieties of PHT and 7-COOH-CBD instead of the above hydantoin–resorcinol
tethering. For comparisons of the electrostatic potential surfaces of PHT and selected cannabinoid
metabolites, this latter alignment was used.

Figure 3. Alternative superpositions of PHT (gold carbon atoms) and CBD (green carbon atoms) by tethering the
hydantoin C-5 atom and the cyclohexenyl C-3 atom, and (A) by tethering the two carbonyl and resorcinol
oxygens of PHT and CBD, respectively, according to Ref. 50; or (B) by tethering the C-2 carbonyl group
of PHT and the carbonyl group of 7-COOH-CBD. Hydrogens are shown on heteroatoms only. Two views
rotated by 90° about the vertical axis.

Figure 4 shows the EPMs projected onto the electron density surface of PHT, CBD, 7-
COOH-CBD and 7-OH-CBDV. As seen, the EPMs of PHT and CBD show significant
differences. For the weak acid PHT, the hydantoin ring, which would correspond to the branched
allylic system bearing the 7-CH3 of CBD, is able to participate in multiple hydrogen bond
 7

interactions: the exposed C=O groups, as the most electron-rich regions (red), may act as
hydrogen bond acceptors while the amide/imide hydrogen atoms (blue) are available as hydrogen
bond donors. In CBD, the area around the 7-CH3 group bears essentially ‘zero potential’ (green);
the lone pairs of electrons (electron rich regions; red) of the resorcinol oxygens point toward
limonenyl moiety of CBD and appear to be buried between the two rings thus (possibly)
inaccessible for hydrogen bonding as acceptors; consequently, in the minimum-energy
conformation the two phenolic hydrogens (blue) point away from the limonenyl moiety and may
act as hydrogen bond donors only. Compared to the sterically compact PHT, the hydrophobic
pentyl side chain of CBD could occupy an additional hydrophobic cavity of the target site and
may facilitate membrane penetration also. However, the remarkable similarities in the EPMs of
the polar functionalities of PHT and 7-COOH-CBD are readily recognizable: the hydantoin
system and the carboxylic acid moiety show similar electron distribution (compare the respective
red and blue regions in Fig. 4) which supports our hypothesis on the hydantoin–carboxylic acid
bioisosterism for this pair of compounds. Likewise, the EPMs of PHT and 7-OH-CBDV also
show a certain degree of similarity around the polar functionalities (Fig. 4); the 7-OH group of
the cannabinoid metabolite can be involved in hydrogen bonding interactions though not as
extensively as a carboxylic acid species.

Figure 4. Electrostatic potential maps of PHT, CBD, 7-COOH-CBD and 7-OH-CBDV in their minimum energy
conformations.
 8

Insufficient structure-activity relationship (SAR) data preclude the formulation of a

rigorous pharmacophore model for the anticonvulsant cannabinoids. Notwithstanding, the present
study have revealed steric and electrostatic similarities between the cannabinoid metabolites and
PHT which suggest a common pharmacophore orientation shown in Fig. 3B. Accordingly: (1)
like the hydantoin ring in PHT, the exposed 7-OH or 7-COOH polar headgroups of the
cannabinoid metabolites function as hydrogen bond donors and/or acceptors; and (2) similar to
the spatial arrangement two phenyl rings in PHT, the similar positioning of the limonenyl and
substituted-aryl groups of the cannabinoids facilitate hydrophobic interactions, which are likely
strengthened by hydrogen bonds due to the phenolic hydroxyl(s) at the target site. The
importance of at least one free phenolic group in the antiseizure effect of CBD or metabolites
cannot be neglected: upon sequential O-methylation of the resorcinol moiety the activity
gradually diminishes.71
Although not related to anticonvulsant effects, it is interestingly to note that 5,5-di-
phenylhydantoins72 and related thiohydantoins73 alkylated at the imidic nitrogen atom have been
found to be CB1 receptor ligands, typically antagonists, although no data for PHT have been
reported.

Figure 5. Superposition 7-COOH-CBD (green carbon atoms) and ∆2(E)-VPA (gold carbon atoms).

We have also examined the similarity of 7-COOH-CBD and the anticonvulsant drug
metabolite ∆2(E)-VPA by superimposing their minimum-energy structures (Fig. 5). Not
surprisingly, there is an excellent overlap between the respective α,β-unsaturated (cyclo)alkenoic
acid fragments of ∆2(E)-VPA and 7-COOH-CBD. It is of note, that a molecular model-based
pharmacophore for the anticonvulsant potency and sodium ion channel binding efficiency has
been proposed for PHT, carbamazepine, and valproic acid and its amide derivatives.51,52
 9

Figure 6. Superpositions of (R,R)-CBD (green carbon atoms) and (S,S)-CBD (gold carbon atoms) based either on
balanced steric + electrostatic properties (A), or by tethering the respective C-1’, C-3’ and C-5’ resorcinol
atoms of the enantiomers (B). Hydrogen atoms are omitted.

Finally, the lack of stereoselectivity observed in mice for the anticonvulsant effect of
natural (–)-(R,R)-CBD and its synthetic (+)-(S,S)-enantiomer74–76 might be explained by a
remarkably close overlap of the two enantiomeric molecules when superimposed (Fig. 6).
Reasonably, the cyclohexene ring assumes a half-chair conformation placing the bulky resorcinol
moiety into the energetically favourable pseudo-equatorial position in both enantiomers, and this
results in their similar overall shape. Oxidative metabolites of CBD enantiomers may also attain
similar shapes which are further tuned by electrostatic interactions with the target site involved in
the anticonvulsant effects. While the effects of the trans-CBD enantiomers and their 7-OH and 7-
COOH metabolites on various components of the endocannabinoid system and other targets have
been studied,77–80 there are no pharmacological data on cis-CBD, that is the (R,S)- or (S,R)-CBD
isomers.81–83 The impact of chirality of PHT-related 5-(cyclo)alkyl-5-phenylhydantoins on
sodium ion channel pore binding has been discussed.53

CONCLUSION
Multiple lines of evidence indicate similarities between the anticonvulsant effects of PHT – and
to some extent VPA – and CBD suggesting common mechanism of action. The molecular
modeling studies presented here have revealed stereoelectronic similarities between PHT and the
C–7-oxidized metabolites of CBD and CBDV. The lack of information on the actual molecular
targets and on the structural requirements responsible for the anticonvulsant activity of CBD
precludes a comparative SAR study of established AEDs and of CBD or its metabolites and
prevents the formulation of a valid pharmacophore model. Our hypothesis can be tested, for
example, by applying the information obtained during the plethora of SAR studies of PHT and
related AEDs to CBD-type substances. It would also be of interest to devise phenytoin–CBD
hybrid molecules. Importantly, however, further studies in vitro with 7-OH and 7-COOH
metabolites of CBD and CBDV are required to establish the exact mechanism(s) responsible for
their biological activity in general and their involvement in the anticonvulsant effect of cannabis-
containing preparations in particular.
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Author Disclosure Statement

No competing financial interest.

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 15

Supplementary material

Methods and materials

For structural input for calculations in general, the molecules were manually built based on conformations
described earlier. For phenytoin (PHT), structural input used data from crystallographic1-and
computational studies,2-10 while for the structure of the valproic acid derivative data from molecular
modeling experiments were consulted.11,12 For cannabidiol (CBD), crystallographic13-15 and solution NMR
experiments,16,17 as well as molecular modeling studies16-21 provided guidance. Accordingly, the
cyclohexene moiety of CBD assumes a half-chair conformation with the resorcinol group in a pseudo-
equatorial and the isopropenyl group in an equatorial position; for calculations, the n-pentyl side chain in a
fully extended conformation was chosen. Electrostatic potential maps (EPMs) projected onto the electron
density surface of the energy minimized molecules were calculated by ωB97X-D/6-31G* density
functional method using the C-PCM continuum solvation model (water) (Spartan’16 Version 2.0.7,
Wavefunction, Inc., Irvine, CA, USA). The surfaces were color-coded according to the potential with
electron rich regions colored red and electron poor regions colored blue. Figure 4 displays the molecules
in similar orientation as derived from their overlays (as in Figure 3; vide infra) by five tethered atom pairs
of PHT and 7-COOH-CBD (atoms of the hydantoin imidic -CONH with -COOH of the CBD metabolite,
and atoms of the pivot bond connecting the hydantoin and phenyl rings of PHT or the cyclohexenyl and
aryl moieties of the cannabinoid). Superpositions shown in Figures 3, 5 and 6 were done using Discovery
Studio Visualizer 4.1 (Accelrys/BIOVIA, San Diego, CA, USA) software. The molecules were manually
built, their energy minimized (CHARMm); alignments were done either by balanced (50:50) steric +
electrostatic fields overlay or by selected atom–atom tethers according to command options in the
Structure/Superimpose/Molecular Overlay menu of the software. Hydrogen atoms are omitted except
where indicated.

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 16

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