Cannabinoids by www.benzo-fury.me.uk

Filed under Cannabinoids by admin

 

Cannabinoids are a class of chemical compounds which include the phytocannabinoids (oxygen-containing C21 aromatic hydrocarbon compounds found in the cannabis plant), and chemical compounds which mimic the actions of phytocannabinoids or have a similar structure (e.g. endocannabinoids, found in the nervous and immune systems of animals and that activate cannabinoid receptors). The most notable of the cannabinoids is ?9-tetrahydrocannabinol (?9-THC—the primary psychoactive compound of cannabis).

 

Synthetic cannabinoids encompass a variety of distinct chemical classes: the classical cannabinoids structurally related to THC, the nonclassical cannabinoids including the aminoalkylindoles, 1,5-diarylpyrazoles, quinolines and arylsulphonamides, as well as eicosanoids related to the endocannabinoids.

 

 

 

Cannabinoid receptors

 

Before the 1980s, it was often speculated that cannabinoids produced their physiological and behavioral effects via nonspecific interaction with cell membranes, instead of interacting with specific membrane-bound receptors. The discovery of the first cannabinoid receptors in the 1980s helped to resolve this debate. These receptors are common in animals, and have been found in mammals, birds, fish, and reptiles. At present, there are two known types of cannabinoid receptors, termed CB1 and CB2, with mounting evidence of more. In a recent study it has been found that humans have these receptors as well.

 

 

 

Cannabinoid receptor type 1

 

CB1 receptors are found primarily in the brain, to be specific in the basal ganglia and in the limbic system, including the hippocampus. They are also found in the cerebellum and in both male and female reproductive systems. CB1 receptors are absent in the medulla oblongata, the part of the brain stem responsible for respiratory and cardiovascular functions. Thus, there is not the risk of respiratory or cardiovascular failure that can be produced by some drugs. CB1 receptors appear to be responsible for the euphoric and anticonvulsive effects of cannabis.

 

 

 

 

 

Cannabinoid receptor type 2

 

CB2 receptors are predominantly found in the immune system, or immune-derived cells with the greatest density in the spleen. While found only in the peripheral nervous system, a report does indicate that CB2 is expressed by a subpopulation of microglia in the human cerebellum .CB2 receptors appear to be responsible for the anti-inflammatory and possibly other therapeutic effects of cannabis.

 

 

 

Phytocannabinoids

 

Phytocannabinoids, also called natural cannabinoids, herbal cannabinoids, and classical cannabinoids, are only known to occur naturally in significant quantity in the cannabis plant, and are concentrated in a viscous resin that is produced in glandular structures known as trichomes. In addition to cannabinoids, the resin is rich in terpenes, which are largely responsible for the odour of the cannabis plant.

 

Phytocannabinoids are nearly insoluble in water but are soluble in lipids, alcohols, and other non-polar organic solvents. However, as phenols, they form more water-soluble phenolate salts under strongly alkaline conditions.

 

All-natural cannabinoids are derived from their respective 2-carboxylic acids (2-COOH) by decarboxylation (catalyzed by heat, light, or alkaline conditions).

 

 

 

Types

 

At least 85 cannabinoids have been isolated from the cannabis plant[7] To the right the main classes of natural cannabinoids are shown. All classes derive from cannabigerol-type compounds and differ mainly in the way this precursor is cyclized.

 

Tetrahydrocannabinol (THC), cannabidiol (CBD) and cannabinol (CBN) are the most prevalent natural cannabinoids and have received the most study. Other common cannabinoids are listed below:

 

* CBG Cannabigerol

* CBC Cannabichromene

* CBL Cannabicyclol

* CBV Cannabivarin

* THCV Tetrahydrocannabivarin

* CBDV Cannabidivarin

* CBCV Cannabichromevarin

* CBGV Cannabigerovarin

* CBGM Cannabigerol Monoethyl Ether

Type      Skeleton              Cyclization

Cannabigerol-type

CBG        Chemical structure of a CBG-type cannabinoid.                 Chemical structure of the CBG-type cyclization of cannabinoids.

Cannabichromene-type

CBC        Chemical structure of a CBC-type cannabinoid.                 Chemical structure of the CBC-type cyclization of cannabinoids.

Cannabidiol-type

CBD        Chemical structure of a CBD-type cannabinoid.                 Chemical structure of the CBD-type cyclization of cannabinoids.

Tetrahydrocannabinol-

and

Cannabinol-type

THC, CBN             Chemical structure of a CBN-type cannabinoid.                Chemical structure of the CBN-type cyclization of cannabinoids.

Cannabielsoin-type

CBE        Chemical structure of a CBE-type cannabinoid.                 Chemical structure of the CBE-type cyclization of cannabinoids.

iso-

Tetrahydrocannabinol-

type

iso-THC                Chemical structure of an iso-CBN-type cannabinoid.      Chemical structure of the iso-CBN-type cyclization of cannabinoids.

Cannabicyclol-type

CBL         Chemical structure of a CBL-type cannabinoid. Chemical structure of the CBL-type cyclization of cannabinoids.

Cannabicitran-type

CBT        Chemical structure of a CBT-type cannabinoid.                 Chemical structure of the CBT-type cyclization of cannabinoids.

Main classes of natural cannabinoids

 

Tetrahydrocannabinol

 

Tetrahydrocannabinol (THC) is the primary psychoactive component of the plant. It appears to ease moderate pain (analgetic) and to be neuroprotective. THC has approximately equal affinity for the CB1 and CB2 receptors.

 

Delta-9-Tetrahydrocannabinol (?9-THC, THC) and delta-8-tetrahydrocannabinol (?8-THC), mimic the action of anandamide, a neurotransmitter produced naturally in the body. The THCs produce the high associated with cannabis by binding to the CB1 cannabinoid receptors in the brain.

 

 

 

Cannabidiol

 

Cannabidiol (CBD) is not particularly psychoactive in and of itself, and was thought not to affect the psychoactivity of THC. However, recent evidence shows that smokers of cannabis with a higher CBD/THC ratio were less likely to experience schizophrenia-like symptoms.This is supported by psychological tests, in which participants experience less intense psychotic-like effects when intravenous THC was co-administered with CBD (as measured with a PANSS test). Cannabidiol has no affinity for CB1 and CB2 receptors but acts as an indirect antagonist of cannabinoid agonists. Recently it was found to be an antagonist at the putative new cannabinoid receptor, GPR55, a GPCR expressed in the caudate nucleus and putamen. Cannabidiol has also been shown to act as a 5-HT1A receptor agonist, an action which is involved in its antidepressant, anxiolytic, and neuroprotective effects.

 

It appears to relieve convulsion, inflammation, anxiety, and nausea. CBD has a greater affinity for the CB2 receptor than for the CB1 receptor.

 

CBD shares a precursor with THC and is the main cannabinoid in low-THC Cannabis strains. CBD apparently plays a role in preventing the short-term memory loss associated with THC in mammals.

 

Cannabinol

 

Cannabinol (CBN) is the primary product of THC degradation, and there is usually little of it in a fresh plant. CBN content increases as THC degrades in storage, and with exposure to light and air. It is only mildly psychoactive. Its affinity to the CB2 receptor is higher than for the CB1 receptor.

 

 

 

Cannabigerol

 

Cannabigerol (CBG) is non-psychotomimetic but still affects the overall effects of Cannabis. It acts as an a2-adrenergic receptor agonist, 5-HT1A receptor antagonist, and CB1 receptor antagonist.[22] It also binds to the CB2 receptor.

 

 

 

Tetrahydrocannabivarin

 

Tetrahydrocannabivarin (THCV) is prevalent in certain South African and Southeast Asian strains of Cannabis. It is an antagonist of THC at CB1 receptors and attenuates the psychoactive effects of THC.

 

Cannabichromene

 

Cannabichromene (CBC) is non-psychoactive and does not affect the psychoactivity of THC .

 

 

 

Double bond position

 

In addition, each of the compounds above may be in different forms depending on the position of the double bond in the alicyclic carbon ring. There is potential for confusion because there are different numbering systems used to describe the position of this double bond. Under the dibenzopyran numbering system widely used today, the major form of THC is called ?9-THC, while the minor form is called ?8-THC. Under the alternate terpene numbering system, these same compounds are called ?1-THC and ?6-THC, respectively.

 

 

 

Length

 

Most herbal cannabinoid compounds are 21-carbon compounds. However, some do not follow this rule, primarily because of variation in the length of the side-chain attached to the aromatic ring. In THC, CBD, and CBN, this side-chain is a pentyl (5-carbon) chain. In the most common homologue, the pentyl chain is replaced with a propyl (3-carbon) chain. Cannabinoids with the propyl side-chain are named using the suffix varin, and are designated, for example, THCV, CBDV, or CBNV.

 

 

 

 

 

Plant profile

 

Cannabis plants can exhibit wide variation in the quantity and type of cannabinoids they produce. The mixture of cannabinoids produced by a plant is known as the plant’s cannabinoid profile. Selective breeding has been used to control the genetics of plants and modify the cannabinoid profile. For example, strains that are used as fiber (commonly called hemp) are bred such that they are low in psychoactive chemicals like THC. Strains used in medicine are often bred for high CBD content, and strains used for recreational purposes are usually bred for high THC content or for a specific chemical balance.

 

Quantitative analysis of a plant’s cannabinoid profile is usually determined by gas chromatography (GC), or more reliably by gas chromatography combined with mass spectrometry (GC/MS). Liquid chromatography (LC) techniques are also possible, although these are often only semi-quantitative or qualitative. There have been systematic attempts to monitor the cannabinoid profile of cannabis over time, but their accuracy is impeded by the illegal status of the plant in many countries.

 

 

 

Pharmacology

 

Cannabinoids can be administered by smoking, vaporizing, oral ingestion, transdermal patch, intravenous injection, sublingual absorption, or rectal suppository. Once in the body, most cannabinoids are metabolized in the liver, especially by cytochrome P450 mixed-function oxidases, mainly CYP 2C9. Thus supplementing with CYP 2C9 inhibitors leads to extended intoxication.

 

Some is also stored in fat in addition to being metabolized in liver. ?9-THC is metabolized to 11-hydroxy-?9-THC, which is then metabolized to 9-carboxy-THC. Some cannabis metabolites can be detected in the body several weeks after administration. These metabolites are the chemicals recognized by common antibody-based “drug tests”; in the case of THC et al., these loads do not represent intoxication (compare to ethanol breath tests which measure instantaneous blood alcohol levels) but an integration of past consumption over an approximately month-long window.

 

 

 

 

 

Plant synthesis

 

Cannabinoid production starts when an enzyme causes geranyl pyrophosphate and olivetolic acid to combine and form CBG. Next, CBG is independently converted to either CBD or CBC by two separate synthase enzymes. CBD is then enzymatically cyclized to THC. For the propyl homologues (THCV, CBDV and CBNV), there is a similar pathway that is based on CBGV.

 

 

 

 

 

Separation

 

Cannabinoids can be separated from the plant by extraction with organic solvents. Hydrocarbons and alcohols are often used as solvents. However, these solvents are flammable and many are toxic. Butane may be used, which evaporates extremely quickly. Supercritical solvent extraction with carbon dioxide is an alternative technique. Although this process requires high pressures (73 atmospheres or more), there is minimal risk of fire or toxicity, solvent removal is simple and efficient, and extract quality can be well-controlled. Once extracted, cannabinoid blends can be separated into individual components using wiped film vacuum distillation or other distillation techniques. However, to produce high purity cannabinoids, chemical synthesis or semisynthesis is generally required.

 

 

 

History

 

Cannabinoids were first discovered in the 1940s, when CBD and CBN were identified. The structure of THC was first determined in 1964.

 

Due to molecular similarity and ease of synthetic conversion, CBD was originally believed to be a natural precursor to THC. However, it is now known that CBD and THC are produced independently in the cannabis plant.

 

 

 

Endocannabinoids

 

Anandamide, an endogenous ligand of CB1 and CB2

 

 

 

Endocannabinoids are substances produced from within the body that activate cannabinoid receptors. After the discovery of the first cannabinoid receptor in 1988, scientists began searching for an endogenous ligand for the receptor.

 

 

 

Types of endocannabinoid ligands

 

* Arachidonoylethanolamine (Anandamide or AEA)

 

In 1992, in Raphael Mechoulam’s Israeli lab, the first such compound was identified as arachidonoyl ethanolamine and named anandamide, a name derived from the Sanskrit word for bliss and -amide. Anandamide is derived from the essential fatty acid arachidonic acid. It has a pharmacology similar to THC, although its chemical structure is different. Anandamide binds to the central (CB1) and, to a lesser extent, peripheral (CB2) cannabinoid receptors, where it acts as a partial agonist. Anandamide is about as potent as THC at the CB1 receptor. It is found in nearly all tissues in a wide range of animals.

 

Two analogs of anandamide, 7,10,13,16-docosatetraenoylethanolamide and homo-?-linolenoylethanolamine, have similar pharmacology. All of these are members of a family of signalling lipids called N-acylethanolamides, which also includes the noncannabimimetic palmitoylethanolamide and oleoylethanolamine, which possess anti-inflammatory and orexigenic effects, respectively. Many N-acylethanolamines have also been identified in plant seeds and in molluscs.

 

* 2-arachidonoyl glycerol (2-AG)

 

Another endocannabinoid, 2-arachidonoyl glycerol, binds to both the CB1 and CB2 receptors with similar affinity, acting as a full agonist at both. 2-AG is present at significantly higher concentrations in the brain than anandamide, and there is some controversy over whether 2-AG rather than anandamide is chiefly responsible for endocannabinoid signalling in vivo. In particular, one in vitro study suggests that 2-AG is capable of stimulating higher G-protein activation than anandamide, although the physiological implications of this finding are not yet known.

 

* 2-arachidonyl glyceryl ether (noladin ether)

 

In 2001, a third, ether-type endocannabinoid, 2-arachidonyl glyceryl ether (noladin ether), was isolated from porcine brain. Prior to this discovery, it had been synthesized as a stable analog of 2-AG; indeed, some controversy remains over its classification as an endocannabinoid, as another group failed to detect the substance at “any appreciable amount” in the brains of several different mammalian species. It binds to the CB1 cannabinoid receptor (Ki = 21.2 nmol/L) and causes sedation, hypothermia, intestinal immobility, and mild antinociception in mice. It binds primarily to the CB1 receptor, and only weakly to the CB2 receptor.

 

* N-arachidonoyl-dopamine (NADA)

 

Discovered in 2000, NADA preferentially binds to the CB1 receptor. Like anandamide, NADA is also an agonist for the vanilloid receptor subtype 1 (TRPV1), a member of the vanilloid receptor family.

 

* Virodhamine (OAE)

 

A fifth endocannabinoid, virodhamine, or O-arachidonoyl-ethanolamine (OAE), was discovered in June 2002. Although it is a full agonist at CB2 and a partial agonist at CB1, it behaves as a CB1 antagonist in vivo. In rats, virodhamine was found to be present at comparable or slightly lower concentrations than anandamide in the brain, but 2- to 9-fold higher concentrations peripherally.

 

 

 

Function

 

Endocannabinoids serve as intercellular ‘lipid messengers’, signaling molecules that are released from one cell and activating the cannabinoid receptors present on other nearby cells. Although in this intercellular signaling role they are similar to the well-known monoamine neurotransmitters, such as acetylcholine and dopamine, endocannabinoids differ in numerous ways from them. For instance, they use retrograde signaling. Furthermore, endocannabinoids are lipophilic molecules that are not very soluble in water. They are not stored in vesicles, and exist as integral constituents of the membrane bilayers that make up cells. They are believed to be synthesized ‘on-demand’ rather than made and stored for later use. The mechanisms and enzymes underlying the biosynthesis of endocannabinoids remain elusive and continue to be an area of active research.

 

The endocannabinoid 2-AG has been found in bovine and human maternal milk.

 

 

 

Retrograde signal

 

Conventional neurotransmitters are released from a ‘presynaptic’ cell and activate appropriate receptors on a ‘postsynaptic’ cell, where presynaptic and postsynaptic designate the sending and receiving sides of a synapse, respectively. Endocannabinoids, on the other hand, are described as retrograde transmitters because they most commonly travel ‘backwards’ against the usual synaptic transmitter flow. They are, in effect, released from the postsynaptic cell and act on the presynaptic cell, where the target receptors are densely concentrated on axonal terminals in the zones from which conventional neurotransmitters are released. Activation of cannabinoid receptors temporarily reduces the amount of conventional neurotransmitter released. This endocannabinoid mediated system permits the postsynaptic cell to control its own incoming synaptic traffic. The ultimate effect on the endocannabinoid-releasing cell depends on the nature of the conventional transmitter being controlled. For instance, when the release of the inhibitory transmitter GABA is reduced, the net effect is an increase in the excitability of the endocannabinoid-releasing cell. On the converse, when release of the excitatory neurotransmitter glutamate is reduced, the net effect is a decrease in the excitability of the endocannabinoid-releasing cell.

 

 

 

Range

 

Endocannabinoids are hydrophobic molecules. They cannot travel unaided for long distances in the aqueous medium surrounding the cells from which they are released, and therefore act locally on nearby target cells. Hence, although emanating diffusely from their source cells, they have much more restricted spheres of influence than do hormones, which can affect cells throughout the body.

Other thoughts

 

Endocannabinoids constitute a versatile system for affecting neuronal network properties in the nervous system.

 

Scientific American published an article in December 2004, entitled “The Brain’s Own Marijuana” discussing the endogenous cannabinoid system.

 

The current understanding recognizes the role that endocannabinoids play in almost every major life function in the human body.

 

 

 

U.S. Patent # 6630507

 

In 2003 The U.S.A.’s Government as represented by the Department of Health and Human Services was awarded a patent on cannabinoids as antioxidants and neuroprotectants. U.S. Patent 6630507.

 

 

 

 

 

Synthetic and patented cannabinoids

 

Historically, laboratory synthesis of cannabinoids were often based on the structure of herbal cannabinoids, and a large number of analogs have been produced and tested, especially in a group led by Roger Adams as early as 1941 and later in a group led by Raphael Mechoulam. Newer compounds are no longer related to natural cannabinoids or are based on the structure of the endogenous cannabinoids.

 

Synthetic cannabinoids are particularly useful in experiments to determine the relationship between the structure and activity of cannabinoid compounds, by making systematic, incremental modifications of cannabinoid molecules.

 

Medications containing natural or synthetic cannabinoids or cannabinoid analogs:

 

* Dronabinol (Marinol), is ?9-tetrahydrocannabinol (THC), used as an appetite stimulant, anti-emetic, and analgesic

* Nabilone (Cesamet), a synthetic cannabinoid and an analog of Marinol. It is Schedule II unlike Marinol, which is Schedule III

* Sativex, a cannabinoid extract oral spray containing THC, CBD, and other cannabinoids used for neuropathic pain and spasticity in 22 countries including England, Canada and Spain. Sativex develops whole-plant cannabinoid medicines

* Rimonabant (SR141716), a selective cannabinoid (CB1) receptor inverse agonist used as an anti-obesity drug under the proprietary name Acomplia. It is also used for smoking cessation

 

Other notable synthetic cannabinoids include:

 

* JWH-018, a potent synthetic cannabinoid agonist discovered by Dr. John W. Huffman at Clemson University. It is being increasingly sold in legal smoke blends collectively known as “spice”. Several countries and states have moved to ban it legally.

* CP-55940, produced in 1974, this synthetic cannabinoid receptor agonist is many times more potent than THC.

* Dimethylheptylpyran

* HU-210, about 100 times as potent as THC

* HU-331 a potential anti-cancer drug derived from cannabidiol that specifically inhibits topoisomerase II.

* SR144528, a CB2 receptor antagonist

* WIN 55,212-2, a potent cannabinoid receptor agonist

* JWH-133, a potent selective CB2 receptor agonist

* Levonantradol (Nantrodolum), an anti-emetic and analgesic but not currently in use in medicine

 

 

Table of natural cannabinoids

Cannabigerol-type (CBG)

Chemical structure of cannabigerol.Cannabigerol

(E)-CBG-C5          Chemical structure of cannabigerol monomethyl ether.Cannabigerol

monomethyl ether

(E)-CBGM-C5 A Chemical structure of cannabinerolic acid A.Cannabinerolic acid A

(Z)-CBGA-C5 A   Chemical structure of cannabigerovarin.Cannabigerovarin

(E)-CBGV-C3      

Chemical structure of cannabigerolic acid A.Cannabigerolic acid A

(E)-CBGA-C5 A   Chemical structure of cannabigerolic acid A monomethyl ether.Cannabigerolic acid A

monomethyl ether

(E)-CBGAM-C5 A               Chemical structure of cannabigerovarinic acid A.Cannabigerovarinic acid A

(E)-CBGVA-C3 A                               

Cannabichromene-type (CBC)

Chemical structure of cannabichromene.(±)-Cannabichromene

CBC-C5                 Chemical structure of cannabichromenic acid A.(±)-Cannabichromenic acid A

CBCA-C5 A          Chemical structure of cannabichromevarine.(±)-Cannabivarichromene,

(±)-Cannabichromevarin

CBCV-C3              Chemical structure of cannabichromevarinic acid A.(±)-Cannabichromevarinic

acid A

CBCVA-C3 A      

Cannabidiol-type (CBD)

Chemical structure of cannabidiol.(−)-Cannabidiol

CBD-C5                 Chemical structure of cannabidiol momomethyl ether.Cannabidiol

momomethyl ether

CBDM-C5             Chemical structure of cannabidiol-C4Cannabidiol-C4

CBD-C4                 Chemical structure of cannabidivarin.(−)-Cannabidivarin

CBDV-C3              Chemical structure of cannabidiorcol.Cannabidiorcol

CBD-C1

Chemical structure of cannabidiolic acid.Cannabidiolic acid

CBDA-C5              Chemical structure of cannabidivarinic acid.Cannabidivarinic acid

CBDVA-C3                                          

Cannabinodiol-type (CBND)

Chemical structure of cannabinodiol.Cannabinodiol

CBND-C5              Chemical structure of cannabinodivarin.Cannabinodivarin

CBND-C3                                             

Tetrahydrocannabinol-type (THC)

Chemical structure of Δ9-tetrahydrocannabinol.Δ9-Tetrahydrocannabinol

Δ9-THC-C5           Chemical structure of Δ9-tetrahydrocannabinol-C4Δ9-Tetrahydrocannabinol-C4

Δ9-THC-C4           Chemical structure of Δ9-tetrahydrocannabivarin.Δ9-Tetrahydrocannabivarin

Δ9-THCV-C3        Chemical structure of tetrahydrocannabiorcol.Δ9-Tetrahydrocannabiorcol

Δ9-THCO-C1      

Chemical structure of Δ9-tetrahydrocannabinolic acid A.Δ9-Tetrahydro-

cannabinolic acid A

Δ9-THCA-C5 A    Chemical structure of Δ9-tetrahydrocannabinolic acid B.Δ9-Tetrahydro-

cannabinolic acid B

Δ9-THCA-C5 B    Chemical structure of Δ9-tetrahydrocannabinolic acid-C4Δ9-Tetrahydro-

cannabinolic acid-C4

A and/or B

Δ9-THCA-C4 A and/or B                 Chemical structure of Δ9-tetrahydrocannabivarinic acid A.Δ9-Tetrahydro-

cannabivarinic acid A

Δ9-THCVA-C3 A                 Chemical structure of Δ9-tetrahydrocannabiorcolic acid.Δ9-Tetrahydro-

cannabiorcolic acid

A and/or B

Δ9-THCOA-C1 A and/or B

Chemical structure of Δ8-tetrahydrocannabinol.(−)-Δ8-trans-(6aR,10aR)-

Δ8-Tetrahydrocannabinol

Δ8-THC-C5           Chemical structure of Δ8-tetrahydrocannabinolic acid A.(−)-Δ8-trans-(6aR,10aR)-

Tetrahydrocannabinolic

acid A

Δ8-THCA-C5 A    Chemical structure of cis-Δ9tetrahydrocannabinol.(−)-(6aS,10aR)-Δ9-

Tetrahydrocannabinol

(−)-cis-Δ9-THC-C5                           

Cannabinol-type (CBN)

Chemical structure of cannabinol.Cannabinol

CBN-C5                 Chemical structure of cannabinol-C4Cannabinol-C4

CBN-C4                 Chemical structure of cannabivarin.Cannabivarin

CBN-C3                 Chemical structure of cannabinol-C2Cannabinol-C2

CBN-C2                 Chemical structure of cannabiorcol.Cannabiorcol

CBN-C1

Chemical structure of cannabinolic acid A.Cannabinolic acid A

CBNA-C5 A          Chemical structure of cannabinol methyl ether.Cannabinol methyl ether

CBNM-C5                                            

Cannabitriol-type (CBT)

Chemical structure of (-)-trans-cannabitriol.(−)-(9R,10R)-trans-

Cannabitriol

(−)-trans-CBT-C5              Chemical structure of (+)-trans-cannabitriol.(+)-(9S,10S)-Cannabitriol

(+)-trans-CBT-C5              Chemical structure of cis-cannabitriol.(±)-(9R,10S/9S,10R)-

Cannabitriol

(±)-cis-CBT-C5   Chemical structure of trans-cannabitriol ethyl ether.(−)-(9R,10R)-trans-

10-O-Ethyl-cannabitriol

(−)-trans-CBT-OEt-C5     Chemical structure of trans-cannabitriol-C3(±)-(9R,10R/9S,10S)-

Cannabitriol-C3

(±)-trans-CBT-C3

Chemical structure of 8,9-dihydroxy-Δ6a(10a)-tetrahydrocannabinol.8,9-Dihydroxy-Δ6a(10a)-

tetrahydrocannabinol

8,9-Di-OH-CBT-C5            Chemical structure of cannabidiolic acid A cannabitriol ester.Cannabidiolic acid A

cannabitriol ester

CBDA-C5 9-OH-CBT-C5 ester       Chemical structure of cannabiripsol.(−)-(6aR,9S,10S,10aR)-

9,10-Dihydroxy-

hexahydrocannabinol,

Cannabiripsol

Cannabiripsol-C5             Chemical structure of cannabitetrol.(−)-6a,7,10a-Trihydroxy-

Δ9-tetrahydrocannabinol

(−)-Cannabitetrol            Chemical structure of 10-oxo-Δ6a10a-tetrahydrocannabinol.10-Oxo-Δ6a(10a)-

tetrahydrocannabinol

OTHC

Cannabielsoin-type (CBE)

Chemical structure of cannabielsoin.(5aS,6S,9R,9aR)-

Cannabielsoin

CBE-C5 Chemical structure of C3-cannabielsoin.(5aS,6S,9R,9aR)-

C3-Cannabielsoin

CBE-C3 Chemical structure of cannabielsoic acid A.(5aS,6S,9R,9aR)-

Cannabielsoic acid A

CBEA-C5 A           Chemical structure of cannabielsoic acid B.(5aS,6S,9R,9aR)-

Cannabielsoic acid B

CBEA-C5 B           Chemical structure of C3-cannabielsoic acid B.(5aS,6S,9R,9aR)-

C3-Cannabielsoic acid B

CBEA-C3 B

Chemical structure of cannabiglendol-C3Cannabiglendol-C3

OH-iso-HHCV-C3              Chemical structure of dehydrocannabifuran.Dehydrocannabifuran

DCBF-C5               Chemical structure of cannabifuran.Cannabifuran

CBF-C5                 

Isocannabinoids

Chemical structure of Δ7-trans-isotetrahydrocannabinol.(−)-Δ7-trans-(1R,3R,6R)-

Isotetrahydrocannabinol             Chemical structure of Δ7-isotetrahydrocannabivarin.(±)-Δ7-1,2-cis-

(1R,3R,6S/1S,3S,6R)-

Isotetrahydro-

cannabivarin      Chemical structure of Δ7-trans-isotetrahydrocannabivarin.(−)-Δ7-trans-(1R,3R,6R)-

Isotetrahydrocannabivarin                         

Cannabicyclol-type (CBL)

Chemical structure of cannabicyclol.(±)-(1aS,3aR,8bR,8cR)-

Cannabicyclol

CBL-C5 Chemical structure of cannabicyclolic acid A.(±)-(1aS,3aR,8bR,8cR)-

Cannabicyclolic acid A

CBLA-C5 A           Chemical structure of cannabicyclovarin.(±)-(1aS,3aR,8bR,8cR)-

Cannabicyclovarin

CBLV-C3                              

Cannabicitran-type (CBT)

Chemical structure of cannabicitran.Cannabicitran

CBT-C5                                                 

Cannabichromanone-type (CBCN)

Chemical structure of cannabichromanone.Cannabichromanone

CBCN-C5              Chemical structure of cannabichromanone-C3Cannabichromanone-C3

CBCN-C3              Chemical structure of cannabicoumaronone.Cannabicoumaronone

CBCON-C5          

 

Cannabinoids

Plant cannabinoids        

 

CBCV · CBD · CBDV · CBGM · CBGV · CBN · CBG · CBV · CBL · THC · THC-C4 · THCV

Cannabinoid metabolites           

 

8,11-DiOH-THC · 11-COOH-THC · 11-OH-THC

Endogenous cannabinoids         

 

Arachidonoyl ethanolamide (Anandamide or AEA) · 2-Arachidonoylglycerol (2-AG) · 2-Arachidonyl glyceryl ether (noladin ether) · Virodhamine · Palmitoylethanolamide (PEA) · N-Arachidonoyl dopamine (NADA) · Oleamide · RVD-Hpα

Synthetic cannabinoid

receptor agonists           

Classical cannabinoids

(Dibenzopyrans)

               

 

A-40174 · A-41988 · A-42574 · Ajulemic acid · AM-087 · AM-411 · AM-855 · AM-905 · AM-906 · AM-919 · AM-926 · AM-938 · AM-4030 · AMG-1 · AMG-3 · AMG-36 · AMG-41 · Dexanabinol (HU-211) · DMHP · Dronabinol · HHC · HU-210 · JWH-051 · JWH-133 · JWH-139 · JWH-161 · JWH-229 · JWH-359 · L-759,633 · L-759,656 · Levonantradol (CP 50,5561) · Nabazenil · Nabidrox (Canbisol) · Nabilone · Nabitan · Naboctate · O-581 · O-774 · O-806 · O-823 · O-1057 · O-1125 · O-1238 · O-2365 · O-2372 · O-2373 · O-2383 · O-2426 · O-2484 · O-2545 · O-2694 · O-2715 · O-2716 · O-3226 · Parahexyl · Perrottetinene · Pirnabine · THC-O-acetate · THC-O-phosphate

Nonclassical cannabinoids

               

 

Cannabicyclohexanol · CP 47,497 · CP 55,244 · CP 55,940 · HU-308 · HU-331 · HU-336 · Nonabine · O-1376 · O-1422 · O-1601 · O-1656 · O-1657 · O-1660 · O-1871 · SPA-229 · Tinabinol · 2-Isopropyl-5-methyl-1-(2,6-dihydroxy-4-nonylphenyl)cyclohex-1-ene

Benzoylindoles

               

 

1-Pentyl-3-(4-methoxybenzoyl)indole · AM-630 · AM-679 · AM-694 · AM-1241 · AM-2233 · GW-405,833 (L-768,242) · Pravadoline · WIN 54,461

Naphthoylindoles

               

 

AM-1220 · AM-1221 · AM-1235 · AM-2201 · AM-2232 · JWH-007 · JWH-015 · JWH-018 · JWH-019 · JWH-073 · JWH-081 · JWH-098 · JWH-116 · JWH-122 · JWH-149 · JWH-164 · JWH-182 · JWH-193 · JWH-198 · JWH-200 · JWH-210 · JWH-398 · JWH-424 · WIN 55,212-2

Naphthylmethylindoles

               

 

JWH-175 · JWH-184 · JWH-185 · JWH-192 · JWH-194 · JWH-195 · JWH-196 · JWH-197 · JWH-199

Phenylacetylindoles

               

 

1-(2-Cyclohexylethyl)-3-(2-methoxyphenylacetyl)indole · JWH-167 · JWH-203 · JWH-249 · JWH-250 · JWH-251 · JWH-302

Naphthoylpyrroles

               

 

JWH-030 · JWH-147 · JWH-307

Eicosanoids

               

 

AM-883 · Arachidonyl-2′-chloroethylamide · Arachidonylcyclopropylamide · Methanandamide · O-585 · O-689 · O-1812 · O-1860 · O-1861

Others

               

 

A-796,260 · A-834,735 · A-836,339 · Abnormal cannabidiol · AM-1248 · AZ-11713908 · BAY 38-7271 · BAY 59-3074 · CB-13 · GW-842,166X · JWH-171 · JWH-176 · JTE 7-31 · Leelamine · MDA19 · O-1918 · O-2220 · Org 28312 · Org 28611 · SER-601 · VSN-16 · WIN 56,098

Allosteric modulators of

cannabinoid receptors

 

Org 27569 · Org 27759 · Org 29647

Endocannabinoid

activity enhancers          

 

AM-404 · CAY-10401 · CAY-10402 · JZL184 · JZL195 · N-arachidonoyl-serotonin · O-1624 · PF-04457845 · PF-622 · PF-750 · PF-3845 · URB-447 · URB-597 · URB-602 · URB-754 · Genistein · Arvanil · Olvanil · Kaempferol · Biochanin A

Cannabinoid receptor

antagonists and

inverse agonists              

 

AM-251 · AM-281 · AM-630 · BML-190 · CAY-10508 · CB-25 · CB-52 · CB-86 · Drinabant · Hemopressin · Ibipinabant (SLV319) · JTE-907 · LY-320,135 · Taranabant (MK-0364) · MK-9470 · NESS-0327 · O-1184 · O-1248 · O-2050 · O-2654 · Otenabant · Rimonabant (SR141716) · SR144528 · Surinabant (SR147778) · VCHSR