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Comparison of phytocannabinoids

Cannabinoids (/kəˈnæbənɔɪdzˌ ˈkænəbənɔɪdz/) are compounds found in the cannabis plant or synthetic compounds that can interact with the endocannabinoid system.^[1]^[2] The most notable cannabinoid is the phytocannabinoid tetrahydrocannabinol (THC) (Delta-9-THC), the primary intoxicating compound in cannabis.^[3]^[4] Cannabidiol (CBD) is another major constituent of some cannabis plants.^[5] Conversion of CBD to THC can occur when CBD is heated to temperatures between 250–300 °C (480 to 570°F), potentially leading to its partial transformation into THC.^[6]

At least 113 distinct cannabinoids have been isolated from cannabis.^[7] This article gives comparative structures of some of the more common natural and synthetic cannabinoids, as well as showing structures of legally banned and sanctioned cannabinoids.

Structures

Cannabinoid	2D Structure	3D Structure
CBC
CBCV
CBD
CBDD
CBDH
CBDO
CBDP
CBDV
CBE
CBG
CBGV
CBL
CBN
CBND
CBTC
CBV
delta-3-THC
delta-4-THC
delta-7-THC
delta-8-THC
delta-10-THC
delta-11-THC
THC
THCC
THCB
THCH
THCP
THCV

Legality

Cannabinoid	Quasi-psychedelic	Drug precursor	Legal status
CBCA, CBC			Legal in most countries
CBCVA, CBCV
CBDA, CBD	No	THC^[6]	See Cannabidiol § Legal status
CBDD
CBDH
CBDO
CBDPA, CBDP
CBDVA, CBDV
CBEA, CBE
CBGA, CBG
CBGVA, CBGV
CBLA, CBL
CBNA, CBN
CBNDA, CBND
CBTA, CBT
CBVA, CBV
delta-3-THC	Yes		Legal in most countries
delta-4-THC	Yes		Legal in most countries
delta-7-THC	Yes		Legal in most countries
delta-8-THC	Yes		Legal in most countries
delta-10-THC	Yes		Legal in most countries
delta-11-THC	Yes		Legal in most countries
THCA, THC	Yes		UN Convention on Psychotropic Substances
THCB
THCCA, THCC
THCH	Yes		Legal in most countries
THCPA, THCP	Yes		Legal in most countries
THCVA, THCV

Thermal properties

Conversion temperatures

Main article: Conversion of CBD to THC

Cyclization reaction	Temperature
CBD → THC	250 °C (482 °F) to 300 °C (572 °F)^[6]

Decarboxylation temperatures

All cannabinoids listed here and their acids are found naturally in the plant to varying degrees.

Decarboxylation reaction	Temperature
CBCA → CBC
CBCVA → CBCV
CBDA → CBD
CBDPA → CBDP
CBDVA → CBDV
CBEA → CBE
CBGA → CBG
CBGVA → CBGV
CBLA → CBL
CBNA → CBN
CBNDA → CBND
CBTA → CBT
CBVA → CBV
THCA → THC	230 °F (110 °C) to 250 °F (121 °C)^[8]^[9]
THCCA → THCC
THCPA → THCP
THCVA → THCV

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Upon heating, cannabinoid acids decarboxylate to give their psychoactive cannabinoid. For example, Delta-9-tetrahydrocannabinol (THC) is the main psychoactive compound found in cannabis and is responsible for the "high" feeling when consumed. However, cannabis does not naturally contain significant amounts of THC. Instead, tetrahydrocannabinolic acid (THCA) is found naturally in raw and live cannabis and is non-intoxicating. Over time, THCA slowly converts to THC through a process of decarboxylation over the course of roughly a year, but can be sped up with exposure to high temperatures. When heated under conditions of 110 °C, decarboxylation generally occurs in 30–45 minutes. The decarboxylated THCA (THC) is added to cannabis edibles, as THCA is not orally active. When consumed orally, the liver breaks down and metabolizes THC into the more potent 11-hydroxy-THC.

Vaporization temperatures

Dry-herb vaporizers can be used to inhale cannabis in its flower form. There are 483 identifiable chemical constituents known to exist in the cannabis plant, and at least 85 different cannabinoids have been isolated from the plant.^[10] The aromatic terpenoids begin to vaporize at 126.0 °C (258.8 °F), but the more bioactive tetrahydrocannabinol (THC), and other cannabinoids also found in cannabis (often legally sold as cannabinoid isolates) like cannabidiol (CBD), cannabichromene (CBC), cannabigerol (CBG), cannabinol (CBN), do not vaporize until near their respective boiling points.

The cannabinoids listed here are found in the plant but only in trace amounts. However, they have also been extracted and sold as isolates online. Third party certification may help ensure buyers to avoid synthetic cannabinoids.

Cannabinoid	Boiling point
CBC	220 °C (428 °F)^[11]
CBCV
CBD	160 °C (320 °F)-180 °C (356 °F)^[11]
CBDD	?
CBDO
CBDP
CBDV
CBE
CBG	185 °C (365 °F)^[12]
CBGV
CBL
CBN	185 °C (365 °F)^[11]
CBT
CBV
delta-3-THC	?
delta-4-THC	?
delta-7-THC	?
delta-8-THC	175 °C (347 °F)-178 °C (352 °F)^[11]
delta-10-THC	?
delta-11-THC	?
THC	157 °C (315 °F)^[11]
THCB
THCC
THCP
THCV	<220^[11]

Structural scheduling

Table of plant cannabinoids^[13]
Cannabigerol-type (CBG)
Cannabigerol (E)-CBG-C₅	Cannabigerol monomethyl ether (E)-CBGM-C₅ A	Cannabinerolic acid A (Z)-CBGA-C₅ A	Cannabigerovarin (E)-CBGV-C₃
Cannabigerolic acid A (E)-CBGA-C₅ A	Cannabigerolic acid A monomethyl ether (E)-CBGAM-C₅ A		Cannabigerovarinic acid A (E)-CBGVA-C₃ A
Cannabichromene-type (CBC)
(±)-Cannabichromene CBC-C₅	(±)-Cannabichromenic acid A CBCA-C₅ A	(±)-Cannabivarichromene, (±)-Cannabichromevarin CBCV-C₃	(±)-Cannabichromevarinic acid A CBCVA-C₃ A
Cannabidiol-type (CBD)
(−)-Cannabidiol CBD-C₅	Cannabidiol momomethyl ether CBDM-C₅	Cannabidiol-C₄ CBD-C₄	(−)-Cannabidivarin CBDV-C₃	Cannabidiorcol CBD-C₁
Cannabidiolic acid CBDA-C₅			Cannabidivarinic acid CBDVA-C₃
Cannabinodiol-type (CBND)
Cannabinodiol CBND-C₅	Cannabinodivarin CBND-C₃
Tetrahydrocannabinol-type (THC)
Δ⁹-Tetrahydrocannabinol Δ⁹-THC-C₅		Δ⁹-Tetrahydrocannabinol-C₄ Δ⁹-THC-C₄	Δ⁹-Tetrahydrocannabivarin Δ⁹-THCV-C₃	Δ⁹-Tetrahydrocannabiorcol Δ⁹-THCO-C₁
Δ⁹-Tetrahydro- cannabinolic acid A Δ⁹-THCA-C₅ A	Δ⁹-Tetrahydro- cannabinolic acid B Δ⁹-THCA-C₅ B	Δ⁹-Tetrahydro- cannabinolic acid-C₄ A and/or B Δ⁹-THCA-C₄ A and/or B	Δ⁹-Tetrahydro- cannabivarinic acid A Δ⁹-THCVA-C₃ A	Δ⁹-Tetrahydro- cannabiorcolic acid A and/or B Δ⁹-THCOA-C₁ A and/or B
(−)-Δ⁸-trans-(6aR,10aR)- Δ⁸-Tetrahydrocannabinol Δ⁸-THC-C₅	(−)-Δ⁸-trans-(6aR,10aR)- Tetrahydrocannabinolic acid A Δ⁸-THCA-C₅ A	(−)-(6aS,10aR)-Δ⁹- Tetrahydrocannabinol *(−)-cis-Δ⁹-THC-C₅*
Cannabinol-type (CBN)
Cannabinol CBN-C₅	Cannabinol-C₄ CBN-C₄	Cannabivarin CBN-C₃	Cannabinol-C₂ CBN-C₂	Cannabiorcol CBN-C₁
Cannabinolic acid A CBNA-C₅ A	Cannabinol methyl ether CBNM-C₅
Cannabitriol-type (CBT)
(−)-(9R,10R)-trans- Cannabitriol *(−)-trans-CBT-C₅*	(+)-(9S,10S)-Cannabitriol *(+)-trans-CBT-C₅*	(±)-(9R,10S/9S,10R)- Cannabitriol *(±)-cis-CBT-C₅*	(−)-(9R,10R)-trans- 10-O-Ethyl-cannabitriol *(−)-trans-CBT-OEt-C₅*	(±)-(9R,10R/9S,10S)- Cannabitriol-C₃ *(±)-trans-CBT-C₃*
8,9-Dihydroxy-Δ^6a(10a)- tetrahydrocannabinol 8,9-Di-OH-CBT-C₅	Cannabidiolic acid A cannabitriol ester CBDA-C₅ 9-OH-CBT-C₅ ester	(−)-(6aR,9S,10S,10aR)- 9,10-Dihydroxy- hexahydrocannabinol, Cannabiripsol Cannabiripsol-C₅	(−)-6a,7,10a-Trihydroxy- Δ⁹-tetrahydrocannabinol (−)-Cannabitetrol	10-Oxo-Δ^6a(10a)- tetrahydrocannabinol OTHC
Cannabielsoin-type (CBE)
(5aS,6S,9R,9aR)- Cannabielsoin CBE-C₅		(5aS,6S,9R,9aR)- C₃-Cannabielsoin CBE-C₃
(5aS,6S,9R,9aR)- Cannabielsoic acid A CBEA-C₅ A	(5aS,6S,9R,9aR)- Cannabielsoic acid B CBEA-C₅ B	(5aS,6S,9R,9aR)- C₃-Cannabielsoic acid B CBEA-C₃ B
Cannabiglendol-C₃ OH-iso-HHCV-C₃	Dehydrocannabifuran DCBF-C₅	Cannabifuran CBF-C₅
Isocannabinoids
(−)-Δ⁷-trans-(1R,3R,6R)- Isotetrahydrocannabinol	(±)-Δ⁷-1,2-cis- (1R,3R,6S/1S,3S,6R)- Isotetrahydro- cannabivarin	(−)-Δ⁷-trans-(1R,3R,6R)- Isotetrahydrocannabivarin
Cannabicyclol-type (CBL)
(±)-(1aS,3aR,8bR,8cR)- Cannabicyclol CBL-C₅	(±)-(1aS,3aR,8bR,8cR)- Cannabicyclolic acid A CBLA-C₅ A	(±)-(1aS,3aR,8bR,8cR)- Cannabicyclovarin CBLV-C₃
Cannabicitran-type (CBT)
Cannabicitran CBT-C₅
Cannabichromanone-type (CBCN)
Cannabichromanone CBCN-C₅	Cannabichromanone-C₃ CBCN-C₃	Cannabicoumaronone CBCON-C₅

References

↑ Abyadeh M, Gupta V, Paulo JA, Gupta V, Chitranshi N, Godinez A, et al. (September 2021). "A Proteomic View of Cellular and Molecular Effects of Cannabis". Biomolecules. 11 (10): 1411–1428. doi:10.3390/biom11101411. PMC 8533448. PMID 34680044.
↑ "Marijuana, also called: Cannabis, Ganja, Grass, Hash, Pot, Weed". Medline Plus. 3 July 2017.
↑ Lambert DM, Fowler CJ (August 2005). "The endocannabinoid system: drug targets, lead compounds, and potential therapeutic applications". Journal of Medicinal Chemistry. 48 (16): 5059–5087. doi:10.1021/jm058183t. PMID 16078824.
↑ Pertwee R, ed. (2005). Cannabinoids. Springer-Verlag. p. 2. ISBN 978-3-540-22565-2.
↑ "Bulletin on Narcotics – 1962 Issue 3 – 004". UNODC (United Nations Office of Drugs and Crime). 1962-01-01. Retrieved 2014-01-15.
1 2 3 Czégény Z, Nagy G, Babinszki B, Bajtel Á, Sebestyén Z, Kiss T, et al. (April 2021). "CBD, a precursor of THC in e-cigarettes". Scientific Reports. 11 (1): 8951. Bibcode:2021NatSR..11.8951C. doi:10.1038/s41598-021-88389-z. PMC 8076212. PMID 33903673.
↑ Aizpurua-Olaizola O, Soydaner U, Öztürk E, Schibano D, Simsir Y, Navarro P, et al. (February 2016). "Evolution of the Cannabinoid and Terpene Content during the Growth of Cannabis sativa Plants from Different Chemotypes". Journal of Natural Products. 79 (2): 324–331. doi:10.1021/acs.jnatprod.5b00949. PMID 26836472.
↑ Wang M, Wang YH, Avula B, Radwan MM, Wanas AS, van Antwerp J, et al. (1 December 2016). "Decarboxylation Study of Acidic Cannabinoids: A Novel Approach Using Ultra-High-Performance Supercritical Fluid Chromatography/Photodiode Array-Mass Spectrometry". Cannabis and Cannabinoid Research. 1 (1): 262–271. doi:10.1089/can.2016.0020. PMC 5549281. PMID 28861498.
↑ Wang M, Wang YH, Avula B, Radwan MM, Wanas AS, van Antwerp J, et al. (2016). "Decarboxylation Study of Acidic Cannabinoids: A Novel Approach Using Ultra-High-Performance Supercritical Fluid Chromatography/Photodiode Array-Mass Spectrometry". Cannabis and Cannabinoid Research. 1 (1): 262–271. doi:10.1089/can.2016.0020. PMC 5549281. PMID 28861498.
↑ El-Alfy AT, Ivey K, Robinson K, Ahmed S, Radwan M, Slade D, et al. (June 2010). "Antidepressant-like effect of delta9-tetrahydrocannabinol and other cannabinoids isolated from Cannabis sativa L". Pharmacology, Biochemistry, and Behavior. 95 (4): 434–442. doi:10.1016/j.pbb.2010.03.004. PMC 2866040. PMID 20332000.
1 2 3 4 5 6 "Phytocannabinoid Boiling Points" (PDF). projectcbd.org. Archived (PDF) from the original on 2019-04-08. Retrieved 20 August 2021.
↑ "CompTox Chemicals Dashboard". comptox.epa.gov. Retrieved 10 April 2024.^{[dead link]}
↑ "Table of Natural Cannabinoids" (PDF).

Cannabinoids

Phytocannabinoids
(comparison)

Cannabibutols	CBB
Cannabichromenes	CBC CBCA CBCA-A CBCB CBCBA CBCP CBCPA CBCV CBCVA CBCQ
Cannabicyclols	CBL CBLA CBLB CBLP CBLPA CBLV CBLVA
Cannabidiols	CBD CBDA CBD-C1 CBD-C5 CBDB CBDBA CBDD CBDH CBDP CBDPA CBDM CBDMA CBDV CBDVA CBDQ
Cannabielsoins	CBE CBEA CBEA-A CBEA-B CBEB CBEP CBEPA CBEV
Cannabigerols	CBG CBGA CBGB CBGBA CBGM CBGAM CBGP CBGPA CBNR CBNRA CBNRA-A CBGV CBGVA CBGVA-A CBGQ
Cannabiphorols	CBP
Cannabinols	CBN CBNA CBN-C1 CBN-C2 CBN-C4 CBNM CBND CBNDA CBNP CBNPA CBVD CBVDA
Cannabitriols	CBT CBTA CBTB CBTV CBTVA CBTP CBTPA
Cannabivarins	CBV CBVA
Delta-3-tetrahydrocannabinols	Delta-3-THC
Delta-4-tetrahydrocannabinols	Delta-4-THC
Delta-7-tetrahydrocannabinols	Delta-7-THC
Delta-8-tetrahydrocannabinols	Delta-8-THC Delta-8-THCA Delta-8-THCA-A Delta-8-THCB Delta-8-THCP Delta-8-THCV
Delta-9-tetrahydrocannabinols	Delta-9-THC (THC) THCA THCMA THCA-A THCA-B THCBA THCA-C4 THCC THCA-C1 THCA-A-C1 THCA-B-C1 THCB THCH THCP THCPA THCV THCVA THCQ
Delta-10-Tetrahydrocannabinols	Delta-10-THC
Delta-11-Tetrahydrocannabinols	Delta-11-THC
Miscellaneous cannabinoids	Δ8-iso-THC Δ4(8)-iso-THC 7,8-Dihydrocannabinol 8,9-Dihydrocannabidiol CBCF Cannabicitran CBF Cannabiglendol CBM CBR CBRPA Caryophyllene DCBF Alkylamides Epigallocatechin gallate Gallocatechol Hexahydrocannabinol (HHC) Perrottetinene Serinolamide A Yangonin
Active metabolites	3'-OH-THC 7-OH-CBD 8,11-DiOH-THC 11-COOH-THC 11-OH-CBN 11-OH-HHC 11-OH-Δ8-THC 11-OH-Δ9-THC

Endocannabinoids

Arachidonoyl ethanolamide (AEA; anandamide)
2-Arachidonoylglycerol (2-AG)
2-Arachidonyl glyceryl ether (2-AGE; noladin ether)
2-Oleoylglycerol (2-OG)
N-Arachidonoyl dopamine (NADA)
N-Arachidonylglycine (NAGly)
2-Arachidonoyl lysophosphatidylinositol (2-ALPI)
N-Arachidonoyl serotonin (AA-5-HT)
Docosatetraenoylethanolamide (DEA)
Lysophosphatidylinositol (LPI)
Oleamide
Oleoylethanolamide (OEA)
Palmitoylethanolamide (PEA)
RVD-Hpα
Stearoylethanolamide (SEA)
O-Arachidonoyl ethanolamine (O-AEA; virodhamine)

Synthetic
cannabinoid
receptor
agonists /
neocannabinoids

Classical cannabinoids (dibenzopyrans)	1,2-Didehydro-3-oxo-THCO 9-OH-HHC 9-Nor-9β-HHC 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-2389 AM-4030 AM-7438 AM-11245 AMG-1 AMG-3 AMG-36 AMG-41 Cis-THC CP 42,096 Dexanabinol (HU-211) DMHP Dronabinol HHCP-O-acetate HHCH HU-210 HU-243 Iso-THC JWH-051 JWH-056 JWH-057 JWH-065 JWH-091 JWH-102 JWH-103 JWH-124 JWH-130 JWH-133 JWH-138 JWH-139 JWH-142 JWH-143 JWH-161 JWH-186 JWH-187 JWH-188 JWH-189 JWH-190 JWH-191 JWH-215 JWH-216 JWH-217 JWH-224 JWH-225 JWH-226 JWH-227 JWH-229 JWH-230 JWH-233 JWH-247 JWH-254 JWH-256 JWH-277 JWH-278 JWH-298 JWH-299 JWH-300 JWH-301 JWH-310 JWH-336 JWH-338 JWH-339 JWH-340 JWH-341 JWH-349 JWH-350 JWH-352 JWH-353 JWH-354 JWH-355 JWH-356 JWH-357 JWH-358 JWH-359 JWH-360 JWH-361 JWH-362 KM-233 L-759,633 L-759,656 Levonantradol (CP 50,5561) Menabitan Nabazenil Nabidrox (Canbisol) Nabilone Nabitan Naboctate O-224 O-581 O-774 O-806 O-823 O-1057 O-1125 O-1191 O-1238 O-2048 O-2113 O-2365 O-2372 O-2373 O-2383 O-2426 O-2484 O-2545 O-2694 O-2715 O-2716 O-3223 O-3226 Parahexyl Pirnabine SP-111 THC hemisuccinate THC-O-acetate THC-O-phosphate THCP-O-acetate ZYN-001 (THC O-glyceric acid)
Non-classical cannabinoids	Cannabicyclohexanol Cannabinor CBD-DMH CP 47,497 (C6)-CP 47,497 (C9)-CP 47,497 CP 55,244 CP 55,940 Delta-6-Cannabidiol Etrinabdione HU-320 HU-331 HU-336 HU-345 HU-446 HU-465 HU-910 HUF-101 Nonabine O-1376 O-1422 O-1601 O-1656 O-1657 O-1660 O-1663 O-1871 Onternabez (HU-308) SPA-229 Tinabinol
Adamantoylindoles	5F-AKB-48 APICA STS-135
Benzimidazoles	AZ-11713908 AZD-1940 BIM-018 FUBIMINA MCHB-1 PF-03550096 RQ-00202730
Benzoylindoles	1-Butyl-3-(2-methoxybenzoyl)indole 1-Butyl-3-(4-methoxybenzoyl)indole 1-Pentyl-3-(2-methoxybenzoyl)indole AM-630 AM-679 AM-694 AM-1241 AM-2233 GW-405,833 (L-768,242) Pravadoline RCS-4 WIN 54,461
Cyclohexylphenols	CP-47,947 CP-55,940
Eicosanoids	AM-883 AM-1346 ACEA ACPA Methanandamide (AM-356) O-585 O-689 O-1812 O-1860 O-1861
Indazole-3- carboxamides	4F-MDMB-BINACA 4'Cl-CUMYL-PINACA 4'F-CUMYL-5F-PINACA 5Cl-APINACA 5F-ADB 5F-ADB-PINACA 5F-AMB 5F-APINACA 5F-CUMYL-PINACA 5F-EDMB-PINACA 5F-EMB-PINACA A-CHMINACA AB-CHMINACA AB-FUBINACA AB-FUBINACA 2-fluorobenzyl isomer AB-PINACA ADB-BINACA ADB-BUTINACA ADB-CHMINACA ADB-HEXINACA ADB-FUBINACA ADB-PINACA ADB-4en-PINACA ADB-5'Br-PINACA ADMB-3TMS-PRINACA Adamantyl-THPINACA ADSB-FUB-187 AMB-CHMINACA AMB-FUBINACA APINACA (AKB48) APP-FUBINACA CUMYL-3TMS-PRINACA CUMYL-4CN-BINACA CUMYL-CBMINACA CUMYL-CHSINACA CUMYL-EINACA CUMYL-FUBINACA CUMYL-NBMINACA CUMYL-PINACA CUMYL-THPINACA CUMYL-TSINACA EMB-FUBINACA FUB-APINACA MDMB-4en-PINACA MDMB-5Br-INACA MDMB-BINACA MDMB-CHMINACA MDMB-FUBINACA MN-18 PX-2 PX-3 THQ-PINACA
Indole-3-carboxamides	4'F-CUMYL-5F-PICA 5F-ADBICA 5F-EDMB-PICA 5F-MDMB-PICA 5F-NNE1 5F-PCN 5F-SDB-006 AB-FUBICA AB-PICA ADBICA ADB-FUBICA APICA BMS-F CUMYL-BICA CUMYL-CBMICA CUMYL-CHMICA CUMYL-NBMICA CUMYL-PICA CUMYL-5F-PICA FDU-NNE1 MDMB-CHMICA MMB-CHMICA MMB-2201 MN-25 (UR-12) NNE1 PX-1 Org 28312 Org 28611 SDB-006 STS-135
Indole-3-carboxylates	5F-PB-22 FDU-PB-22 FUB-PB-22 QUCHIC (BB-22) QUPIC (PB-22) NM-2201
Naphthoylindazoles	THJ-018 THJ-2201
Naphthoylindoles	5F-JWH-398 AM-1220 AM-1221 AM-1235 AM-2201 AM-2232 CHM-081 EAM-2201 FUB-JWH-018 JWH-004 JWH-007 JWH-009 JWH-011 JWH-015 JWH-016 JWH-018 JWH-019 JWH-020 JWH-042 JWH-043 JWH-046 JWH-047 JWH-048 JWH-049 JWH-050 JWH-070 JWH-072 JWH-073 JWH-076 JWH-077 JWH-079 JWH-080 JWH-081 JWH-082 JWH-083 JWH-093 JWH-094 JWH-095 JWH-096 JWH-097 JWH-098 JWH-099 JWH-100 JWH-116 JWH-120 JWH-122 JWH-148 JWH-149 JWH-151 JWH-153 JWH-159 JWH-160 JWH-163 JWH-164 JWH-165 JWH-166 JWH-180 JWH-181 JWH-182 JWH-189 JWH-193 JWH-198 JWH-200 JWH-210 JWH-211 JWH-212 JWH-213 JWH-234 JWH-235 JWH-236 JWH-239 JWH-240 JWH-241 JWH-242 JWH-258 JWH-259 JWH-260 JWH-261 JWH-262 JWH-265 JWH-266 JWH-267 JWH-268 JWH-387 JWH-398 JWH-416 JWH-417 JWH-422 JWH-423 JWH-424 JWH-425 MAM-1220 MAM-2201 NE-CHMIMO
Naphthoylpyrroles	JWH-030 JWH-031 JWH-032 JWH-033 JWH-036 JWH-044 JWH-045 JWH-145 JWH-146 JWH-147 JWH-150 JWH-156 JWH-243 JWH-244 JWH-245 JWH-246 JWH-292 JWH-293 JWH-307 JWH-308 JWH-309 JWH-346 JWH-347 JWH-348 JWH-363 JWH-364 JWH-365 JWH-366 JWH-367 JWH-368 JWH-369 JWH-370 JWH-371 JWH-372 JWH-373
Naphthylmethylindenes	JWH-171 JWH-176 JWH-220
Naphthylmethylindoles	JWH-175 JWH-184 JWH-185 JWH-192 JWH-194 JWH-195 JWH-196 JWH-197 JWH-199
Phenylacetylindoles	Cannabipiperidiethanone JWH-167 JWH-201 JWH-202 JWH-203 JWH-204 JWH-205 JWH-206 JWH-207 JWH-208 JWH-209 JWH-237 JWH-248 JWH-249 JWH-250 JWH-251 JWH-252 JWH-253 JWH-302 JWH-303 JWH-304 JWH-305 JWH-306 JWH-311 JWH-312 JWH-313 JWH-314 JWH-315 JWH-316 RCS-8
Pyrazolecarboxamides	5F-AB-FUPPYCA 5F-AMPPPCA AB-CHFUPYCA Z8526711350
Tetramethylcyclo- propanoylindazoles	FAB-144
Tetramethylcyclo- propanoylindoles	5Br-UR-144 5Cl-UR-144 A-796,260 A-834,735 FUB-144 UR-144 XLR-11 XLR-12
Others	2F-QMPSB 4-HTMPIPO 4CN-CUMYL-BUT7AICA 5F-3-pyridinoylindole 5F-ADB-P7AICA 5F-CUMYL-P7AICA 5F-CUMYL-PEGACLONE 5F-PY-PICA 5F-PY-PINACA A-836,339 A-955,840 A-PBITMO A-PONASA AB-001 ADB-FUBHQUCA ADB-FUBIATA ADB-P7AICA AM-1248 AM-1714 Abnormal cannabidiol BAY 38-7271 BAY 59-3074 BzODZ-EPyr CB-13 CB-86 CBS-0550 CUMYL-4CN-B7AICA CUMYL-CB-MEGACLONE CUMYL-CH-MEGACLONE CUMYL-PEGACLONE EG-018 GSK-554,418A GW-842,166X JTE 7-31 LASSBio-881 LBP-1 Leelamine MDA-19 MDA-7 MEPIRAPIM NESS-040C5 NMDMSB NMP-7 O-1269 O-1270 O-1399 O-1602 O-2220 O-889 Olorinab PF-03550096 PSB-SB-1202 PTI-1 PTI-2 PTI-3 QMPSB S-444,823 S-777,469 SER-601 Tedalinab URB-447 VSN-16 Vicasinabin WIN 55,212-2 WIN 56,098

Allosteric CBRTooltip Cannabinoid receptor ligands

AEF0117
GAT100
Org 27569
Org 27759
Org 29647
PSNCBAM-1
Pregnenolone
RTI-371
ZCZ-011

Endocannabinoid
enhancers
(inactivation inhibitors)

4-Nonylphenylboronic acid
AM-404
Arachidonoyl serotonin
ART26.12
Arvanil
BIA 10-2474
Biochanin A
CAY-10401
CAY-10429
Genistein
Guineesine
IDFP
JNJ 1661010
JNJ-42165279
JZL184
JZL195
Kaempferol
LY-2183240
MK-4409
O-1624
O-2093
O-7460
Oleoylethanolamide (OEA)
Olvanil
Palmitoylethanolamide (PEA)
PF-04457845
PF-622
PF-750
PF-3845
PHOP
UCM707
URB-447
URB-597
URB-602
URB-754
VDM-11

Anticannabinoids
(antagonists/inverse
agonists/antibodies)

ABD459
AM-251
AM-281
AM-630
AM-1387
AM-4113
AM-6527
AM-6545
Amauromine
ANEB-001
AZD-2207
BML-190
CAY-10508
CB-25
CB-52
CB-86
CE-178253
COR170
Drinabant (AVE1625)
Hemopressin
Ibipinabant (SLV319)
JD-5037
JTE-907
LH-21
LY-320,135
MDA-77
MJ-15
MK-9470
Monlunabant
MRL-650
NESS-0327
NIDA-41020
O-606
O-1184
O-1248
O-1918
O-2050
O-2654
Otenabant (CP-945,598)
PF-514273
PGN36
PipISB
PSB-SB-487
Rezosicone
Rimonabant (SR141716)
Rosonabant (E-6776)
SLV 319
SR-144,528
Surinabant (SR147778)
Taranabant (MK-0364)
TC-C 14G
TM-38837
VCHSR
Voacamine
Zevaquenabant

See also: Cannabinoid receptor modulators (cannabinoids by pharmacology)
List of: AM cannabinoids
JWH cannabinoids
Designer drugs § Synthetic cannabimimetics

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