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. Author manuscript; available in PMC: 2021 Jan 1.
Published in final edited form as: J Dual Diagn. 2019 Oct 9;16(1):106–119. doi: 10.1080/15504263.2019.1668100

Table 1:

An organized table listing the various drugs used in pre-clinical and clinical studies discussed in the paper.

Drug Abreviation Drug Full Name Derivative Specificity
AGONISTS
WIN 55212-2 WIN 55212-2 Synthetic CB1R Full Agonist
CB2R Full Agnoist
Indole Indole Synthetic Peripherally restricted CB1R agonist
Indene Indene Synthetic Peripherally restricted CB1R agonist
URB937 URB937 Synthetic Peripherally restricted CB1R agonist
ZCZ011 ZCZ011 Synthetic CB1R Allosteric Modulator
AZD1940 AZD1940 Synthetic Peripherally restricted CB1R agonist
AZD1704 AZD1704 Synthetic Peripherally restricted CB1R agonist
CP-55,940 CP-55,940 Synthetic CB1R Full Agonist
CB2R Full Agnoist
HU-210 HU-210 Synthetic CB1R Full Agonist
CB2R Full Agnoist
Δ 9-THC Δ9-tetrahydrocannabinol Plant-based Derivative CB1R Full Agonist
CB2R Full Agnoist
Anandamide N-arachidonoylethanolamine Endogenous CB1R Partial Agonist
CB2R Partial Agnoist
2-AG 2-arachidonoylglycerol Endogenous CB1R Full Agonist
CB2R Partial Agnoist
ACEA Arachidonyl-2-chloroethylamide Endogenous CB1R Full Agonist
ANTAGONISTS
ACPA Arachidonylcyclopropylamide Synthetic CB1R Antagonist
SR141716 [3H]rimonabant Synthetic CB1R Antagonist
This table is meant to be a reference and assist the reader throughout the article of distingusihing important drug informaiton and how it pertains to the experimental results described.

Note. CB1R = cannabinoid receptor type 1; CB2R = cannabinoid receptor type 2.