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The absolute configuration of δ1-tetrahydrocannabinol, the major active constituent of hashish.

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This article is published in Tetrahedron Letters.The article was published on 1967-01-01. It has received 189 citations till now. The article focuses on the topics: Hashish.

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International Union of Pharmacology. XXVII. Classification of Cannabinoid Receptors

TL;DR: It is considered premature to rename cannabinoid receptors after an endogenous agonist as is recommended by the International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification, because pharmacological evidence for the existence of additional types of cannabinoid receptor is emerging and other kinds of supporting evidence are still lacking.
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The Endocannabinoid System as an Emerging Target of Pharmacotherapy

TL;DR: A comprehensive overview on the current state of knowledge of the endocannabinoid system as a target of pharmacotherapy is provided.
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Molecular targets for cannabidiol and its synthetic analogues: effect on vanilloid VR1 receptors and on the cellular uptake and enzymatic hydrolysis of anandamide.

TL;DR: Results suggest that VR1 receptors, or increased levels of endogenous AEA, might mediate some of the pharmacological effects of CBD and its analogues, and (−)‐5′‐DMH‐CBD represents a valuable candidate for further investigation as inhibitor of AEA uptake and a possible new therapeutic agent.
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Chemical constituents of marijuana: The complex mixture of natural cannabinoids

TL;DR: The chemical constituents of the plant are discussed with particular emphasis on the cannabinoids as the class of compounds responsible for the drug's psychological properties.
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Cannabinoid physiology and pharmacology: 30 years of progress

TL;DR: Delta9-Tetrahydrocannabinol from Cannabis sativa is mimicked by cannabimimetic analogs such as CP55940 and WIN55212-2, and antagonized by rimonabant and SR144528, through G-protein-coupled receptors, CB1 in the brain, and CB2 in the immune system.
References
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Journal ArticleDOI

Isolation, Structure, and Partial Synthesis of an Active Constituent of Hashish

TL;DR: In this paper, the extinction coefficients of stilbene, stil bene-, and stilben-2 were determined for tetrahydrofuran, 2-methyltetrahydrlfurfh-fragments, and 1,2-dime thoxye thane.
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Hashish. I. The Structure of Cannabidiol

TL;DR: Cannabidiol, one of the major components of hashish, has been shown to possess structure IIIa.
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Hashish—VII : The isomerization of cannabidiol to tetrahydrocannabinols

TL;DR: Adams as mentioned in this paper showed that the physiologically active products obtained by Adams on isomerization of the inactive cannabidiol (Ia) with acids are either Δ 1(6) tetrahydrocannabinol (II) or a mixture of II, Δ 1 tetrahedrocannabinols (IIIa), and the two isomers of 1-ethoxy hexahydricannabinol(VIIIa, VIIIb).
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