| Weight | 310.437 g/mol |
|---|---|
| Formula | C21H26O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 4 |
cannabinol (521-35-7)
Score:
#1554 in Biochemistry
,
#4499 in Chemistry
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- A comparison of the pharmacological activity in man of intravenously administered 1368-11368-11368-1, cannabinol, and cannabidiol (Cellular and Molecular Life Sciences, 1973)
- Cannabinol derivatives: binding to cannabinoid receptors and inhibition of adenylylcyclase. (Journal of Medicinal Chemistry, 1997)
- Pharmacokinetics and Metabolism of the Plant Cannabinoids, 9-Tetrahydrocannibinol, Cannabidiol and Cannabinol (Handbook of experimental pharmacology, 2005)
- Cytochrome P450 enzymes involved in the metabolism of tetrahydrocannabinols and cannabinol by human hepatic microsomes. (Life Sciences, 2007)
- Cannabidiol and cannabinol in man (Cellular and Molecular Life Sciences, 1973)
- Delta(9)-tetrahydrocannabinol and cannabinol activate capsaicin-sensitive sensory nerves via a CB1 and CB2 cannabinoid receptor-independent mechanism (The Journal of Neuroscience, 2002)
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SMILESCCCCCC1=CC2=C(C(=C1)O)C3=C(C=CC(=C3)C)C(O2)(C)C
-
InChIKeyVBGLYOIFKLUMQG-UHFFFAOYSA-N
- Pubchem - cannabinol
- Wikipedia - cannabinol
Cannabinol (CBN) is a non-psychoactive cannabinoid found only in trace amounts in Cannabis, and is mostly found in aged Cannabis. Pharmacologically relevant quantities are formed as a metabolite of tetrahydrocannabinol (THC). CBN acts as a partial agonist at the CB1 receptors, but has a higher affinity to CB2 receptors; however, it has lower affinities relative to THC.
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