| Identification | Back Directory | [Name]
1,3-Benzenediol, 2-[(1R,4S,6R)-4-hydroxy-3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl- | [CAS]
58940-28-6 | [Synonyms]
6α-Hydroxycannabidiol 6a-Hydroxycannabidiol (?)-6α-hydroxy Cannabidiol 6α-Hydroxycannabidiol (1.0mg/ml in Acetonitrile) 1,3-Benzenediol, 2-[(1R,4S,6R)-4-hydroxy-3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl- | [Molecular Formula]
C21H30O3 | [MOL File]
58940-28-6.mol | [Molecular Weight]
330.46 |
| Chemical Properties | Back Directory | [Boiling point ]
506.5±50.0 °C(Predicted) | [density ]
1.088±0.06 g/cm3(Predicted) | [storage temp. ]
-10 to -25°C | [solubility ]
DMF: 50 mg/ml; DMSO: 60 mg/ml; DMSO:PBS (pH 7.2) (1:3): 0.25 mg/ml; Ethanol: 35 mg/ml | [form ]
A crystalline solid | [pka]
9?+-.0.45(Predicted) |
| Hazard Information | Back Directory | [Uses]
(-)-6α-Hydroxy cannabidiol is a metabolite of Cannabidiol[1]. | [Definition]
ChEBI:6alpha-hydroxycannabidiol is a hydroxy-cannabidiol that is cannabidiol in which the 6-pro-S hydrogen of the cyclohexene ring has been replaced by a hydroxy group. It is one of the main metabolites of cannabidiol by human liver microsomes, produced by CYP2C19 and CYP3A. It has a role as a human xenobiotic metabolite. It is a hydroxy-cannabidiol, a member of resorcinols, an olefinic compound and a secondary alcohol. | [References]
[1] Jiang R, et al. Identification of cytochrome P450 enzymes responsible for metabolism of cannabidiol by human liver microsomes. Life Sci. 2011 Aug 1;89(5-6):165-70. DOI:10.1016/j.lfs.2011.05.018 |
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