| Identification | Back Directory | [Name]
(+/-)-4R-[4-(1,1-DIMETHYLHEPTYL)-2,6-DIMETHOXYPHENYL]-6,6-DIMETHYL-1R,5R-BICYCLO[3.1.1]HEPT-2-ENE-2-METHANOL | [CAS]
256934-39-1 | [Synonyms]
HU-308
4-[4-(1,1-Dimethylheptyl)-2,6-dimethoxyphenyl]-6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-methanol
(+/-)-4R-[4-(1,1-DIMETHYLHEPTYL)-2,6-DIMETHOXYPHENYL]-6,6-DIMETHYL-1R,5R-BICYCLO[3.1.1]HEPT-2-ENE-2-METHANOL
[(1S,2S,5S)-2-[2,6-dimethoxy-4-(2-methyloctan-2-yl)phenyl]-6,6-dimethyl-4-bicyclo[3.1.1]hept-3-enyl]methanol
(1R,4R,5R)-rel-(+)-4-[4-(1,1-DiMethylheptyl)-2,6-diMethoxyphenyl]-6,6-diMethylbicyclo[3.1.1]hept-2-ene-2-Methanol
Bicyclo[3.1.1]hept-2-ene-2-methanol, 4-[4-(1,1-dimethylheptyl)-2,6-dimethoxyphenyl]-6,6-dimethyl-, (1R,4R,5R)-rel-(+)- | [Molecular Formula]
C27H42O3 | [MDL Number]
MFCD03412032 | [MOL File]
256934-39-1.mol | [Molecular Weight]
414.62 |
| Chemical Properties | Back Directory | [Boiling point ]
508.7±50.0 °C(Predicted) | [density ]
0.999 | [storage temp. ]
Store at -20°C | [solubility ]
Soluble in DMSO | [form ]
solution in methyl acetate | [pka]
14.77±0.10(Predicted) | [color ]
white to dark beige | [optical activity]
[α]/D 180.0 to 130.0°, c =0.5 in chloroform-d |
| Hazard Information | Back Directory | [Uses]
A specific CB2-specific agonist that inhibits forskolin-stimulated cAMP production in CB2-transfected cells. It reduces blood pressure, blocks defecation, and elicits anti-inflammatory and peripheral analgesic activity and thus may lead to new therapies for hypertension, inflammation, and pain.
Controlled Substance. | [Definition]
ChEBI: HU-308 is a carbobicyclic compound that is bicyclo[3.1.1]hept-2-ene which is substituted by a hydroxymethyl group at position 2, a 2,6-dimethoxy-4-(2-methyloctan-2-yl)phenyl group at position 4, and two methyl groups at position 6 (the 1S,4S,5S stereoisomer). A highly selective and effective cannabinoid type-2 agonist and the enantiomer of HU-433. It has a role as a CB2 receptor agonist, an anti-inflammatory agent, a bone density conservation agent, an apoptosis inhibitor and an antihypertensive agent. It is a bridged compound, a carbobicyclic compound, an aromatic ether, a synthetic cannabinoid and a primary allylic alcohol. | [Biological Activity]
Potent and selective CB 2 receptor agonist (K i values are 22.7 nM and > 10 μ M for CB 2 and CB 1 receptors respectively, EC 50 = 5.57 nM). Displays antiallodynic activity in the rat hindpaw incision model of postoperative pain. | [storage]
Store at -20°C |
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