Chemical Structure : BNS808
Catalog No.: PC-24424Not For Human Use, Lab Use Only.
BNS808 is a potent, peripherally selective cannabinoid-1 receptor (CB1R) antagonist with Ki values of 0.7 nM for both mouse and human CB1R and IC50 of 0.8 nM (hCB1R), >2000-fold selective over CB2R.
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BNS808 is a potent, peripherally selective cannabinoid-1 receptor (CB1R) antagonist with Ki values of 0.7 nM for both mouse and human CB1R and IC50 of 0.8 nM (hCB1R), >2000-fold selective over CB2R.
BNS808 does not induce CNS-mediated side effects.
BNS808 treatment (1 mg/kg/day, oral doses for 24 days.) reduced body weigh and fat mass and increases lean body mass in diet-induced obese mice.
Chronic BNS808 administration (1 mg/kg/day for 24 days) reduces HFD-induced hepatic steatosis and liver injury in diet-induced obese mice.
M.Wt | 548.86 | |
Formula | C25H20Cl3N3O3S | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Gammal A, et al. J Med Chem. 2025 Apr 21. doi: 10.1021/acs.jmedchem.4c03132.
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