Chemical Structure : BMS-193885
CAS No.: 186185-03-5
Catalog No.: PC-26144Not For Human Use, Lab Use Only.
BMS-193885 is a potent, selective neuropeptide Y(1) receptor (Y1R) antagonist with binding Ki of 3.3 nM, demonstrates full functional antagonism with Kb of 4.54 nM in forskolin-stimulated c-AMP production assay using CHO cells expressing human Y(1) receptor.
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|---|---|---|---|
| 5 mg | $78 | In stock | |
| 10 mg | $118 | In stock | |
| 25 mg | $198 | In stock | |
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BMS-193885 is a potent, selective neuropeptide Y(1) receptor (Y1R) antagonist with binding Ki of 3.3 nM, demonstrates full functional antagonism with Kb of 4.54 nM in forskolin-stimulated c-AMP production assay using CHO cells expressing human Y(1) receptor.
BMS-193885 inhibited NPY-induced feeding in satiated rats when dosed at 3.0 and 10.0 mg/kg (ip), and also decreased spontaneous overnight food consumption in rats at doses of 10 and 20 mg/kg (ip).
BMS-193885 (10 mg/kg) also reduced one-hour neuropeptide Y-induced food intake in satiated rats, as well as spontaneous overnight food consumption.
| M.Wt | 590.72 | |
| Formula | C33H42N4O6 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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| Chemical Name/SMILES |
Dimethyl 4-(3-(3-(3-(4-(3-methoxyphenyl)piperidin-1-yl)propyl)ureido)phenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate |
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1. Antal-Zimanyi I, et al. Eur J Pharmacol. 2008 Aug 20;590(1-3):224-32.
2. Poindexter GS, et al. Bioorg Med Chem. 2004 Jan 15;12(2):507-21.

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