Chemical Structure : PD176252
CAS No.: 204067-01-6
Catalog No.: PC-27296Not For Human Use, Lab Use Only.
PD176252 is a potent antagonist of neuromedin-B preferring (BB1, NMBR) and gastrin-releasing peptide-preferring (BB2) receptor (GRPR) with Kis of 0.17 nM and 1 nM for human BB1 and BB2 receptors, and 0.66 nM, 16 nM for Rat BB1 and BB2 receptors, respectively.
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|---|---|---|---|
| 10 mg | $88 | In stock | |
| 25 mg | $138 | In stock | |
| 50 mg | $238 | In stock | |
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PD176252 is a potent antagonist of neuromedin-B preferring (BB1, NMBR) and gastrin-releasing peptide-preferring (BB2) receptor (GRPR) with Kis of 0.17 nM and 1 nM for human BB1 and BB2 receptors, and 0.66 nM, 16 nM for Rat BB1 and BB2 receptors, respectively.
PD176252 inhibits (125I-Tyr0) neuromedin B binding with IC50 of 50 nM.
PD176252 (1 uM) significantly inhibited colony number using a proliferation assay in vitro.
| M.Wt | 584.68 | |
| Formula | C32H36N6O5 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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| Chemical Name/SMILES |
(S)-3-(1H-Indol-3-yl)-N-((1-(5-methoxypyridin-2-yl)cyclohexyl)methyl)-2-methyl-2-(3-(4-nitrophenyl)ureido)propanamide |
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1. Ashwood V, et al. Bioorg Med Chem Lett. 1998 Sep 22;8(18):2589-94.
2. Moody TW, et al. Eur J Pharmacol. 2000 Dec 8;409(2):133-42.

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