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PD176252

Chemical Structure : PD176252

CAS No.: 204067-01-6

PD176252 (PD 176252, PD-176252)

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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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

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.

Physicochemical Properties

M.Wt 584.68
Formula C32H36N6O5
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

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

References

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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