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NMS-P118

カタログ番号GC19264

NMS-P118 は、癌治療のための強力で経口投与可能な選択性の高い PARP-1 阻害剤です。

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NMS-P118 化学構造

Cas No.: 1262417-51-5

サイズ 価格 在庫数 個数
2mg
$54.00
在庫あり
5mg
$80.00
在庫あり
10mg
$141.00
在庫あり
25mg
$265.00
在庫あり
50mg
$495.00
在庫あり

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Sample solution is provided at 25 µL, 10mM.

Description Protocol Chemical Properties Product Documents Related Products

NMS-P118 is a potent, orally available, and highly selective PARP-1 Inhibitor for cancer therapy.

NMS-P118 is found to be less myelotoxic in vitro than olaparib (now marketed as Lynparza), a dual PARP-1/-2 inhibitor. NMS-P118 proves to be metabolically stable, it modestly inhibites two cytochrome P450 family members (CYP-2B6 IC50: 8.15 uM; CYP-2D6 IC50: 9.51 uM) out of eight isoforms tested. Its ability in hampering the proliferation of bone marrow cells is from 5 to > 60 times lower then olaparib according to the species[1].

NMS-P118 is a potent (KD=0.009 uM) PARP-1 inhibitor, showing 150-fold selectivity over PARP-2 (KD=1.39 uM). NMS-P118 possesses excellent pharmacokinetic profile and nearly complete oral bioavailability both in mice and rats. It proved to be highly efficacious in vivo both as single agent in MDA-MB-436 human breast cancer tumors and in combination with temozolomide in CAPAN-1 human pancreatic tumors growing as xenografts in the mouse. The compound is well tolerated at highly efficacious doses and is endowed with an excellent ADME profile[1].

References:
[1]. Papeo G, et al. Discovery of 2-[1-(4,4-Difluorocyclohexyl)piperidin-4-yl]-6-fluoro-3-oxo-2,3-dihydro-1H-isoindole-4-carboxamide (NMS-P118): A Potent, Orally Available, and Highly Selective PARP-1 Inhibitor for Cancer Therapy. J Med Chem. 2015 Sep 10;58(17):6875-98.

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Average Rating: 5 ★★★★★ (Based on Reviews and 34 reference(s) in Google Scholar.)

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