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首页-小分子抑制剂&激动剂-GPCR-Protease-activated Receptor (PAR)-SCH 79797 dihydrochloride
SCH 79797 dihydrochloride

Chemical Structure : SCH 79797 dihydrochloride

CAS No.: 1216720-69-2

SCH 79797 dihydrochloride (SCH79797;SCH-79797)

货号: PC-61305Not For Human Use, Lab Use Only.

SCH79797 dihydrochloride is a potent, selective competitive and nonpeptide PAR-1 antagonist with IC50 of 70 nM.

规格 价格 库存 数量
5 mg ¥1280 In stock
10 mg ¥1980 In stock
25 mg ¥3380 In stock
50 mg Get quote
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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

SCH79797 dihydrochloride is a potent, selective competitive and nonpeptide PAR-1 antagonist with IC50 of 70 nM.
SCH79797 inhibits α-thrombin- and haTRAP-induced aggregation of human platelets, but does inhibits human platelet aggregation induced by the tethered ligand agonist for PAR-4, γ-thrombin, ADP, or collagen.
SCH79797 also blocks angiogenesis association with endothelial cell growth suppression and induction of apoptosis.

物理化学性质&存储条件

分子量 444.41
分子式 C23H25N5.2HCl
外观性状 Solid
CAS No.
储存条件
固体粉末
-20 °C 12 个月; 4°C 6 个月
配置液
-80 °C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

N3-Cyclopropyl-7-[[4-(1-methylethyl)phenyl]methyl]-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine dihydrochloride

参考文献

1. Ahn HS, et al. Biochem Pharmacol. 2000 Nov 15;60(10):1425-34.

2. Ahn HS, et al. Bioorg Med Chem Lett. 1999 Jul 19;9(14):2073-8.

3. Zania P, et al. J Pharmacol Exp Ther. 2006 Jul;318(1):246-54.

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