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首页-小分子抑制剂&激动剂-Apoptosis-IAP-UC-112
UC-112

Chemical Structure : UC-112

CAS No.: 383392-66-3

UC-112 (UC112)

货号: PC-43254Not For Human Use, Lab Use Only.

UC-112 is a novel IAP inhibitor that potently inhibits human melanoma (A375 and M14) and human prostate (PC-3 and DU145) cancer cell lines with IC50 of 0.7-3.4 uM.

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

UC-112 is a novel IAP inhibitor that potently inhibits human melanoma (A375 and M14) and human prostate (PC-3 and DU145) cancer cell lines with IC50 of 0.7-3.4 uM.
UC-112 also potently inhibits the growth of P-gp-overexpressed multidrug-resistant cancer cells, strongly activates caspase-3/7 and caspase-9 activities, and selectively downregulates survivin level at 1 uM.
UC-112 strongly inhibits tumor growth and reduces both X chromosome-linked IAP and survivin levels in an A375 human melanoma xenograft model in vivo.

物理化学性质&存储条件

分子量 348.4382
分子式 C22H24N2O2
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

8-Quinolinol, 5-[(phenylmethoxy)methyl]-7-(1-pyrrolidinylmethyl)-

参考文献

1. Wang J, et al. J Pharmacol Exp Ther. 2014 May;349(2):319-29.

2. Xiao M, et al. PLoS One. 2015 Jun 12;10(6):e0129807.

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