Chemical Structure : A-800141
货号: PC-63347Not For Human Use, Lab Use Only.
A-800141 is a potent, highly specific, orally bioavailable MetAP2 inhibitor with IC50 of 12 nM, shows no inhibition for MetAP1 (IC50>30 uM).
大包装,大折扣!
E-mail: sales@probechem.com
Tech Support: tech@probechem.com
A-800141 is a potent, highly specific, orally bioavailable MetAP2 inhibitor with IC50 of 12 nM, shows no inhibition for MetAP1 (IC50>30 uM).
A-800141 also shows a greater selectivity against other aminopeptidases, as well as a CEREP panel of >80 receptors.
A-800141 causes the formation of GAPDH variants with an unprocessed N-terminal methionine in cell cultures in vitro.
A-800141 exhibits an antiangiogenesis effect and a broad anticancer activity in a variety of tumor xenografts including B cell lymphoma, neuroblastoma, and prostate and colon carcinomas, either as a single agent or in combination with cytotoxic agents.
A-800141 blocks tumor growth and MetAP2 activity in mouse models, which are causally connected to MetAP2 inhibition in vivo.
分子量 | 442.574 | |
分子式 | C24H30N2O4S | |
外观性状 | Solid | |
储存条件 |
|
|
Solubility |
10 mM in DMSO |
1. Wang J, et al. Proc Natl Acad Sci U S A. 2008 Feb 12;105(6):1838-43.
备案号:沪ICP备16042516号-1 Copyright © 2022 probechem.com. All Rights Reserved. probechem Copyright