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Chemical Structure : A-800141
Catalog No.: 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).
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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.
| M.Wt | 442.574 | |
| Formula | C24H30N2O4S | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Wang J, et al. Proc Natl Acad Sci U S A. 2008 Feb 12;105(6):1838-43.
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