4.7 Article

Fumarranol, a rearranged fumagillin analogue that inhibits angiogenesis in vivo

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JOURNAL OF MEDICINAL CHEMISTRY
卷 49, 期 19, 页码 5645-5648

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AMER CHEMICAL SOC
DOI: 10.1021/jm060559v

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The fumagillin family of natural products inhibits angiogenesis through the irreversible inhibition of the type 2 methionine aminopeptidase (MetAP2). Herein is reported a novel fumagillin analogue named fumarranol. It is shown that, like fumagillin, fumarranol selectively inhibits MetAP2 and endothelial cell proliferation. It is also active in a mouse model of angiogenesis in vivo. Unlike TNP-470, fumarranol does not covalently bind to MetAP2. Fumarranol may serve as a lead for a new class of angiogenesis inhibitors.

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