4.7 Article

Fumarranol, a rearranged fumagillin analogue that inhibits angiogenesis in vivo

Journal

JOURNAL OF MEDICINAL CHEMISTRY
Volume 49, Issue 19, Pages 5645-5648

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jm060559v

Keywords

-

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available