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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Discovery and structural modification of inhibitors of methionine aminopeptidases from Escherichia coli and Saccharomyces cerevisiae.

A series of pyridine-2-carboxylic acid derivatives were synthesized according to the leads from the screening, and potent inhibitors have been obtained by structural modification. They have shown submicromolar inhibition of the enzymes (for example, for 9n, IC(50) = 130 nM for EcMetAP1 and IC(50) = 380 nM for ScMetAP1). They represent small-molecule MetAP inhibitors with novel structures different from alkylating fumagillin derivatives and peptidic bestatin-based MetAP inhibitor.[1]

References

  1. Discovery and structural modification of inhibitors of methionine aminopeptidases from Escherichia coli and Saccharomyces cerevisiae. Luo, Q.L., Li, J.Y., Liu, Z.Y., Chen, L.L., Li, J., Qian, Z., Shen, Q., Li, Y., Lushington, G.H., Ye, Q.Z., Nan, F.J. J. Med. Chem. (2003) [Pubmed]
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