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C6 modification of the pyridinone core of thrombin inhibitor L-374,087 as a means of enhancing its oral absorption

Authors :
C. M. Cooper
Elizabeth P. Baskin
Elizabeth A. Lyle
J.J. Lynch
Lucas R
I.-W. Chen
Jacquelynn J. Cook
Sanderson Philip E
Kellie J. Cutrona
Kari Vastag
S. D. Lewis
M. G. Solinsky
Christina L. Newton
Richard C.A. Isaacs
Maria T. Stranieri
J. P. Vacca
Stephen J. Gardell
Adel M. Naylor-Olsen
Source :
Bioorganicmedicinal chemistry letters. 8(13)
Publication Year :
1999

Abstract

1 (L-374,087) is a potent, selective, efficacious, and orally bioavailable thrombin inhibitor that contains a core 3-amino-2-pyridinone moiety. Replacement of the C6 pyridinone methyl group of 1 by a propyl group gave 5 (L-375,052), which retained all the excellent properties of 1, and also yielded higher plasma levels after oral dosing in dogs and rats.

Details

ISSN :
0960894X
Volume :
8
Issue :
13
Database :
OpenAIRE
Journal :
Bioorganicmedicinal chemistry letters
Accession number :
edsair.doi.dedup.....ce0cae6c611da785a9c22fd3e180c35c