Potent inhibition of thymidylate synthase by two series of nonclassical quinazolines
The synthesis and biological activity of two series of nonclassical thymidylate synthase (TS) inhibitors are described. The first is a series of 10-propargyl-5.8-dideazafolic acid derivatives (10a-j) and the second is a series of the analogous 2-desamino
McNamara,Berman,Fry,Werbel
p. 2045 - 2051
(2007/10/02)
Substituted quinazolinones as anticancer agents
Novel 6-substituted-4(3H)-quinazolinones are described as well as methods for the preparation and pharmaceutical composition of same, which inhabit the enzyme thymidylate synthase (TS) and are thus useful as anticancer agents.
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(2008/06/13)
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