42417-69-6Relevant academic research and scientific papers
Folate-based inhibitors of thymidylate synthase: Synthesis and antitumor activity of γ-linked sterically hindered dipeptide analogues of 2-desamino- 2-methyl-N10-propargyl-5,8-dideazafolic acid (ICI 198583)
Bavetsias, Vassilios,Jackman, Ann L.,Marriott, Jonathan H.,Kimbell, Rosemary,Gibson, William,Boyle, F. Thomas,Bisset, Graham M. F.
, p. 1495 - 1510 (2007/10/03)
In an effort to synthesize inhibitors of thymidylate synthase (TS) that do not undergo polyglutamation, a series of γ-linked sterically hindered dipeptide analogues of 2-desamino-2-methyl-N10-propargyl-5,8-dideazafolic acid (ICI 198583) was pre
Thymidylate synthase inhibiting quinazolinones
-
, (2008/06/13)
Quinazolines of the formula STR1 wherein R1 is typically methyl, hydrogen or amino; R2 is typically methyl or propargyl; Ar is typically phenylene or 2'-fluorophenylene; R3 is the residue of a dipeptide substituted, typically by methyl, at position (a), (b) or (c), shown in the following partial formula: STR2 R4, R5, R6 and R8 are typically hydrogen, R7 is typically hydrogen or methyl; or a pharmaceutically acceptable salt, ester or amide thereof are of value in the treatment of cancer.
