Non-glutamate Type Pyrrolo[2, 3-d]pyrimidine Antifolates. I : Synthesis and Biological Properties of Pyrrolo[2, 3-d]pyrimidine Antifolates Containing Tetrazole Congener of Glutamic Acid

Abstract

Either the α- or γ-carboxyl group of the glutamic acid moiety of N-[4-[3-(2, 4-diamino-7H-pyrrolo[2, 3-d]pyrimidin-5-yl)propyl]benzoyl]-L-glutamic acid (1b, TNP-351) and its related compound (1a) was replaced with a 1H-tetrazle ring, and the inhibitory effects of the resulting compounds on dihydrofolate reductase (DHFR) and the growth of murine fibrosarcoma Meth A cells were examined. The γ-tetrazole analogs (2) were found to be much more potent DHFR inhibitors than TNP-351, and strongly inhibited the growth of Meth A cells. On the other hand, the α-tetrazole analogs (3) were much less active against Meth A cells, even though their DHFR-inhibitory activity was comparable to that of TNP-351. These findings suggest that the α-carboxyl group plays an important role in effective uptake via the reduced folate carrier, and a novel DHFR inhibitor could be obtained by chemically modifying the γ-carboxyl moiety while leaving the α-carboxyl group intact.