The structure of Pneumocystis carinii dihydrofolate reductase to 1.9. Å resolution
Champness, J. N.; Achari, A.; Ballantine, S. P.; Bryant, P. K.; Delves, C. J.; Stammers, D. K. The structure of Pneumocystis carinii Dihydrofolate Reductase to 1.9. Å Resolution. Structure 1994, 2, 915-924.
Identification and cloning of the Mycobacterium avium FolA gene, required for dihydrofolate reductase activity
Ginkel, S. Z.; Dooley, T. P.; Suling, W. J.; Barrow, W. W. Identification and Cloning of the Mycobacterium avium FolA Gene, Required for Dihydrofolate Reductase Activity. FEMS Microbiol. Lett. 1997, 156, 69-78.
2,4-Diaminothieno[2,3-d]pyrimidines as antifolates and antimalarials. 3. Synthesis of 5,6-disubstituted derivatives and related tetracyclic analogs
Rosowsky, A.; Chen, K. K. N.; Lin, M. 2,4-Diaminothieno[2,3-d]pyrimidines as Antifolates and Antimalarials. 3. Synthesis of 5,6-Disubstituted Derivatives and Related Tetracyclic Analogs. J. Med. Chem. 1973, 16, 191-194.
2,4-Diaminothieno[2,3-d]pyrimidine analogs of trimetrexate and piritrexim as potential inhibitors of Pneumocystis carinii and Toxoplasma gondii dihydrofolate reductase
Rosowsky, A.; Mota, C. E.; Wright, J. E.; Freisheim, J. H.; Heusner, J. J.; McCormack, J. J.; Queener, S. F. 2,4-Diaminothieno[2,3-d]pyrimidine Analogs of Trimetrexate and Piritrexim as Potential Inhibitors of Pneumocystis carinii and Toxoplasma gondii Dihydrofolate Reductase. J. Med. Chem. 1993, 36, 3103-3112.
Synthesis and DHFR inhibitory activity of a series of 6-substituted-2,4-diaminothieno-[2,3-d]pyrimidines
Donkor, I. O.; Li, H.; Queener, S. F. Synthesis and DHFR Inhibitory Activity of a Series of 6-Substituted-2,4-diaminothieno-[2,3-d]pyrimidines. Eur. J. Med. Chem. 2003, 38, 605-611.
Synthesis and dihydrofolate reductase inhibitory activities of 2,4-diamino-5-deaza and 2,4-diamino-5,10-dideaza lipophilic antifolates
Gangjee, A.; Devraj, R.; Queener, S. F. Synthesis and Dihydrofolate Reductase Inhibitory Activities of 2,4-Diamino-5-deaza and 2,4-Diamino-5,10- dideaza Lipophilic Antifolates. J. Med. Chem. 1997, 40, 470-478.
Conformational analysis of human dihydrofolate reductase inhibitor complexes: Crystal structure determination of wild type and F31 mutant binary and ternary inhibitor complexes
Cody, V.; Wojtczak, A.; Kalman, T. I.; Friesheim, J. H.; Blakley, R. L. Conformational Analysis of Human Dihydrofolate Reductase Inhibitor Complexes: Crystal Structure Determination of Wild Type and F31 Mutant Binary and Ternary Inhibitor Complexes. Adv. Exp. Med. Biol. 1993, 338, 481-486.
A one-step ring transformation/ring annulation approach to pyrrolo[2,3-d]pyrimidines. A new synthesis of the potent dihydrofolate reductase inhibitor TNP-351
Taylor, E. C.; Patel, H. H.; Jun, J.-G. A One-Step Ring Transformation/Ring Annulation Approach to Pyrrolo[2,3-d]pyrimidines. A New Synthesis of the Potent Dihydrofolate Reductase Inhibitor TNP-351. J. Org. Chem. 1995, 60, 6684-6687.
2-Amino-4-oxo-5-substituted-pyrrolo[2,3-d]pyrimidines as nonclassical antifolate inhibitors of thymidylate synthase
Gangjee, A.; Mavandadi, F.; Kisliuk, R. L.; McGuire, J. J.; Queener, S. F. 2-Amino-4-oxo-5-substituted-pyrrolo[2,3-d]pyrimidines as Nonclassical Antifolate Inhibitors of Thymidylate Synthase. J. Med. Chem. 1996, 39, 4563-4568.