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Structure-Based Design and Synthesis of Lipophilic 2,4-Diamino-6-Substituted Quinazolines and Their Evaluation as Inhibitors of Dihydrofolate Reductases and Potential Antitumor Agents1

โœ Scribed by Galitsky, Nikolai; Luft, Joe R.; Pangborn, Walter; Gangjee, Aleem; Vidwans, Anup P.; Vasudevan, Anil; Queener, Sherry F.; Kisliuk, Roy L.; Cody, Vivian; Li, Ruming


Book ID
111987748
Publisher
American Chemical Society
Year
1998
Tongue
English
Weight
132 KB
Volume
41
Category
Article
ISSN
0022-2623

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Nine novel nonclassical 2,4-diamino-6-methyl-5-thioarylsubstituted-7H-pyrrolo [2,3-d]pyrimidines 2-10 were synthesized as potential inhibitors of dihydrofolate reductase and as antitumor agents. The analogues contain various electron donating and electron withdrawing substituents on the phenylsulfan