1,2-Dihydropyrido[3,4-b]pyrazines: structure-activity relationships

• Published in: Journal of medicinal chemistry 1983-01, Vol.26 (1), p.91-95
• Main Authors: Temple, Carroll, Wheeler, Glynn P, Elliott, Robert D, Rose, Jerry D, Comber, Robert N, Montgomery, John A
• Format: Article
• Language: English
• Subjects: Animals; Antineoplastic Agents - chemical synthesis; Cell Survival - drug effects; Cells, Cultured; Leukemia L1210 - drug therapy; Mice; Mitosis - drug effects; Pyrazines - chemical synthesis; Pyrazines - pharmacology; Pyridines - chemical synthesis; Pyridines - pharmacology; Structure-Activity Relationship
• ISSN: 0022-2623; 1520-4804
• DOI: 10.1021/jm00355a018

Certain derivatives containing the 1,2-dihydropyrido[3,4-b]pyrazine (1-deaza-7,8-dihydropteridine) ring system are active against experimental neoplasms in mice. The mechanism of action of these agents has been attributed to the accumulation of cells at mitosis. Identification of the structural features that are necessary for activity was accomplished by evaluation of modified 1-deazapteridines and ring and ring-opened analogues. Relative to ethyl 4-amino-1-deaza-7,8-dihydro-6-[(N-methylanilino)methyl]pteridine-2-carbamate (11) and the corresponding 6-phenyl compound (12), no antitumor activity was observed with 7,8-dihydropteridines, 3-deaza-7,8-dihydropteridines, and the corresponding heteroaromatic compounds. Also, activity was diminished or destroyed when 1-deaza-7,8-dihydropteridines were oxidized to 1-deazapteridines or reduced to 1-deaza-5,6,7,8-tetrahydropteridines. In addition, replacement of the 4-amino group with other substituents destroyed activity. The presence of a 6-substituent containing an aryl group appeared to be necessary for activity, which was increased when a methyl group was substituted at the 7-position.