CAS: 925705-73-3; 3-(2,4-Diaminopteridin-6-yl)Phenol

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3-hydroxyphenylglyoxal 2,4,5,6-tetraaminopyrimidine sulfate acetone oxime

📜3-Hydroxyphenylglyoxal,2,4,5,6-四氨基嘧啶硫酸盐置于盐酸,丙酮肟体系中,化学反应 10.0H,以96.5%的收率获得产物3-(2,4-二氨基蝶呤-6-基)苯酚
参考文献:Discovery Of 3,3'-(2,4-Diaminopteridine-6,7-Diyl)Diphenol As An Isozyme-Selective Inhibitor Of Pi3K For The Treatment Of Ischemia Reperfusion Injury Associated With Myocardial Infarction
标题:Discovery Of 3,3'-(2,4-Diaminopteridine-6,7-Diyl)Diphenol As An Isozyme-Selective Inhibitor Of Pi3K For The Treatment Of Ischemia Reperfusion Injury Associated With Myocardial Infarction
摘要:In Studies Aimed Toward Identifying Effective And Safe Inhibitors Of Kinase Signaling Cascades That Underlie Ischemia/reperfusion (I/r) Injury,We Synthesized A Series Of Pteridines And Pyridopyrazines. The Design Strategy Was Inspired By The Examination Of Naturally occurring Pi3K Inhibitors Such As Wortmannin And Quercetin,And Building A Pharmacophore-Based Model Used For Optimization. Structural Modifications Led To Hybrid Molecules Which Incorporated Aminopyrimidine And Aminopyridine Moieties With Atp Mimetic Characteristics Into The Pharmacophore Motifs To Modulate Kinase Affinity And Selectivity. Elaborations Involving Substitutions Of The 2 And 4 Positions Of The Pyrimidine Or Pyridine Ring And The 6 And 7 Positions Of The Central Pyrazine Ring Resulted In In Vivo Activity Profiles Which Identified Potent Inhibitors Of Vascular Endothelial Growth Factor (Vegf) Induced Vascular Leakage. Pathway Analysis Identified A Diaminopteridine-Diphenol As A Potent And Selective Phosphatidylinositol-3-Kinase (Pi3K) Inhibitor. The Structure-Activity Relationship Studies Of Various Analogues Of Diaminopteridine-Diphenol-Based On Biochemical Assays Resulted In Potent Inhibitors Of Pi3K.
DOI:10.1021/jm051056C