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Synthesis and structure-activity relationship of ribofuranosyl echiguanine analogs as inhibitors of phosphatidylinositol 4-kinase

Y Saito, K Kato, K Umezawa

文献索引：Saito, Yoshio; Kato, Kuniki; Umezawa, Kazuo Tetrahedron, 1998 ,  vol. 54,  # 17  p. 4251 - 4266

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被引用次数: 7

摘要

N-Substituted-2-amino-4 (3H)-7H-oxopyrrolo [2, 3-d] pyrimidine-5-carboxamides and their ribofuranosyl and 2′, 3′-dideoxyribofuranosyl derivatives were prepared as membrane permeable echiguanine analogs and tested for their ability to inhibit phosphatidylinositol (PI) 4-kinase. Compounds 5 and 6 were found to inhibit the enzyme approximately at the same level as echiguanines A and B. It is noteworthy that ribofuranosides 18, 19, and 20 and ...