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Synthesis of ribofuranosyl glycosides of echiguanines A and B, inhibitors of phosphatidylinositol 4-kinase

✍ Scribed by Kasumi Sanpei; Yoshio Saito; Masaya Imoto; Kazuo Umezawa; Kuniki Kato


Book ID
103983583
Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
195 KB
Volume
6
Category
Article
ISSN
0960-894X

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✦ Synopsis


The synthesis of ribofuranosyl glycosides of echiguanines A and B, PI 4-kinase inhibitors, was achieved from 2-amino-4-chloropyrrolo[2,3-d]pyrimidine and 2,3-O-isopropylidene-5-O-(t-butyl) dimethylsilyl-o~-D-ribofuranosyl chloride. The ribofuranosyl echiguanine A weakly inhibited PI 4-kinase.


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Synthesis and structure-activity relatio
✍ Yoshio Saito; Kuniki Kato; Kazuo Umezawa πŸ“‚ Article πŸ“… 1998 πŸ› Elsevier Science 🌐 French βš– 923 KB

N-Substituted-2-amino-4(3/-/)-7H-oxopyrrolo[2,3-d]pyrimidine-5-carboxamides and their ribofuranosyl and 2',3'-dideoxyribofuranosyl derivatives were ixcpared as membrane permeable Β’chiguanine analogs and tested for their ability to inhibit phosphatidylinositol (PI) 4-kinase. Compounds 5 and 6 were fo