Synthesis and biological activity of benzo-fused 7-deazaadenosine analogues. 5- and 6-substituted 4-amino- or 4-alkylpyrimido[4,5-b]indole ribonucleosides-Reference-Cited by-同舟云学术

Synthesis and biological activity of benzo-fused 7-deazaadenosine analogues. 5- and 6-substituted 4-amino- or 4-alkylpyrimido[4,5-b]indole ribonucleosides

Published:2013-09 Issue:17 Volume:21 Page:5362-5372
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Tichý Michal,Pohl Radek,Tloušt’ová Eva,Weber Jan,Bahador Gina,Lee Yu-Jen,Hocek Michal

Funder

Academy of Sciences of the Czech Republic

Czech Science Foundation

Gilead Sciences, Inc

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference28 articles.

1. 6-(Het)aryl-7-Deazapurine Ribonucleosides as Novel Potent Cytostatic Agents

2. Synthesis and Significant Cytostatic Activity of 7-Hetaryl-7-deazaadenosines

3. Sugar-modified derivatives of cytostatic 6-(het)aryl-7-deazapurine nucleosides: 2′-C-methylribonucleosides, arabinonucleosides and 2′-deoxy-2′-fluoroarabinonucleosides

4. CycloSal-phosphate Pronucleotides of Cytostatic 6-(Het)aryl-7-deazapurine Ribonucleosides: Synthesis, Cytostatic Activity, and Inhibition of Adenosine Kinases

5. Phosphoramidate pronucleotides of cytostatic 6-aryl-7-deazapurine ribonucleosides

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