Volume 22, Issue 39
Natural Products
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ChemInform Abstract: Synthesis and Anticancer Activity of Various 3′-Deoxy Pyrimidine Nucleoside Analogues and Crystal Structure of 1-(3-Deoxy-β-D- threo-pentofuranosyl)cytosine.

T.-S. LIN

T.-S. LIN

Dep. Pharm. Compreh. Cancer Center, Yale Univ. School Med., New Haven, CT 06510, USA

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J.-H. YANG

J.-H. YANG

Dep. Pharm. Compreh. Cancer Center, Yale Univ. School Med., New Haven, CT 06510, USA

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M.-C. LIU

M.-C. LIU

Dep. Pharm. Compreh. Cancer Center, Yale Univ. School Med., New Haven, CT 06510, USA

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Z.-Y. SHEN

Z.-Y. SHEN

Dep. Pharm. Compreh. Cancer Center, Yale Univ. School Med., New Haven, CT 06510, USA

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Y.-C. CHENG

Y.-C. CHENG

Dep. Pharm. Compreh. Cancer Center, Yale Univ. School Med., New Haven, CT 06510, USA

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W. H. PRUSOFF

W. H. PRUSOFF

Dep. Pharm. Compreh. Cancer Center, Yale Univ. School Med., New Haven, CT 06510, USA

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G. I. BIRNBAUM

G. I. BIRNBAUM

Dep. Pharm. Compreh. Cancer Center, Yale Univ. School Med., New Haven, CT 06510, USA

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J. GIZIEWICZ

J. GIZIEWICZ

Dep. Pharm. Compreh. Cancer Center, Yale Univ. School Med., New Haven, CT 06510, USA

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I. GHAZZOULI

I. GHAZZOULI

Dep. Pharm. Compreh. Cancer Center, Yale Univ. School Med., New Haven, CT 06510, USA

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V. BRANKOVAN

V. BRANKOVAN

Dep. Pharm. Compreh. Cancer Center, Yale Univ. School Med., New Haven, CT 06510, USA

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J.-S. FENG

J.-S. FENG

Dep. Pharm. Compreh. Cancer Center, Yale Univ. School Med., New Haven, CT 06510, USA

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G.-D. HSIUNG

G.-D. HSIUNG

Dep. Pharm. Compreh. Cancer Center, Yale Univ. School Med., New Haven, CT 06510, USA

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First published: October 1, 1991

Abstract

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

ChemInform Abstract

A series of 3′-deoxy pyrimidine nucleosides such as (II) are synthesized in multi-step syntheses starting with uridine (I). Some derivatives, e.g. (IIa) and (IIb), show significant antitumor activity against several cancer cell lines in vitro.

chemical structure image

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