Synthesis of D-ring-substituted (5′R)- and (5′S)-17β-pyrazolinylandrostene epimers and comparison of their potential anticancer activities-Reference-Cited by-同舟云学术

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Synthesis of D-ring-substituted (5′R)- and (5′S)-17β-pyrazolinylandrostene epimers and comparison of their potential anticancer activities

Published:2012-04 Issue:5 Volume:77 Page:566-574
ISSN:0039-128X
Container-title:Steroids
language:en
Short-container-title:Steroids

Author:

Iványi Zoltán,Szabó Nikoletta,Huber Judit,Wölfling János,Zupkó István,Szécsi Mihály,Wittmann Tibor,Schneider Gyula

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Pharmacology,Endocrinology,Molecular Biology,Biochemistry

Reference31 articles.

1. Synthetic cardenolides and related compounds;Schneider;Curr Org Chem,2004

2. 17-Imidazolyl, pyrazolyl and isoxazolyl androstene derivatives. Novel steroid inhibitors of human cytochrome C17,20-lyase (P45017α);Ling;J Med Chem,1997

3. Novel 17-azolyl steroids, potent inhibitors of human cytochrome 17α-hydroxylase-C17,20-lyase (P45017α): potent agent for the treatment of prostate cancer;Njar;J Med Chem,1998

4. Neighbouring group participation. Part 15. Stereoselective synthesis of some steroidal tetrahydrooxazin-2-ones, as novel presumed inhibitors of human 5α-reductase;Wölfling;Steroids,2004

5. Stereoselective synthesis of some 17β-dihydrooxazinyl steroids, as novel presumed inhibitors of 17α-hydroxylase-C17,20-lyase;Wölfling;Steroids,2006

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