Synthesis and Structure−Activity Relationships of 17β-Substituted 14β-Hydroxysteroid 3-(α-l-Rhamnopyranoside)s: Steroids That Bind to the Digitalis Receptor-Reference-Cited by-同舟云学术

Synthesis and Structure−Activity Relationships of 17β-Substituted 14β-Hydroxysteroid 3-(α-l-Rhamnopyranoside)s: Steroids That Bind to the Digitalis Receptor

Published:1997-05-01 Issue:10 Volume:40 Page:1439-1446
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Templeton John F.¹,Ling Yangzhi¹,Marat Kirk¹,LaBella Frank S.¹

Affiliation:

1. Faculty of Pharmacy and Department of Chemistry, University of Manitoba, Winnipeg, Manitoba R3T 2N2, Canada, and Department of Pharmacology and Therapeutics, Faculty of Medicine, University of Manitoba, Winnipeg, Manitoba R3E 0W3, Canada

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm960880l

Reference27 articles.

1. Synthesis of 20-hydroxy-, 20-amino-, and 20-nitro-14-hydroxy-21-nor-5.beta.,14.beta.-pregnane C-3 glycosides and related derivatives: structure-activity relationships of pregnanes that bind to the digitalis receptor

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4. 17β-O-Aminoalkyloximes of 5β-Androstane-3β,14β-diol with Digitalis-like Activity: Synthesis, Cardiotonic Activity, Structure−Activity Relationships, and Molecular Modeling of the Na+,K+-ATPase Receptor;Journal of Medicinal Chemistry;2000-05-17

5. A Short Review on Cardiotonic Steroids and Their Aminoguanidine Analogues;Molecules;2000-01-21