Literature DB >> 146738

Cardenolide analogues. 7. Synthesis and biological activity of some new steroidal guanylhydrazones.

A Gelbart, R Thomas.   

Abstract

The synthesis, proof of structure, and biological activity of some new steroidal 17beta-formyl guanylhydrazones are described. The guanylhydrazones of nondigitalis-like steroids inhibited myocardial Na+,K+-ATPase but had only a depressant effect on myocardial contractility. By comparison, the corresponding guanylhydrazone of a digitalis-like steroid gave a positive inotropic effect in concentrations that also inhibited Na+,K+-ATPase. The nondigitalis-like guanylhydrazones also inhibited membrane Mg2+-ATPase and this may infer that the compounds act nonspecifically by membrane stabilization rather than by interaction with stereoselective receptors. Biological activity was determined in the guinea pig.

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Year:  1978        PMID: 146738     DOI: 10.1021/jm00201a010

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  3 in total

1.  14 beta-Hydroxyprogesterone binds to the digitalis receptor, inhibits the sodium pump and enhances cardiac contractility.

Authors:  D Bose; D Elliott; T Kobayashi; J F Templeton; V P Kumar; F S LaBella
Journal:  Br J Pharmacol       Date:  1988-02       Impact factor: 8.739

2.  Active-site directed inactivation of rat ovarian 20 alpha-hydroxysteroid dehydrogenase.

Authors:  J W Ricigliano; T M Penning
Journal:  Biochem J       Date:  1986-12-15       Impact factor: 3.857

3.  The lead structure in cardiac glycosides is 5 beta, 14 beta-androstane-3 beta 14-diol.

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Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1985-06       Impact factor: 3.000

  3 in total

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