Literature DB >> 3097318

Synthesis and biological evaluation of irreversible inhibitors of aldose reductase.

J J Ares, P F Kador, D D Miller.   

Abstract

5-Isothiocyanatoalrestatin (1b) and 5-azidoalrestatin (1c) were prepared synthetically and examined as potential affinity and photoaffinity inhibitors of rat lens aldose reductase. Both compound 1b and 1c under appropriate conditions at 10(-4) M produced a 70% irreversible inactivation of aldose reductase within 1 min. The enzyme could, in part, be protected by preincubation with sorbinil 2, a known potent inhibitor of aldose reductase.

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Year:  1986        PMID: 3097318     DOI: 10.1021/jm00161a040

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


  4 in total

1.  New approach for preparation of 2,3,7-trisubstituted 3,4-dihydroisoquinolinone libraries on solid phase.

Authors:  Y Ni; V Krchnak; M Lebl
Journal:  Mol Divers       Date:  2000       Impact factor: 2.943

2.  Synthesis and the Biological Activity of Phosphonylated 1,2,3-Triazolenaphthalimide Conjugates.

Authors:  Iwona E Głowacka; Rafał Gulej; Piotr Grzonkowski; Graciela Andrei; Dominique Schols; Robert Snoeck; Dorota G Piotrowska
Journal:  Molecules       Date:  2016-10-26       Impact factor: 4.411

3.  Design, antiviral and cytostatic properties of isoxazolidine-containing amonafide analogues.

Authors:  Kamil Kokosza; Graciela Andrei; Dominique Schols; Robert Snoeck; Dorota G Piotrowska
Journal:  Bioorg Med Chem       Date:  2015-05-06       Impact factor: 3.641

Review 4.  Sulforaphane and Its Bifunctional Analogs: Synthesis and Biological Activity.

Authors:  Łukasz Janczewski
Journal:  Molecules       Date:  2022-03-07       Impact factor: 4.411

  4 in total

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