Literature DB >> 9507669

Benzisothiazole-1,1-dioxide alkanoic acid derivatives as inhibitors of rat lens aldose reductase.

G Primofiore1, F Da Settimo, C La Motta, F Simorini, A Minutolo, E Boldrini.   

Abstract

Derivatives of 4-substituted 1,2-benzisothiazole-1,1-dioxide alkanoic acids were prepared and their in vitro aldose reductase inhibitory activity was tested in rat lens enzyme. The acetic derivatives 10, 12, and 16a-d proved to be much more potent inhibitors than the propionic derivatives 11, 13, and 17a-d. The presence of an acyl moiety on the amino group in position 4 of the acetic derivatives 16a-d led to a significant increase in activity with respect to the parent compound 14. One of the most active compounds in vitro, 10, was also evaluated in vivo as an inhibitor of glutathione lens depletion in galactosemic rats, but it did not show any activity in maintaining the rat lens glutathione level, probably due to problems of ocular bioavailability or metabolism.

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Year:  1997        PMID: 9507669

Source DB:  PubMed          Journal:  Farmaco        ISSN: 0014-827X


  2 in total

1.  2-(3-Methyl-but-2-en-1-yl)-1,2-benziso-thia-zol-3(2H)-one 1,1-dioxide.

Authors:  Muhammad Nadeem Arshad; M Nawaz Tahir; Islam Ullah Khan; Muhammad Humayun Bilal; Hafiz Mubashar-Ur-Rehman
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2009-04-08

2.  A new approach to control the enigmatic activity of aldose reductase.

Authors:  Antonella Del-Corso; Francesco Balestri; Elisa Di Bugno; Roberta Moschini; Mario Cappiello; Stefania Sartini; Concettina La-Motta; Federico Da-Settimo; Umberto Mura
Journal:  PLoS One       Date:  2013-09-03       Impact factor: 3.240

  2 in total

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