Several methyl benzothiazolyloxybenzoates, S-isosters, and the corresponding benzoic acids were synthesized and tested as aldose reductase inhibitors (ARIs). Out of this series, the ester derivative 2a-7 was found to exhibit the highest enzyme-inhibitoric activity. In order to investigate this unexpected result, further modifications were carried out which allowed us to explain this finding and to open a path to a novel class of ARIs.

Synthesis of novel benzoic acid derivatives with benzothiazolyl subunit and evaluation as aldose reductase inhibitors / Rakowitz, D; Hennig, B; Nagano, M; Steger, S; Costantino, Luca; Matuszczak, B.. - In: ARCHIV DER PHARMAZIE. - ISSN 0365-6233. - STAMPA. - 338:(2005), pp. 411-418. [10.1002/ardp.200500101]

Synthesis of novel benzoic acid derivatives with benzothiazolyl subunit and evaluation as aldose reductase inhibitors

COSTANTINO, Luca;
2005

Abstract

Several methyl benzothiazolyloxybenzoates, S-isosters, and the corresponding benzoic acids were synthesized and tested as aldose reductase inhibitors (ARIs). Out of this series, the ester derivative 2a-7 was found to exhibit the highest enzyme-inhibitoric activity. In order to investigate this unexpected result, further modifications were carried out which allowed us to explain this finding and to open a path to a novel class of ARIs.
2005
338
411
418
Synthesis of novel benzoic acid derivatives with benzothiazolyl subunit and evaluation as aldose reductase inhibitors / Rakowitz, D; Hennig, B; Nagano, M; Steger, S; Costantino, Luca; Matuszczak, B.. - In: ARCHIV DER PHARMAZIE. - ISSN 0365-6233. - STAMPA. - 338:(2005), pp. 411-418. [10.1002/ardp.200500101]
Rakowitz, D; Hennig, B; Nagano, M; Steger, S; Costantino, Luca; Matuszczak, B.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/3307
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