PMID

Data

Article Title

Organization

Soft docking and multiple receptor conformations in virtual screening.

University of California San Francisco

Effect of Polygonum hydropiper sulfated flavonoids on lens aldose reductase and related enzymes.

Fukuyama University

 

Benzothiazol-2-ylcarboxylic acids with diverse spacers: A novel class of potent, orally active aldose reductase inhibitors

TBA

Aldose reductase and protein tyrosine phosphatase 1B inhibitors as a promising therapeutic approach for diabetes mellitus.

Aristotle University of Thessaloniki

Rational design of an indolebutanoic acid derivative as a novel aldose reductase inhibitor based on docking and 3D QSAR studies of phenethylamine derivatives.

Yonsei University

Novel, highly potent aldose reductase inhibitors: (R)-(-)-2-(4-bromo-2-fluorobenzyl)-1,2,3,4- tetrahydropyrrolo[1,2-a]pyrazine -4-spiro-3'-pyrrolidine-1,2',3,5'-tetrone (AS-3201) and its congeners.

Dainippon Pharmaceutical