Synthesis of pyrrolo[3,4-c]pyridine derivatives possessing an acid group and their in vitro and in vivo evaluation as aldose reductase inhibitors

By Da Settimo A.   Primofiore G.   Da Settimo F.   Simorini F.   La Motta C.   Martinelli A.   Boldrini E.  

European Journal of Medicinal Chemistry, Vol. 31, Iss. 1, 1996-01 ,pp. : 49-58

Elsevier

Access to resources Recommend Favorite

On the prodrug potential of novel aldose reductase inhibitors with diphenylmethyleneaminooxycarboxylic acid structure

By Rakowitz D.   Matuszczak B.   Gritsch S.   Hofbauer P.   Krassnigg A.   Costantino L.  

European Journal of Pharmaceutical Sciences, Vol. 15, Iss. 1, 2002-02 ,pp. : 11-20

Elsevier

Access to resources Recommend Favorite

Aldose Reductase Inhibitors from the Nature

By  

Current Medicinal Chemistry, Vol. 10, Iss. 15, 2003-08 ,pp. : 1353-1374

Bentham Science Publishers

Access to resources Recommend Favorite

7-Hydroxy-2-substituted-4-H-1-benzopyran-4-one derivatives as aldose reductase inhibitors: a SAR study

By Costantino L.   Del Corso A.   Rastelli G.   Petrash J.M.   Mura U.  

European Journal of Medicinal Chemistry, Vol. 36, Iss. 9, 2001-09 ,pp. : 697-703

Elsevier

Access to resources Recommend Favorite

Structure-Activity Relationship Study Reveals Benzazepine Derivatives of Luteolin as New Aldose Reductase Inhibitors for Diabetic Cataract

By  

Current Drug Discovery Technologies, Vol. 13, Iss. 3, 2016-10 ,pp. : 152-163

Bentham Science Publishers

Access to resources Recommend Favorite