ARTICLE;
DIABETES MELLITUS;
DRUG ACTIVITY;
DRUG MECHANISM;
DRUG POTENCY;
DRUG SCREENING;
DRUG SYNTHESIS;
ENZYME ACTIVITY;
ENZYME INHIBITION;
IC 50;
IN VITRO STUDY;
PHARMACOPHORE;
PRIORITY JOURNAL;
The aldo-keto reductase superfamily. cDNAs and deduced aminoacid sequences of human aldehyde and aldose reductases
Bohren K.M., Bullock B., Wermuth B., Gabbay K.H. The aldo-keto reductase superfamily. cDNAs and deduced aminoacid sequences of human aldehyde and aldose reductases. J. Biol. Chem. 264:1989;9547-9551.
Synthesis, activity, and molecular modeling of a new series of tricyclic pyridazinones as selective aldose reductase inhibitors
Costantino L., Rastelli G., Vescovini K., Cignarella G., Vianello P., Del Corso A., Cappiello M., Mura U., Barlocco D. Synthesis, activity, and molecular modeling of a new series of tricyclic pyridazinones as selective aldose reductase inhibitors. J. Med. Chem. 39:1996;4396-4405.
Relation between serum 3-deoxyglucosone and development of diabetic microangiopathy
Kotsunori H., Miyata S., Ohara T., Liu B.-F., Urihara A., Kojima H., Suzuki K., Myiazaki H., Yamashita Y., Inaba K., Kasuga M. Relation between serum 3-deoxyglucosone and development of diabetic microangiopathy. Diabetes care. 26:2003;1889-1894.
Novel spirosuccinimide aldose reductase inhibitors derived from isoquinoline-1,3-diones: 2-[(4-bromo-2-fluorophenyl)methyl]-6-fluorospiro- isoquinoline-[4(1H)-3′-pyrrolidine]-1,2′,3,5′(2H)-tetrone and congeners. Part 1
Malamas M.S., Hohman T.C., Millen J. Novel spirosuccinimide aldose reductase inhibitors derived from isoquinoline-1,3-diones: 2-[(4-bromo-2- fluorophenyl)methyl]-6-fluorospiro-isoquinoline-[4(1H)-3′-pyrrolidine]-1, 2′,3,5′(2H)-tetrone and congeners. Part 1. J. Med. Chem. 37:1994;2043-2058.
Approaches to the rational design of enzyme inhibitors
Wolff, M. (Ed.), Wiley, New York
Muscate, A., Kenion, G.L., 1995. Approaches to the rational design of enzyme inhibitors. In: Wolff, M. (Ed.), Burger's Medicinal Chemistry and Drug Discovery, vol. 1, Principles and Practice. Wiley, New York, p. 733.
A highly selective, non hydantoin, non carboxylic acid inhibitor of aldose reductase with potent oral activity in diabetic rat models: 6-(5-chloro-3-methylbenzofuran-2-sulfonyl)-2-H-pyridazin-3-one
Mylari B.L., Armento S.J., Beebe D.A., Conn E.L., Coutcher J.B., Dina M.S., O'Gorman M.T., Linhares M.C., Martin W.H., Oates D.J., Tess D.A., Withbroe G.J., Zembrowski W.J. A highly selective, non hydantoin, non carboxylic acid inhibitor of aldose reductase with potent oral activity in diabetic rat models: 6-(5-chloro-3-methylbenzofuran-2-sulfonyl)-2-H-pyridazin-3- one. J. Med. Chem. 46:2003;2283-2286.
Evaluation of a sorbitol dehydrogenase inhibitor on diabetic peripheral nerve metabolism: A prevention study
Obrosova I.G., Fathallah I., Lang H.J., Greene D.A. Evaluation of a sorbitol dehydrogenase inhibitor on diabetic peripheral nerve metabolism: a prevention study. Diabetologia. 42:1999;1187-1194.
Synthesis and pharmacological evaluation of 4,4a,5,6-tetrahydro-2H- thieno[2,3-h]-cinnolin-3-ones bioisosters of antihypertensive and antithrombotic benzo[h]-cinnolinones
Pinna G.A., Barlocco D. Synthesis and pharmacological evaluation of 4,4a,5,6-tetrahydro-2H-thieno[2,3-h]-cinnolin-3-ones bioisosters of antihypertensive and antithrombotic benzo[h]-cinnolinones. Eur. J. Med. Chem. 26:1991;787-790.
Synthesis and evaluation of novel 2-aryl-2,5,6,7-tetrahydro-3H- thieno[2′,3′:6,7]cyclohepta[1,2-c]pyridazin-3-ones and 2-aryl-5,6-dihydrothieno[2,3-h]cinnolin-3(2H)-ones as anxiolytics
Tanaka H., Kirihara S., Yasumatsu H., Yakushiji T., Nakao T. Synthesis and evaluation of novel 2-aryl-2,5,6,7-tetrahydro-3H-thieno[2′,3′:6, 7]cyclohepta[1,2-c]pyridazin-3-ones and 2-aryl-5,6-dihydrothieno[2,3-h]cinnolin- 3(2H)-ones as anxiolytics. Eur. J. Med. Chem. Chim. Ther. 32:1997;607-615.
Wilson, D.K., Qhiocho, F.A., Petrash, J.M., 1997. Structural studies of aldose reductase inhibition. In: Veerapandian, P. (Ed.), Structure-Based Drug Design. Marcel Dekker, New York, pp. 229-246.
Aldose reductase in glucose toxicity: A potential target for the prevention of diabetic complications
Yabe-Nishimura C. Aldose reductase in glucose toxicity: a potential target for the prevention of diabetic complications. Pharmacol. Rev. 50:1998;21-33.