Banavara L. Mylari
Pfizer Global Research and Development
Groton Laboratories
Groton
Connecticut 06340
USA
Name/email consistency: high
- A novel series of non-carboxylic acid, non-hydantoin inhibitors of aldose reductase with potent oral activity in diabetic rat models: 6-(5-chloro-3-methylbenzofuran-2-sulfonyl)-2H-pyridazin-3-one and congeners. 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, P.J., Tess, D.A., Withbroe, G.J., Zembrowski, W.J. J. Med. Chem. (2005)
- 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, P.J., Tess, D.A., Withbroe, G.J., Zembrowski, W.J. J. Med. Chem. (2003)
- Design and synthesis of a novel family of triazine-based inhibitors of sorbitol dehydrogenase with oral activity: 1-[4-[3R,5S-dimethyl-4-(4-methyl-[1,3,5]triazin-2-yl)-piperazin-1-yl]-[1,3,5]triazin-2-yl]-(R) ethanol. Mylari, B.L., Withbroe, G.J., Beebe, D.A., Brackett, N.S., Conn, E.L., Coutcher, J.B., Oates, P.J., Zembrowski, W.J. Bioorg. Med. Chem. (2003)
- A sorbitol dehydrogenase inhibitor of exceptional in vivo potency with a long duration of action: 1-(R)-[4-[4-(4,6-dimethyl[1,3,5]triazin-2-yl)- 2R,6S-dimethylpiperazin-1-yl]pyrimidin-2- yl]ethanol. Mylari, B.L., Oates, P.J., Zembrowski, W.J., Beebe, D.A., Conn, E.L., Coutcher, J.B., O'Gorman, M.T., Linhares, M.C., Withbroe, G.J. J. Med. Chem. (2002)