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Banavara L. Mylari

Pfizer Global Research and Development

Groton Laboratories

Groton

Connecticut 06340

USA

[email]@aol.com

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Pfizer Global Research and Development, Groton Laboratories, Groton, Connecticut 06340, USA. 2002 - 2005

References

  1. 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) [Pubmed]
  2. 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) [Pubmed]
  3. 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) [Pubmed]
  4. 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) [Pubmed]
 
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