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Page 1
Indole-2-carboxamide inhibitors of human liver glycogen phosphorylase.
Hoover DJ, Lefkowitz-Snow S, Burgess-Henry JL, Martin WH, Armento SJ, Stock IA, McPherson RK, Genereux PE, Gibbs EM, Treadway JL. Hoover DJ, et al. Among authors: armento sj. J Med Chem. 1998 Jul 30;41(16):2934-8. doi: 10.1021/jm980264k. J Med Chem. 1998. PMID: 9685232 No abstract available.
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 BL, Armento SJ, Beebe DA, Conn EL, Coutcher JB, Dina MS, O'Gorman MT, Linhares MC, Martin WH, Oates PJ, Tess DA, Withbroe GJ, Zembrowski WJ. Mylari BL, et al. Among authors: armento sj. J Med Chem. 2003 Jun 5;46(12):2283-6. doi: 10.1021/jm034065z. J Med Chem. 2003. PMID: 12773033
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 BL, Armento SJ, Beebe DA, Conn EL, Coutcher JB, Dina MS, O'Gorman MT, Linhares MC, Martin WH, Oates PJ, Tess DA, Withbroe GJ, Zembrowski WJ. Mylari BL, et al. Among authors: armento sj. J Med Chem. 2005 Oct 6;48(20):6326-39. doi: 10.1021/jm050462t. J Med Chem. 2005. PMID: 16190759