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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Saleem Ahmad

Research & Development

Bristol-Myers Squibb Co

PO Box 4000


United States


Name/email consistency: high



  • Research & Development, Bristol-Myers Squibb Co, PO Box 4000, Princeton, United States. 2010
  • Bristol-Myers Squibb Research & Development, P.O. Box 4000, Princeton, New Jersey 08543, USA. 2001 - 2008


  1. Tricyclic dihydroquinazolinones as novel 5-HT2C selective and orally efficacious anti-obesity agents. Ahmad, S., Ngu, K., Miller, K.J., Wu, G., Hung, C.P., Malmstrom, S., Zhang, G., O'Tanyi, E., Keim, W.J., Cullen, M.J., Rohrbach, K.W., Thomas, M., Ung, T., Qu, Q., Gan, J., Narayanan, R., Pelleymounter, M.A., Robl, J.A. Bioorg. Med. Chem. Lett. (2010) [Pubmed]
  2. (3R,5S,E)-7-(4-(4-fluorophenyl)-6-isopropyl-2-(methyl(1-methyl-1h-1,2,4-triazol-5-yl)amino)pyrimidin-5-yl)-3,5-dihydroxyhept-6-enoic acid (BMS-644950): a rationally designed orally efficacious 3-hydroxy-3-methylglutaryl coenzyme-a reductase inhibitor with reduced myotoxicity potential. Ahmad, S., Madsen, C.S., Stein, P.D., Janovitz, E., Huang, C., Ngu, K., Bisaha, S., Kennedy, L.J., Chen, B.C., Zhao, R., Sitkoff, D., Monshizadegan, H., Yin, X., Ryan, C.S., Zhang, R., Giancarli, M., Bird, E., Chang, M., Chen, X., Setters, R., Search, D., Zhuang, S., Nguyen-Tran, V., Cuff, C.A., Harrity, T., Darienzo, C.J., Li, T., Reeves, R.A., Blanar, M.A., Barrish, J.C., Zahler, R., Robl, J.A. J. Med. Chem. (2008) [Pubmed]
  3. Tetrahydronaphthalene-derived amino alcohols and amino ketones as potent and selective inhibitors of the delayed rectifier potassium current IKs. Ahmad, S., Doweyko, L., Ashfaq, A., Ferrara, F.N., Bisaha, S.N., Schmidt, J.B., DiMarco, J., Conder, M.L., Jenkins-West, T., Normandin, D.E., Russell, A.D., Smith, M.A., Levesque, P.C., Lodge, N.J., Lloyd, J., Stein, P.D., Atwal, K.S. Bioorg. Med. Chem. Lett. (2004) [Pubmed]
  4. Aminoimidazoles as bioisosteres of acylguanidines: novel, potent, selective and orally bioavailable inhibitors of the sodium hydrogen exchanger isoform-1. Ahmad, S., Ngu, K., Combs, D.W., Wu, S.C., Weinstein, D.S., Liu, W., Chen, B.C., Chandrasena, G., Dorso, C.R., Kirby, M., Atwal, K.S. Bioorg. Med. Chem. Lett. (2004) [Pubmed]
  5. Arylcyclopropanecarboxyl guanidines as novel, potent, and selective inhibitors of the sodium hydrogen exchanger isoform-1. Ahmad, S., Doweyko, L.M., Dugar, S., Grazier, N., Ngu, K., Wu, S.C., Yost, K.J., Chen, B.C., Gougoutas, J.Z., DiMarco, J.D., Lan, S.J., Gavin, B.J., Chen, A.Y., Dorso, C.R., Serafino, R., Kirby, M., Atwal, K.S. J. Med. Chem. (2001) [Pubmed]
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