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

Robert J. Altenbach

Neuroscience Research

Global Pharmaceutical Research and Development

Abbott Laboratories

100 Abbott Park Road

United States


Name/email consistency: high



  • Neuroscience Research, Global Pharmaceutical Research and Development, Abbott Laboratories, 100 Abbott Park Road, United States. 2002 - 2010


  1. Diaryldiamines with dual inhibition of the histamine H(3) receptor and the norepinephrine transporter and the efficacy of 4-(3-(methylamino)-1-phenylpropyl)-6-(2-(pyrrolidin-1-yl)ethoxy)naphthalen-1-ol in pain. Altenbach, R.J., Black, L.A., Strakhova, M.I., Manelli, A.M., Carr, T.L., Marsh, K.C., Wetter, J.M., Wensink, E.J., Hsieh, G.C., Honore, P., Garrison, T.R., Brioni, J.D., Cowart, M.D. J. Med. Chem. (2010) [Pubmed]
  2. Structure-activity studies on a series of a 2-aminopyrimidine-containing histamine H4 receptor ligands. Altenbach, R.J., Adair, R.M., Bettencourt, B.M., Black, L.A., Fix-Stenzel, S.R., Gopalakrishnan, S.M., Hsieh, G.C., Liu, H., Marsh, K.C., McPherson, M.J., Milicic, I., Miller, T.R., Vortherms, T.A., Warrior, U., Wetter, J.M., Wishart, N., Witte, D.G., Honore, P., Esbenshade, T.A., Hancock, A.A., Brioni, J.D., Cowart, M.D. J. Med. Chem. (2008) [Pubmed]
  3. Synthesis, potency, and in vivo profiles of quinoline containing histamine H3 receptor inverse agonists. Altenbach, R.J., Liu, H., Banfor, P.N., Browman, K.E., Fox, G.B., Fryer, R.M., Komater, V.A., Krueger, K.M., Marsh, K., Miller, T.R., Pan, J.B., Pan, L., Sun, M., Thiffault, C., Wetter, J., Zhao, C., Zhou, D., Esbenshade, T.A., Hancock, A.A., Cowart, M.D. J. Med. Chem. (2007) [Pubmed]
  4. Effects of substitution on 9-(3-bromo-4-fluorophenyl)-5,9-dihydro-3H,4H-2,6-dioxa-4- azacyclopenta[b]naphthalene-1,8-dione, a dihydropyridine ATP-sensitive potassium channel opener. Altenbach, R.J., Brune, M.E., Buckner, S.A., Coghlan, M.J., Daza, A.V., Fabiyi, A., Gopalakrishnan, M., Henry, R.F., Khilevich, A., Kort, M.E., Milicic, I., Scott, V.E., Smith, J.C., Whiteaker, K.L., Carroll, W.A. J. Med. Chem. (2006) [Pubmed]
  5. Synthesis and structure-activity studies on N-[5-(1H-imidazol-4-yl)-5,6,7,8-tetrahydro-1-naphthalenyl]methanesulfonamide, an imidazole-containing alpha(1A)-adrenoceptor agonist. Altenbach, R.J., Khilevich, A., Kolasa, T., Rohde, J.J., Bhatia, P.A., Patel, M.V., Searle, X.B., Yang, F., Bunnelle, W.H., Tietje, K., Bayburt, E.K., Carroll, W.A., Meyer, M.D., Henry, R., Buckner, S.A., Kuk, J., Daza, A.V., Milicic, I.V., Cain, J.C., Kang, C.H., Ireland, L.M., Carr, T.L., Miller, T.R., Hancock, A.A., Nakane, M., Esbenshade, T.A., Brune, M.E., O'Neill, A.B., Gauvin, D.M., Katwala, S.P., Holladay, M.W., Brioni, J.D., Sullivan, J.P. J. Med. Chem. (2004) [Pubmed]
  6. N-[3-(1H-imidazol-4-ylmethyl)phenyl]ethanesulfonamide (ABT-866, 1),(1) a novel alpha(1)-adrenoceptor ligand with an enhanced in vitro and in vivo profile relative to phenylpropanolamine and midodrine. Altenbach, R.J., Khilevich, A., Meyer, M.D., Buckner, S.A., Milicic, I., Daza, A.V., Brune, M.E., O'Neill, A.B., Gauvin, D.M., Cain, J.C., Nakane, M., Holladay, M.W., Williams, M., Brioni, J.D., Sullivan, J.P. J. Med. Chem. (2002) [Pubmed]
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