Bioorganic & Medicinal Chemistry, 1464-3391

Journal

  1. 2018
  2. Kok, T., Wapenaar, H., Wang, K., Neochoritis, C. G., Zarganes-Tzitzikas, T., Proietti, G., ... Dekker, F. J. (2018). Discovery of chromenes as inhibitors of macrophage migration inhibitory factor. Bioorganic & Medicinal Chemistry, 26(5), 999-1005. https://doi.org/10.1016/j.bmc.2017.12.032
  3. 2017
  4. Juergens, S., Scalcon, V., Estrada-Ortiz, N., Folda, A., Tonolo, F., Jandl, C., ... Casini, A. (2017). Exploring the theme: Synthesis and biological properties of tridentate cyclometalated gold(III) complexes. Bioorganic & Medicinal Chemistry, 25(20), 5452-5460. https://doi.org/10.1016/j.bmc.2017.08.001
  5. Barroso, M. V., Cattani-Cavalieri, I., de Brito-Gitirana, L., Fautrel, A., Lagente, V., Schmidt, M., ... Lanzetti, M. (2017). Propolis reversed cigarette smoke-induced emphysema through macrophage alternative activation independent of Nrf2. Bioorganic & Medicinal Chemistry, 25(20), 5557-5568. https://doi.org/10.1016/j.bmc.2017.08.026
  6. 2015
  7. 2014
  8. Szymanski, W., Zwolinska, M., Klossowski, S., Mlynarczuk-Bialy, I., Bialy, L., Issat, T., ... Ostaszewski, R. (2014). Synthesis of novel, peptidic kinase inhibitors with cytostatic/cytotoxic activity. Bioorganic & Medicinal Chemistry, 22(5), 1773-1781. https://doi.org/10.1016/j.bmc.2014.01.005
  9. 2013
  10. 2012
  11. 2011
  12. 2010
  13. Garibotto, F. M., Garro, A. D., Masman, M. F., Rodriguez, A. M., Luiten, P. G. M., Raimondi, M., ... Enriz, R. D. (2010). New small-size peptides possessing antifungal activity. Bioorganic & Medicinal Chemistry, 18(1), 158-167. https://doi.org/10.1016/j.bmc.2009.11.009
  14. 2009
  15. 2008
  16. 2006
  17. Messori, L., Gabbiani, C., Casini, A., Siragusa, M., Vincieri, FF., & Bilia, AR. (2006). The reaction of artemisinins with hemoglobin: A unified picture. Bioorganic & Medicinal Chemistry, 14(9), 2972-2977. https://doi.org/10.1016/j.bmc.2005.12.038
  18. 2005
  19. Oberwinkler - Marchais, S., Nowicki, B., Pike, VW., Halldin, C., Sandell, J., Chou, YH., ... Wikstrom, H. V. (2005). N-Oxide analogs of WAY-100635: new high affinity 5-HT (1A) receptor antagonists. Bioorganic & Medicinal Chemistry, 13(3), 883-893. https://doi.org/10.1016/j.bmc.2004.10.033
  20. 2003
  21. 2001
  22. Marchais, S., Nowicki, B., Wikstrom, H., Brennum, LT., Halldin, C., & Pike, VW. (2001). Short and efficient syntheses of analogues of WAY-100635: New and potent 5-HT1A receptor antagonists. Bioorganic & Medicinal Chemistry, 9(3), 695-702.
  23. 2000
  24. 1999
  25. Leenders, RGG., Damen, EWP., Bijsterveld, EJA., Scheeren, HW., Houba, PHJ., van der Meulen-Muileman, IH., ... Haisma, HJ. (1999). Novel anthracycline-spacer-beta-glucuronide, -beta-glucoside, and -beta-galactoside prodrugs for application in selective chemotherapy. Bioorganic & Medicinal Chemistry, 7(8), 1597-1610.
  26. Homan, E. J., Copinga, S., Unelius, L., Jackson, D., Wikström, H. V., & Grol, C. (1999). Synthesis and pharmacology of the enantiomers of the potential atypical antipsychotic agents 5-OMe-BPAT and 5-OMe-(2,6-di-OMe)-BPAT. Bioorganic & Medicinal Chemistry, 7(7), 1263 - 1271.
  27. Homan, EJ., Kroodsma, E., Copinga, S., Unelius, L., Mohell, N., Wikstrom, HV., & Grol, CJ. (1999). Structural analogues of 5-OMe-BPAT: Synthesis and interactions with dopamine D-2, D-3, and serotonin 5-HT1A receptors. Bioorganic & Medicinal Chemistry, 7(6), 1111-1121.
  28. Homan, E. J., Kroodsma, E., Copinga, S., Unelius, L., Mohell, N., Wikström, H. V., & Grol, C. (1999). Structural analogues of 5-OMe-BPAT: Synthesis and interactions with dopamine D2, D3, and serotonin 5-HT 1A receptors. Bioorganic & Medicinal Chemistry, 1111 - 1121.
  29. 1998
  30. Barf, T., Wikstrom, H., Pauwels, PJ., Palmier, C., Tardif, S., Lundmark, M., & Sundell, S. (1998). 5-(sulfonyl)oxy-tryptamines and ethylamino side chain restricted derivatives. Structure-affinity relationships for h5-HT1B and h5-HT1D receptors. Bioorganic & Medicinal Chemistry, 6(9), 1469-1479.
  31. Barf, T. A., Wikström, H. V., Pauwels, P. J., Palmier, C., Tardif, S., Lundmark, M., & Sundell, S. (1998). 5-(Sulfonyl)oxy-tryptamines and ethylamino side chain restricted derivatives. Structure-affinity relationships for h5-HT 1B and h5-HT 1D receptors. Bioorganic & Medicinal Chemistry, 1469 - 1479.
  32. 1997
  33. 1996
  34. Jansen, JM., Copinga, S., Gruppen, G., Molinari, EJ., Dubocovich, ML., & Grol, CJ. (1996). The high affinity melatonin binding site probed with conformationally restricted ligands .1. Pharmacophore and minireceptor models. Bioorganic & Medicinal Chemistry, 4(8), 1321-1332.
  35. Kozaikowski, A., Liao, Y., Tuckmantel, W., Wang, S., Pshenichkin, S., Surin, A., ... Wrobleuski, J. (1996). Synthesis and biology of the regidified glutamate analogue, trans-2-carboxyazetidine-3-acetic acid (t-CAA). Bioorganic & Medicinal Chemistry, 2559 - 2564.
  36. Jansen, J. M., Copinga, S., Gruppen, G., Molinari, E. J., Dubocovich, M. L., & Grol, C. (1996). The high affinity melatonin binding site probed with conformationally restricted ligands- I. Pharmacophore and minireceptor models. Bioorganic & Medicinal Chemistry, 8, 1321 - 1332.

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