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Journal of Medicinal Chemistry|December 23, 2008
Synthesis, reduction potentials, and antitubercular activity of ring A/B analogues of the bioreductive drug (6S)-2-nitro-6-{[4-(trifluoromethoxy)benzyl]oxy}-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazine (PA-824)Andrew M Thompson, Adrian Blaser, Robert F Anderson, et al.Journal of Medicinal Chemistry|December 23, 2008
Identification of a new G-quadruplex motif in the KRAS promoter and design of pyrene-modified G4-decoys with antiproliferative activity in pancreatic cancer cellsSusanna Cogoi, Manikandan Paramasivam, Vyacheslav Filichev, et al.Journal of Medicinal Chemistry|September 1, 1991
Interphenylene 7-oxabicyclo[2.2.1]heptane thromboxane A2 antagonists. Semicarbazone omega-chainsR N Misra, B R Brown, W C Han, et al.Journal of Medicinal Chemistry|May 23, 2009
Galactosyl prodrug of ketorolac: synthesis, stability, and pharmacological and pharmacokinetic evaluationsAnnalisa Curcio, Oscar Sasso, Daniela Melisi, et al.Journal of Medicinal Chemistry|May 23, 2009
Discovery of tetrasubstituted imidazolines as potent and selective neuropeptide Y Y5 receptor antagonists: reduced human ether-a-go-go related gene potassium channel binding affinity and potent antiobesity effectNagaaki Sato, Makoto Ando, Shiho Ishikawa, et al.Journal of Medicinal Chemistry|May 26, 2009
High-affinity, non-nucleotide-derived competitive antagonists of platelet P2Y12 receptorsYounis Baqi, Kerstin Atzler, Meryem Köse, et al.Journal of Medicinal Chemistry|May 26, 2009
Structurally simple inhibitors of lanosterol 14alpha-demethylase are efficacious in a rodent model of acute Chagas diseasePraveen Kumar Suryadevara, Srinivas Olepu, Jeffrey W Lockman, et al.Journal of Medicinal Chemistry|May 28, 2009
Synthesis and evaluation of sphingosine analogues as inhibitors of sphingosine kinasesLingkai Wong, Sheryl S L Tan, Yulin Lam, et al.Journal of Medicinal Chemistry|May 28, 2009
Targeting human gastrointestinal stromal tumor cells with a quadruplex-binding small moleculeMekala Gunaratnam, Stephen Swank, Shozeb M Haider, et al.Journal of Medicinal Chemistry|May 29, 2009
Substitution of arginine with proline and proline derivatives in melanocyte-stimulating hormones leads to selectivity for human melanocortin 4 receptorHongchang Qu, Minying Cai, Alexander V Mayorov, et al.Pageof 3,141