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Journal of Medicinal Chemistry|January 1, 1992
N-modified analogues of cocaine: synthesis and inhibition of binding to the cocaine receptorP Abraham, J B Pitner, A H Lewin, et al.Journal of Medicinal Chemistry|January 1, 1992
Synthesis and biological activity of new dimers in the 7H-pyrido[4,3-c] carbazole antitumor seriesC Garbay-Jaureguiberry, M C Barsi, A Jacquemin-Sablon, et al.Journal of Medicinal Chemistry|January 24, 1992
Structure-function studies in a series of carboxyl-terminal octapeptide analogues of anaphylatoxin C5aM Kawai, D A Quincy, B Lane, et al.Journal of Medicinal Chemistry|January 24, 1992
A new, general synthetic route to multidentate N,S ligands for use in technetium-99m radiopharmaceuticals. Preparation of diamido disulfur, diamino dithiol, and tripodal N3S3 prototypes. Comparative biodistributions of [99mTcvO-DADS]- analogues which contain 5,5,5- and 5,7,5-membered chelate ring systemsD Stepniak-Biniakiewicz, B H Chen, E DeutschJournal of Medicinal Chemistry|January 24, 1992
Phenyl-substituted analogues of oxotremorine as muscarinic antagonistsB M Nilsson, H M Vargas, B Ringdahl, et al.Journal of Medicinal Chemistry|January 24, 1992
Conformational studies of muscarone analogues: X-ray analysis and molecular mechanics calculationsP J Carroll, M De Amici, C De Micheli, et al.Journal of Medicinal Chemistry|January 24, 1992
Synthesis and antifolate evaluation of the 10-propargyl derivatives of 5-deazafolic acid, 5-deazaaminopterin, and 5-methyl-5-deazaaminopterinJ R Piper, N D Malik, M S Rhee, et al.Journal of Medicinal Chemistry|March 3, 2007
Novel sigma receptor ligands: synthesis and biological profileOrazio Prezzavento, Agata Campisi, Simone Ronsisvalle, et al.Journal of Medicinal Chemistry|September 15, 2006
Design and synthesis of dual peroxisome proliferator-activated receptors gamma and delta agonists as novel euglycemic agents with a reduced weight gain profileYanping Xu, Garret J Etgen, Carol L Broderick, et al.Journal of Medicinal Chemistry|September 15, 2006
Identification of a novel 4-aminomethylpiperidine class of M3 muscarinic receptor antagonists and structural insight into their M3 selectivityYufu Sagara, Takeshi Sagara, Minaho Uchiyama, et al.Pageof 3,134