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Bioorganic & Medicinal Chemistry Letters|November 22, 2002
Natural and synthetic geiparvarins are strong and selective MAO-B inhibitors. Synthesis and SAR studiesAngelo Carotti, Antonio Carrieri, Stefano Chimichi, et al.Bioorganic & Medicinal Chemistry Letters|November 22, 2002
Synthesis and biological evaluation of aristolactamsAxel Couture, Eric Deniau, Pierre Grandclaudon, et al.Bioorganic & Medicinal Chemistry Letters|November 22, 2002
Synthesis and pharmacological evaluation of a new class of peroxisome proliferator-activated receptor modulatorsMarkus Thor, Katarina Beierlein, Graeme Dykes, et al.Bioorganic & Medicinal Chemistry Letters|November 22, 2002
2-(Dimethylaminomethyl)-tetrahydroisoxazolopyridobenzazepine derivatives. Synthesis of a new 5-HT(2C) antagonist with potential anxiolytic propertiesJ Ignacio Andrés, José M Alonso, Javier Fernández, et al.Bioorganic & Medicinal Chemistry Letters|November 22, 2002
Synthetic studies of cis-4-Amino-L-proline derivatives as novel lipid lowering agentsSaibal Kumar Das, V L Narasimha Rao Krovvidi, H Jagadheshan, et al.Bioorganic & Medicinal Chemistry Letters|November 22, 2002
A simple and rapid method for the differentiation of C-13 manoyl oxide epimers in biologically important samples using GC-MS analysis supported with NMR spectroscopy and computational chemistry resultsCostas Demetzos, Antonios Kolocouris, Thalia AnastasakiBioorganic & Medicinal Chemistry Letters|November 22, 2002
Silanediol-based inhibitor of thermolysinJaeseung Kim, Athanasios Glekas, Scott McN SieburthBioorganic & Medicinal Chemistry Letters|November 22, 2002
Inhibition of amine oxidases activity by 1-acetyl-3,5-diphenyl-4,5-dihydro-(1H)-pyrazole derivativesFedele Manna, Franco Chimenti, Adriana Bolasco, et al.Bioorganic & Medicinal Chemistry Letters|November 22, 2002
Unique hole-trapping property of the degenerate base,2-amino-7-deazaadenineAkimitsu Okamoto, Kazuo Tanaka, Isao SaitoBioorganic & Medicinal Chemistry Letters|October 10, 2002
Novel semi-synthetic glycopeptide antibiotics active against methicillin-resistant staphylococcus aureus (MRSA) and vancomycin-resistant Enterococci (VRE): doubly-modified water-soluble derivatives of chloroorienticin BOsamu Yoshida, Tatsuro Yasukata, Yukihito Sumino, et al.Pageof 2,631