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Journal of Medicinal Chemistry|November 7, 1998
A novel class of orally active non-peptide bradykinin B2 receptor antagonists. 4. Discovery of novel frameworks mimicking the active conformationY Abe, H Kayakiri, S Satoh, et al.Journal of Medicinal Chemistry|November 7, 1998
Abasic analogues of TSAO-T as the first sugar derivatives that specifically inhibit HIV-1 reverse transcriptaseS Velázquez, C Chamorro, M J Pérez-Pérez, et al.Journal of Medicinal Chemistry|November 7, 1998
Synthesis and cytotoxicity of 2-acetyl-4,8-dihydrobenzodithiophene-4, 8-dione derivativesY H Chao, S C Kuo, C H Wu, et al.Journal of Medicinal Chemistry|November 7, 1998
New 1alpha,25-dihydroxy-19-norvitamin D3 compounds of high biological activity: synthesis and biological evaluation of 2-hydroxymethyl, 2-methyl, and 2-methylene analoguesR R Sicinski, J M Prahl, C M Smith, et al.Journal of Medicinal Chemistry|October 11, 1996
Derivatives of the triazoloquinazoline adenosine antagonist (CGS15943) are selective for the human A3 receptor subtypeY C Kim, X D Ji, K A JacobsonJournal of Medicinal Chemistry|October 11, 1996
Understanding the mechanism of sweet taste: synthesis of ultrapotent guanidinoacetic acid photoaffinity labeling reagentsS Nagarajan, M S Kellogg, G E DuBois, et al.Journal of Medicinal Chemistry|October 11, 1996
Structure-activity relationships for inhibition of inosine monophosphate dehydrogenase by nuclear variants of mycophenolic acidP H Nelson, S F Carr, B H Devens, et al.Journal of Medicinal Chemistry|October 11, 1996
Hydroxamic acid-based bisubstrate analog inhibitors of Ras farnesyl protein transferaseD V Patel, M G Young, S P Robinson, et al.Journal of Medicinal Chemistry|October 11, 1996
2-alkenyl and 2-alkyl derivatives of adenosine and adenosine-5'-N-ethyluronamide: different affinity and selectivity of E- and Z-diastereomers at A2A adenosine receptorsS Vittori, E Camaioni, E Di Francesco, et al.Journal of Medicinal Chemistry|October 11, 1996
Synthesis, molecular modeling, and K+ channel-blocking activity of dequalinium analogues having semirigid linkersJ Campos Rosa, D Galanakis, C R Ganellin, et al.Pageof 3,141