Showing results (1921-1930 of 31,409) with videos related to
Sort By:
Pageof 3,141
Journal of Medicinal Chemistry|March 4, 1994
Tyrosine kinase inhibitors. 2. Synthesis of 2,2'-dithiobis(1H-indole-3-alkanamides) and investigation of their inhibitory activity against epidermal growth factor receptor and pp60v-src protein tyrosine kinasesA M Thompson, D W Fry, A J Kraker, et al.Journal of Medicinal Chemistry|March 4, 1994
In vitro and in vivo activities of reduced-size antagonists of luteinizing hormone-releasing hormoneF Haviv, T D Fitzpatrick, C J Nichols, et al.Journal of Medicinal Chemistry|April 1, 1994
Synthesis of L-thiocitrulline, L-homothiocitrulline, and S-methyl-L-thiocitrulline: a new class of potent nitric oxide synthase inhibitorsK Narayanan, O W GriffithJournal of Medicinal Chemistry|April 1, 1994
Discovery, synthesis, and bioactivity of bis(heteroaryl)piperazines. 1. A novel class of non-nucleoside HIV-1 reverse transcriptase inhibitorsD L Romero, R A Morge, C Biles, et al.Journal of Medicinal Chemistry|December 24, 1993
The inophyllums, novel inhibitors of HIV-1 reverse transcriptase isolated from the Malaysian tree, Calophyllum inophyllum LinnA D Patil, A J Freyer, D S Eggleston, et al.Journal of Medicinal Chemistry|January 7, 1994
Design and synthesis of novel cyclic RGD-containing peptides as highly potent and selective integrin alpha IIb beta 3 antagonistsS Cheng, W S Craig, D Mullen, et al.Journal of Medicinal Chemistry|February 18, 1994
Copper complexation by 3-hydroxypyridin-4-one iron chelators: structural and iron competition studiesA el-Jammal, P L Howell, M A Turner, et al.Journal of Medicinal Chemistry|July 22, 1994
Synthesis of a series of 4-(arylethynyl)-6-chloro-4-cyclopropyl-3,4-dihydroquinazolin-2(1H)-ones as novel non-nucleoside HIV-1 reverse transcriptase inhibitorsT J Tucker, T A Lyle, C M Wiscount, et al.Journal of Medicinal Chemistry|September 2, 1994
Aza-tricyclic substance P antagonistsJ A Lowe, S E Drozda, S McLean, et al.Journal of Medicinal Chemistry|January 6, 1995
Derivatives of cis-2-amino-8-hydroxy-1-methyltetralin: mixed 5-HT1A-receptor agonists and dopamine D2-receptor antagonistsY Liu, H Yu, N Mohell, et al.Pageof 3,141