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Bioorganic & Medicinal Chemistry Letters|October 7, 2009
Solid-phase synthesis of a library based on biphenyl-containing trypsin-like serine protease inhibitorsShuhao Shi, Shirong Zhu, Samuel W Gerritz, et al.Journal of Microbiology (Seoul, Korea)|January 5, 2018
Application of high-salinity stress for enhancing the lipid productivity of Chlorella sorokiniana HS1 in a two-phase processRamesh Kakarla, Jung-Woon Choi, Jin-Ho Yun, et al.Journal of Medicinal Chemistry|May 20, 2025
Discovery of an Orally Bioavailable and Brain Penetrant Selective Estrogen Receptor DegraderGuobao Zhang, Peter Q Huang, Kevin D Bunker, et al.Journal of Medicinal Chemistry|January 31, 2014
Discovery of a novel class of potent HCV NS4B inhibitors: SAR studies on piperazinone derivativesRamesh Kakarla, Jian Liu, Devan Naduthambi, et al.Journal of Medicinal Chemistry|January 8, 2024
Structure-Activity Relationships and Discovery of (<i>S</i>)-6-Isopropyl-2-methoxy-3-(3-methoxypropoxy)-10-oxo-5,10-dihydro-6<i>H</i>-pyrido[1,2-<i>h</i>][1,7]naphthyridine-9-carboxylic Acid (AB-452), a Novel Orally Available HBV RNA DestabilizerDimitar Gotchev, Bruce D Dorsey, Duyan Nguyen, et al.Journal of Combinatorial Chemistry|December 18, 2008
Design and synthesis of a G-protein-coupled receptor antagonist library of aryloxyalkanolamines using a polymer-supported acyclic acetal linkerJacques Y Roberge, Lalgudi S Harikrishnan, Muthoni G Kamau, et al.Bioorganic & Medicinal Chemistry Letters|September 11, 2012
HCV NS5A replication complex inhibitors. Part 2: investigation of stilbene prolinamidesDenis R St Laurent, Makonen Belema, Min Gao, et al.Journal of Medicinal Chemistry|November 26, 2013
Structure-activity relationship (SAR) optimization of 6-(indol-2-yl)pyridine-3-sulfonamides: identification of potent, selective, and orally bioavailable small molecules targeting hepatitis C (HCV) NS4BNanjing Zhang, Xiaoyan Zhang, Jin Zhu, et al.Pageof 2