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Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|March 12, 2022
Progress in traditional Chinese medicine and natural extracts for the treatment of lupus nephritisYu-Jiao Wang, Ya-Xin Li, Shuo Li, et al.European Journal of Medicinal Chemistry|September 22, 2019
Identification of highly potent and selective Cdc25 protein phosphatases inhibitors from miniaturization click-chemistry-based combinatorial librariesLanlan Jing, Gaochan Wu, Xia Hao, et al.Current Drug Targets|June 24, 2024
Multi-target Compounds against Trypanosomatid Parasites and <i>Mycobacterium tuberculosis</i>Midiane Correia Gomes, Emanuelly Karla Araújo Padilha, Gustavo Rafael Angelo Diniz, et al.European Journal of Medicinal Chemistry|February 24, 2015
Fused heterocycles bearing bridgehead nitrogen as potent HIV-1 NNRTIs. Part 4: design, synthesis and biological evaluation of novel imidazo[1,2-a]pyrazinesBoshi Huang, Xin Liang, Cuicui Li, et al.European Journal of Medicinal Chemistry|October 11, 2022
Design, synthesis and activity evaluation of novel lesinurad analogues containing thienopyrimidinone or pyridine substructure as human urate transporter 1 inhibitorsJian Zhang, Yue Dong, Shenghua Gao, et al.European Journal of Medicinal Chemistry|February 18, 2020
Design, synthesis and structure-activity relationships of 4-phenyl-1H-1,2,3-triazole phenylalanine derivatives as novel HIV-1 capsid inhibitors with promising antiviral activitiesLin Sun, Tianguang Huang, Alexej Dick, et al.Science Advances|May 30, 2025
Development of enhanced HIV-1 non-nucleoside reverse transcriptase inhibitors with improved resistance and pharmacokinetic profilesZhao Wang, Shawn Rumrill, Dongwei Kang, et al.Journal of Medicinal Chemistry|December 7, 2024
Elaborate Structural Modifications Yielding Novel Boron-Containing N-Substituted Oseltamivir Derivatives as Potent Neuraminidase Inhibitors with Significantly Improved Broad-Spectrum Antiresistance ProfilesJiwei Zhang, Ruifang Jia, Huinan Jia, et al.European Journal of Medicinal Chemistry|April 1, 2025
TCM theory-inspired discovery of DNJ-flavonoid conjugates as broad-spectrum anti-SARS-CoV-2 agents by primarily targeting ER-associated glycoprotein folding processYan-Yun Liu, Zheng-Ao Li, Yu-Zheng Zhou, et al.European Journal of Medicinal Chemistry|January 1, 2021
Discovery of highly potent and selective influenza virus neuraminidase inhibitors targeting 150-cavityRuifang Jia, Jian Zhang, Chiara Bertagnin, et al.Pageof 56