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Frontiers in Pharmacology|December 9, 2022
Characterization of three naturally occurring lignans, sesamol, sesamolin, and sesamin, as potent inhibitors of human cytochrome P450 46A1: Implications for treating excitatory neurotoxicityJie Du, Xiaodong Chen, Yongshun Zhao, et al.Food Chemistry|March 19, 2013
Biotransformation of imperatorin by Penicillium janthinellum. Anti-osteoporosis activities of its metabolitesXia Lv, Dan Liu, Jie Hou, et al.European Journal of Medicinal Chemistry|November 18, 2017
Identification of highly potent BTK and JAK3 dual inhibitors with improved activity for the treatment of B-cell lymphomaYang Ge, Changyuan Wang, Shijie Song, et al.Molecular Plant-Microbe Interactions : MPMI|August 21, 2020
NADPH Oxidase ClNOX2 Regulates Melanin-Mediated Development and Virulence in Curvularia lunataFen Wang, Weida Gao, Jiaying Sun, et al.Bioorganic Chemistry|May 25, 2024
Molecular design, construction and analgesic mechanism insights into the novel transdermal fusion peptide ANTP-BgNPBXinmeng Peng, Han Tao, Fengyan Xia, et al.Optics Express|June 29, 2023
True-color light-field display system with large depth-of-field based on joint modulation for size and arrangement of halftone dotsXunbo Yu, Zhaohe Zhang, Boyang Liu, et al.European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|July 13, 2014
PEPT1- and OAT1/3-mediated drug-drug interactions between bestatin and cefixime in vivo and in vitro in rats, and in vitro in humanLi Wang, Changyuan Wang, Qi Liu, et al.Pharmacological Research|September 9, 2015
Dioscin attenuates renal ischemia/reperfusion injury by inhibiting the TLR4/MyD88 signaling pathway via up-regulation of HSP70Meng Qi, Lingli Zheng, Yan Qi, et al.Inorganic Chemistry|April 12, 2022
Deprotonation from an OH on myo-Inositol Promoted by μ2-Bridges with Possible Regioselectivity/Chiral SelectivityLinchen Xie, Anqi He, Da Li, et al.European Journal of Medicinal Chemistry|April 13, 2019
Structure-based modification of carbonyl-diphenylpyrimidines (Car-DPPYs) as a novel focal adhesion kinase (FAK) inhibitor against various stubborn cancer cellsLuhong Wang, Min Ai, Jiawen Yu, et al.Pageof 57