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Ridong Li

Showing results (11-20 of 31) with videos related to

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European Journal of Pharmacology|September 29, 2022
Identification of a new small molecule that initiates ferroptosis in cancer cells by inhibiting the system Xc<sup>-</sup> to deplete GSHXianling Ning, Hailong Qi, Yuyao Yuan, et al.
European Journal of Medicinal Chemistry|March 18, 2019
Synthesis of novel 7-azaindole derivatives containing pyridin-3-ylmethyl dithiocarbamate moiety as potent PKM2 activators and PKM2 nucleus translocation inhibitorsBin Liu, Xia Yuan, Bo Xu, et al.
Organic Letters|May 15, 2020
Ruthenium-Catalyzed Highly Enantioselective Synthesis of <i>cis</i>-3-Quinuclidinols via DKR Asymmetric Transfer HydrogenationZhonghua Luo, Zhongqing Wang, Guodong Sun, et al.
Bioorganic & Medicinal Chemistry|August 10, 2019
Design, synthesis and biological evaluation of novel dithiocarbamate-substituted diphenylaminopyrimidine derivatives as BTK inhibitorsZheng Zhai, Ridong Li, Xinyu Bai, et al.
European Journal of Medicinal Chemistry|February 28, 2018
Discovery and optimization of 2-thio-5-amino substituted benzoquinones as potent anticancer agentsYuqiong Zhao, Yihuan Lu, Ridong Li, et al.
European Journal of Medicinal Chemistry|July 9, 2017
Discovery of novel naphthoquinone derivatives as inhibitors of the tumor cell specific M2 isoform of pyruvate kinaseXianling Ning, Hailong Qi, Ridong Li, et al.
Bioorganic & Medicinal Chemistry|June 22, 2017
Synthesis and biological activity of peptide proline-boronic acids as proteasome inhibitorsLiqiang Han, Yanzhao Wen, Ridong Li, et al.
European Journal of Medicinal Chemistry|May 27, 2019
Discovery of 2,4-diarylaminopyrimidine derivatives bearing dithiocarbamate moiety as novel FAK inhibitors with antitumor and anti-angiogenesis activitiesYue Su, Ridong Li, Xianling Ning, et al.
European Journal of Medicinal Chemistry|June 27, 2025
Molecular hybridization-driven FAK inhibitors: N-2,4-diarylaminopyrimidine-3-sulfamoyl-benzamide derivatives with improved antitumor potencyLidong Gong, Zichao Liang, Xianling Ning, et al.
Bioorganic & Medicinal Chemistry|June 18, 2015
New pyridin-3-ylmethyl carbamodithioic esters activate pyruvate kinase M2 and potential anticancer lead compoundsYu Zhang, Bin Liu, Xingyu Wu, et al.
Pageof 4

Showing results (11-20 of 31) with videos related to

Sort By:
Pageof 4
European Journal of Pharmacology|September 29, 2022
Identification of a new small molecule that initiates ferroptosis in cancer cells by inhibiting the system Xc<sup>-</sup> to deplete GSHXianling Ning, Hailong Qi, Yuyao Yuan, et al.
European Journal of Medicinal Chemistry|March 18, 2019
Synthesis of novel 7-azaindole derivatives containing pyridin-3-ylmethyl dithiocarbamate moiety as potent PKM2 activators and PKM2 nucleus translocation inhibitorsBin Liu, Xia Yuan, Bo Xu, et al.
Organic Letters|May 15, 2020
Ruthenium-Catalyzed Highly Enantioselective Synthesis of <i>cis</i>-3-Quinuclidinols via DKR Asymmetric Transfer HydrogenationZhonghua Luo, Zhongqing Wang, Guodong Sun, et al.
Bioorganic & Medicinal Chemistry|August 10, 2019
Design, synthesis and biological evaluation of novel dithiocarbamate-substituted diphenylaminopyrimidine derivatives as BTK inhibitorsZheng Zhai, Ridong Li, Xinyu Bai, et al.
European Journal of Medicinal Chemistry|February 28, 2018
Discovery and optimization of 2-thio-5-amino substituted benzoquinones as potent anticancer agentsYuqiong Zhao, Yihuan Lu, Ridong Li, et al.
European Journal of Medicinal Chemistry|July 9, 2017
Discovery of novel naphthoquinone derivatives as inhibitors of the tumor cell specific M2 isoform of pyruvate kinaseXianling Ning, Hailong Qi, Ridong Li, et al.
Bioorganic & Medicinal Chemistry|June 22, 2017
Synthesis and biological activity of peptide proline-boronic acids as proteasome inhibitorsLiqiang Han, Yanzhao Wen, Ridong Li, et al.
European Journal of Medicinal Chemistry|May 27, 2019
Discovery of 2,4-diarylaminopyrimidine derivatives bearing dithiocarbamate moiety as novel FAK inhibitors with antitumor and anti-angiogenesis activitiesYue Su, Ridong Li, Xianling Ning, et al.
European Journal of Medicinal Chemistry|June 27, 2025
Molecular hybridization-driven FAK inhibitors: N-2,4-diarylaminopyrimidine-3-sulfamoyl-benzamide derivatives with improved antitumor potencyLidong Gong, Zichao Liang, Xianling Ning, et al.
Bioorganic & Medicinal Chemistry|June 18, 2015
New pyridin-3-ylmethyl carbamodithioic esters activate pyruvate kinase M2 and potential anticancer lead compoundsYu Zhang, Bin Liu, Xingyu Wu, et al.
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