Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Yechun Xu

Showing results (71-80 of 154) with videos related to

Pageof 16
Sort By:
Biochemical Pharmacology|December 13, 2022
Dipyridamole interacts with the N-terminal domain of HSP90 and antagonizes the function of the chaperone in multiple cancer cell linesJing Gao, Chen Zhou, Yan Zhong, et al.
Analytical and Bioanalytical Chemistry|February 6, 2010
An enzyme-linked immunosorbent assay to compare the affinity of chemical compounds for β-amyloid peptide as a monomerChunyi Jiang, Yu Feng, Xiaotong Huang, et al.
Journal of Medicinal Chemistry|October 20, 2015
Discovery of a Novel Series of Imidazo[1,2-a]pyrimidine Derivatives as Potent and Orally Bioavailable Lipoprotein-Associated Phospholipase A2 InhibitorsXinde Chen, Wenwei Xu, Kai Wang, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 27, 2013
Free energy landscape for the binding process of Huperzine A to acetylcholinesteraseFang Bai, Yechun Xu, Jing Chen, et al.
European Journal of Medicinal Chemistry|January 17, 2018
Design and synthesis of 2-(4,5,6,7-tetrahydrothienopyridin-2-yl)-benzoimidazole carboxamides as novel orally efficacious Poly(ADP-ribose)polymerase (PARP) inhibitorsXuxing Chen, Xiajuan Huan, Qiufeng Liu, et al.
European Journal of Medicinal Chemistry|December 3, 2014
Novel fatty acid binding protein 4 (FABP4) inhibitors: virtual screening, synthesis and crystal structure determinationHaiyan Cai, Qiufeng Liu, Dingding Gao, et al.
Angewandte Chemie (International Ed. in English)|December 1, 2021
Potent and Selective RIPK1 Inhibitors Targeting Dual-Pockets for the Treatment of Systemic Inflammatory Response Syndrome and SepsisXiangbo Yang, Huimin Lu, Hang Xie, et al.
Journal of Medicinal Chemistry|December 16, 2022
Discovery of 10<i>H</i>-Benzo[<i>b</i>]pyrido[2,3-<i>e</i>][1,4]oxazine AXL Inhibitors <i>via</i> Structure-Based Drug Design Targeting c-Met KinaseZhengsheng Zhan, Yinchun Ji, Haixia Su, et al.
Journal of Advanced Research|September 24, 2025
Orthosteric-allosteric dual inhibitors of PI5P4Kγ with potent antitumor activity in non-small cell lung cancerLiang Xiong, Lei Tang 唐磊, Wenfeng Zhao, et al.
Journal of Virology|April 27, 2026
SARS-CoV-2 3CLpro mutations T21I and E166A confer differential resistance to simnotrelvir, bofutrelvir, and ensitrelvirLu Chen, Haixia Su, Weijuan Shang, et al.
Pageof 16

Showing results (71-80 of 154) with videos related to

Sort By:
Pageof 16
Biochemical Pharmacology|December 13, 2022
Dipyridamole interacts with the N-terminal domain of HSP90 and antagonizes the function of the chaperone in multiple cancer cell linesJing Gao, Chen Zhou, Yan Zhong, et al.
Analytical and Bioanalytical Chemistry|February 6, 2010
An enzyme-linked immunosorbent assay to compare the affinity of chemical compounds for β-amyloid peptide as a monomerChunyi Jiang, Yu Feng, Xiaotong Huang, et al.
Journal of Medicinal Chemistry|October 20, 2015
Discovery of a Novel Series of Imidazo[1,2-a]pyrimidine Derivatives as Potent and Orally Bioavailable Lipoprotein-Associated Phospholipase A2 InhibitorsXinde Chen, Wenwei Xu, Kai Wang, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 27, 2013
Free energy landscape for the binding process of Huperzine A to acetylcholinesteraseFang Bai, Yechun Xu, Jing Chen, et al.
European Journal of Medicinal Chemistry|January 17, 2018
Design and synthesis of 2-(4,5,6,7-tetrahydrothienopyridin-2-yl)-benzoimidazole carboxamides as novel orally efficacious Poly(ADP-ribose)polymerase (PARP) inhibitorsXuxing Chen, Xiajuan Huan, Qiufeng Liu, et al.
European Journal of Medicinal Chemistry|December 3, 2014
Novel fatty acid binding protein 4 (FABP4) inhibitors: virtual screening, synthesis and crystal structure determinationHaiyan Cai, Qiufeng Liu, Dingding Gao, et al.
Angewandte Chemie (International Ed. in English)|December 1, 2021
Potent and Selective RIPK1 Inhibitors Targeting Dual-Pockets for the Treatment of Systemic Inflammatory Response Syndrome and SepsisXiangbo Yang, Huimin Lu, Hang Xie, et al.
Journal of Medicinal Chemistry|December 16, 2022
Discovery of 10<i>H</i>-Benzo[<i>b</i>]pyrido[2,3-<i>e</i>][1,4]oxazine AXL Inhibitors <i>via</i> Structure-Based Drug Design Targeting c-Met KinaseZhengsheng Zhan, Yinchun Ji, Haixia Su, et al.
Journal of Advanced Research|September 24, 2025
Orthosteric-allosteric dual inhibitors of PI5P4Kγ with potent antitumor activity in non-small cell lung cancerLiang Xiong, Lei Tang 唐磊, Wenfeng Zhao, et al.
Journal of Virology|April 27, 2026
SARS-CoV-2 3CLpro mutations T21I and E166A confer differential resistance to simnotrelvir, bofutrelvir, and ensitrelvirLu Chen, Haixia Su, Weijuan Shang, et al.
Pageof 16