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

Chang Bai

Showing results (51-60 of 72) with videos related to

Pageof 8
Sort By:
ACS Omega|August 29, 2019
Discovery of SHR9352: A Highly Potent G Protein-Biased μ-Opioid Receptor AgonistXin Li, Wei He, Yang Chen, et al.
ACS Medicinal Chemistry Letters|March 18, 2022
Discovery of SHR5133, a Highly Potent and Novel HBV Capsid Assembly ModulatorXin Li, Zhigao Zhang, Yang Chen, et al.
Bioorganic & Medicinal Chemistry Letters|July 6, 2016
WITHDRAWN: Discovery of SHR1977: A highly potent and selective ROMK inhibitorXin Li, Yun Zhang, Yang Chen, et al.
ACS Medicinal Chemistry Letters|June 22, 2019
Discovery of SHR1653, a Highly Potent and Selective OTR Antagonist with Improved Blood-Brain Barrier PenetrationXin Li, Zhigao Zhang, Yang Chen, et al.
Oncotarget|April 16, 2016
Efficient therapeutic delivery by a novel cell-permeant peptide derived from KDM4A protein for antitumor and antifibrosisHu Wang, Jie-Lan Ma, Ying-Gui Yang, et al.
Nature Communications|November 13, 2021
Regio- and enantioselective umpolung gem-difluoroallylation of hydrazones via palladium catalysis enabled by N-heterocyclic carbene ligandShuai Huang, Fei-Fei Tong, Da-Chang Bai, et al.
Bioorganic & Medicinal Chemistry Letters|March 11, 2022
Discovery of novel spiro compound as RAF kinase inhibitor with in vitro potency against KRAS mutant cancerPeng Zhao, Xiangzhu Wang, Linghang Zhuang, et al.
Fish & Shellfish Immunology|September 15, 2024
A molecular mechanism underlies grass carp (Ctenopharyngodon idella) TARBP2 regulating PKR-mediated cell apoptosisMiao-Miao Li, Chang-Bai Tao, Mei-Feng Li, et al.
ACS Medicinal Chemistry Letters|February 19, 2021
Discovery of Hydroxyamidine Derivatives as Highly Potent, Selective Indoleamine-2,3-dioxygenase 1 InhibitorsFangfang Jin, Qiyue Hu, Hongbo Fei, et al.
Bioorganic & Medicinal Chemistry|November 15, 2011
Discovery of selective glucocorticoid receptor modulator MK-5932Christopher J Bungard, George D Hartman, Jesse J Manikowski, et al.
Pageof 8

Showing results (51-60 of 72) with videos related to

Sort By:
Pageof 8
ACS Omega|August 29, 2019
Discovery of SHR9352: A Highly Potent G Protein-Biased μ-Opioid Receptor AgonistXin Li, Wei He, Yang Chen, et al.
ACS Medicinal Chemistry Letters|March 18, 2022
Discovery of SHR5133, a Highly Potent and Novel HBV Capsid Assembly ModulatorXin Li, Zhigao Zhang, Yang Chen, et al.
Bioorganic & Medicinal Chemistry Letters|July 6, 2016
WITHDRAWN: Discovery of SHR1977: A highly potent and selective ROMK inhibitorXin Li, Yun Zhang, Yang Chen, et al.
ACS Medicinal Chemistry Letters|June 22, 2019
Discovery of SHR1653, a Highly Potent and Selective OTR Antagonist with Improved Blood-Brain Barrier PenetrationXin Li, Zhigao Zhang, Yang Chen, et al.
Oncotarget|April 16, 2016
Efficient therapeutic delivery by a novel cell-permeant peptide derived from KDM4A protein for antitumor and antifibrosisHu Wang, Jie-Lan Ma, Ying-Gui Yang, et al.
Nature Communications|November 13, 2021
Regio- and enantioselective umpolung gem-difluoroallylation of hydrazones via palladium catalysis enabled by N-heterocyclic carbene ligandShuai Huang, Fei-Fei Tong, Da-Chang Bai, et al.
Bioorganic & Medicinal Chemistry Letters|March 11, 2022
Discovery of novel spiro compound as RAF kinase inhibitor with in vitro potency against KRAS mutant cancerPeng Zhao, Xiangzhu Wang, Linghang Zhuang, et al.
Fish & Shellfish Immunology|September 15, 2024
A molecular mechanism underlies grass carp (Ctenopharyngodon idella) TARBP2 regulating PKR-mediated cell apoptosisMiao-Miao Li, Chang-Bai Tao, Mei-Feng Li, et al.
ACS Medicinal Chemistry Letters|February 19, 2021
Discovery of Hydroxyamidine Derivatives as Highly Potent, Selective Indoleamine-2,3-dioxygenase 1 InhibitorsFangfang Jin, Qiyue Hu, Hongbo Fei, et al.
Bioorganic & Medicinal Chemistry|November 15, 2011
Discovery of selective glucocorticoid receptor modulator MK-5932Christopher J Bungard, George D Hartman, Jesse J Manikowski, et al.
Pageof 8