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Xiangyi Jiang

Showing results (11-20 of 45) with videos related to

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Expert Opinion on Drug Discovery|November 30, 2022
The current progress in the use of boron as a platform for novel antiviral drug designShuo Wang, Yujie Ren, Zhao Wang, et al.
Bioorganic Chemistry|August 31, 2025
Design, synthesis, and biological evaluation of dual-site HIV-1 inhibitors simultaneously targeting the NNRTI binding pocket and an adjacent site with favorable resistance profilesXiangkai Ji, Xiangyi Jiang, Xing Huang, et al.
Journal of Medicinal Chemistry|February 17, 2022
Contemporary Medicinal Chemistry Strategies for the Discovery and Development of Novel HIV-1 Non-nucleoside Reverse Transcriptase InhibitorsZhao Wang, Srinivasulu Cherukupalli, Minghui Xie, et al.
Medicinal Research Reviews|April 20, 2019
Molecular design opportunities presented by solvent-exposed regions of target proteinsXiangyi Jiang, Ji Yu, Zhongxia Zhou, et al.
European Journal of Medicinal Chemistry|March 23, 2020
In situ click chemistry-based rapid discovery of novel HIV-1 NNRTIs by exploiting the hydrophobic channel and tolerant regions of NNIBPDongwei Kang, Da Feng, Lanlan Jing, et al.
ACS Infectious Diseases|July 4, 2020
Structure-Activity Relationship Exploration of NNIBP Tolerant Region I Leads to Potent HIV-1 NNRTIsDongwei Kang, Yanying Sun, N Arul Murugan, et al.
Journal of Medicinal Chemistry|September 17, 2025
Exploring the HIV-1 Reverse Transcriptase p51/p66 Interface: Structure-Based Design and Optimization of Novel 2,4,6-Trisubstituted Pyrimidines as Potent NNRTIs with Improved Resistance ProfilesXiangkai Ji, Xiangyi Jiang, Zhen Gao, et al.
Molecules (Basel, Switzerland)|September 23, 2022
Design, Synthesis, and Evaluation of a Set of Carboxylic Acid and Phosphate Prodrugs Derived from HBV Capsid Protein Allosteric Modulator NVR 3-778Xiangkai Ji, Xiangyi Jiang, Chisa Kobayashi, et al.
European Journal of Medicinal Chemistry|October 6, 2024
Identification of novel diarylpyrimidine derivatives as potent HIV-1 non-nucleoside reverse transcriptase inhibitors against wild-type and K103N mutant virusesXiangyi Jiang, Waleed A Zalloum, Zhen Gao, et al.
European Journal of Medicinal Chemistry|December 6, 2020
Exploiting the tolerant region I of the non-nucleoside reverse transcriptase inhibitor (NNRTI) binding pocket. Part 2: Discovery of diarylpyrimidine derivatives as potent HIV-1 NNRTIs with high Fsp<sup>3</sup> values and favorable drug-like propertiesXiangyi Jiang, Boshi Huang, Fisayo A Olotu, et al.
Pageof 5

Showing results (11-20 of 45) with videos related to

Sort By:
Pageof 5
Expert Opinion on Drug Discovery|November 30, 2022
The current progress in the use of boron as a platform for novel antiviral drug designShuo Wang, Yujie Ren, Zhao Wang, et al.
Bioorganic Chemistry|August 31, 2025
Design, synthesis, and biological evaluation of dual-site HIV-1 inhibitors simultaneously targeting the NNRTI binding pocket and an adjacent site with favorable resistance profilesXiangkai Ji, Xiangyi Jiang, Xing Huang, et al.
Journal of Medicinal Chemistry|February 17, 2022
Contemporary Medicinal Chemistry Strategies for the Discovery and Development of Novel HIV-1 Non-nucleoside Reverse Transcriptase InhibitorsZhao Wang, Srinivasulu Cherukupalli, Minghui Xie, et al.
Medicinal Research Reviews|April 20, 2019
Molecular design opportunities presented by solvent-exposed regions of target proteinsXiangyi Jiang, Ji Yu, Zhongxia Zhou, et al.
European Journal of Medicinal Chemistry|March 23, 2020
In situ click chemistry-based rapid discovery of novel HIV-1 NNRTIs by exploiting the hydrophobic channel and tolerant regions of NNIBPDongwei Kang, Da Feng, Lanlan Jing, et al.
ACS Infectious Diseases|July 4, 2020
Structure-Activity Relationship Exploration of NNIBP Tolerant Region I Leads to Potent HIV-1 NNRTIsDongwei Kang, Yanying Sun, N Arul Murugan, et al.
Journal of Medicinal Chemistry|September 17, 2025
Exploring the HIV-1 Reverse Transcriptase p51/p66 Interface: Structure-Based Design and Optimization of Novel 2,4,6-Trisubstituted Pyrimidines as Potent NNRTIs with Improved Resistance ProfilesXiangkai Ji, Xiangyi Jiang, Zhen Gao, et al.
Molecules (Basel, Switzerland)|September 23, 2022
Design, Synthesis, and Evaluation of a Set of Carboxylic Acid and Phosphate Prodrugs Derived from HBV Capsid Protein Allosteric Modulator NVR 3-778Xiangkai Ji, Xiangyi Jiang, Chisa Kobayashi, et al.
European Journal of Medicinal Chemistry|October 6, 2024
Identification of novel diarylpyrimidine derivatives as potent HIV-1 non-nucleoside reverse transcriptase inhibitors against wild-type and K103N mutant virusesXiangyi Jiang, Waleed A Zalloum, Zhen Gao, et al.
European Journal of Medicinal Chemistry|December 6, 2020
Exploiting the tolerant region I of the non-nucleoside reverse transcriptase inhibitor (NNRTI) binding pocket. Part 2: Discovery of diarylpyrimidine derivatives as potent HIV-1 NNRTIs with high Fsp<sup>3</sup> values and favorable drug-like propertiesXiangyi Jiang, Boshi Huang, Fisayo A Olotu, et al.
Pageof 5