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San-Qi Zhang

Showing results (1-10 of 77) with videos related to

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Drug Development Research|January 6, 2023
Progress of small molecules for targeted protein degradation: PROTACs and other technologiesHong-Yi Zhao, Minhang Xin, San-Qi Zhang
Bioorganic Chemistry|August 14, 2022
Overcoming C797S mutation: The challenges and prospects of the fourth-generation EGFR-TKIsHong-Yi Zhao, Xiao-Xiao Xi, Minhang Xin, et al.
Bioorganic & Medicinal Chemistry Letters|August 7, 2020
Research advances on selective phosphatidylinositol 3 kinase δ (PI3Kδ) inhibitorsJiajia Sun, Yifan Feng, Yuan Huang, et al.
Bioorganic & Medicinal Chemistry Letters|March 23, 2017
Design and synthesis of novel 6-aryl substituted 4-anilinequinazoline derivatives as potential PI3Kδ inhibitorsMinhang Xin, Yuan-Yuan Hei, Hao Zhang, et al.
Yao Xue Xue Bao = Acta Pharmaceutica Sinica|September 30, 2008
[Preparation and liver targeting of floxuridinyl dibutyrate solid lipid nanoparticles]Jin-juan Li, Guang-de Yang, Hong-ying Wang, et al.
Zhongguo Zhong Yao Za Zhi = Zhongguo Zhongyao Zazhi = China Journal of Chinese Materia Medica|August 4, 2007
[Application of macroporous resin in purification for effective part from Polygonum cuspidatum]Dan Liu, Hai-feng Tang, San-qi Zhang, et al.
Expert Opinion on Therapeutic Patents|February 24, 2022
Menin-MLL protein-protein interaction inhibitors: a patent review (2014-2021)Huanrong Bai, San-Qi Zhang, Hao Lei, et al.
Bioorganic & Medicinal Chemistry Letters|November 8, 2015
Discovery of novel 2-benzylisoquinolin-1(2H)-ones as potent vasodilative agentsBo-Rui Kang, Sen Li, Shuai Mao, et al.
Bioorganic & Medicinal Chemistry|October 11, 2025
Synthesis and degradation effect of PROTACs targeting EGFR triple mutantsXiao-Xiao Xi, Hong-Yi Zhao, Minhang Xin, et al.
Bioorganic & Medicinal Chemistry|August 23, 2019
Synthesis and biological evaluation of 4-(piperid-3-yl)amino substituted 6-pyridylquinazolines as potent PI3Kδ inhibitorsYifan Feng, Weiming Duan, Shu Fan, et al.
Pageof 8

Showing results (1-10 of 77) with videos related to

Sort By:
Pageof 8
Drug Development Research|January 6, 2023
Progress of small molecules for targeted protein degradation: PROTACs and other technologiesHong-Yi Zhao, Minhang Xin, San-Qi Zhang
Bioorganic Chemistry|August 14, 2022
Overcoming C797S mutation: The challenges and prospects of the fourth-generation EGFR-TKIsHong-Yi Zhao, Xiao-Xiao Xi, Minhang Xin, et al.
Bioorganic & Medicinal Chemistry Letters|August 7, 2020
Research advances on selective phosphatidylinositol 3 kinase δ (PI3Kδ) inhibitorsJiajia Sun, Yifan Feng, Yuan Huang, et al.
Bioorganic & Medicinal Chemistry Letters|March 23, 2017
Design and synthesis of novel 6-aryl substituted 4-anilinequinazoline derivatives as potential PI3Kδ inhibitorsMinhang Xin, Yuan-Yuan Hei, Hao Zhang, et al.
Yao Xue Xue Bao = Acta Pharmaceutica Sinica|September 30, 2008
[Preparation and liver targeting of floxuridinyl dibutyrate solid lipid nanoparticles]Jin-juan Li, Guang-de Yang, Hong-ying Wang, et al.
Zhongguo Zhong Yao Za Zhi = Zhongguo Zhongyao Zazhi = China Journal of Chinese Materia Medica|August 4, 2007
[Application of macroporous resin in purification for effective part from Polygonum cuspidatum]Dan Liu, Hai-feng Tang, San-qi Zhang, et al.
Expert Opinion on Therapeutic Patents|February 24, 2022
Menin-MLL protein-protein interaction inhibitors: a patent review (2014-2021)Huanrong Bai, San-Qi Zhang, Hao Lei, et al.
Bioorganic & Medicinal Chemistry Letters|November 8, 2015
Discovery of novel 2-benzylisoquinolin-1(2H)-ones as potent vasodilative agentsBo-Rui Kang, Sen Li, Shuai Mao, et al.
Bioorganic & Medicinal Chemistry|October 11, 2025
Synthesis and degradation effect of PROTACs targeting EGFR triple mutantsXiao-Xiao Xi, Hong-Yi Zhao, Minhang Xin, et al.
Bioorganic & Medicinal Chemistry|August 23, 2019
Synthesis and biological evaluation of 4-(piperid-3-yl)amino substituted 6-pyridylquinazolines as potent PI3Kδ inhibitorsYifan Feng, Weiming Duan, Shu Fan, et al.
Pageof 8