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Jinfeng Luo

Showing results (31-40 of 53) with videos related to

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Journal of Medicinal Chemistry|March 26, 2013
Discovery and optimization of 3-(2-(Pyrazolo[1,5-a]pyrimidin-6-yl)ethynyl)benzamides as novel selective and orally bioavailable discoidin domain receptor 1 (DDR1) inhibitorsMingshan Gao, Lei Duan, Jinfeng Luo, et al.
Bioorganic & Medicinal Chemistry Letters|May 9, 2016
Design and synthesis of N-(4-aminopyridin-2-yl)amides as B-Raf(V600E) inhibitorsXiaokai Li, Jiayi Shen, Li Tan, et al.
RSC Advances|February 25, 2025
Alkyne dichotomy and hydrogen migration in binuclear cyclopentadienylmetal alkyne complexesHuidong Li, Jinfeng Luo, Haoyu Chen, et al.
Cancer Medicine|March 14, 2018
YL143, a novel mutant selective irreversible EGFR inhibitor, overcomes EGFR<sup>L858R, T790M</sup> -mutant resistance in vitro and in vivoZhang Zhang, Jian Zou, Lei Yu, et al.
European Journal of Medicinal Chemistry|February 8, 2019
Quinolone antibiotic derivatives as new selective Axl kinase inhibitorsLi Tan, Zhang Zhang, Donglin Gao, et al.
ACS Medicinal Chemistry Letters|March 19, 2020
Design and Optimization of 3'-(Imidazo[1,2-<i>a</i>]pyrazin-3-yl)-[1,1'-biphenyl]-3-carboxamides as Selective DDR1 InhibitorsCheng Mo, Zhang Zhang, Yupeng Li, et al.
Journal of Drug Targeting|October 11, 2018
GZD2202, a novel TrkB inhibitor, suppresses BDNF-mediated proliferation and metastasis in neuroblastoma modelsJian Zou, Zhang Zhang, Fang Xu, et al.
Translational Oncology|April 5, 2020
GZD824 as a FLT3, FGFR1 and PDGFRα Inhibitor Against Leukemia In Vitro and In VivoYuting Wang, Lenghe Zhang, Xia Tang, et al.
The Laryngoscope|November 2, 2023
Difference of Antrochoanal Polyps Between Children and Adults in the Chinese PopulationYanyi Tu, Tianjiao Jiang, Yisha Wu, et al.
Journal of Medicinal Chemistry|June 28, 2019
Design, Synthesis, and Structure-Activity Relationships of 1,2,3-Triazole Benzenesulfonamides as New Selective Leucine-Zipper and Sterile-α Motif Kinase (ZAK) InhibitorsJianzhang Yang, Marthandam Asokan Shibu, Lulu Kong, et al.
Pageof 6

Showing results (31-40 of 53) with videos related to

Sort By:
Pageof 6
Journal of Medicinal Chemistry|March 26, 2013
Discovery and optimization of 3-(2-(Pyrazolo[1,5-a]pyrimidin-6-yl)ethynyl)benzamides as novel selective and orally bioavailable discoidin domain receptor 1 (DDR1) inhibitorsMingshan Gao, Lei Duan, Jinfeng Luo, et al.
Bioorganic & Medicinal Chemistry Letters|May 9, 2016
Design and synthesis of N-(4-aminopyridin-2-yl)amides as B-Raf(V600E) inhibitorsXiaokai Li, Jiayi Shen, Li Tan, et al.
RSC Advances|February 25, 2025
Alkyne dichotomy and hydrogen migration in binuclear cyclopentadienylmetal alkyne complexesHuidong Li, Jinfeng Luo, Haoyu Chen, et al.
Cancer Medicine|March 14, 2018
YL143, a novel mutant selective irreversible EGFR inhibitor, overcomes EGFR<sup>L858R, T790M</sup> -mutant resistance in vitro and in vivoZhang Zhang, Jian Zou, Lei Yu, et al.
European Journal of Medicinal Chemistry|February 8, 2019
Quinolone antibiotic derivatives as new selective Axl kinase inhibitorsLi Tan, Zhang Zhang, Donglin Gao, et al.
ACS Medicinal Chemistry Letters|March 19, 2020
Design and Optimization of 3'-(Imidazo[1,2-<i>a</i>]pyrazin-3-yl)-[1,1'-biphenyl]-3-carboxamides as Selective DDR1 InhibitorsCheng Mo, Zhang Zhang, Yupeng Li, et al.
Journal of Drug Targeting|October 11, 2018
GZD2202, a novel TrkB inhibitor, suppresses BDNF-mediated proliferation and metastasis in neuroblastoma modelsJian Zou, Zhang Zhang, Fang Xu, et al.
Translational Oncology|April 5, 2020
GZD824 as a FLT3, FGFR1 and PDGFRα Inhibitor Against Leukemia In Vitro and In VivoYuting Wang, Lenghe Zhang, Xia Tang, et al.
The Laryngoscope|November 2, 2023
Difference of Antrochoanal Polyps Between Children and Adults in the Chinese PopulationYanyi Tu, Tianjiao Jiang, Yisha Wu, et al.
Journal of Medicinal Chemistry|June 28, 2019
Design, Synthesis, and Structure-Activity Relationships of 1,2,3-Triazole Benzenesulfonamides as New Selective Leucine-Zipper and Sterile-α Motif Kinase (ZAK) InhibitorsJianzhang Yang, Marthandam Asokan Shibu, Lulu Kong, et al.
Pageof 6