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Heyao Wang

Showing results (31-40 of 41) with videos related to

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Scientific Reports|August 10, 2016
Repositioning organohalogen drugs: a case study for identification of potent B-Raf V600E inhibitors via docking and bioassayYisu Li, Binbin Guo, Zhijian Xu, et al.
Journal of Chemical Information and Modeling|September 30, 2011
Computational screening for active compounds targeting protein sequences: methodology and experimental validationFei Wang, Dongxiang Liu, Heyao Wang, et al.
Bioorganic & Medicinal Chemistry Letters|August 4, 2012
Combining pharmacophore, docking and substructure search approaches to identify and optimize novel B-RafV600E inhibitorsZhijian Xu, Guirui Yan, Gaihong Wang, 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.
Journal of Medicinal Chemistry|September 3, 2014
Design, synthesis, and structure-activity and structure-pharmacokinetic relationship studies of novel [6,6,5] tricyclic fused oxazolidinones leading to the discovery of a potent, selective, and orally bioavailable FXa inhibitorTao Xue, Shi Ding, Bin Guo, et al.
Archiv Der Pharmazie|April 15, 2015
Design, synthesis, and pharmacological evaluation of highly potent and selective dipeptidyl peptidase-4 inhibitorsTao Jiang, Yuren Zhou, Jianming Zhu, et al.
The Journal of Endocrinology|November 8, 2018
Vincamine as a GPR40 agonist improves glucose homeostasis in type 2 diabetic miceTe Du, Liu Yang, Xu Xu, et al.
ACS Medicinal Chemistry Letters|May 26, 2015
Design, Synthesis, and Pharmacological Evaluation of Fused β-Homophenylalanine Derivatives as Potent DPP-4 InhibitorsTao Jiang, Yuren Zhou, Zhuxi Chen, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|November 29, 2024
Slow Metabolism-Driven Amplification of Hepatic PPARγ Agonism Mediates Benzbromarone-Induced Obesity-Specific Liver InjuryGuanting Li, Yourong Hu, Han Zhao, et al.
Oncotarget|January 16, 2017
Impact of NUDT15 polymorphisms on thiopurines-induced myelotoxicity and thiopurines tolerance doseDandan Yin, Xuyang Xia, Junlong Zhang, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Scientific Reports|August 10, 2016
Repositioning organohalogen drugs: a case study for identification of potent B-Raf V600E inhibitors via docking and bioassayYisu Li, Binbin Guo, Zhijian Xu, et al.
Journal of Chemical Information and Modeling|September 30, 2011
Computational screening for active compounds targeting protein sequences: methodology and experimental validationFei Wang, Dongxiang Liu, Heyao Wang, et al.
Bioorganic & Medicinal Chemistry Letters|August 4, 2012
Combining pharmacophore, docking and substructure search approaches to identify and optimize novel B-RafV600E inhibitorsZhijian Xu, Guirui Yan, Gaihong Wang, 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.
Journal of Medicinal Chemistry|September 3, 2014
Design, synthesis, and structure-activity and structure-pharmacokinetic relationship studies of novel [6,6,5] tricyclic fused oxazolidinones leading to the discovery of a potent, selective, and orally bioavailable FXa inhibitorTao Xue, Shi Ding, Bin Guo, et al.
Archiv Der Pharmazie|April 15, 2015
Design, synthesis, and pharmacological evaluation of highly potent and selective dipeptidyl peptidase-4 inhibitorsTao Jiang, Yuren Zhou, Jianming Zhu, et al.
The Journal of Endocrinology|November 8, 2018
Vincamine as a GPR40 agonist improves glucose homeostasis in type 2 diabetic miceTe Du, Liu Yang, Xu Xu, et al.
ACS Medicinal Chemistry Letters|May 26, 2015
Design, Synthesis, and Pharmacological Evaluation of Fused β-Homophenylalanine Derivatives as Potent DPP-4 InhibitorsTao Jiang, Yuren Zhou, Zhuxi Chen, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|November 29, 2024
Slow Metabolism-Driven Amplification of Hepatic PPARγ Agonism Mediates Benzbromarone-Induced Obesity-Specific Liver InjuryGuanting Li, Yourong Hu, Han Zhao, et al.
Oncotarget|January 16, 2017
Impact of NUDT15 polymorphisms on thiopurines-induced myelotoxicity and thiopurines tolerance doseDandan Yin, Xuyang Xia, Junlong Zhang, et al.
Pageof 5