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Oncotarget
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May 11, 2017
Eg5 inhibitor YL001 induces mitotic arrest and inhibits tumor proliferation
Yufei Wang, Xingyu Wu, Mufeng Du, et al.
European Journal of Medicinal Chemistry
|
October 29, 2024
Design, synthesis, and pharmacological characterization of sulfonylurea-based NLRP3 inhibitors: Towards an effective therapeutic strategy for Alzheimer's disease
Weiping Lyu, Tongfei Gao, Cheng Shi, et al.
Organic & Biomolecular Chemistry
|
December 18, 2015
A stereo configuration-activity study of 3-iodo-4-(2-methylcyclohexyloxy)-6-phenethylpyridin-2(2H)-ones as potency inhibitors of HIV-1 variants
Shaotong Wu, Qianqian Yin, Liang Zhao, et al.
Journal of Medicinal Chemistry
|
May 3, 2021
Discovery of Novel and Potent <i>N</i>-Methyl-d-aspartate Receptor Positive Allosteric Modulators with Antidepressant-like Activity in Rodent Models
Zhongtang Li, Guanxing Cai, Fan Fang, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
November 5, 2024
Targeting SLITRK4 Restrains Proliferation and Liver Metastasis in Colorectal Cancer via Regulating PI3K/AKT/NFκB Pathway and Tumor-Associated Macrophage
Xiaojiao Sun, Junling Zhang, Bingqi Dong, et al.
European Journal of Medicinal Chemistry
|
June 10, 2022
Discovery of 2-(furan-2-ylmethylene)hydrazine-1-carbothioamide derivatives as novel inhibitors of SARS-CoV-2 main protease
Xiaodong Dou, Qi Sun, Guofeng Xu, et al.
Journal of Virology
|
January 2, 2025
Discovery of small molecules against porcine reproductive and respiratory syndrome virus replication by targeting NendoU activity
Jiaqi Zhu, Yunqiang Lai, Mengqi Cheng, et al.
Cell Reports
|
June 20, 2019
Direct Gating of the TRPM2 Channel by cADPR via Specific Interactions with the ADPR Binding Pocket
Peilin Yu, Zhenming Liu, Xiafei Yu, et al.
Journal of Medicinal Chemistry
|
July 30, 2025
Structure-Based Discovery of Quinazolin-2-amine Derivatives as Potent ROR1 Pseudokinase Inhibitors with <i>In Vitro</i> and <i>In Vivo</i> Efficacy against Triple-Negative Breast Cancer
Dehua Lu, Weiping Lyu, Xiaowei Chi, et al.
Journal of Medicinal Chemistry
|
June 30, 2026
Design and Synthesis of a Novel Covalent Dihydropteridinone Derivative as a Highly Potent and Orally Bioavailable PLK1 Inhibitor for the Treatment of Chronic Myeloid Leukemia
Jiaxu Zhou, Zhongtang Li, Xiaojiao Sun, et al.
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of 17
Search research articles
Search
Showing results (151-160 of 163) with videos related to
Sort By:
Page
of 17
Oncotarget
|
May 11, 2017
Eg5 inhibitor YL001 induces mitotic arrest and inhibits tumor proliferation
Yufei Wang, Xingyu Wu, Mufeng Du, et al.
European Journal of Medicinal Chemistry
|
October 29, 2024
Design, synthesis, and pharmacological characterization of sulfonylurea-based NLRP3 inhibitors: Towards an effective therapeutic strategy for Alzheimer's disease
Weiping Lyu, Tongfei Gao, Cheng Shi, et al.
Organic & Biomolecular Chemistry
|
December 18, 2015
A stereo configuration-activity study of 3-iodo-4-(2-methylcyclohexyloxy)-6-phenethylpyridin-2(2H)-ones as potency inhibitors of HIV-1 variants
Shaotong Wu, Qianqian Yin, Liang Zhao, et al.
Journal of Medicinal Chemistry
|
May 3, 2021
Discovery of Novel and Potent <i>N</i>-Methyl-d-aspartate Receptor Positive Allosteric Modulators with Antidepressant-like Activity in Rodent Models
Zhongtang Li, Guanxing Cai, Fan Fang, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
November 5, 2024
Targeting SLITRK4 Restrains Proliferation and Liver Metastasis in Colorectal Cancer via Regulating PI3K/AKT/NFκB Pathway and Tumor-Associated Macrophage
Xiaojiao Sun, Junling Zhang, Bingqi Dong, et al.
European Journal of Medicinal Chemistry
|
June 10, 2022
Discovery of 2-(furan-2-ylmethylene)hydrazine-1-carbothioamide derivatives as novel inhibitors of SARS-CoV-2 main protease
Xiaodong Dou, Qi Sun, Guofeng Xu, et al.
Journal of Virology
|
January 2, 2025
Discovery of small molecules against porcine reproductive and respiratory syndrome virus replication by targeting NendoU activity
Jiaqi Zhu, Yunqiang Lai, Mengqi Cheng, et al.
Cell Reports
|
June 20, 2019
Direct Gating of the TRPM2 Channel by cADPR via Specific Interactions with the ADPR Binding Pocket
Peilin Yu, Zhenming Liu, Xiafei Yu, et al.
Journal of Medicinal Chemistry
|
July 30, 2025
Structure-Based Discovery of Quinazolin-2-amine Derivatives as Potent ROR1 Pseudokinase Inhibitors with <i>In Vitro</i> and <i>In Vivo</i> Efficacy against Triple-Negative Breast Cancer
Dehua Lu, Weiping Lyu, Xiaowei Chi, et al.
Journal of Medicinal Chemistry
|
June 30, 2026
Design and Synthesis of a Novel Covalent Dihydropteridinone Derivative as a Highly Potent and Orally Bioavailable PLK1 Inhibitor for the Treatment of Chronic Myeloid Leukemia
Jiaxu Zhou, Zhongtang Li, Xiaojiao Sun, et al.
Page
of 17