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European Journal of Medicinal Chemistry
|
September 5, 2025
Discovery and SAR study of highly selective and potent 1,2,4-oxadiazole-based S1PR1 agonists
Tianyu Ye, Jinling Yu, Yuxian Fang, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 21, 2022
Design, synthesis and biological evaluation of pteridine-7(8H)-one derivatives as potent and selective CDK4/6 inhibitors
Huan He, Qi Liu, Lu Chen, et al.
Bioorganic & Medicinal Chemistry
|
February 26, 2013
Substituted indolin-2-ones as p90 ribosomal S6 protein kinase 2 (RSK2) inhibitors: Molecular docking simulation and structure-activity relationship analysis
Ye Zhong, Mengzhu Xue, Xue Zhao, et al.
Organic & Biomolecular Chemistry
|
January 23, 2023
A simple monoselective C-H oxygenation approach for the synthesis of ursane triterpenoids
Wenyi Mei, Sisi Fan, Yufei Han, et al.
American Journal of Translational Research
|
June 21, 2021
Guanosine ameliorates positive symptoms of schizophrenia <i>via</i> modulating 5-HT<sub>1A</sub> and 5-HT<sub>2A</sub> receptors
Yu Mao, Yao Xing, Jie Li, et al.
Pesticide Biochemistry and Physiology
|
September 14, 2024
Fluorinated plant activators induced dual-pathway signal transduction and long-lasting ROS burst in chloroplast
Qinjie Shi, Jianmian Fu, Yiqing Zhou, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
August 14, 2023
Targeting DHODH reveals therapeutic opportunities in ATRA-resistant acute promyelocytic leukemia
Tingyuan Yang, Xiayu Shi, Shiliang Li, et al.
Journal of Medicinal Chemistry
|
September 24, 2013
Discovery of pteridin-7(8H)-one-based irreversible inhibitors targeting the epidermal growth factor receptor (EGFR) kinase T790M/L858R mutant
Wei Zhou, Xiaofeng Liu, Zhengchao Tu, et al.
European Journal of Medicinal Chemistry
|
February 23, 2013
Optimization of heterocyclic substituted benzenesulfonamides as novel carbonic anhydrase IX inhibitors and their structure activity relationship
Rui Gao, Sha Liao, Chen Zhang, et al.
Scientific Reports
|
June 21, 2017
Structure-Guided Design of C4-alkyl-1,4-dihydro-2H-pyrimido[4,5-d][1,3]oxazin-2-ones as Potent and Mutant-Selective Epidermal Growth Factor Receptor (EGFR) L858R/T790M Inhibitors
Yongjia Hao, Jiankun Lyu, Rong Qu, et al.
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Search research articles
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Showing results (31-40 of 93) with videos related to
Sort By:
Page
of 10
European Journal of Medicinal Chemistry
|
September 5, 2025
Discovery and SAR study of highly selective and potent 1,2,4-oxadiazole-based S1PR1 agonists
Tianyu Ye, Jinling Yu, Yuxian Fang, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 21, 2022
Design, synthesis and biological evaluation of pteridine-7(8H)-one derivatives as potent and selective CDK4/6 inhibitors
Huan He, Qi Liu, Lu Chen, et al.
Bioorganic & Medicinal Chemistry
|
February 26, 2013
Substituted indolin-2-ones as p90 ribosomal S6 protein kinase 2 (RSK2) inhibitors: Molecular docking simulation and structure-activity relationship analysis
Ye Zhong, Mengzhu Xue, Xue Zhao, et al.
Organic & Biomolecular Chemistry
|
January 23, 2023
A simple monoselective C-H oxygenation approach for the synthesis of ursane triterpenoids
Wenyi Mei, Sisi Fan, Yufei Han, et al.
American Journal of Translational Research
|
June 21, 2021
Guanosine ameliorates positive symptoms of schizophrenia <i>via</i> modulating 5-HT<sub>1A</sub> and 5-HT<sub>2A</sub> receptors
Yu Mao, Yao Xing, Jie Li, et al.
Pesticide Biochemistry and Physiology
|
September 14, 2024
Fluorinated plant activators induced dual-pathway signal transduction and long-lasting ROS burst in chloroplast
Qinjie Shi, Jianmian Fu, Yiqing Zhou, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
August 14, 2023
Targeting DHODH reveals therapeutic opportunities in ATRA-resistant acute promyelocytic leukemia
Tingyuan Yang, Xiayu Shi, Shiliang Li, et al.
Journal of Medicinal Chemistry
|
September 24, 2013
Discovery of pteridin-7(8H)-one-based irreversible inhibitors targeting the epidermal growth factor receptor (EGFR) kinase T790M/L858R mutant
Wei Zhou, Xiaofeng Liu, Zhengchao Tu, et al.
European Journal of Medicinal Chemistry
|
February 23, 2013
Optimization of heterocyclic substituted benzenesulfonamides as novel carbonic anhydrase IX inhibitors and their structure activity relationship
Rui Gao, Sha Liao, Chen Zhang, et al.
Scientific Reports
|
June 21, 2017
Structure-Guided Design of C4-alkyl-1,4-dihydro-2H-pyrimido[4,5-d][1,3]oxazin-2-ones as Potent and Mutant-Selective Epidermal Growth Factor Receptor (EGFR) L858R/T790M Inhibitors
Yongjia Hao, Jiankun Lyu, Rong Qu, et al.
Page
of 10