이경

전체 410건 중 101번부터 110번까지의 결과를 표시합니다.

2022

Article

Suppression of Tumor Growth and Cell Migration by Indole-Based Benzenesulfonamides and Their Synergistic Effects in Combination with Doxorubicin

Article

Metal/catalyst-free sequential C-N bond forming cascades at room temperature: environment-friendly one-pot synthesis of 5-aminoimidazoles from aryl glyoxals, anilines, and amidines

Article

PRR16/Largen Induces Epithelial-Mesenchymal Transition through the Interaction with ABI2 Leading to the Activation of ABL1 Kinase

Conference

Synthesis, Structure Activity Relationship (SAR) and Target Identification Study of Novel Stilbenes as Potential Anticancer Agent

Conference

Design, synthesis, molecular docking, and biological evaluation of novel 4-Anilinoquinazoline-based benzenesulfonamides as nanomolar carbonic anhydrase inhibitors possessing promising anticancer prof

Conference

Inhibition of Cancer Cell Growth by Targeting Mitochondrial Respiration Using the Novel HIF-1α Inhibitor LW1564

Conference

Design, Synthesis, and Biological Evaluation of Indole-Based Benzenesulfonamide Derivatives as Novel, Potent and Selective Human Carbonic Anhydrase II Inhibitors

Conference

Development of protein-protein interaction inhibitors targeting AIMP2-DX2 as potential cancer therapeutics

Conference

Total Synthesis of Cudraisoflavone J and Its Enantiomers

Article

AIMP2-DX2 provides therapeutic interface to control KRAS-driven tumorigenesis

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Suppression of Tumor Growth and Cell Migration by Indole-Based Benzenesulfonamides and Their Synergistic Effects in Combination with Doxorubicin

Metal/catalyst-free sequential C-N bond forming cascades at room temperature: environment-friendly one-pot synthesis of 5-aminoimidazoles from aryl glyoxals, anilines, and amidines

PRR16/Largen Induces Epithelial-Mesenchymal Transition through the Interaction with ABI2 Leading to the Activation of ABL1 Kinase

Synthesis, Structure Activity Relationship (SAR) and Target Identification Study of Novel Stilbenes as Potential Anticancer Agent

Design, synthesis, molecular docking, and biological evaluation of novel 4-Anilinoquinazoline-based benzenesulfonamides as nanomolar carbonic anhydrase inhibitors possessing promising anticancer prof

Inhibition of Cancer Cell Growth by Targeting Mitochondrial Respiration Using the Novel HIF-1α Inhibitor LW1564

Design, Synthesis, and Biological Evaluation of Indole-Based Benzenesulfonamide Derivatives as Novel, Potent and Selective Human Carbonic Anhydrase II Inhibitors

Development of protein-protein interaction inhibitors targeting AIMP2-DX2 as potential cancer therapeutics

Total Synthesis of Cudraisoflavone J and Its Enantiomers

AIMP2-DX2 provides therapeutic interface to control KRAS-driven tumorigenesis