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Virtual Screening and Biological Activity Evaluation of New Potent Inhibitors Targeting Hexokinase-II
by
Liu, Ruijuan
, Liu, Xuewei
in
Adenosine triphosphate
/ Amino acids
/ Cancer
/ Care and treatment
/ Cell growth
/ Cytotoxicity
/ Diagnosis
/ Enzymes
/ Force and energy
/ Glucose
/ Glucose metabolism
/ Hexokinase-II
/ Hydrogen bonds
/ inhibitor
/ Kinases
/ Libraries
/ Ligands
/ Metabolism
/ molecular docking
/ Oncology, Experimental
/ Phosphorylation
/ Physiological aspects
/ Proteins
/ small molecule
/ virtual screen
2022
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Virtual Screening and Biological Activity Evaluation of New Potent Inhibitors Targeting Hexokinase-II
by
Liu, Ruijuan
, Liu, Xuewei
in
Adenosine triphosphate
/ Amino acids
/ Cancer
/ Care and treatment
/ Cell growth
/ Cytotoxicity
/ Diagnosis
/ Enzymes
/ Force and energy
/ Glucose
/ Glucose metabolism
/ Hexokinase-II
/ Hydrogen bonds
/ inhibitor
/ Kinases
/ Libraries
/ Ligands
/ Metabolism
/ molecular docking
/ Oncology, Experimental
/ Phosphorylation
/ Physiological aspects
/ Proteins
/ small molecule
/ virtual screen
2022
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Virtual Screening and Biological Activity Evaluation of New Potent Inhibitors Targeting Hexokinase-II
by
Liu, Ruijuan
, Liu, Xuewei
in
Adenosine triphosphate
/ Amino acids
/ Cancer
/ Care and treatment
/ Cell growth
/ Cytotoxicity
/ Diagnosis
/ Enzymes
/ Force and energy
/ Glucose
/ Glucose metabolism
/ Hexokinase-II
/ Hydrogen bonds
/ inhibitor
/ Kinases
/ Libraries
/ Ligands
/ Metabolism
/ molecular docking
/ Oncology, Experimental
/ Phosphorylation
/ Physiological aspects
/ Proteins
/ small molecule
/ virtual screen
2022
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Virtual Screening and Biological Activity Evaluation of New Potent Inhibitors Targeting Hexokinase-II
Journal Article
Virtual Screening and Biological Activity Evaluation of New Potent Inhibitors Targeting Hexokinase-II
2022
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Overview
Hexokinase-II (HK-II), the rate-limiting step enzyme in the glycolysis pathway, expresses high levels of cancer cells compared with normal cells. Due to its pivotal role in the different aspects of cancer physiology including cellular proliferation, metastasis, and apoptosis, HK-II provides a new therapeutic target for cancer therapy. The structure-based virtual screening targeting HK-II was used to hit identifications from small molecule databases, and the select compounds were further evaluated in biological assays. Forty-seven compounds with the lowest binding energies were identified as potential HK-II inhibitors. Among them, nine compounds displayed the highest cytotoxicity to three different cancer cells. Based on the mechanism study, compounds 4244-3659 and K611-0094 showed an obvious inhibitory effect on the HK-II enzyme. This study identified two potential inhibitors of HK-II and can be helpful for developing potential drugs targeting HK-II in tumor therapy.
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