Design, synthesis, crystallization and biological evaluation of new symmetrical biscationic compounds as selective inhibitors of human Choline Kinase α1 (ChoKα1). [electronic resource]
Producer: 20170127Description: 23793 p. digitalISSN:- 2045-2322
- Antineoplastic Agents -- chemical synthesis
- Binding Sites
- Butanes -- chemistry
- Cations
- Cell Line
- Cell Line, Tumor
- Cell Proliferation -- drug effects
- Choline Kinase -- antagonists & inhibitors
- Crystallization
- Drug Design
- Enzyme Inhibitors -- chemical synthesis
- Humans
- Molecular Docking Simulation
- Organ Specificity
- Protein Binding
- Pyridinium Compounds -- chemical synthesis
- Quantitative Structure-Activity Relationship
- Quinolinium Compounds -- chemical synthesis
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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