Synthesis, anticancer evaluation, and molecular docking studies of some novel 4,6-disubstituted pyrazolo[3,4-d]pyrimidines as cyclin-dependent kinase 2 (CDK2) inhibitors. [electronic resource]
Producer: 20190221Description: 46-59 p. digitalISSN:- 1090-2120
- Animals
- Antineoplastic Agents -- chemical synthesis
- Catalytic Domain
- Cell Line, Tumor
- Cyclin-Dependent Kinase 2 -- antagonists & inhibitors
- Drug Design
- Humans
- Molecular Docking Simulation
- Molecular Structure
- Protein Kinase Inhibitors -- chemical synthesis
- Pyrazoles -- chemical synthesis
- Pyrimidines -- chemical synthesis
- Spodoptera
- Structure-Activity Relationship
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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