Exploring DOXP-reductoisomerase binding limits using phosphonated N-aryl and N-heteroarylcarboxamides as DXR inhibitors. [electronic resource]
Producer: 20140121Description: 4332-41 p. digitalISSN:- 1464-3391
- Aldose-Ketose Isomerases -- antagonists & inhibitors
- Amides -- chemical synthesis
- Binding Sites
- Carbamates -- chemical synthesis
- Drug Design
- Enzyme Activation -- drug effects
- Enzyme Inhibitors -- chemistry
- Magnetic Resonance Spectroscopy
- Models, Molecular
- Molecular Structure
- Protein Binding -- drug effects
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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