Receptor site topographies for phencyclidine-like and sigma drugs: predictions from quantitative conformational, electrostatic potential, and radioreceptor analyses. [electronic resource]
Producer: 19890123Description: 863-79 p. digitalISSN:- 0026-895X
- Animals
- Electrochemistry
- Hydrogen Bonding
- In Vitro Techniques
- Isomerism
- Male
- Models, Molecular
- Molecular Conformation
- Quantum Theory
- Radioligand Assay
- Rats
- Rats, Inbred Strains
- Receptors, N-Methyl-D-Aspartate
- Receptors, Neurotransmitter -- metabolism
- Receptors, Opioid -- metabolism
- Receptors, Phencyclidine
- Receptors, sigma
- Stereoisomerism
- Structure-Activity Relationship
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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