Weight | 371.824 g/mol |
---|---|
Formula | C19H18ClN3O3 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 0 |
Aromatic Rings | 2 |
Rotatable Bonds | 2 |
Camazepam (36104-80-0)
B-5833 · B 5833 · SB 5833
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- Determination of camazepam and bromazepam in human serum by adsorptive stripping voltammetry (Analyst, 1987)
- Hypnotic activity and effects on performance of lormetazepam and camazepam-analogues of temazepam. (British Journal of Clinical Pharmacology, 1982)
- Relationship between camazepam, Nmethyloxazepam and oxazepam brain concentrations and antileptazol effect in the rat (Journal of Pharmacy and Pharmacology, 1981)
- Enantiomer resolution of camazepam and its derivatives and enantioselective metabolism of camazepam by human liver microsomes. (Journal of Chromatography A, 1994)
- Achiral and chiral analysis of camazepam and metabolites by packed-column supercritical fluid chromatography. (Journal of Chromatography B: Biomedical Sciences and Applications, 1995)
- Species differences in the disposition and metabolism of camazepam. (Xenobiotica, 1985)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - B-5833
- B 5833
- SB 5833
- S-58-33
-
SMILESCN1C2=C(C=C(C=C2)Cl)C(=NC(C1=O)OC(=O)N(C)C)C3=CC=CC=C3
-
InChIKeyPXBVEXGRHZFEOF-UHFFFAOYSA-N
- Pubchem - Camazepam
- Wikipedia - camazepam
Camazepam is a benzodiazepine psychoactive drug, marketed under the brand names Albego, Limpidon and Paxor. It is the dimethyl carbamate ester of temazepam, a metabolite of diazepam. While it possesses anxiolytic, anticonvulsant, skeletal muscle relaxant and hypnotic properties it differs from other benzodiazepines in that its anxiolytic properties are particularly prominent but has comparatively limited anticonvulsant, hypnotic and skeletal muscle relaxant properties.
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