| Weight | 324.811 g/mol |
|---|---|
| Formula | C19H17ClN2O |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
prazepam (2955-38-6)
Centrax · United Drug Brand of Prazepam · Mono Demetrin
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- Desmethyldiazepam kinetics in the elderly after oral prazepam (Clinical Pharmacology & Therapeutics, 1980)
- Comparative single-dose kinetics and dynamics of lorazepam, alprazolam, prazepam, and placebo. (Clinical Pharmacology & Therapeutics, 1988)
- Prazepam and lorazepam, two new benzodiazepines. (The New England Journal of Medicine, 1978)
- Prazepam metabolism by man. (Clinical Pharmacology & Therapeutics, 1970)
- Cyclometallated derivatives of palladium(II) with 1,4-benzodiazepin-2-ones. Crystal structure of (L-H)Pd(PPh3)ClCHCl3 (L = Prazepam: 7-chloro-1-cyclopropylmethyl-1,3-dihydro-5-phenyl-2H-1,4-benzodiazepin-2-one). Synthesis of isoindolo[2,1-d][1,4]benzodiazepine derivatives by reaction of [(L-H)PdCl]2 species with carbon monoxide (Journal of Organometallic Chemistry, 1991)
- Carcinogenesis bioassay of prazepam (verstran) in rats and mice (Toxicology and Applied Pharmacology, 1981)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Centrax
- United Drug Brand of Prazepam
- Mono Demetrin
- Demetrin
- Lysanxia
- Pfizer Brand of Prazepam
- Reapam
- Warner-Lambert Brand of Prazepam
- Parke Davis Brand of Prazepam
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SMILESC1CC1CN2C(=O)CN=C(C3=C2C=CC(=C3)Cl)C4=CC=CC=C4
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InChIKeyMWQCHHACWWAQLJ-UHFFFAOYSA-N
- Pubchem - prazepam
- Wikipedia - prazepam
Prazepam is a benzodiazepine derivative drug developed by Warner-Lambert in the 1960s. It possesses anxiolytic, anticonvulsant, sedative and skeletal muscle relaxant properties. Prazepam is a prodrug for desmethyldiazepam which is responsible for the therapeutic effects of prazepam.
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prazepam
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