Weight | 386.801 g/mol |
---|---|
Formula | C17H11ClF4N2S |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 2 |
Rotatable Bonds | 2 |
quazepam (36735-22-5)
Doral · Quiedorm · Sch 16134
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- Comparison of short and long halflife benzodiazepine hypnotics: Triazolam and quazepam (Clinical Pharmacology & Therapeutics, 1986)
- Quazepam and flurazepam: Long-term use and extended withdrawal (Clinical Pharmacology & Therapeutics, 1982)
- Hyperphagic and anorectic effects of -carbolines in a palatable food consumption test: Comparisons with triazolam and quazepam (European Journal of Pharmacology, 1986)
- Insomnia in Generalized Anxiety Disorder: Polysomnographic, Psychometric and Clinical Investigations before, during and after Therapy with a Long- versus a Short-Half-Life Benzodiazepine (Quazepam versus Triazolam) (Neuropsychobiology, 1994)
- Drug interaction between St John's Wort and quazepam. (British Journal of Clinical Pharmacology, 2004)
- A Comparative 25Night Sleep Laboratory Study on the Effects of Quazepam and Triazolam on Chronic Insomniacs (The Journal of Clinical Pharmacology, 1984)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Doral
- Quiedorm
- Sch 16134
-
SMILESC1C(=S)N(C2=C(C=C(C=C2)Cl)C(=N1)C3=CC=CC=C3F)CC(F)(F)F
-
InChIKeyIKMPWMZBZSAONZ-UHFFFAOYSA-N
- Pubchem - quazepam
- Wikipedia - quazepam
Quazepam (marketed under brand names Doral, Dormalin) is a relatively long-acting benzodiazepine derivative drug developed by the Schering Corporation in the 1970s. Quazepam is indicated for the treatment of insomnia including sleep induction and sleep maintenance. Quazepam induces impairment of motor function and has relatively (and uniquely) selective hypnotic and anticonvulsant properties with considerably less overdose potential than other benzodiazepines (due to its novel receptor-subtype selectively).
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