Weight | 315.716 g/mol |
---|---|
Formula | C15H10ClN3O3 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 1 |
Aromatic Rings | 2 |
Rotatable Bonds | 2 |
clonazepam (1622-61-3)
Rivotril · Ro 5-4023 · Ro 54023
Score:
#37 in Neurology
,
#196 in Neuroscience
,
#914 in Biology
,
#1010 in Chemistry
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- Treatment of social phobia with clonazepam and placebo. (Journal of Clinical Psychopharmacology, 1993)
- Clonazepam and imipramine in the treatment of panic attacks : a double-blind comparison of efficacy and side effects (The Journal of Clinical Psychiatry, 1990)
- Topical clonazepam in stomatodynia: a randomised placebo-controlled study. (Pain, 2004)
- Clonazepam release from core-shell type nanoparticles in vitro (Journal of Controlled Release, 1998)
- CLINICAL, BIOCHEMICAL, AND PHYSIOLOGICAL FEATURES DISTINGUISHING MYOCLONUS RESPONSIVE TO 5-HYDROXYTRYPTOPHAN, TRYPTOPHAN WITH A MONOAMINE OXIDASE INHIBITOR, AND CLONAZEPAM (Brain, 1977)
- Clonazepam suppresses GABAB-mediated inhibition in thalamic relay neurons through effects in nucleus reticularis (Journal of Neurophysiology, 1994)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Rivotril
- Ro 5-4023
- Ro 54023
- Antelepsin
-
SMILESC1C(=O)NC2=C(C=C(C=C2)[N+](=O)[O-])C(=N1)C3=CC=CC=C3Cl
-
InChIKeyDGBIGWXXNGSACT-UHFFFAOYSA-N
- Pubchem - clonazepam
- Wikipedia - clonazepam
Clonazepam, sold under the brand name Klonopin among others, is a medication used to prevent and treat seizures, panic disorder, and for the movement disorder known as akathisia. It is a tranquilizer of the benzodiazepine class. It is taken by mouth.
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Synthesis
N-[2-(2-chlorobenzoyl)-4-nitrophenyl]acetamide
+
Glycine p-nitroanilide
(Imine formation from aldehyde)
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