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BioModels Ontology
Last uploaded:
April 3, 2012
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| Preferred Name | clonazepam | |
| Synonyms |
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| Definitions |
1,3-Dihydro-2H-1,4-benzodiazepin-2-one in which the hydrogens at positions 5 and 7 are substituted by 2-chlorophenyl and nitro groups, respectively. It is used in the treatment of all types of epilepsy and seizures, as well as myoclonus and associated abnormal movements, and panic disorders. However, its use can be limited by the development of tolerance and by sedation. |
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| ID |
http://purl.obolibrary.org/obo/CHEBI_3756 |
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| alternative term |
InChI=1S/C15H10ClN3O3/c16-12-4-2-1-3-10(12)15-11-7-9(19(21)22)5-6-13(11)18-14(20)8-17-15/h1-7H,8H2,(H,18,20) [O-][N+](=O)c1ccc2NC(=O)CN=C(c3ccccc3Cl)c2c1 1,3-dihydro-7-nitro-5-(2-chlorophenyl)-2H-1,4.benzodiazepin-2-one C15H10ClN3O3 clonazepamum 5-(o-chlorophenyl)-7-nitro-1,3-dihydro-2H-1,4-benzodiazepin-2-one clonazepam InChIKey=DGBIGWXXNGSACT-UHFFFAOYSA-N 5-(2-chlorophenyl)-7-nitro-1H-benzo[e][1,4]diazepin-2(3H)-one CLONAZEPAM 5-(2-chlorophenyl)-7-nitro-1,3-dihydro-2H-1,4-benzodiazepin-2-one 5-(2-Chloro-phenyl)-7-nitro-1,3-dihydro-benzo[e][1,4]diazepin-2-one
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| definition |
1,3-Dihydro-2H-1,4-benzodiazepin-2-one in which the hydrogens at positions 5 and 7 are substituted by 2-chlorophenyl and nitro groups, respectively. It is used in the treatment of all types of epilepsy and seizures, as well as myoclonus and associated abnormal movements, and panic disorders. However, its use can be limited by the development of tolerance and by sedation.
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| has role |
http://purl.obolibrary.org/obo/CHEBI_50268 |
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| label |
clonazepam
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| prefixIRI |
CHEBI:3756
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| prefLabel |
clonazepam
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| subClassOf |
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