U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C18H18BrClN2O
Molecular Weight 393.705
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of METACLAZEPAM

SMILES

COCC1CN=C(C2=C(Cl)C=CC=C2)C3=C(C=CC(Br)=C3)N1C

InChI

InChIKey=WABYCCJHARSRBH-UHFFFAOYSA-N
InChI=1S/C18H18BrClN2O/c1-22-13(11-23-2)10-21-18(14-5-3-4-6-16(14)20)15-9-12(19)7-8-17(15)22/h3-9,13H,10-11H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C18H18BrClN2O
Molecular Weight 393.705
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

PubMed

PubMed

TitleDatePubMed
General pharmacology of the anxiolytic compound metaclazepam in comparison to other benzodiazepines.
1985

Sample Use Guides

In Vivo Use Guide
patients with anxiety syndrome were treated either with placebo, or with 15 mg or with 30 mg metaclazepam/day for two weeks
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:40:07 UTC 2023
Edited
by admin
on Fri Dec 15 17:40:07 UTC 2023
Record UNII
C2N2B1303L
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
METACLAZEPAM
INN   MI   WHO-DD  
INN  
Official Name English
KC-2547
Code English
METUCLAZEPAM
Common Name English
metaclazepam [INN]
Common Name English
METACLAZEPAM [MI]
Common Name English
Metaclazepam [WHO-DD]
Common Name English
7-BROMO-5-(2-CHLOROPHENYL)-2,3-DIHYDRO-2-(METHOXYMETHYL)-1-METHYL-1H-1,4-BENZODIAZEPINE
Systematic Name English
1H-1,4-BENZODIAZEPINE, 7-BROMO-5-(2-CHLOROPHENYL)-2,3-DIHYDRO-2-(METHOXYMETHYL)-1-METHYL-
Systematic Name English
7-BROMO-5-(O-CHLOROPHENYL)-2,3-DIHYDRO-2-(METHOXYMETHYL)-1-METHYL-1H-1,4-BENZODIAZEPINE
Common Name English
KA-2547
Code English
BROMETAZEPAM
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C1012
Created by admin on Fri Dec 15 17:40:08 UTC 2023 , Edited by admin on Fri Dec 15 17:40:08 UTC 2023
Code System Code Type Description
CAS
84031-17-4
Created by admin on Fri Dec 15 17:40:08 UTC 2023 , Edited by admin on Fri Dec 15 17:40:08 UTC 2023
PRIMARY
EPA CompTox
DTXSID40905121
Created by admin on Fri Dec 15 17:40:08 UTC 2023 , Edited by admin on Fri Dec 15 17:40:08 UTC 2023
PRIMARY
FDA UNII
C2N2B1303L
Created by admin on Fri Dec 15 17:40:08 UTC 2023 , Edited by admin on Fri Dec 15 17:40:08 UTC 2023
PRIMARY
EVMPD
SUB08800MIG
Created by admin on Fri Dec 15 17:40:08 UTC 2023 , Edited by admin on Fri Dec 15 17:40:08 UTC 2023
PRIMARY
ChEMBL
CHEMBL1290783
Created by admin on Fri Dec 15 17:40:08 UTC 2023 , Edited by admin on Fri Dec 15 17:40:08 UTC 2023
PRIMARY
MERCK INDEX
m7260
Created by admin on Fri Dec 15 17:40:08 UTC 2023 , Edited by admin on Fri Dec 15 17:40:08 UTC 2023
PRIMARY Merck Index
SMS_ID
100000081172
Created by admin on Fri Dec 15 17:40:08 UTC 2023 , Edited by admin on Fri Dec 15 17:40:08 UTC 2023
PRIMARY
RXCUI
614654
Created by admin on Fri Dec 15 17:40:08 UTC 2023 , Edited by admin on Fri Dec 15 17:40:08 UTC 2023
PRIMARY
NCI_THESAURUS
C83941
Created by admin on Fri Dec 15 17:40:08 UTC 2023 , Edited by admin on Fri Dec 15 17:40:08 UTC 2023
PRIMARY
DRUG CENTRAL
1716
Created by admin on Fri Dec 15 17:40:08 UTC 2023 , Edited by admin on Fri Dec 15 17:40:08 UTC 2023
PRIMARY
INN
4495
Created by admin on Fri Dec 15 17:40:08 UTC 2023 , Edited by admin on Fri Dec 15 17:40:08 UTC 2023
PRIMARY
WIKIPEDIA
METACLAZEPAM
Created by admin on Fri Dec 15 17:40:08 UTC 2023 , Edited by admin on Fri Dec 15 17:40:08 UTC 2023
PRIMARY
PUBCHEM
71272
Created by admin on Fri Dec 15 17:40:08 UTC 2023 , Edited by admin on Fri Dec 15 17:40:08 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY