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Details

Stereochemistry ACHIRAL
Molecular Formula C15H10ClN3O3
Molecular Weight 315.711
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CLONAZEPAM

SMILES

[O-][N+](=O)C1=CC2=C(NC(=O)CN=C2C3=C(Cl)C=CC=C3)C=C1

InChI

InChIKey=DGBIGWXXNGSACT-UHFFFAOYSA-N
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)

HIDE SMILES / InChI
Molecular Formula C15H10ClN3O3
Molecular Weight 315.711
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:55:06 UTC 2023
Edited
by admin
on Sat Dec 16 16:55:06 UTC 2023
Record UNII
5PE9FDE8GB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CLONAZEPAM
EP   HSDB   INN   MART.   MI   ORANGE BOOK   USAN   USP   VANDF   WHO-DD  
USAN   INN  
Official Name English
NSC-179913
Code English
CLONAZEPAM [JAN]
Common Name English
RIVOTRIL
Brand Name English
RO-5-4023
Code English
CLONAZEPAM [MART.]
Common Name English
RIVATRIL
Brand Name English
RO 5-4023
Code English
2H-1,4-BENZODIAZEPIN-2-ONE, 5-(2-CHLOROPHENYL)-1,3-DIHYDRO-7-NITRO-
Systematic Name English
Clonazepam [WHO-DD]
Common Name English
CLONAZEPAM [ORANGE BOOK]
Common Name English
5-(O-CHLOROPHENYL)-1,3-DIHYDRO-7-NITRO-2H-1,4-BENZODIAZEPIN-2-ONE
Common Name English
CLONAZEPAM [MI]
Common Name English
KLONOPIN
Brand Name English
CLONAZEPAM [EP MONOGRAPH]
Common Name English
RO-54023
Code English
clonazepam [INN]
Common Name English
RAVOTRIL
Brand Name English
CLONAZEPAM [VANDF]
Common Name English
CLONAZEPAM CIV [USP-RS]
Common Name English
CLONAZEPAM [HSDB]
Common Name English
CLONAZEPAM CIV
USP-RS  
Common Name English
CLONAZEPAM [USAN]
Common Name English
CLONAZEPAM [USP MONOGRAPH]
Common Name English
Classification Tree Code System Code
NDF-RT N0000175694
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
WHO-VATC QN03AE01
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
NCI_THESAURUS C264
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
FDA ORPHAN DRUG 243507
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
WHO-ATC N03AE01
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
NDF-RT N0000007542
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
NCI_THESAURUS C1012
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
DEA NO. 2737
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
LIVERTOX NBK548030
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
FDA ORPHAN DRUG 82794
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
Code System Code Type Description
PUBCHEM
2802
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
PRIMARY
WIKIPEDIA
CLONAZEPAM
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
PRIMARY
SMS_ID
100000084528
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
PRIMARY
RXCUI
2598
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
PRIMARY RxNorm
DRUG CENTRAL
703
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
PRIMARY
NSC
179913
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
PRIMARY
LACTMED
Clonazepam
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
PRIMARY
DAILYMED
5PE9FDE8GB
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
PRIMARY
DRUG BANK
DB01068
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
PRIMARY
CAS
1622-61-3
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
PRIMARY
MESH
D002998
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
PRIMARY
RS_ITEM_NUM
1140305
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
PRIMARY
CHEBI
3756
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
PRIMARY
MERCK INDEX
m3649
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
216-596-2
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
PRIMARY
EPA CompTox
DTXSID1022845
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
PRIMARY
INN
2765
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
PRIMARY
NCI_THESAURUS
C28935
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
PRIMARY
FDA UNII
5PE9FDE8GB
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
PRIMARY
EVMPD
SUB06728MIG
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
PRIMARY
ChEMBL
CHEMBL452
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
PRIMARY
HSDB
3265
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
PRIMARY
IUPHAR
6963
Created by admin on Sat Dec 16 16:55:07 UTC 2023 , Edited by admin on Sat Dec 16 16:55:07 UTC 2023
PRIMARY
Related Record Type Details
GABAA RECEPTOR
TARGET->POSITIVE ALLOSTERIC MODULATOR (PAM)
ARYLAMINE N-ACETYLTRANSFERASE 2
METABOLIC ENZYME -> SUBSTRATE
Structure of CLONAZEPAM HYDROCHLORIDE
SALT/SOLVATE -> PARENT
PLASMA PROTEIN FRACTION (HUMAN)
BINDER->LIGAND
BINDING
Related Record Type Details
Structure of 7-ACETAMINOCLONAZEPAM
METABOLITE INACTIVE -> PARENT
Structure of 7-AMINOCLONAZEPAM
METABOLITE INACTIVE -> PARENT
Related Record Type Details
Structure of 2-AMINO-2'-CHLORO-5-NITROBENZOPHENONE
IMPURITY -> PARENT
Structure of 3-AMINO-4-(2-CHLOROPHENYL)-6-NITROCARBOSTYRIL
IMPURITY -> PARENT
Related Record Type Details
Structure of CLONAZEPAM
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
MAXIMUM TOLERATED DOSE TOXICITY
Biological Half-life PHARMACOKINETIC
ORAL BIOAVAILABILITY PHARMACOKINETIC
Volume of Distribution PHARMACOKINETIC
Tmax PHARMACOKINETIC
PROTEIN BINDING PHARMACOKINETIC
Route of Elimination PHARMACOKINETIC
Biological Half-life PHARMACOKINETIC
NIH
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