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

Details

Stereochemistry ACHIRAL
Molecular Formula C7H4ClNO2
Molecular Weight 169.565
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CHLORZOXAZONE

SMILES

ClC1=CC=C2OC(=O)NC2=C1

InChI

InChIKey=TZFWDZFKRBELIQ-UHFFFAOYSA-N
InChI=1S/C7H4ClNO2/c8-4-1-2-6-5(3-4)9-7(10)11-6/h1-3H,(H,9,10)

HIDE SMILES / InChI

Molecular Formula C7H4ClNO2
Molecular Weight 169.565
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 05:13:25 UTC 2023
Edited
by admin
on Sat Dec 16 05:13:25 UTC 2023
Record UNII
H0DE420U8G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CHLORZOXAZONE
INN   JAN   MART.   MI   ORANGE BOOK   USP   USP-RS   VANDF   WHO-DD  
INN  
Official Name English
CHLORZOXAZONE [MART.]
Common Name English
chlorzoxazone [INN]
Common Name English
Chlorzoxazone [WHO-DD]
Common Name English
CHLORZOXAZONE [USP-RS]
Common Name English
5-Chloro-2-benzoxazolinone
Systematic Name English
STRIFON
Brand Name English
CHLORZOXAZONE [JAN]
Common Name English
CHLORZOXAZONE [USP IMPURITY]
Common Name English
PARAFLEX
Brand Name English
CHLORZOXAZONE [MI]
Common Name English
CHLORZOXAZONE [ORANGE BOOK]
Common Name English
PARAFON
Brand Name English
CHLORZOXAZONE [VANDF]
Common Name English
CHLORZOXAZONE [USP MONOGRAPH]
Common Name English
2(3H)-BENZOXAZOLONE, 5-CHLORO-
Systematic Name English
Classification Tree Code System Code
LIVERTOX NBK548137
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
NDF-RT N0000175737
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
WHO-VATC QM03BB53
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
WHO-ATC M03BB03
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
WHO-VATC QM03BB03
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
WHO-ATC M03BB53
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
NDF-RT N0000175730
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
WHO-ATC M03BB73
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
NCI_THESAURUS C29696
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
WHO-VATC QM03BB73
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
Code System Code Type Description
ECHA (EC/EINECS)
202-403-9
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
PRIMARY
EPA CompTox
DTXSID9022813
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
PRIMARY
MESH
D002753
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
PRIMARY
FDA UNII
H0DE420U8G
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
PRIMARY
DAILYMED
H0DE420U8G
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
PRIMARY
IUPHAR
2322
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
PRIMARY
CAS
95-25-0
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
PRIMARY
EVMPD
SUB06215MIG
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
PRIMARY
WIKIPEDIA
CHLORZOXAZONE
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
PRIMARY
RXCUI
2410
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
PRIMARY RxNorm
ChEMBL
CHEMBL1371
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
PRIMARY
CHEBI
3655
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
PRIMARY
INN
748
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
PRIMARY
MERCK INDEX
m3471
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
PRIMARY Merck Index
RS_ITEM_NUM
1130505
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
PRIMARY
SMS_ID
100000081896
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
PRIMARY
NCI_THESAURUS
C28926
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
PRIMARY
DRUG CENTRAL
626
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
PRIMARY
PUBCHEM
2733
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
PRIMARY
DRUG BANK
DB00356
Created by admin on Sat Dec 16 05:13:25 UTC 2023 , Edited by admin on Sat Dec 16 05:13:25 UTC 2023
PRIMARY
Related Record Type Details
BINDER->LIGAND
BINDING
METABOLIC ENZYME -> SUBSTRATE
EXCRETED UNCHANGED
Related Record Type Details
METABOLITE INACTIVE -> PARENT
MAJOR
URINE
METABOLITE -> PARENT
further metabolized to glucoronide
MAJOR
PLASMA
Related Record Type Details
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Volume of Distribution PHARMACOKINETIC
Biological Half-life PHARMACOKINETIC
Cmax PHARMACOKINETIC ROUTE OF ADMINISTRATION
PHARMACOKINETIC
DOSE
PHARMACOKINETIC
Tmax PHARMACOKINETIC ROUTE OF ADMINISTRATION
PHARMACOKINETIC
DOSE
PHARMACOKINETIC