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Details

Stereochemistry ACHIRAL
Molecular Formula C14H17ClN2O3S
Molecular Weight 328.814
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CLOREXOLONE

SMILES

NS(=O)(=O)C1=CC2=C(CN(C3CCCCC3)C2=O)C=C1Cl

InChI

InChIKey=VPMWFZKOWULPGT-UHFFFAOYSA-N
InChI=1S/C14H17ClN2O3S/c15-12-6-9-8-17(10-4-2-1-3-5-10)14(18)11(9)7-13(12)21(16,19)20/h6-7,10H,1-5,8H2,(H2,16,19,20)

HIDE SMILES / InChI

Molecular Formula C14H17ClN2O3S
Molecular Weight 328.814
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 Fri Dec 15 16:17:35 UTC 2023
Edited
by admin
on Fri Dec 15 16:17:35 UTC 2023
Record UNII
Q2PLT3FS05
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CLOREXOLONE
INN   JAN   MART.   MI   USAN   WHO-DD  
INN   USAN  
Official Name English
CLOREXOLONE [USAN]
Common Name English
Clorexolone [WHO-DD]
Common Name English
clorexolone [INN]
Common Name English
6-Chloro-2-cyclohexyl-3-oxo-5-isoindolinesulfonamide
Systematic Name English
CLOREXOLONE [MART.]
Common Name English
1H-ISOINDOLE-5-SULFONAMIDE, 6-CHLORO-2-CYCLOHEXYL-2,3-DIHYDRO-3-OXO-
Systematic Name English
CLOREXOLONE [MI]
Common Name English
CLOREXOLONE [JAN]
Common Name English
Classification Tree Code System Code
WHO-VATC QC03BA82
Created by admin on Fri Dec 15 16:17:35 UTC 2023 , Edited by admin on Fri Dec 15 16:17:35 UTC 2023
NCI_THESAURUS C448
Created by admin on Fri Dec 15 16:17:35 UTC 2023 , Edited by admin on Fri Dec 15 16:17:35 UTC 2023
WHO-VATC QC03BA12
Created by admin on Fri Dec 15 16:17:35 UTC 2023 , Edited by admin on Fri Dec 15 16:17:35 UTC 2023
WHO-ATC C03BA12
Created by admin on Fri Dec 15 16:17:35 UTC 2023 , Edited by admin on Fri Dec 15 16:17:35 UTC 2023
WHO-ATC C03BA82
Created by admin on Fri Dec 15 16:17:35 UTC 2023 , Edited by admin on Fri Dec 15 16:17:35 UTC 2023
Code System Code Type Description
INN
1795
Created by admin on Fri Dec 15 16:17:35 UTC 2023 , Edited by admin on Fri Dec 15 16:17:35 UTC 2023
PRIMARY
EVMPD
SUB06754MIG
Created by admin on Fri Dec 15 16:17:35 UTC 2023 , Edited by admin on Fri Dec 15 16:17:35 UTC 2023
PRIMARY
MESH
C017137
Created by admin on Fri Dec 15 16:17:35 UTC 2023 , Edited by admin on Fri Dec 15 16:17:35 UTC 2023
PRIMARY
ChEMBL
CHEMBL2106167
Created by admin on Fri Dec 15 16:17:35 UTC 2023 , Edited by admin on Fri Dec 15 16:17:35 UTC 2023
PRIMARY
DRUG BANK
DB13617
Created by admin on Fri Dec 15 16:17:35 UTC 2023 , Edited by admin on Fri Dec 15 16:17:35 UTC 2023
PRIMARY
MERCK INDEX
m1084
Created by admin on Fri Dec 15 16:17:35 UTC 2023 , Edited by admin on Fri Dec 15 16:17:35 UTC 2023
PRIMARY Merck Index
WIKIPEDIA
Clorexolone
Created by admin on Fri Dec 15 16:17:35 UTC 2023 , Edited by admin on Fri Dec 15 16:17:35 UTC 2023
PRIMARY
NCI_THESAURUS
C81075
Created by admin on Fri Dec 15 16:17:35 UTC 2023 , Edited by admin on Fri Dec 15 16:17:35 UTC 2023
PRIMARY
CAS
2127-01-7
Created by admin on Fri Dec 15 16:17:35 UTC 2023 , Edited by admin on Fri Dec 15 16:17:35 UTC 2023
PRIMARY
SMS_ID
100000084024
Created by admin on Fri Dec 15 16:17:35 UTC 2023 , Edited by admin on Fri Dec 15 16:17:35 UTC 2023
PRIMARY
EPA CompTox
DTXSID4057683
Created by admin on Fri Dec 15 16:17:35 UTC 2023 , Edited by admin on Fri Dec 15 16:17:35 UTC 2023
PRIMARY
ECHA (EC/EINECS)
218-342-6
Created by admin on Fri Dec 15 16:17:35 UTC 2023 , Edited by admin on Fri Dec 15 16:17:35 UTC 2023
PRIMARY
PUBCHEM
16473
Created by admin on Fri Dec 15 16:17:35 UTC 2023 , Edited by admin on Fri Dec 15 16:17:35 UTC 2023
PRIMARY
DRUG CENTRAL
712
Created by admin on Fri Dec 15 16:17:35 UTC 2023 , Edited by admin on Fri Dec 15 16:17:35 UTC 2023
PRIMARY
FDA UNII
Q2PLT3FS05
Created by admin on Fri Dec 15 16:17:35 UTC 2023 , Edited by admin on Fri Dec 15 16:17:35 UTC 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY