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

Details

Stereochemistry ACHIRAL
Molecular Formula C16H17ClN2O4S
Molecular Weight 368.835
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-(2-(5-CHLORO-2-METHOXYBENZAMIDO)ETHYL)PHENYLSULFONAMIDE

SMILES

COC1=CC=C(Cl)C=C1C(=O)NCCC2=CC=C(C=C2)S(N)(=O)=O

InChI

InChIKey=KVWWTCSJLGHLRM-UHFFFAOYSA-N
InChI=1S/C16H17ClN2O4S/c1-23-15-7-4-12(17)10-14(15)16(20)19-9-8-11-2-5-13(6-3-11)24(18,21)22/h2-7,10H,8-9H2,1H3,(H,19,20)(H2,18,21,22)

HIDE SMILES / InChI

Molecular Formula C16H17ClN2O4S
Molecular Weight 368.835
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Q96P20|||Q59H68
Gene ID: 114548.0
Gene Symbol: NLRP3
Target Organism: Homo sapiens (Human)
PubMed

PubMed

TitleDatePubMed
Liquid chromatography-electrospray tandem mass spectrometry method for determination of indapamide in serum for single/multiple dose bioequivalence studies of sustained release formulations.
2005 Feb 25
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:09:14 GMT 2023
Edited
by admin
on Fri Dec 15 18:09:14 GMT 2023
Record UNII
8TF6P2NUB5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-(2-(5-CHLORO-2-METHOXYBENZAMIDO)ETHYL)PHENYLSULFONAMIDE
Systematic Name English
BENZAMIDE, N-(2-(4-(AMINOSULFONYL)PHENYL)ETHYL)-5-CHLORO-2-METHOXY-
Systematic Name English
GLYBURIDE RELATED COMPOUND A [USP-RS]
Common Name English
4-(2-(2-METHOXY-5-CHLOROBENZENE-1-CARBOXAMIDO)ETHYL)BENZENESULFONAMIDE
Systematic Name English
O-ANISAMIDE, 5-CHLORO-N-(P-SULFAMOYLPHENETHYL)-
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
240-722-5
Created by admin on Fri Dec 15 18:09:14 GMT 2023 , Edited by admin on Fri Dec 15 18:09:14 GMT 2023
PRIMARY
PUBCHEM
85542
Created by admin on Fri Dec 15 18:09:14 GMT 2023 , Edited by admin on Fri Dec 15 18:09:14 GMT 2023
PRIMARY
FDA UNII
8TF6P2NUB5
Created by admin on Fri Dec 15 18:09:14 GMT 2023 , Edited by admin on Fri Dec 15 18:09:14 GMT 2023
PRIMARY
EPA CompTox
DTXSID1057660
Created by admin on Fri Dec 15 18:09:14 GMT 2023 , Edited by admin on Fri Dec 15 18:09:14 GMT 2023
PRIMARY
CAS
16673-34-0
Created by admin on Fri Dec 15 18:09:14 GMT 2023 , Edited by admin on Fri Dec 15 18:09:14 GMT 2023
PRIMARY
RS_ITEM_NUM
1295516
Created by admin on Fri Dec 15 18:09:14 GMT 2023 , Edited by admin on Fri Dec 15 18:09:14 GMT 2023
PRIMARY
Related Record Type Details
INNOVATOR->PARENT