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Details

Stereochemistry RACEMIC
Molecular Formula C18H17ClNO4S.Na
Molecular Weight 401.84
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Z-335 sodium

SMILES

[Na+].[O-]C(=O)CC1=CC2=C(CC(CNS(=O)(=O)C3=CC=C(Cl)C=C3)C2)C=C1

InChI

InChIKey=UEPBEZPJELQKJV-UHFFFAOYSA-M
InChI=1S/C18H18ClNO4S.Na/c19-16-3-5-17(6-4-16)25(23,24)20-11-13-8-14-2-1-12(10-18(21)22)7-15(14)9-13;/h1-7,13,20H,8-11H2,(H,21,22);/q;+1/p-1

HIDE SMILES / InChI

Molecular Formula Na
Molecular Weight 22.98976928
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C18H17ClNO4S
Molecular Weight 378.85
Charge -1
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Mechanism of hepatobiliary transport of a novel thromboxane A2 receptor antagonist, [2-(4-chlorophenylsulfonylaminomethyl)indan-5-yl]acetate (Z-335), and its xenobiotic taurine conjugate (Z-335-Tau) in rats.
2003-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:25:11 GMT 2025
Edited
by admin
on Mon Mar 31 22:25:11 GMT 2025
Record UNII
STR7DVQ85U
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Z-335
Preferred Name English
Z-335 sodium
Code English
1H-Indene-5-acetic acid, 2-[[[(4-chlorophenyl)sulfonyl]amino]methyl]-2,3-dihydro-, sodium salt (1:1)
Systematic Name English
1H-Indene-5-acetic acid, 2-[[[(4-chlorophenyl)sulfonyl]amino]methyl]-2,3-dihydro-, monosodium salt
Systematic Name English
Sodium 2-(2-(((4-chlorophenyl)sulfonamido)methyl)-2,3-dihydro-1h-inden-5-yl)acetate
Systematic Name English
Code System Code Type Description
PUBCHEM
23669776
Created by admin on Mon Mar 31 22:25:11 GMT 2025 , Edited by admin on Mon Mar 31 22:25:11 GMT 2025
PRIMARY
FDA UNII
STR7DVQ85U
Created by admin on Mon Mar 31 22:25:11 GMT 2025 , Edited by admin on Mon Mar 31 22:25:11 GMT 2025
PRIMARY
CAS
146731-14-8
Created by admin on Mon Mar 31 22:25:11 GMT 2025 , Edited by admin on Mon Mar 31 22:25:11 GMT 2025
PRIMARY
EPA CompTox
DTXSID20932899
Created by admin on Mon Mar 31 22:25:11 GMT 2025 , Edited by admin on Mon Mar 31 22:25:11 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY