Z-335 Free Acid

OC(=O)CC1=CC=C2CC(CNS(=O)(=O)C3=CC=C(Cl)C=C3)CC2=C1

InChIKey=PNAKMOCXPDQBOS-UHFFFAOYSA-N

InChI=1S/C18H18ClNO4S/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)

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

PubMed

Title	Date	PubMed
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	12486683

Patents

Substance Class	Chemical Created by `admin` on `Wed Apr 02 21:10:39 GMT 2025` Edited by `admin` on `Wed Apr 02 21:10:39 GMT 2025`
Record UNII	LM4TK5EY6B
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

1H-Indene-5-acetic acid, 2-[[[(4-chlorophenyl)sulfonyl]amino]methyl]-2,3-dihydro-

Preferred Name

English

Z-335 Free Acid

Code

English

2-[[[(4-Chlorophenyl)sulfonyl]amino]methyl]-2,3-dihydro-1H-indene-5-acetic acid

Systematic Name

English

2-{2-[(4-chlorobenzenesulfonamido)methyl]-2,3-dihydro-1H-inden-5-yl}acetic acid

Systematic Name

English

Code System Code Type Description

CAS

146737-36-2

Created by admin on Wed Apr 02 21:10:39 GMT 2025 , Edited by admin on Wed Apr 02 21:10:39 GMT 2025

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FDA UNII

LM4TK5EY6B

Created by admin on Wed Apr 02 21:10:39 GMT 2025 , Edited by admin on Wed Apr 02 21:10:39 GMT 2025

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PUBCHEM

219052

Created by admin on Wed Apr 02 21:10:39 GMT 2025 , Edited by admin on Wed Apr 02 21:10:39 GMT 2025

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