LEXOFENAC

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C14H14O3
Molecular Weight	230.2592
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of LEXOFENAC

Structure Search

SMILES

OC(=O)CC1=CC=C(C=C1)C2=CC(=O)CCC2

InChI

InChIKey=SRJYOCXLFRUMBY-UHFFFAOYSA-N

InChI=1S/C14H14O3/c15-13-3-1-2-12(9-13)11-6-4-10(5-7-11)8-14(16)17/h4-7,9H,1-3,8H2,(H,16,17)

HIDE SMILES / InChI

Molecular Formula	C14H14O3
Molecular Weight	230.2592
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Description
Sources: Elks, J. (2014) The Dictionary of Drugs: Chemical Data, page 731, retrieved from: https://books.google.ru/books?id=0vXTBwAAQBAJ | https://apps.who.int/iris/bitstream/handle/10665/275695/WHO-EMP-RHT-TSN-2018.1-eng.pdf | Negwer, M. (1994) Organic-chemical drugs and their synonyms, page 861, retrieved from: https://books.google.ru/books?id=1ghtAAAAMAAJ

Lexofenac is an ibufenac derivative. It was developed as anti-inflammatory and analgesic agent.

Approval Year

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:22:45 GMT 2025` Edited by `admin` on `Mon Mar 31 18:22:45 GMT 2025`
Record UNII	3578QN1B5H
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

LEXOFENAC

Official Name

English

(P-(3-OXO-1-CYCLOHEXEN-1-YL)PHENYL)ACETIC ACID

Preferred Name

English

lexofenac [INN]

Common Name

English

Classification Tree Code System Code

NCI_THESAURUS

C257

Created by admin on Mon Mar 31 18:22:45 GMT 2025 , Edited by admin on Mon Mar 31 18:22:45 GMT 2025

Code System Code Type Description

FDA UNII

3578QN1B5H

Created by admin on Mon Mar 31 18:22:45 GMT 2025 , Edited by admin on Mon Mar 31 18:22:45 GMT 2025

PRIMARY

INN

4218

Created by admin on Mon Mar 31 18:22:45 GMT 2025 , Edited by admin on Mon Mar 31 18:22:45 GMT 2025

PRIMARY

PUBCHEM

3038504

Created by admin on Mon Mar 31 18:22:45 GMT 2025 , Edited by admin on Mon Mar 31 18:22:45 GMT 2025

PRIMARY

EPA CompTox

DTXSID50194327

Created by admin on Mon Mar 31 18:22:45 GMT 2025 , Edited by admin on Mon Mar 31 18:22:45 GMT 2025

PRIMARY

CAS

41387-02-4

Created by admin on Mon Mar 31 18:22:45 GMT 2025 , Edited by admin on Mon Mar 31 18:22:45 GMT 2025

PRIMARY

EVMPD

SUB08500MIG

Created by admin on Mon Mar 31 18:22:45 GMT 2025 , Edited by admin on Mon Mar 31 18:22:45 GMT 2025

PRIMARY

SMS_ID

100000082307

Created by admin on Mon Mar 31 18:22:45 GMT 2025 , Edited by admin on Mon Mar 31 18:22:45 GMT 2025

PRIMARY

ChEMBL

CHEMBL2104357

Created by admin on Mon Mar 31 18:22:45 GMT 2025 , Edited by admin on Mon Mar 31 18:22:45 GMT 2025

PRIMARY

NCI_THESAURUS

C66011

Created by admin on Mon Mar 31 18:22:45 GMT 2025 , Edited by admin on Mon Mar 31 18:22:45 GMT 2025

PRIMARY

Related Record Type Details


					3578QN1B5H

LEXOFENAC

ACTIVE MOIETY