TETRIPROFEN

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

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C15H18O2
Molecular Weight	230.3022
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of TETRIPROFEN

Structure Search

SMILES

CC(C(O)=O)C1=CC=C(C=C1)C2=CCCCC2

InChI

InChIKey=CVBPQTZKZQWEFX-UHFFFAOYSA-N

InChI=1S/C15H18O2/c1-11(15(16)17)12-7-9-14(10-8-12)13-5-3-2-4-6-13/h5,7-11H,2-4,6H2,1H3,(H,16,17)

HIDE SMILES / InChI

Molecular Formula	C15H18O2
Molecular Weight	230.3022
Charge	0
Count

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

Description
Sources: https://worldwide.espacenet.com/publicationDetails/biblio?DB=EPODOC&II=0&ND=3&adjacent=true&locale=en_EP&FT=D&date=&CC=DE&NR=987C&KC=C

Tetriprofen is a hydratropic acid derivative patented by Swiss chemical company CIBA Ltd as an antinociceptive and anti-inflammatory agent.

Originator

Approval Year

Patents

Patents

Substance Class	Chemical Created by `admin` on `Fri Dec 15 15:47:24 GMT 2023` Edited by `admin` on `Fri Dec 15 15:47:24 GMT 2023`
Record UNII	8JG5454O0D
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

TETRIPROFEN

Official Name

English

tetriprofen [INN]

Common Name

English

2-(4-(CYCLOHEXEN-1-YL)PHENYL)PROPANOIC ACID

Common Name

English

4-(1-CYCLOHEXEN-1-YL)-.ALPHA.-METHYLBENZENEACETIC ACID

Common Name

English

BENZENEACETIC ACID, 4-(1-CYCLOHEXEN-1-YL)-.ALPHA.-METHYL-

Systematic Name

English

HYDRATROPIC ACID, P-1-CYCLOHEXEN-1-YL-

Common Name

English

P-1-CYCLOHEXEN-1-YLHYDRATROPIC ACID

Common Name

English

Classification Tree Code System Code

NCI_THESAURUS

C257

Created by admin on Fri Dec 15 15:47:24 GMT 2023 , Edited by admin on Fri Dec 15 15:47:24 GMT 2023

Code System Code Type Description

ChEMBL

CHEMBL2104691

Created by admin on Fri Dec 15 15:47:24 GMT 2023 , Edited by admin on Fri Dec 15 15:47:24 GMT 2023

PRIMARY

PUBCHEM

163312

Created by admin on Fri Dec 15 15:47:24 GMT 2023 , Edited by admin on Fri Dec 15 15:47:24 GMT 2023

PRIMARY

FDA UNII

8JG5454O0D

Created by admin on Fri Dec 15 15:47:24 GMT 2023 , Edited by admin on Fri Dec 15 15:47:24 GMT 2023

PRIMARY

CAS

28168-10-7

Created by admin on Fri Dec 15 15:47:24 GMT 2023 , Edited by admin on Fri Dec 15 15:47:24 GMT 2023

PRIMARY

EVMPD

SUB10949MIG

Created by admin on Fri Dec 15 15:47:24 GMT 2023 , Edited by admin on Fri Dec 15 15:47:24 GMT 2023

PRIMARY

SMS_ID

100000082720

Created by admin on Fri Dec 15 15:47:24 GMT 2023 , Edited by admin on Fri Dec 15 15:47:24 GMT 2023

PRIMARY

NCI_THESAURUS

C90907

Created by admin on Fri Dec 15 15:47:24 GMT 2023 , Edited by admin on Fri Dec 15 15:47:24 GMT 2023

PRIMARY

INN

3334

Created by admin on Fri Dec 15 15:47:24 GMT 2023 , Edited by admin on Fri Dec 15 15:47:24 GMT 2023

PRIMARY

EPA CompTox

DTXSID20865416

Created by admin on Fri Dec 15 15:47:24 GMT 2023 , Edited by admin on Fri Dec 15 15:47:24 GMT 2023

PRIMARY

Related Record Type Details


					7ZK53999QF

TETRIPROFEN SODIUM

SALT/SOLVATE -> PARENT


					G97SCV6KL6

TETRIPROFEN, (-)-

ENANTIOMER -> RACEMATE


					D4D4P67PK9

TETRIPROFEN, (+)-

ENANTIOMER -> RACEMATE

Related Record Type Details


					8JG5454O0D

ACTIVE MOIETY