CRESOTAMIDE

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

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C8H9NO2
Molecular Weight	151.1626
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of CRESOTAMIDE

Structure Search

SMILES

CC1=CC=CC(C(N)=O)=C1O

InChI

InChIKey=NWULWVPYPIRXAU-UHFFFAOYSA-N

InChI=1S/C8H9NO2/c1-5-3-2-4-6(7(5)10)8(9)11/h2-4,10H,1H3,(H2,9,11)

HIDE SMILES / InChI

Molecular Formula	C8H9NO2
Molecular Weight	151.1626
Charge	0
Count

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

Description
Sources: https://www.ncbi.nlm.nih.gov/pubmed/15615546 | https://www.ncbi.nlm.nih.gov/pubmed/13888148

Cresotamide of o-cresotinic acid with analgesic, antipyretic and anti-inflammatory action.

Approval Year

PubMed

PubMed

Title	Date	PubMed
Drug evolution concept in drug design: 1. Hybridization method.	2004 Dec 30	15615546

Substance Class	Chemical Created by `admin` on `Fri Dec 15 16:30:51 GMT 2023` Edited by `admin` on `Fri Dec 15 16:30:51 GMT 2023`
Record UNII	5748P7L6IT
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

CRESOTAMIDE

Official Name

English

Cresotamide [WHO-DD]

Common Name

English

cresotamide [INN]

Common Name

English

2,3-CRESOTAMIDE

Common Name

English

Classification Tree Code System Code

NCI_THESAURUS

C257

Created by admin on Fri Dec 15 16:30:51 GMT 2023 , Edited by admin on Fri Dec 15 16:30:51 GMT 2023

Code System Code Type Description

EPA CompTox

DTXSID40161225

Created by admin on Fri Dec 15 16:30:51 GMT 2023 , Edited by admin on Fri Dec 15 16:30:51 GMT 2023

PRIMARY

SMS_ID

100000083717

Created by admin on Fri Dec 15 16:30:51 GMT 2023 , Edited by admin on Fri Dec 15 16:30:51 GMT 2023

PRIMARY

EVMPD

SUB06818MIG

Created by admin on Fri Dec 15 16:30:51 GMT 2023 , Edited by admin on Fri Dec 15 16:30:51 GMT 2023

PRIMARY

INN

3321

Created by admin on Fri Dec 15 16:30:51 GMT 2023 , Edited by admin on Fri Dec 15 16:30:51 GMT 2023

PRIMARY

CAS

14008-60-7

Created by admin on Fri Dec 15 16:30:51 GMT 2023 , Edited by admin on Fri Dec 15 16:30:51 GMT 2023

PRIMARY

MESH

C004629

Created by admin on Fri Dec 15 16:30:51 GMT 2023 , Edited by admin on Fri Dec 15 16:30:51 GMT 2023

PRIMARY

PUBCHEM

26392

Created by admin on Fri Dec 15 16:30:51 GMT 2023 , Edited by admin on Fri Dec 15 16:30:51 GMT 2023

PRIMARY

ChEMBL

CHEMBL2104183

Created by admin on Fri Dec 15 16:30:51 GMT 2023 , Edited by admin on Fri Dec 15 16:30:51 GMT 2023

PRIMARY

NCI_THESAURUS

C77351

Created by admin on Fri Dec 15 16:30:51 GMT 2023 , Edited by admin on Fri Dec 15 16:30:51 GMT 2023

PRIMARY

ECHA (EC/EINECS)

237-821-0

Created by admin on Fri Dec 15 16:30:51 GMT 2023 , Edited by admin on Fri Dec 15 16:30:51 GMT 2023

PRIMARY

FDA UNII

5748P7L6IT

Created by admin on Fri Dec 15 16:30:51 GMT 2023 , Edited by admin on Fri Dec 15 16:30:51 GMT 2023

PRIMARY

Related Record Type Details


					5748P7L6IT

ACTIVE MOIETY