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Details

Stereochemistry ACHIRAL
Molecular Formula C10H10O4
Molecular Weight 194.184
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CRESOPIRINE

SMILES

CC(=O)OC1=C(C=CC=C1C)C(O)=O

InChI

InChIKey=XRBMKGUDDJPAMH-UHFFFAOYSA-N
InChI=1S/C10H10O4/c1-6-4-3-5-8(10(12)13)9(6)14-7(2)11/h3-5H,1-2H3,(H,12,13)

HIDE SMILES / InChI

Molecular Formula C10H10O4
Molecular Weight 194.184
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Cresopirine is benzoic acid derivative and o-Cresotic Acid ester with anti-inflammatory activity.

Originator

Sources: Justus Liebigs Annalen der Chemie (1911), 379, 333-50.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
[De-acetalization and elimination in vivo of some salicylate derivatives: acetylsalicylic acid (aspirin) and acetylorthocresotic acid (cresopirin); calculation of hemicresis time and protorrhea].
1954 Oct-Dec
Patents

Patents

Sample Use Guides

Mouse: 200 mg. per kg
Route of Administration: Other
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:05:32 GMT 2023
Edited
by admin
on Sat Dec 16 08:05:32 GMT 2023
Record UNII
2G83E641HZ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CRESOPIRINE
Common Name English
2-(ACETYLOXY)-3-METHYLBENZOIC ACID
Systematic Name English
NSC-49105
Code English
BENZOIC ACID, 2-(ACETYLOXY)-3-METHYL-
Systematic Name English
AGN-357
Code English
ACETYL-O-CRESOTIC ACID
Common Name English
2-ACETOXY-3-METHYLBENZOIC ACID
Systematic Name English
CRESOPYRINE
Common Name English
2,3-CRESOTIC ACID, ACETATE
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID40195964
Created by admin on Sat Dec 16 08:05:32 GMT 2023 , Edited by admin on Sat Dec 16 08:05:32 GMT 2023
PRIMARY
NSC
49105
Created by admin on Sat Dec 16 08:05:32 GMT 2023 , Edited by admin on Sat Dec 16 08:05:32 GMT 2023
PRIMARY
FDA UNII
2G83E641HZ
Created by admin on Sat Dec 16 08:05:32 GMT 2023 , Edited by admin on Sat Dec 16 08:05:32 GMT 2023
PRIMARY
CAS
4386-39-4
Created by admin on Sat Dec 16 08:05:32 GMT 2023 , Edited by admin on Sat Dec 16 08:05:32 GMT 2023
PRIMARY
ECHA (EC/EINECS)
224-499-1
Created by admin on Sat Dec 16 08:05:32 GMT 2023 , Edited by admin on Sat Dec 16 08:05:32 GMT 2023
PRIMARY
PUBCHEM
78094
Created by admin on Sat Dec 16 08:05:32 GMT 2023 , Edited by admin on Sat Dec 16 08:05:32 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY