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Details

Stereochemistry RACEMIC
Molecular Formula C16H14N2O2
Molecular Weight 266.2946
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MIROPROFEN

SMILES

CC(C(O)=O)C1=CC=C(C=C1)C2=CN3C=CC=CC3=N2

InChI

InChIKey=OJGQFYYLKNCIJD-UHFFFAOYSA-N
InChI=1S/C16H14N2O2/c1-11(16(19)20)12-5-7-13(8-6-12)14-10-18-9-3-2-4-15(18)17-14/h2-11H,1H3,(H,19,20)

HIDE SMILES / InChI

Molecular Formula C16H14N2O2
Molecular Weight 266.2946
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Miroprofen, an imidazopyridine derivative, possesses anti-inflammatory properties. It was shown that this compound could be effective in suppressing pain responses and acute inflammation accompanied by increased vascular permeability. Analgesic effect of this compound was studied in post-extraction pain. However, information about the current study of this agent is not available.

Approval Year

PubMed

PubMed

TitleDatePubMed
Anti-inflammatory activity of an imidazopyridine derivative (miroprofen).
1981
[Double blind controlled study of miroprofen in acute upper respiratory tract infections--comparison with ibuprofen].
1982 May
[Analgesic effects of miroprofen in post-extraction pain].
1983 May
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:09:10 UTC 2023
Edited
by admin
on Fri Dec 15 16:09:10 UTC 2023
Record UNII
S00I5XG484
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MIROPROFEN
INN  
INN  
Official Name English
miroprofen [INN]
Common Name English
MIROPROFEN [JAN]
Common Name English
P-IMIDAZO(1,2-A)PYRIDIN-2-YLHYDRATROPIC ACID
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C257
Created by admin on Fri Dec 15 16:09:10 UTC 2023 , Edited by admin on Fri Dec 15 16:09:10 UTC 2023
Code System Code Type Description
MESH
C017978
Created by admin on Fri Dec 15 16:09:10 UTC 2023 , Edited by admin on Fri Dec 15 16:09:10 UTC 2023
PRIMARY
ChEMBL
CHEMBL2106551
Created by admin on Fri Dec 15 16:09:10 UTC 2023 , Edited by admin on Fri Dec 15 16:09:10 UTC 2023
PRIMARY
PUBCHEM
68752
Created by admin on Fri Dec 15 16:09:10 UTC 2023 , Edited by admin on Fri Dec 15 16:09:10 UTC 2023
PRIMARY
CHEBI
76249
Created by admin on Fri Dec 15 16:09:10 UTC 2023 , Edited by admin on Fri Dec 15 16:09:10 UTC 2023
PRIMARY
FDA UNII
S00I5XG484
Created by admin on Fri Dec 15 16:09:10 UTC 2023 , Edited by admin on Fri Dec 15 16:09:10 UTC 2023
PRIMARY
WIKIPEDIA
Miroprofen
Created by admin on Fri Dec 15 16:09:10 UTC 2023 , Edited by admin on Fri Dec 15 16:09:10 UTC 2023
PRIMARY
NCI_THESAURUS
C90910
Created by admin on Fri Dec 15 16:09:10 UTC 2023 , Edited by admin on Fri Dec 15 16:09:10 UTC 2023
PRIMARY
SMS_ID
100000080647
Created by admin on Fri Dec 15 16:09:10 UTC 2023 , Edited by admin on Fri Dec 15 16:09:10 UTC 2023
PRIMARY
EVMPD
SUB08994MIG
Created by admin on Fri Dec 15 16:09:10 UTC 2023 , Edited by admin on Fri Dec 15 16:09:10 UTC 2023
PRIMARY
EPA CompTox
DTXSID30866515
Created by admin on Fri Dec 15 16:09:10 UTC 2023 , Edited by admin on Fri Dec 15 16:09:10 UTC 2023
PRIMARY
CAS
55843-86-2
Created by admin on Fri Dec 15 16:09:10 UTC 2023 , Edited by admin on Fri Dec 15 16:09:10 UTC 2023
PRIMARY
INN
4938
Created by admin on Fri Dec 15 16:09:10 UTC 2023 , Edited by admin on Fri Dec 15 16:09:10 UTC 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY