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Details

Stereochemistry ACHIRAL
Molecular Formula C21H17FN2O2
Molecular Weight 348.3703
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TIMAPIPRANT

SMILES

CC1=C(CC2=NC3=C(C=CC=C3)C=C2)C4=C(C=CC(F)=C4)N1CC(O)=O

InChI

InChIKey=FATGTHLOZSXOBC-UHFFFAOYSA-N
InChI=1S/C21H17FN2O2/c1-13-17(11-16-8-6-14-4-2-3-5-19(14)23-16)18-10-15(22)7-9-20(18)24(13)12-21(25)26/h2-10H,11-12H2,1H3,(H,25,26)

HIDE SMILES / InChI

Molecular Formula C21H17FN2O2
Molecular Weight 348.3703
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 04:36:09 UTC 2023
Edited
by admin
on Sat Dec 16 04:36:09 UTC 2023
Record UNII
04XB9TB8OL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TIMAPIPRANT
INN  
INN  
Official Name English
OC-000459
Code English
CHF-6532
Code English
OC000459
Code English
OC459
Code English
1H-INDOLE-1-ACETIC ACID, 5-FLUORO-2-METHYL-3-(2-QUINOLINYLMETHYL)-
Systematic Name English
OC-459
Common Name English
ODC-9101
Common Name English
Timapiprant [WHO-DD]
Common Name English
timapiprant [INN]
Common Name English
(5-FLUORO-2-METHYL-3-QUINOLIN-2-YLMETHYLINDO-1-YL)-ACETIC ACID
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C574
Created by admin on Sat Dec 16 04:36:09 UTC 2023 , Edited by admin on Sat Dec 16 04:36:09 UTC 2023
Code System Code Type Description
ChEMBL
CHEMBL560993
Created by admin on Sat Dec 16 04:36:09 UTC 2023 , Edited by admin on Sat Dec 16 04:36:09 UTC 2023
PRIMARY
SMS_ID
300000008740
Created by admin on Sat Dec 16 04:36:09 UTC 2023 , Edited by admin on Sat Dec 16 04:36:09 UTC 2023
PRIMARY
NCI_THESAURUS
C152633
Created by admin on Sat Dec 16 04:36:09 UTC 2023 , Edited by admin on Sat Dec 16 04:36:09 UTC 2023
PRIMARY
DRUG BANK
DB11900
Created by admin on Sat Dec 16 04:36:09 UTC 2023 , Edited by admin on Sat Dec 16 04:36:09 UTC 2023
PRIMARY
CAS
851723-84-7
Created by admin on Sat Dec 16 04:36:09 UTC 2023 , Edited by admin on Sat Dec 16 04:36:09 UTC 2023
PRIMARY
FDA UNII
04XB9TB8OL
Created by admin on Sat Dec 16 04:36:09 UTC 2023 , Edited by admin on Sat Dec 16 04:36:09 UTC 2023
PRIMARY
EPA CompTox
DTXSID00234343
Created by admin on Sat Dec 16 04:36:09 UTC 2023 , Edited by admin on Sat Dec 16 04:36:09 UTC 2023
PRIMARY
INN
10483
Created by admin on Sat Dec 16 04:36:09 UTC 2023 , Edited by admin on Sat Dec 16 04:36:09 UTC 2023
PRIMARY
PUBCHEM
11462174
Created by admin on Sat Dec 16 04:36:09 UTC 2023 , Edited by admin on Sat Dec 16 04:36:09 UTC 2023
PRIMARY
CAS
1422181-22-3
Created by admin on Sat Dec 16 04:36:09 UTC 2023 , Edited by admin on Sat Dec 16 04:36:09 UTC 2023
NO STRUCTURE GIVEN
Related Record Type Details
TARGET -> INHIBITOR
A post hoc analysis revealed that the greatest improvement of lung function by timapiprant was observed in patients with active eosinophilia (≥250/μl peripheral blood) and—even more pronounced—in younger patients (90). This applies also for the humanized murine IL-5 antibody mepolizumab, which is most effective and only given in asthma patients with severe eosinophilic airway inflammation (91). In eosinophil esophagitis, timapiprant significantly reduced the esophageal eosinophil load and induced some clinical improvement (92). Timapiprant also successfully reduced nasal and ocular symptoms in allergic subjects exposed to grass pollen (93).
Related Record Type Details
ACTIVE MOIETY