ChemicalBook--->CAS DataBase List--->872365-14-5

872365-14-5

872365-14-5 Structure

872365-14-5 Structure
IdentificationBack Directory
[Name]

Fevipiprant
[CAS]

872365-14-5
[Synonyms]

QAW039
CS-2449
Fevipipran
NVP-QAW039
Fevipiprant
NVP-QAW039;QAW039
Fevipiprant (QAW039)
Fevipiprant(NVP-QAW039)
NVP-QAW039; QAW039;QAW039;QAW-039;QAW 039;FEVIPIPRANT
NVP-QAW039; NVP-QAW 039; NVP-QAW-039 QAW-039; QAW039; QAW 039; FEVIPIPRANT
2-Methyl-1-[[4-(methylsulfonyl)-2-(trifluoromethyl)phenyl]methyl]-1H-pyrrolo[2,3-b]pyridine-3-acetic acid
1H-Pyrrolo[2,3-b]pyridine-3-acetic acid, 2-methyl-1-[[4-(methylsulfonyl)-2-(trifluoromethyl)phenyl]methyl]-
[Molecular Formula]

C19H17F3N2O4S
[MDL Number]

MFCD22548206
[MOL File]

872365-14-5.mol
[Molecular Weight]

426.41
Chemical PropertiesBack Directory
[Boiling point ]

637.6±55.0 °C(Predicted)
[density ]

1.44±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMF: 10 mg/mL; DMF:PBS(pH7.2) (1:2): 0.33 mg/mL; DMSO: 10 mg/mL; Ethanol: 1 mg/mL
[form ]

A crystalline solid
[pka]

3.33±0.30(Predicted)
[color ]

White to off-white
[InChI]

InChI=1S/C19H17F3N2O4S/c1-11-15(9-17(25)26)14-4-3-7-23-18(14)24(11)10-12-5-6-13(29(2,27)28)8-16(12)19(20,21)22/h3-8H,9-10H2,1-2H3,(H,25,26)
[InChIKey]

GFPPXZDRVCSVNR-UHFFFAOYSA-N
[SMILES]

C12N(CC3=CC=C(S(C)(=O)=O)C=C3C(F)(F)F)C(C)=C(CC(O)=O)C1=CC=CN=2
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H335-H302+H312+H332-H315
[Precautionary statements ]

P280-P301+P312-P362+P364
[HS Code ]

2933998090
Hazard InformationBack Directory
[Uses]

Fevipiprant is used in the oral treatment of asthma and has been successful in targeting severe eosinophilic asthma.Fevipiprant is a novel oral prostaglandin D2 receptor 2 (DP2; known as CRTh2) antagonist and currently in development for the treatment of severe asthma and atopic dermatitis.
[in vivo]

Fevipiprant (10 mg/kg; in the drinking water) reduces CaCl2-induced AAA (abdominal aortic aneurysm) formation in mouse[3].

Animal Model:C57Bl/6 mice[3]
Dosage:10 mg/kg
Administration:In the drinking water
Result:Efficiently reduced CaCl2-induced AAA formation with diminished elastin degradation, aortic macrophage infiltration, MPO accumulation and MCP-1 expression.
[IC 50]

DP2: 1.14 nM (Kd)
[storage]

Store at -20°C
Spectrum DetailBack Directory
[Spectrum Detail]

Fevipiprant(872365-14-5)1HNMR
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