ChemicalBook--->CAS DataBase List--->351071-62-0

351071-62-0

351071-62-0 Structure

351071-62-0 Structure
IdentificationBack Directory
[Name]

4(1H)-Quinolinone, 8-(2-methylphenoxy)-2-(4-morpholinyl)-
[CAS]

351071-62-0
[Synonyms]

TGX115
TGX-115
TGX 115
4(1H)-Quinolinone, 8-(2-methylphenoxy)-2-(4-morpholinyl)-
[Molecular Formula]

C20H20N2O3
[MDL Number]

MFCD12922524
[MOL File]

351071-62-0.mol
[Molecular Weight]

336.38
Chemical PropertiesBack Directory
[Boiling point ]

475.1±45.0 °C(Predicted)
[density ]

1.249±0.06 g/cm3(Predicted)
[pka]

2.20±0.20(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362
Hazard InformationBack Directory
[Uses]

TGX-115 is a cytopermeable and potent PI3-K isomer p110β/p110δ inhibitor (p110β IC50 value of 0.13 μM, p110δ IC50 value of 0.63 μM).TGX-115 is an enzyme that regulates platelet adhesion process and inhibits phosphoinosine 3-kinase. TGX-115 can be used in the study of cardiovascular diseases such as coronary artery occlusion, stroke, acute coronary syndrome, acute myocardial infarction, restenosis, arteriosclerosis and unstable angina[1].
[Definition]

ChEBI: 8-(2-methylphenoxy)-2-(4-morpholinyl)-1H-quinolin-4-one is an aminoquinoline.
[IC 50]

PI3Kβ: 0.13 μM (IC50); PI3Kδ: 0.63 μM (IC50)
[References]

[1] Popovici-Muller J, et al. Discovery of AG-120 (Ivosidenib): a first-in-class mutant IDH1 inhibitor for the treatment of IDH1 mutant cancers[J]. ACS medicinal chemistry letters, 2018, 9(4): 300-305. DOI:10.1021/acsmedchemlett.7b00421
Spectrum DetailBack Directory
[Spectrum Detail]

4(1H)-Quinolinone, 8-(2-methylphenoxy)-2-(4-morpholinyl)-(351071-62-0)1HNMR
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