ChemicalBook--->CAS DataBase List--->168425-64-7

168425-64-7

168425-64-7 Structure

168425-64-7 Structure
IdentificationBack Directory
[Name]

COMPOUND 401
[CAS]

168425-64-7
[Synonyms]

CS-315
Morpholino a
Compound 401, >=98%
COMPOUND401;COMPOUND-401
2-Morpholino-4H-pyrimido[2,1-a]isoquinolin-4-one
2-(Morpholin-4-yl)pyrimido[2,1-a]isoquinolin-4-one
2-Morpholino-4H-pyrimido[2,1-a]isoquinolin-4-one>
2-(4-Morpholinyl)-4H-pyrimido[2,1-a]isoquinolin-4-one
4H-PyriMido[2,1-a]isoquinolin-4-one, 2-(4-Morpholinyl)-
2-Morpholino-4H-pyrimido[2,1-a]isoquinolin-4-one
[Molecular Formula]

C16H15N3O2
[MDL Number]

MFCD10568147
[MOL File]

168425-64-7.mol
[Molecular Weight]

281.314
Chemical PropertiesBack Directory
[Melting point ]

184-186℃ (ethanol )
[Boiling point ]

456.9±55.0 °C(Predicted)
[density ]

1.36±0.1 g/cm3 (20 ºC 760 Torr)
[storage temp. ]

Store at RT
[solubility ]

DMSO : 6 mg/mL (21.33 mM; Need ultrasonic and warming)
[form ]

powder to crystal
[pka]

1.01±0.20(Predicted)
[color ]

White to Light yellow
[CAS DataBase Reference]

168425-64-7
Safety DataBack Directory
[HS Code ]

2934.99.4400
Hazard InformationBack Directory
[Uses]

Compound 401 is a selective inhibitor of DNA-PK and FRAP.
[Biological Activity]

Reversible and selective inhibitor of DNA-dependent protein kinase (DNA-PK) and mammalian target of rapamycin (mTOR) (IC 50 values are 0.28 and 5.3 μ M respectively). Displays little affinity for other commonly studied kinases including PI 3-K, ATM and ATR (IC 50 values are all > 100 μ M). Induces apoptosis in vitro .
[IC 50]

DNA-PK: 0.28 μM (IC50); mTOR: 5.3 μM (IC50)
[storage]

Store at RT
Spectrum DetailBack Directory
[Spectrum Detail]

COMPOUND 401(168425-64-7)1HNMR
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