ChemicalBook--->CAS DataBase List--->1202055-34-2

1202055-34-2

1202055-34-2 Structure

1202055-34-2 Structure
IdentificationBack Directory
[Name]

NMS-P715
[CAS]

1202055-34-2
[Synonyms]

CS-1822
NMS-P715
NMS P715 analog
NMS-P715 analog
NMS-P 715 analog
NMS P715 ANALOG;NMS-P 715 ANALOG
1H-Pyrazolo[4,3-h]quinazoline-3-carboxamide, N-(2,6-diethylphenyl)-4,5-dihydro-8-[[2-methoxy-4-[[(1-methyl-4-piperidinyl)amino]carbonyl]phenyl]amino]-1-methyl-
N-(2,6-diethylphenyl)-1-Methyl-8-({4-[(1-Methylpiperidin-4-yl)carbaMoyl]-2-(trifluoroMethoxy)phenyl}aMino)-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxaMide
N-(2,6-diethylphenyl)-1-methyl-8-((4-((1-methylpiperidin-4-yl)carbamoyl)-2-(trifluoromethoxy)phenyl)amino)-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide NMS-P715
[Molecular Formula]

C35H42N8O3
[MDL Number]

MFCD19443684
[MOL File]

1202055-34-2.mol
[Molecular Weight]

622.76
Chemical PropertiesBack Directory
[density ]

1.32±0.1 g/cm3(Predicted)
[storage temp. ]

-70°C
[solubility ]

Soluble in DMSO
[form ]

Powder
[pka]

11.75±0.70(Predicted)
Safety DataBack Directory
[WGK Germany ]

WGK 1
[Storage Class]

10 - Combustible liquids
Hazard InformationBack Directory
[Uses]

An orally bioavailable, ATP-competitive, pyrazolo-quinazoline, MPS1 inhibitor (IC50 = 182 nM, Ki = 0.99 nM) that is shown to act in a reversible and time-dependent manner. It demonstrates selectivity for MPS1 against a panel of 60 kinases, displaying activity against only three kinases, CK2, MELK, and NEK6 (<10 µM), but not against other mitotic kinases including PLK1, CDK1, Aurora A, Aurora B, or the SAC kinase BUB1, in an in vitro kinase assay. It promotes massive SAC (spindle assembly checkpoint) override (EC50 = 65 nM) in nocodazole-arrested U20S cells and elicits a reduction in the G1 and G2/M phase of the cell cycle in A2780 ovarian cancer cells, similar to RNAi-mediated MPS1 silencing. In addition, it is shown to inactivate SAC, delocalize kinetochore components, and inhibit the proliferation of select cancer cell lines (IC50 ~ 1 µM), without marked activity among a panel of 127 normal cell lines. Also, it inhibits A2780 tumor xenograft growth in mice (90 mg/kg/day, o.s., in vivo) by 53% without marked body weight loss.
[Biological Activity]

Cell permeable: yes''Primary Target
MPS1''Reversible: yes
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