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1613191-99-3

1613191-99-3 Structure

1613191-99-3 Structure
IdentificationBack Directory
[Name]

2-amino-6-fluoro-N-(5-fluoro-4-(4-(4-(oxetan-3-yl)piperazine-1-carbonyl)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide(WXC04788)
[CAS]

1613191-99-3
[Synonyms]

VX-803
M-4344
ATR inhibitor 2
2-amino-6-fluoro-N-(5-fluoro-4-(4-(4-(oxetan-3-yl)piperazine-1-carbonyl)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide
Pyrazolo[1,5-a]pyrimidine-3-carboxamide, 2-amino-6-fluoro-N-[5-fluoro-4-[4-[[4-(3-oxetanyl)-1-piperazinyl]carbonyl]-1-piperidinyl]-3-pyridinyl]-
2-amino-6-fluoro-N-(5-fluoro-4-(4-(4-(oxetan-3-yl)piperazine-1-carbonyl)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide(WXC04788)
[Molecular Formula]

C25H29F2N9O3
[MDL Number]

MFCD31803930
[MOL File]

1613191-99-3.mol
[Molecular Weight]

541.55
Chemical PropertiesBack Directory
[density ]

1?+-.0.1 g/cm3(Predicted)
[form ]

Solid
[pka]

4.89±0.46(Predicted)
[color ]

Light yellow to yellow
Hazard InformationBack Directory
[Uses]

2-Amino-6-fluoro-N-[5-fluoro-4-[4-[[4-(oxetan-3-yl)piperazin-1-yl]carbonyl]-1-piperidyl]-3-pyridyl]pyrazolo[1,5-a]pyrimidine-3-carboxamide is an ATP-competitive and selective ATR inhibitor. Exhibits antitumor activity. Useful for monotherapy.
[in vivo]

In monotherapy efficacy studies Gartisertib shows tumor stasis to regression in tumor models with alternative lengthening of telomeres (ALT). In combination with PARP inhibitors, tumor regression could be observed in triple-negative breast cancer xenograft models[1].

[IC 50]

ATR: <150 pM (Ki)
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