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ChemicalBook--->CAS DataBase List--->1891087-61-8

1891087-61-8

1891087-61-8 Structure

1891087-61-8 Structure
IdentificationBack Directory
[Name]

BAY-1816032
[CAS]

1891087-61-8
[Synonyms]

BAY-1816032
BAY-1816032 (BAY1816032)
2-[3,5-Difluoro-4-[[3-[5-methoxy-4-[(3-methoxy-4-pyridinyl)amino]-2-pyrimidinyl]-1H-indazol-1-yl]methyl]phenoxy]ethanol
Ethanol, 2-[3,5-difluoro-4-[[3-[5-methoxy-4-[(3-methoxy-4-pyridinyl)amino]-2-pyrimidinyl]-1H-indazol-1-yl]methyl]phenoxy]-
[Molecular Formula]

C27H24F2N6O4
[MDL Number]

MFCD31657337
[MOL File]

1891087-61-8.mol
[Molecular Weight]

534.51
Chemical PropertiesBack Directory
[Boiling point ]

640.8±55.0 °C(Predicted)
[density ]

1.40±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO:37.5(Max Conc. mg/mL);70.16(Max Conc. mM)
[form ]

A solid
[pka]

14.05±0.10(Predicted)
[color ]

Off-white to yellow
Hazard InformationBack Directory
[Uses]

BAY-1816032 is a potent and oral available BUB1 (budding uninhibited by benzimidazoles 1) kinase inhibitor with an IC50 of 7 nM.
[Biological Activity]

BAY 1816032 is an orally activeATP-competitive (Ki = 1.2 μM)highly potent and selective BUB1 inhibitor (IC50 = 6.1 nM with 10 μM ATP; affinity Kd = 3.3 nM/BUB1 vs 57 nM/STK10850 nM/DMPK22.3 μM/DDR1 and >2.3 μM toward more than 390 other kinases) th at effectively targets BUB1-dependent cellular signaling (H2A-pThr120 IC50 = 29 nM post 1h treatment of nocodazole-arrested HeLa cells) and tumor cell proliferation in vitro (IC50 range from 0.5 to 5.8 μM in 43 human and mouse cancer cultures) and in human triple-negative breast xenograft models in vivo (25-50 mg/kg twice daily p.o.; SUM-149 and MDA-MB-436).
[in vivo]

In tumor xenograft studies BAY 1816032 only marginally inhibits tumor growth as single agent upon oral administration, however, upon combination with paclitaxel or docetaxel a strong and statistically significant reduction of tumor size as compared to the respective monotherapy is observed[1].

[storage]

Store at -20°C
[References]

[1] Siemeister G, et al. BAY 1816032, a novel BUB1 kinase inhibitor with potent antitumor activity [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2017; 2017 Apr 1-5; Ishington, DC. Philadelphia (PA): AACR; Cancer Res 2017;77(13 Suppl):Abstract nr 287. doi:10.1158/1538-7445.AM2017-287
Spectrum DetailBack Directory
[Spectrum Detail]

BAY-1816032(1891087-61-8)1HNMR
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