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ChemicalBook--->CAS DataBase List--->1820889-23-3

1820889-23-3

1820889-23-3 Structure

1820889-23-3 Structure
IdentificationBack Directory
[Name]

incb057643
[CAS]

1820889-23-3
[Synonyms]

INCB
CS-2906
incb057643
2H-1,4-Benzoxazin-3(4H)-one, 8-(6,7-dihydro-6-methyl-7-oxo-1H-pyrrolo[2,3-c]pyridin-4-yl)-2,2,4-trimethyl-6-(methylsulfonyl)-
[Molecular Formula]

C20H21N3O5S
[MDL Number]

MFCD31657400
[MOL File]

1820889-23-3.mol
[Molecular Weight]

415.46
Chemical PropertiesBack Directory
[Boiling point ]

787.7±60.0 °C(Predicted)
[density ]

1.370±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMF: 30 mg/ml; DMSO: 30 mg/ml; DMSO:PBS (pH 7.2) (1:6): 0.14 mg/ml
[form ]

A crystalline solid
[pka]

14.74±0.40(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

INCB-057643, is a novel, orally bioavailable BET inhibitor.
[in vivo]

Production of several cytokines, including IL-6, IL-10 and MIP-1α, is repressed by INCB-057643 in human and mouse whole blood stimulated ex vivo with LPS. Oral administration of INCB-057643 results in significant anti-tumor efficacy in xenograft models of AML, myeloma, and DLBCL. Additionally, combining INCB-057643 with standard of care agents used for the treatment of DLBCL including rituximab and bendamustine results in enhanced anti-tumor efficacy relative to that achieved with single agent therapies at doses that are well tolerated[1].

[storage]

Store at -20°C
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