ChemicalBook--->CAS DataBase List--->1312691-33-0

1312691-33-0

1312691-33-0 Structure

1312691-33-0 Structure
IdentificationBack Directory
[Name]

TAK-659
[CAS]

1312691-33-0
[Synonyms]

TAK-659
Mivavotinib
Tak-659 free base
MIVAVOTINIB;TAK 659;TAK659
TAK-659 free base(Mivavotinib)
6-((1R,2S)-2-Aminocyclohexylamino)-7-fluoro-4-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[3,4-c]pyridin-3(2H)-one
3H-Pyrrolo[3,4-c]pyridin-3-one, 6-[[(1R,2S)-2-aminocyclohexyl]amino]-7-fluoro-1,2-dihydro-4-(1-methyl-1H-pyrazol-4-yl)-
[EINECS(EC#)]

604-604-1
[Molecular Formula]

C17H21FN6O
[MDL Number]

MFCD30829411
[MOL File]

1312691-33-0.mol
[Molecular Weight]

344.39
Chemical PropertiesBack Directory
[Boiling point ]

661.7±55.0 °C(Predicted)
[density ]

1.58±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

Soluble in DMSO
[pka]

10.90±0.20(Predicted)
Hazard InformationBack Directory
[Uses]

Mivavotinib is employed in the discovery of Lanraplenib, a tyrosine kinase inhibitor for autoimmune diseases.
[in vivo]

TAK-659 (100 mg/kg/day; p.o.; for 10 days) treatment totally abrogates splenomegaly and tumor development in LMP2A/MYC mice in both pretumor and tumor cell transfer experiments[4].
TAK-659 treatment kills tumor cells, but not host cells within the spleen and tumors[4].
TAK-659 treatment abrogates metastasis of tumor cells into bone marrow[4].

Animal Model:LMP2A/MYC double transgenic mice[4]
Dosage:100 mg/kg/day
Administration:Oral gavage; for 10 days
Result:Inhibited LMP2A-induced tumor cell survival in vivo.
[storage]

Store at -20°C
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