ChemicalBook--->CAS DataBase List--->1076235-04-5

1076235-04-5

1076235-04-5 Structure

1076235-04-5 Structure
IdentificationBack Directory
[Name]

CBS9106 (BMS566419)
[CAS]

1076235-04-5
[Synonyms]

SL-801
S-03747
CBS-9106
CBS9106 (BMS566419)
Felezonexor,CBS9106
1-[[6-chloro-5-(trifluoromethyl)pyridin-2-yl]amino]-3-(3,3-dimethylbutoxymethyl)-4-methylpyrrole-2,5-dione
1-((6-chloro-5-(trifluoromethyl)pyridin-2-yl)amino)-3-((3,3-dimethylbutoxy)methyl)-4-methyl-1H-pyrrole-2,5-dione
1H-Pyrrole-2,5-dione, 1-[[6-chloro-5-(trifluoromethyl)-2-pyridinyl]amino]-3-[(3,3-dimethylbutoxy)methyl]-4-methyl-
[Molecular Formula]

C18H21ClF3N3O3
[MDL Number]

MFCD28502170
[MOL File]

1076235-04-5.mol
[Molecular Weight]

419.826
Chemical PropertiesBack Directory
[form ]

Solid
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

CBS9106 (SL-801) is a reversible oral CRM1 inhibitor with CRM1 degrading and antitumor activities. CBS9106, inhibits CRM1-dependent nuclear export, causing arrest of the cell cycle and inducing apoptosis in a time- and dose-dependent manner for a broad spectrum of cancer cells[1].
[in vivo]

CBS9106 (31.25-62.5 mg/kg for 5 times weekly, 125 mg/kg for 3 times weekly; p.o.; 2 weeks) significantly suppresses tumor growth at dose levels of 62.5 or 125 mg/kg in mice bearing human MM xenograft models[1].

Animal Model:SCID mice with RPMI-8226 cells[1]
Dosage:31.25, 62.5, 125 mg/kg
Administration:Oal administration; 5 times weekly (31.25 and 62.5 mg/kg), 3 times weekly (125 mg/kg); 2 weeks
Result:Showed statistically significant tumor growth inhibition at dose levels of 62.5 mg/kg or 125 mg/kg.
[References]

[1] Sakakibara K, et al. CBS9106 is a novel reversible oral CRM1 inhibitor with CRM1 degrading activity. Blood. 2011 Oct 6;118(14):3922-31. DOI:10.1182/blood-2011-01-333138
Spectrum DetailBack Directory
[Spectrum Detail]

CBS9106 (BMS566419)(1076235-04-5)1HNMR
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