ChemicalBook--->CAS DataBase List--->1458630-17-5

1458630-17-5

1458630-17-5 Structure

1458630-17-5 Structure
IdentificationBack Directory
[Name]

CHR 6494 trifluoroacetate
[CAS]

1458630-17-5
[Synonyms]

CHR 6494 TFA
CHR 6494 trifluoroacetate
3-(1H-Indazol-5-yl)-N-propylimidazo[1,2-b]pyridazin-6-amine trifluoroacetate
3-(1H-Indazol-5-yl)-N-propylimidazo[1,2-b]pyridazin-6-amine 2,2,2-trifluoroacetate
CHR-6494,inhibit,apoptosis,Haspin Kinase,NRAS mutant melanoma cells,CHR 6494,mitotic catastrophe,Inhibitor,mice,CHR6494,cancer cells,CHR6494 TFA,BRAFV600E mutant melanoma cells,CHR 6494 TFA
[Molecular Formula]

C18H17F3N6O2
[MDL Number]

MFCD24849399
[MOL File]

1458630-17-5.mol
[Molecular Weight]

406.362
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

Soluble in DMSO
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
Hazard InformationBack Directory
[Uses]

CHR6494 is a small-molecule inhibitor of histone kinase haspin, with a wide spectrum of anticancer effects.
[in vivo]

CHR-6494 (TFA; 50 mg/kg; i.p. in two cycles of five consecutive days for 15 days) inhibits the growth of tumor in nude mice bearing HCT-116 human colorectal cancer cells[1].
CHR-6494 (TFA; 20 mg/kg; intraperitoneal injection for 15 consecutive days) inhibits the tumor growth in nude mice bearing MDA-MB-231 xenograft tumors[3].

Animal Model:Male 4-5 weeks old athymic nu/nu mice harboring HCT-116 cells xenograft tumor with a tumor volume of 200?mm3[1]
Dosage:50?mg/kg (diluted in a solution of 10% DMSO/20% 2-hydroxypropyl-b-cyclodextrin)
Administration:i.p. in two cycles of five consecutive days for 15 days
Result:Dose-dependent tumor growth inhibition was demonstrated.
Did not change the body weight of mice.
Animal Model:4‐week‐old female nude mice bearing MDA-MB-231 xenograft tumors
Dosage:20 mg/kg in a final formulation in 10% DMSO/20% 2‐hydroxypropyl‐β‐cyclodextrin
Administration:i.p. for 15 consecutive days
Result:Inhibited the tumor volume and weight compared with the control group in nude mice bearing MDA-MB-231 xenograft tumors.
Enhanced the tumor volume and weight inhibition of MLN8237 (20 mg/kg; p.o.) in vivo.
[IC 50]

haspin: 2 nM (IC50)
[storage]

Store at +4°C
Spectrum DetailBack Directory
[Spectrum Detail]

CHR 6494 trifluoroacetate(1458630-17-5)1HNMR
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