ChemicalBook--->CAS DataBase List--->1247000-76-5

1247000-76-5

1247000-76-5 Structure

1247000-76-5 Structure
IdentificationBack Directory
[Name]

CFI-400437
[CAS]

1247000-76-5
[Synonyms]

CS-2656
CFI-400437
CFI-400437 HCl
CFI 400437;CFI400437
[Molecular Formula]

C29H29ClN6O2
[MDL Number]

MFCD31922709
[MOL File]

1247000-76-5.mol
[Molecular Weight]

529.04
Chemical PropertiesBack Directory
[storage temp. ]

4°C, protect from light
[solubility ]

DMSO : 12.5 mg/mL (22.10 mM; Need ultrasonic)
[form ]

Solid
[color ]

Brown to orange
Safety DataBack Directory
[Symbol(GHS) ]


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]

(1E)-CFI-400437 dihydrochloride is a potent PLK4 (IC50= 0.6 nM) inhibitor and selective against other members of the PLK family (>10 μM). (1E)-CFI-400437 dihydrochloride inhibits Aurora A, Aurora B, KDR and FLT-3 with IC50s of 0.37, 0.21, 0.48, and 0.18 μM, respectively. Antiproliferative activity[1].
[in vivo]

(1E)-CFI-400437 (25 mg/kg; intraperitoneal injection; daily for 21 days) dihydrochloride shows effective in a mouse xenograft model of tumor growth[1].
The plasma levels of (1E)-CFI-400437 (50 mg/kg; IP; mice) dihydrochloride shows a Cmax of 92 ng/mL and AUC of 190 ng?h/mL, respectively. The mouse plasma protein binding measurement for (1E)-CFI-400437 is 99%, i.e., unbound compound in plasma is 1%[1].

Animal Model:6-8 week old female CB-17 SCID mice (MDA-MB-468 mouse xenograft model)[1]
Dosage:25 mg/kg
Administration:Intraperitoneal injection; daily for 21 days
Result:Effective in a mouse xenograft model of tumor growth. In this study, (1E)-CFI-400437 is weighed and suspended in PEG400:water (30:70) and sonicated at rt for 30 min. The compound is dispensed in aliquots and stored at ?20 C° for the duration of the study, and each aliquot was thawed at room temperature before each dose.
[IC 50]

PLK4: 0.6 nM (IC50)
[storage]

4°C, protect from light
[References]

[1] Laufer R, et al. The discovery of PLK4 inhibitors: (E)-3-((1H-Indazol-6-yl)methylene)indolin-2-ones as novel antiproliferative agents. J Med Chem. 2013;56(15):6069-6087. DOI:10.1021/jm400380m
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