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Cat. Number
10-1037
Chemical Name
ZM-447439
CAS Number
331771-20-1
Mol. Formula
C29H31N5O4
Mol. Weight
513.59
Qty 1
5mg
Qty 2
25mg
Appearance
White solid
Application Notes
98% by TLC
Synonym
N-[4-[[6-Methoxy-7-[3-(4-morpholinyl)propoxy]-4-quinazolinyl]amino]phenyl]benzamide
Solubility
Soluble in DMSO (up to 50 mg/ml) or in Ethanol (up to 25 mg/ml).
Storage condition
RT
Stability
Stable for 1 year as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 3 months.
References

ZM-447439 (331771-20-1) is a selective ATP-competitive inhibitor of Aurora kinase B1 (IC50 = 50 nM, Aur A IC50 = 1 μM, Aur C IC50 = 250 nM at physiological ATP concentrations2, Ref.1 lists Aur A IC50 = 110nM and Aur B IC50 = 113nM). ZM-447439 did not significantly inhibit a panel of 14 other kinases including mitotic kinases CDK1 and PLK1. It prevents chromosome alignment, spindle checkpoint function and cytokinesis.1,2

 

References/Citations
1) Ditchfield et al (2003) Aurora B couples chromosome alignment with anaphase by targeting BubR1, Mad2, and Cenp-E to kinetochores; J.Cell Biol. 161 267
2) Girdler et al. (2006) Validating Aurora B as an anti-cancer drug target; J. Cell Sci. 119 3664

Focus Biomolecules cell signaling reagent supplier, structure of ZM-447439 | Aurora B kinase inhibitor | CAS 331771-20-1

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