Description
An inhibitor of Drosophila Aurora B kinase (Ki = 0.36 µM); specific for Drosophila B kinase, with minimal inhibition of human or X. laevis Aurora B kinases at concentrations up to 100 µM; induces mitotic and cytokinesis defects in Drosophila Kc167 cells; prevents Drosophila S2 cells from assembling a contractile ring during cell division when used at a concentration of 40 µM
Formal name: N’-[1-(3-chloro-4-fluorophenyl)-4-cyano-1H-pyrazol-5-yl]-N,N-dimethyl-methanimidamide
Synonyms:
Molecular weight: 291.7
CAS: 220088-42-6
Purity: ≥98%
Formulation: A solid
Product Type|Biochemicals|Kinase Inhibitors|Aurora||Product Type|Biochemicals|Small Molecule Inhibitors|Kinases||Research Area|Cancer|Cell Cycle|G2/M||Research Area|Cancer|Cell Signaling|Aurora Signaling||Research Area|Cell Biology|Cell Cycle||Research Area|Cell Biology|Cytoskeleton & Motor Proteins