Description
An orally bioavailable inhibitor of Mps1 (TTK; IC50 = 0.27 nM); inactivates the spindle assembly checkpoint, accelerates mitosis, and causes chromosomal misalignment and missegregation
Formal name: N-cyclopropyl-4-[6-(2,3-difluoro-4-methoxyphenoxy)-8-[(3,3,3-trifluoropropyl)amino]imidazo[1,2-b]pyridazin-3-yl]-2-methyl-benzamide
Synonyms:
Molecular weight: 561.5
CAS: 1554458-53-5
Purity: ≥95%
Formulation: A crystalline solid
Product Type|Biochemicals|Kinase Inhibitors|Other Non-Receptor Tyrosine Kinases||Product Type|Biochemicals|Kinase Inhibitors|Other Serine/Threonine Kinases||Product Type|Biochemicals|Small Molecule Inhibitors|Kinases||Research Area|Cancer|Cell Cycle|G2/M||Research Area|Cancer|Cell Signaling