1192754-38-3

IBPR002 Chemical Structure
1192754-38-3

Chemical Structure

IBPR002

  • CAS No.: 1192754-38-3
  • Formula:C34H36N6O4
  • Molecular Weight:592.70

IUPAC Name: 1-(4-(2-((6-(4-(2-(4-hydroxypiperidin-1-yl)ethoxy)phenyl)furo[2,3-d]pyrimidin-4-yl)amino)ethyl)phenyl)-3-phenylurea

InChIKey: WEVRAOPLGYJTLY-UHFFFAOYSA-N

SMILES: O=C(NC=1C=CC=CC1)NC2=CC=C(C=C2)CCNC=3N=CN=C4OC(=CC43)C=5C=CC(OCCN6CCC(O)CC6)=CC5

Biological Activity: IBPR002 is an inhibitor of Aurora kinase A and Aurora kinase B, with IC50 values of 41 nM and 17 nM, respectively. IBPR002 disrupts the nucleation and bundling of kinetochore microtubules, impairs the bipolarity of mitotic spindles, and promotes the binding of non-phosphorylated hepatoma up-regulated protein (HURP) to microtubules derived from the mother centrosome. IBPR002 reduces tumorigenesis levels in a colorectal cancer xenograft model using athymic nude mice. IBPR002 is applicable for research related to colorectal cancer[1].

Cat. No. Product Name Purity Description Pricing
HY-165369
IBPR002 IBPR002 is an inhibitor of Aurora kinase A and Aurora kinase B, with IC50 values of 41 nM and 17 nM, respectively. IBPR002 disrupts the nucleation and bundling of kinetochore microtubules, impairs the bipolarity of mitotic spindles, and promotes the binding of non-phosphorylated hepatoma up-regulated protein (HURP) to microtubules derived from the mother centrosome. IBPR002 reduces tumorigenesis levels in a colorectal cancer xenograft model using athymic nude mice. IBPR002 is applicable for research related to colorectal cancer.
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