Description
A cell-permeable, reversible, ATP-competitive PKC inhibitor (IC50 = 15 nM, rat brain PKC); inhibits PKCα, βI, βII, γ, and ε with IC50 values of 8, 8, 14, 13, and 39 nM, respectively; also inhibits Cdk2 (IC50 = 200 nM) and GSK3α/β; used to activate mesenchymal stem cells and target their delivery to sites of inflammation
Formal name: 3-[8-(aminomethyl)-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-yl]-4-(1-methyl-1H-indol-3-yl)-1H-pyrrole-2,5-dione, monohydrochloride
Synonyms: BIM X|Ro 31-8425
Molecular weight: 461
CAS: 145317-11-9
Purity: ≥98%
Formulation: A solid
Product Type|Biochemicals|Kinase Inhibitors|PKC||Product Type|Biochemicals|Small Molecule Inhibitors|Kinases||Research Area|Cell Biology|Cell Cycle||Research Area|Cell Biology|Cell Signaling||Research Area|Cell Biology|ECM & Adhesion Molecules||Research Area|Cell Biology|Stem Cell Research||Research Area|Immunology & Inflammation