Description
A dual inhibitor of Syk and JAK (IC50s = 32, 12, 6, 8, and 0.5 nM for Syk, JAK1, JAK2, JAK3, and TYK2, respectively); exhibits nanomolar inhibition of other kinases; inhibits JAK1/3-mediated STAT phosphorylation with IC50 values ranging from 0.16 to 1 μM; antitumor activity with IC50 values ranging from 0.05 to 2.1 μM against DLBCL tumor cell lines
Formal name: 4-(cyclopropylamino)-2-[[4-[4-(ethylsulfonyl)-1-piperazinyl]phenyl]amino]-5-pyrimidinecarboxamide
Synonyms: PRT062070|PRT2070
Molecular weight: 445.5
CAS: 1198300-79-6
Purity: ≥98%
Formulation: A crystalline solid
Product Type|Biochemicals|Kinase Inhibitors|JAK Family||Product Type|Biochemicals|Kinase Inhibitors|Other Non-Receptor Tyrosine Kinases||Product Type|Biochemicals|Small Molecule Inhibitors|Kinases||Research Area|Cancer|Cell Death|Apoptosis||Research Area|Cancer|Cell Signaling|JAK/STAT Signaling||Research Area|Cell Biology|Cell Signaling|JAK Signaling||Research Area|Immunology & Inflammation|Adaptive Immunity||Research Area|Immunology & Inflammation|Innate Immunity