PP1
Highly potent and selective Scr family tyrosine kinase inhibitor. Shows anti-Ras cancer potential by blocking Ras-induced activation of PAK1. Antitumor compound. RIP2 inhibitor. Blocks TGF-beta-mediated cellular responses.
Catalog Number | AG-CR1-3562-M001 |
Alternative Name(s) | 4-Amino-5-(methylphenyl)-7-(tert.butyl)pyrazolo-(3,4-d)pyrimidine |
Research Area | Biochemicals, Cancer, Inflammation |
Molecular Formula | C16H19N5 |
CAS# | 172889-26-8 |
Purity | >98% |
Inchi | InChI=1S/C16H19N5/c1-10-5-7-11(8-6-10)13-12-14(17)18-9-19-15(12)21(20-13)16(2,3)4/h5-9H,1-4H3,(H2,17,18,19) |
Inchi Key | ZVPDNRVYHLRXLX-UHFFFAOYSA-N |
SMILES | CC1=CC=C(C=C1)C1=NN(C2=C1C(N)=NC=N2)C(C)(C)C |
Size | 1 mg |
Supplier Page | http://www.adipogen.com/ag-cr1-3562/pp1.html |