529573
PP2
AG 1879, 4-Amino-5-(4-chlorophenyl)-7-(t-butyl)pyrazolo[3,4-d]pyrimidine
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EMD Chemicals, Inc.
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24 May 2012
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A potent, reversible, ATP-competitive, and selective inhibitor of the Src family of protein tyrosine kinases. Inhibits p56lck (IC50 = 4 nM), p59fynT (IC50 = 5 nM), Hck (IC50 = 5 nM), and Src (IC50 = 100 nM). Does not significantly affect the activity of EGFR kinase (IC50 = 480 nM), JAK2 (IC50 > 50 µM), or ZAP-70 (IC50 >100 µM). Inhibits the activation of focal adhesion kinase and its phosphorylation at Tyr577. Also potently inhibits anti-CD3-stimulated tyrosine phosphorylation of human T cells (IC50 = 600 nM). A 10 mM (1 mg/331 µl) solution of PP2 (Cat. No. 529576) in DMSO also available.
| Product information | |||
|---|---|---|---|
| Form | Off-white solid | ||
| Primary Target | p56lck | ||
| Primary Target IC50 | 4 nM | ||
| Secondary target | p59fynT (IC50 = 5 nM), and Hck (IC50 = 5 nM). anti-CD3-stimulated tyrosine phosphorylation of human T cells (IC50 = 600 nM) | ||
| Molar mass | 301.8 | ||
| Packaged under inert gas | Yes | ||
| Purity | ≥95% by HPLC | ||
| Solubility | DMSO | ||
| Chemical formula | C15H16ClN5 | ||
| CAS number | 172889-27-9 | ||
| Store and ship information | |||
|---|---|---|---|
| Storage | -20°C | ||
| Ship |
Ambient Temperature Only
Standard Handling |
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