| 产品详情 |
| Edit |   |
|---|
| Product Name | Src I1 |
|---|
| Description | MW: 373.4. Purity 98% (TLC; 5% CH3OH in CH2Cl2; Rf=0.43); NMR (Conforms). Src kinase inhibitorPotent and selective inhibitor of Bruton's tyrosine kinase (BTK). Inhibits recombinant BTK with an IC50 = 2.5 uM1 and has no activity at other protein kinases (including JAK1, JAK3, HCK, EGFR kinase and insulin receptor kinase) at concentrations up to 300 uM2.Scientific Background: Potent, competitive dual site (ATP- and substrate-binding domains) Src |
|---|
| Size | 0.25 mg, 1 mg |
|---|
| Concentration | n/a |
|---|
| Applications | n/a |
|---|
| Other Names | [LFM-A13; 2-Cyano-N-(2,5-dibromophenyl)-3-hyd-roxy-2-butenamide; 6,7-Dimethoxy-N-(4-phenoxyphenyl)-4-quinazolinamine] |
|---|
| Gene, Accession, CAS # | CAS: 179248-59-0 |
|---|
| Catalog # | MBS515021 |
|---|
| Price | |
|---|
| Order / More Info | Src I1 from MYBIOSOURCE INC. |
|---|
| Product Specific References | 1. S Mahajan et al. J. Biol. Chem. 1999 274:9587 2. A Vassilev et al. J. Biol. Chem. 1999 274:1646 |
|---|
| 产品资料 |
|
|