Powder: -20°C for 3 years | In solvent: -80°C for 1 year
LCB 03-0110 Dihydrochloride is a potent inhibitor of the c-Src kinase (IC50 = 1.3 nM) and tyrosine kinases in the BTK and SYK family, as well as in the DDR2 family. It inhibits LPS-induced activation of macrophages and TGF-β1-induced activation of fibroblasts in vitro, inhibits activation of macrophages and fibroblasts, and inhibits scarring in wound healing models.
説明 | LCB 03-0110 Dihydrochloride is a potent inhibitor of the c-Src kinase (IC50 = 1.3 nM) and tyrosine kinases in the BTK and SYK family, as well as in the DDR2 family. It inhibits LPS-induced activation of macrophages and TGF-β1-induced activation of fibroblasts in vitro, inhibits activation of macrophages and fibroblasts, and inhibits scarring in wound healing models. |
分子量 | 490.45 |
分子式 | C24H25Cl2N3O2S |
CAS No. | 1962928-28-4 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 30 mg/mL (61.17 mM)
You can also refer to dose conversion for different animals. 詳細
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LCB 03-0110 dihydrochloride 1962928-28-4 Angiogenesis Tyrosine Kinase/Adaptors Src LCB 03-0110 LCB 030110 dihydrochloride LCB 03 0110 dihydrochloride LCB 03-0110 Dihydrochloride Inhibitor inhibitor inhibit