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LCB 03-0110 Dihydrochloride 是BTK 和SYK 家族以及DDR2家族中c-Src 激酶(IC50=1.3 nM)和酪氨酸激酶的有效抑制剂。在体外抑制LPS 诱导的巨噬细胞活化和TGF-β1诱导的成纤维细胞活化,抑制巨噬细胞和成纤维细胞的活化,并抑制伤口愈合模型中的瘢痕形成。

LCB 03-0110 Dihydrochloride 是BTK 和SYK 家族以及DDR2家族中c-Src 激酶(IC50=1.3 nM)和酪氨酸激酶的有效抑制剂。在体外抑制LPS 诱导的巨噬细胞活化和TGF-β1诱导的成纤维细胞活化,抑制巨噬细胞和成纤维细胞的活化,并抑制伤口愈合模型中的瘢痕形成。
| 规格 | 价格 | 库存 | 数量 | 
|---|---|---|---|
| 1 mg | ¥ 478  | In stock | |
| 2 mg | ¥ 714  | In stock | |
| 5 mg | ¥ 1,090  | In stock | |
| 10 mg | ¥ 1,590  | In stock | |
| 25 mg | ¥ 2,670  | In stock | |
| 50 mg | ¥ 3,790  | In stock | |
| 100 mg |  待询   | In stock | |
| 1 mL x 10 mM (in DMSO) | ¥ 1,190  | In stock | 
LCB 03-0110 dihydrochloride 相关产品
| 产品描述 | 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.  | 
| 体外活性 | LCB 03-0110处理TGF-β1和I型胶原暴露的细胞时,特别显著地抑制了酪氨酸861的磷酸化,1μM浓度下可使其降低约50%,而3μM浓度几乎完全抑制。  | 
| 分子量 | 490.45 | 
| 分子式 | C24H25Cl2N3O2S | 
| CAS No. | 1962928-28-4 | 
| Smiles | Cl.Cl.Oc1cccc(Nc2ccnc3cc(sc23)-c2cccc(CN3CCOCC3)c2)c1 | 
| 密度 | no data available | 
| 颜色 | White | 
| 物理性状 | Solid | 
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | ||||||||||||||||||||||||||||||
| 溶解度信息 | DMSO: 30 mg/mL (61.17 mM), Sonication is recommended.   | ||||||||||||||||||||||||||||||
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