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Chemical Structure : LCB 03-0110
Catalog No.: PC-63519Not For Human Use, Lab Use Only.
LCB 03-0110 is a potent, ATP-competitive inhibitor of Discoidin domain receptor (DDR) family and c-Src tyrosine kinase family, as well as Btk and Syk.
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LCB 03-0110 is a potent, ATP-competitive inhibitor of Discoidin domain receptor (DDR) family and c-Src tyrosine kinase family, as well as Btk and Syk.
LCB 03-0110 potently inhibits the activated tyrosine kinase activity of DDR2 (IC50=6 nM), and nonactivated form of DDR2 (IC50=145 nM).
LCB 03-0110 suppresses collagen-induced autophosphorylation of DDR1 and DDR2 with IC50 of 164 and 171 nM in cell-based assays.
LCB 03-0110 inhibits all eight Src family kinases with IC50 of 2-20 nM.
LCB 03-0110 suppresses the proliferation and migration of primary dermal fibroblasts induced by TGF β1 and type I collagen (IC50=194 nM), inhibits cell migration and nitric oxide, iNOS, COX2, and TNF-α synthesis in LPS-activated J774A.1 macrophage cells.
LCB 03-0110 suppresses hypertrophic scar formation in wound healing models.
| M.Wt | 417.527 | |
| Formula | C24H23N3O2S | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Sun X, et al. J Pharmacol Exp Ther. 2012 Mar;340(3):510-9.
2. Jung SH, et al. Br J Dermatol. 2013 Jan;168(1):112-9.
3. Kim BH, et al. Exp Dermatol. 2015 Jul;24(7):503-9.
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