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XL092 (JUN04542) is an ATP competitive inhibitor of multiple RTK, including MET, VEGFR2, AXL, and MER, with IC50 values of 15 nM, 1.6 nM, 3.4 nM, and 7.2 nM, respectively, in cell-based assays.
Brand: BCM
Target: VEGFR; c-Met/HGFR; TAM Receptor
Signaling Pathways: Angiogenesis; Tyrosine Kinase/Adaptors
Boiling Point: 840.4±65.0 °C(Predicted)
pKa: 13.14±0.46(Predicted)
Solubility: Soluble in DMSO. Insoluble in Water; Insoluble in Ethanol.
Isomeric SMILES: CNC(=O)C1=CC2=C(C=CN=C2C=C1OC)OC3=CC=C(C=C3)NC(=O)C4(CC4)C(=O)NC5=CC=C(C=C5)F
InChIKey: JSPCKALGNNVYOO-UHFFFAOYSA-N
InChI: InChI=1S/C29H25FN4O5/c1-31-26(35)22-15-21-23(16-25(22)38-2)32-14-11-24(21)39-20-9-7-19(8-10-20)34-28(37)29(12-13-29)27(36)33-18-5-3-17(30)4-6-18/h3-11,14-16H,12-13H2,1-2H3,(H,31,35)(H,33,36)(H,34,37)
Attribute [Synonym] XL092; JUN04542; CL-092 [CAS No.] 2367004-54-2 [MDL No.] MFCD34179545 [Formula] C29H25FN4O5 [Molecular] 528.53 [Form] Solid Powder [Storage] Keep in dark place. Inert atmosphere. Room temperature [Chem Name] 1-N'-(4-fluorophenyl)-1-N-[4-[7-methoxy-6-(methylcarbamoyl)quinolin-4-yl]oxyphenyl]cyclopropane-1,1-dicarboxamide
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