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JNJ-10198409 is a relatively selective, orally active and ATP-competitive inhibitor of platelet-derived growth factor receptor (PDGF-RTK) with an IC50 of 2 nM, It is also a dual-mechanism, anti-angiogenic and anti-tumor cell proliferative agent with good inhibitory activity against PDGFRβ kinase and PDGFRα kinase with IC50 of 4.2 and 45 nM, respectively.
Brand: BCM
pKa: 14.01±0.20(Predicted)
Melting Point: 171-173.5 °C
Boiling Point: 528.8±50.0 °C at 760 mmHg
Flashing Point: 273.6±30.1 °C
Solubility: Soluble in DMSO; soluble in Ethanol. Insoluble in Water.
Attribute [Chem Name] N-(3-Fluorophenyl)-6,7-dimethoxy-1,4-dihydroindeno[1,2-c]pyrazol-3-amine [Synonym] JNJ-10198409 [CAS No.] 627518-40-5 [MDL No.] MFCD11045292 [Formula] C18H16FN3O2 [Molecular] 325.34 [Form] Off-white solid [Storage] −20°C
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