Cat. No.: X24-06-ZQ222
c-MET inhibitor PHA-665752, Purity ≥98%
Synonym: 477575-56-7; c-MET inhibitor; PHA665752
- MDL: MFCD07772270
- CAS Number: 477575-56-7
- Compound CID: 10461815
Product Size
5 mg; 10 mg; 50 mg; 100 mg
Properties
Description
PHA-665752, soluble in DMSO and insoluble in ethanol and water, inhibits the enzymatic activity of the c-Met tyrosine kinase, the receptor of hepatocyte growth factor/scatter factor (HGF/SF), interfering with pathways leading to cell growth and metastasis. It targets Flk1, RON, Aurora A2, c-Abl, c-Met, c-Src, CDK2, EGFR, FGFR1, IGF-1R, and MK2.
Molecular Formula
C32H34Cl2N4O4S
Targets
Flk-1: 200 nM; RON: 68 nM; AuroraA2: >10 μM; c-Abl: 1.4 nM; c-Met: 9 nM; c-Src: 6 nM; CDK2: >10 μM; EGFR: 3.8 μM; FGFR1: 3 μM; IGF-1R: >10 μM; MK2: >10 μM
Solubility
DMSO: 124 mg/mL (193.26 mM); Water: Insoluble; Ethanol: Insoluble
Identity
Confirmed by NMR/HPLC/MS.
Applications
PHA-665752 targets c-MET, facilitating research into therapeutic strategies that disrupt MET signaling in cancer.
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