FIIN-3
FIIN-3 Basic information
- Product Name:
- FIIN-3
- Synonyms:
-
- FIIN3; FIIN 3
- FIIN3; FIIN 3; FIIN-3
- CS-2331
- FIIN-3
- FIN-3
- 2-Propenamide, N-[4-[[[[(2,6-dichloro-3,5-dimethoxyphenyl)amino]carbonyl][6-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-4-pyrimidinyl]amino]methyl]phenyl]-
- Inhibitor,FIIN 3,FIIN-3,HER1,FIIN3,ErbB-1,Epidermal growth factor receptor,inhibit,Fibroblast growth factor receptor,EGFR,FGFR
- FIIN-3, 10 mM in DMSO
- CAS:
- 1637735-84-2
- MF:
- C34H36Cl2N8O4
- MW:
- 691.61
- Mol File:
- 1637735-84-2.mol
FIIN-3 Chemical Properties
- Boiling point:
- 909.4±65.0 °C(Predicted)
- Density
- 1.379±0.06 g/cm3(Predicted)
- storage temp.
- Store at -20°C
- solubility
- Acetonitrile: sparingly soluble; Methanol: sparingly soluble
- form
- A crystalline solid
- pka
- 10.78±0.70(Predicted)
- color
- White to off-white
FIIN-3 Usage And Synthesis
Description
FIIN-3 is an inhibitor of FGF receptors (FGFRs; IC50s = 13, 21, 31, and 35 nM for recombinant FGFR1-4, respectively). It is selective for FGFRs over a panel of 456 kinases at a concentration of 1 μM, however, it does inhibit EGFR (IC50 = 204 nM). FIIN-3 inhibits growth of Ba/F3 cells that are dependent on the kinase activity of wild-type FGFR1-4 as well as gatekeeper mutant FGFR2 and FGFR3 (EC50s = <1-69 nM) and inhibits FGFR-dependent signaling in a concentration-dependent manner in FGFR2TEL/V564M-dependent Ba/F3 cells. FIIN-3 also inhibits growth in a panel of cancer cell lines (EC50s = 1.4-499 nM).
Uses
FIIN-?3 is FGFR inhibitor. It can be used in synthetic preparation and complex with EGFR kinase of crystal structure; development of covalent inhibitors that can overcome resistance to first-generation FGFR kinase inhibitors.
Definition
ChEBI: N-[4-[[[(2,6-dichloro-3,5-dimethoxyanilino)-oxomethyl]-[6-[4-(4-methyl-1-piperazinyl)anilino]-4-pyrimidinyl]amino]methyl]phenyl]-2-propenamide is a member of piperazines.
IC 50
FGFR1: 13.1 nM (IC50); FGFR2: 21 nM (IC50); FGFR3: 31.4 nM (IC50); FGFR4: 35.3 nM (IC50)
FIIN-3Supplier
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- 021-58955995
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