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FIIN-3

FIIN-3 Suppliers list
Company Name: Shanghai Boyle Chemical Co., Ltd.  
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Email: sales@boylechem.com
Company Name: Haoyuan Chemexpress Co., Ltd.  
Tel: 021-58950125
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Company Name: MedChemexpress LLC  
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Company Name: HangZhou YuHao Chemical Technology Co., Ltd.  
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Company Name: Shanghai Lollane Biological Technology Co.,Ltd.  
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FIIN-3 manufacturers

  • FIIN-3
  • FIIN-3 pictures
  • $33.00
  • 2026-07-27
  • CAS:1637735-84-2
  • Purity: 98.92%
  • Supply Ability: 10g
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
EINECS:
Product Categories:
Mol File:1637735-84-2.mol
FIIN-3 Structure
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
pka10.78±0.70(Predicted)
color White to off-white
Safety Information
MSDS Information
FIIN-3 Usage And Synthesis
DescriptionFIIN-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).
UsesFIIN-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.
DefinitionChEBI: 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 50FGFR1: 13.1 nM (IC50); FGFR2: 21 nM (IC50); FGFR3: 31.4 nM (IC50); FGFR4: 35.3 nM (IC50)
FIIN-3 Preparation Products And Raw materials
Tag:FIIN-3(1637735-84-2) Related Product Information
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