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FIIN-2

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Company Name: TargetMol Chemicals Inc.
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Products Intro: Product Name:FIIN-2
CAS:1633044-56-0
Purity:99.65% Package:1mg;35USD|2mg;48USD|5mg;64USD Remarks:REAGENT;FOR LABORATORY USE ONLY
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CAS:1633044-56-0
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CAS:1633044-56-0
Purity:98% Package:5mg Remarks:V0615
Company Name: Nantong HI-FUTURE Biology Co., Ltd.
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Products Intro: Product Name:FIIN-2
CAS:1633044-56-0
Purity:0.98 Package:5mg,10mg,100mg,500mg,1g,5g,10g
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354;
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Products Intro: Product Name:FIIN-2;FIIN 2;FIIN2
CAS:1633044-56-0
Package:1 mL * 10mM (in DMSO);10 mg;2 mg;25 mg;5 mg;50 mg Remarks:REAGENT;FOR LABORATORY USE ONLY

FIIN-2 manufacturers

  • FIIN-2
  • FIIN-2 pictures
  • $35.00 / 1mg
  • 2026-02-01
  • CAS:1633044-56-0
  • Min. Order:
  • Purity: 99.65%
  • Supply Ability: 10g
FIIN-2 Basic information
Product Name:FIIN-2
Synonyms:CS-1618;FIIN2;FIIN-2;FIIN 2;FIIN-2;FIN-2;N-[4-[[3-(3,5-Dimethoxyphenyl)-3,4-dihydro-7-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-2-oxopyrimido[4,5-d]pyrimidin-1(2H)-yl]methyl]phenyl]-2-propenamide;2-Propenamide, N-[4-[[3-(3,5-dimethoxyphenyl)-3,4-dihydro-7-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-2-oxopyrimido[4,5-d]pyrimidin-1(2H)-yl]methyl]phenyl]-;inhibit,FGFR,FIIN2,FIIN 2,Fibroblast growth factor receptor,Inhibitor,FIIN-2;FIIN-2, 10 mM in DMSO
CAS:1633044-56-0
MF:C35H38N8O4
MW:634.73
EINECS:
Product Categories:
Mol File:1633044-56-0.mol
FIIN-2 Structure
FIIN-2 Chemical Properties
density 1.306±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility ≥31.75 mg/mL in DMSO; insoluble in H2O; ≥3.39 mg/mL in EtOH with gentle warming
form solid
pka13.51±0.70(Predicted)
color White to off-white
Safety Information
MSDS Information
FIIN-2 Usage And Synthesis
DescriptionFIIN-2 is an irreversible FGFR inhibitor with IC50 values of 3.09, 4.3, 27, and 45.3 nM for FGFR1, FGFR2, FGFR3, and FGFR4, respectively. It has been shown to inhibit cell proliferation of transformed Ba/F3 cell lines and demonstrates antiproliferative activity in cells dependent upon the gatekeeper mutants of FGFR1 or FGFR2. By inhibiting FGFR in a zebrafish developmental model, FIIN-2 caused mild to severe alterations in tail morphogenesis similar to the phenotypes reported following genetic knockdown of FGFR.
UsesFIIN 2 is FGFR inhibitor. It can be used in biological study of DFG-out mode of inhibition by an irreversible Type-1 inhibitor capable of overcoming gate-keeper mutations in FGF receptors
in vivo

Treatment of fish in the embryonic state with either FIIN-2 causes defects to the posterior mesoderm similar to the phenotypes reported following genetic knockdown of FGFR or treatment with other reported FGFR inhibitors. FIIN-2 causes mild or severe phenotypes to the tail morphogenesis in all treated embryonic zebrafish[1].

IC 50FGFR1: 3.1 nM (IC50); FGFR2: 4.3 nM (IC50); FGFR3: 27 nM (IC50); FGFR4: 45 nM (IC50)
References[1] LI TAN. Development of covalent inhibitors that can overcome resistance to first-generation FGFR kinase inhibitors.[J]. Proceedings of the National Academy of Sciences of the United States of America, 2014, 111 45: E4869-77. DOI: 10.1073/pnas.1403438111
FIIN-2 Preparation Products And Raw materials
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