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Ki8751

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Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
Email: ivan@atkchemical.com
Products Intro: Product Name:Ki 8751
CAS:228559-41-9
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G.100G
Company Name: career henan chemical co
Tel: +86-0371-86658258 +8613203830695
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Products Intro: Product Name: Ki8751
CAS:228559-41-9
Purity:99% Package:1KG;7USD
Company Name: CONIER CHEM AND PHARMA LIMITED
Tel: +8618523575427
Email: sales@conier.com
Products Intro: Product Name:ki 8751
CAS:228559-41-9
Purity:99% Package:1kg
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354; +17819995354
Email: marketing@targetmol.com
Products Intro: Product Name:KI8751
CAS:228559-41-9
Purity:99.9% Package:2mg;31USD|5mg;48USD|10mg;78USD Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Dideu Industries Group Limited
Tel: +86-29-89586680 +86-15129568250
Email: 1026@dideu.com
Products Intro: Product Name:Ki8751
CAS:228559-41-9
Purity:99.9% Package:25kgs/Drum;200kgs/Drum Remarks:FDA GMP CEP Approved Manufacturer

Ki8751 manufacturers

  • KI8751
  • KI8751 pictures
  • $31.00 / 2mg
  • 2026-03-13
  • CAS:228559-41-9
  • Min. Order:
  • Purity: 99.73%
  • Supply Ability: 10g
  • Ki8751
  • 	Ki8751 pictures
  • $7.00 / 1KG
  • 2019-09-02
  • CAS:228559-41-9
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: JD 524
Ki8751 Basic information
Product Name:Ki8751
Synonyms:Ki8751 hydrate;Ki8751, >=98%;KI8751;KI 8751;KI-8751;VEGFR2 Kinase Inhibitor VI, Ki8751;Ki8751;1-(2,4-Difluoro-phenyl)-3-[4-(6,7-dimethoxy-quinolin-4-yloxy)-2-fluoro-phenyl]-urea hydrate;N-(2,4-Difluorophenyl)-N'-[4-[(6,7-dimethoxy-4-quinolinyl)oxy]-2-fluorophenyl]urea;1-(2,4-difluorophenyl)-3-(4-(6,7-diMethoxyquinolin-4-yloxy)-2-fluorophenyl)urea
CAS:228559-41-9
MF:C24H18F3N3O4
MW:469.41
EINECS:
Product Categories:Inhibitors
Mol File:228559-41-9.mol
Ki8751 Structure
Ki8751 Chemical Properties
Melting point 239℃
density 1.429
storage temp. −20°C
solubility Soluble in DMSO (15 mg/ml)
form Off-white solid
color White
Stability:Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
InChI1S/C24H18F3N3O4/c1-32-22-11-15-20(12-23(22)33-2)28-8-7-21(15)34-14-4-6-19(17(27)10-14)30-24(31)29-18-5-3-13(25)9-16(18)26/h3-12H,1-2H3,(H2,29,30,31)
InChIKeyLFKQSJNCVRGFCC-UHFFFAOYSA-N
SMILESFc1c(ccc(c1)F)NC(=O)Nc2c(cc(cc2)Oc3c4c(ncc3)cc(c(c4)OC)OC)F
Safety Information
Hazard Codes Xn
Risk Statements 22-38
Safety Statements 37
WGK Germany WGK 1
Storage Class11 - Combustible Solids
MSDS Information
Ki8751 Usage And Synthesis
DescriptionKi8751 (228559-41-9) is a very potent (IC50 = 0.9 nM) inhibitor of vascular endothelial growth factor receptor 2 (VEGFR-2).1 It also inhibited PDGFRα (IC50 = 67 nM), c-Kit (IC50 = 40 nM), and FGFR2 (IC50 = 170 nM). Ki8751 completely suppressed HUVEC growth at 1 nM. Ki8751 completely inhibited tumor growth in LC-6 human tumor xenografts @ 5mg/kg. Ki8751 displayed anti-influenza A and B activity via disruption of virus entry in a PDGFR/GM3-dependent manner.2
UsesKi8751 is a potent and selective inhibitor of VEGFR2, PDGFRα and c-Kit with IC50 of 0.9 nM, 67 nM and 40 nM, respectively.
UsesKI 8751 is a potent and selective inhibitor of VEGFR-2-tyrosine kinase which inhibits proliferation of human umbilical vein endothelial cells and inhibits tumor growth.
DefinitionChEBI: 1-(2,4-difluorophenyl)-3-[4-[(6,7-dimethoxy-4-quinolinyl)oxy]-2-fluorophenyl]urea is an aromatic ether.
General DescriptionA cell-permeable quinolyloxyphenyl-urea compound that acts as a VEGFR-2-selective inhibitior in both cell-based (IC50 = 0.9 nM in VEGF-induced receptor phosphorylation) and cell-free (IC50 = 4.0 nM in kinase reactions) assays. It inhibits c-Kit, PDGFRα, and FGFR-2 only at much higher concentrations (IC50 = 40, 67, and 170 nM, respectively, in cell-based assays), while exhibiting no effect against eight other commonly studied receptor and non-receptor kinases even at concentrations as high as 10 μM. Effectively blocks VEGF-dependent, but not VEGF-independent, cell proliferation in vitro and tumor growth in mice and rats (5 to 20 mg/kg, daily p.o.) in vivo.
Biological ActivityPotent, selective inhibitor of VEGFR-2 tyrosine kinase (IC 50 = 0.9 nM). Displays some inhibitory activity towards c-Kit, PDGFR α and FGFR-2 (IC 50 values range from 40 to 170 nM) but is highly selective over other receptor tyrosine kinases (IC 50 > 10000 nM for FGFR-2, EGFR and HGFR). Inhibits VEGF-stimulated proliferation of human umbilical vein endothelial cells (HUVEC) and inhibits tumor growth in vivo ; antiangiogenic.
storageStore at +4°C
References[1] KAZUO KUBO. Novel Potent Orally Active Selective VEGFR-2 Tyrosine Kinase Inhibitors: Synthesis, Structure−Activity Relationships, and Antitumor Activities of N-Phenyl-N‘-{4-(4-quinolyloxy)phenyl}ureas[J]. Journal of Medicinal Chemistry, 2005, 48 5: 1359-1366. DOI:10.1021/jm030427r
[2] PIETER VRIJENS. Influenza virus entry via the GM3 ganglioside-mediated platelet-derived growth factor receptor β signalling pathway.[J]. The Journal of general virology, 2019: 583-601. DOI:10.1099/jgv.0.001235
Ki8751 Preparation Products And Raw materials
Tag:Ki8751(228559-41-9) Related Product Information
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