S49076

S49076 Suppliers list
Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
Email: ivan@atkchemical.com
Products Intro: Product Name:S49076
CAS:1265965-22-7
Purity:98% HPLC Package:5MG;10MG;50MG;100MG,1G,5G
Company Name: career henan chemical co
Tel: +86-0371-86658258 15093356674;
Email: factory@coreychem.com
Products Intro: Product Name: S49076
CAS:1265965-22-7
Purity:99% Package:1g;1USD
Company Name: HANGZHOU CLAP TECHNOLOGY CO.,LTD
Tel: 86-571-88216897,88216896 13588875226
Email: sales@hzclap.com
Products Intro: Product Name:S49076
CAS:1265965-22-7
Purity:71299% Package:10kg 25kg 200 kilograms per barrel Remarks:good
Company Name: InvivoChem
Tel: +1-708-310-1919 +1-13798911105
Email: sales@invivochem.cn
Products Intro: Product Name:S-49076
CAS:1265965-22-7
Purity:98% Package:5mg Remarks:V2150
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354
Email: support@targetmol.com
Products Intro: Product Name:S49076
CAS:1265965-22-7
Package:1 mL * 10mM (in DMSO);10 mg;100 mg;2 mg;5 mg;50 mg Remarks:REAGENT;FOR LABORATORY USE ONLY

S49076 manufacturers

  • S49076
  • 	S49076 pictures
  • $1.00 / 1g
  • 2019-12-24
  • CAS:1265965-22-7
  • Min. Order: 1g
  • Purity: 99%
  • Supply Ability: 20kg
S49076 Basic information
Product Name:S49076
Synonyms:S49076;CS-2684;S4 9076;S4-9076;2,4-Thiazolidinedione, 3-[[2,3-dihydro-3-[[4-(4-morpholinylmethyl)-1H-pyrrol-2-yl]methylene]-2-oxo-1H-indol-5-yl]methyl]-;FGFR,S49076,Fibroblast growth factor receptor,inhibit,c-Met/HGFR,S 49076,Inhibitor,S-49076;(Z)-3-((3-((4-(morpholinomethyl)-1H-pyrrol-2-yl)methylene)-2-oxoindolin-5-yl)methyl)thiazolidine-2,4-dione;3-((3-((4-(Morpholinomethyl)-1H-pyrrol-2-yl)methylene)-2-oxoindolin-5-yl)methyl)thiazolidine-2,4-dione
CAS:1265965-22-7
MF:C22H22N4O4S
MW:438.5
EINECS:
Product Categories:
Mol File:1265965-22-7.mol
S49076 Structure
S49076 Chemical Properties
storage temp. Store at -20°C
solubility DMSO : ≥ 31 mg/mL (70.70 mM)
Safety Information
MSDS Information
S49076 Usage And Synthesis
Biological ActivityS49076 is a novel and potent inhibitor of Met (c-Met), AXL/MER and FGFR1/2/3 with IC50 below 20 nM.
in vivo

S49076 effectively inhibits the phosphorylation of MET, AXL and FGFRs in cells, and inhibits their downstream signaling pathways in vitro and in vivo. In cellular models, it inhibits MET and FGFR2-dependent gastric cancer cells, prevents MET-driven migration of lung cancer cells, and inhibits colony formation of liver cancer cells expressing FGFR1/2 and AXL. S49076 inhibits cell viability, motile, three-dimensional colony formation of cancer cells expressing MET, AXL or FGFRs.

in vivoS49076 has significant antitumor activity in MET- and FGFR-dependent tumor grafts. It is highly distributed in tumors, with a half-life of approximately 7 hours in tumors and less than 2 hours in blood at a dose of 3.125 mg/kg. At doses above 6.25 mg/kg, more than 50% of MET phosphorylation was inhibited for 16 hours. S49076 was also active in a bevacizumab-resistant model, and in combination with bevacizumab, completely inhibited the growth of colon cancer xenografts.
target< td style="border-bottom: 1px dotted #ccc;padding: 5px;"> Axl
(Cell-free assay)
TargetValue
Met
(Cell-free assay)
1 nM
Mer
(Cell-free assay)
2 nM
7 nM
FGFR3
(Cell-free assay)
15 nM
FGFR2
(Cell-free assay)
17 nM
S49076 Preparation Products And Raw materials
Raw materials2,4-Thiazolidinedione
Tag:S49076(1265965-22-7) Related Product Information