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Postion:Product Catalog >Biochemical Engineering>Biochemical Reagents>Agonist Inhibitors>AST 487
AST 487
  • AST 487

AST 487

Price $1
Package 1KG
Min. Order: 1KG
Supply Ability: 1ton
Update Time: 2020-01-03

Product Details

Product Name: AST 487 CAS No.: 630124-46-8
EC-No.: 205-525-8 Min. Order: 1KG
Purity: 95-99% Supply Ability: 1ton
Release date: 2020/01/03
contact: Flora@coreychem.com
AST 487 Basic information
Product Name:
AST 487
Synonyms:
AST 487;NVP-AST 487;1-{4-[(4-Ethyl-1-piperazinyl)methyl]-3-(trifluoromethyl)phenyl}-3-(4-{[6-(methylamino)-4-pyrimidinyl]oxy}phenyl)urea;1-(4-((4-ethylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)-3-(4-((6-(methylamino)pyrimidin-4-yl)oxy)phenyl)urea
CAS:
630124-46-8
MF:
C26H30F3N7O2
MW:
529.5573096
EINECS:
 
Product Categories:
-
Mol File:
630124-46-8.mol
Article illustration
 
AST 487 Chemical Properties
Boiling point 
563.1±50.0 °C(Predicted)
density 
1.341±0.06 g/cm3(Predicted)
pka
13.33±0.70(Predicted)
 
Safety Information
MSDS Information
 
 
AST 487 Usage And Synthesis
Uses
AST-487 is an inhibitor of RET (IC50 = 0.88 μM), FLT3 (Ki = 0.52 μM), KDR (IC50 = 0.17 μM), c-Abl (IC50 = 0.02 μM), and c-Kit (IC50 = 0.5 μM). It has been shown to inhibit RET autophosphorylation and activation of downstream effectors and to prevent the growth of human thyroid cancer cell lines with activating mutations of RET but not of lines without RET mutations. In xenografts of NIH3T3 cells expressing oncogenic RET and of the MTC cell line TT in nude mice, AST-487 dose dependently inhibited tumor growth. It also demonstrates antiproliferative effects on primary cells from acute myelocytic leukemia patients and on cell lines expressing FLT3-ITD or FLT3 kinase domain point mutants.[Cayman Chemical]
 
AST 487 Preparation Products And Raw mate

Company Profile Introduction

Established in 2014,Career Henan Chemical Co. is a manufacturerspecializing in the sale of fine chemicals. Mainly deals in the sales of: Pharmaceutical intermediates OLED intermediates: Pharmaceutical intermediates; OLED intermediates;

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