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Postion:Product Catalog >CP-547632
CP-547632
  • CP-547632

CP-547632

Price $1
Package 1g
Min. Order: 1g
Supply Ability: 1ton
Update Time: 2020-01-13

Product Details

Product Name: CP-547632 CAS No.: 252003-65-9
EC-No.: 200-258-5 Min. Order: 1g
Purity: 95-99% Supply Ability: 1ton
Release date: 2020/01/13
contact: Mary@coreychem.com
Common Name
CP-547632
CAS Number
252003-65-9
Molecular Weight
532.402
Density
1.5±0.1 g/cm3
Boiling Point
548.6±50.0 °C at 760 mmHg
Molecular Formula
C20H24BrF2N5O3S
Melting Point
N/A
MSDS
N/A
Flash Point
285.6±30.1 °C

 Use of CP-547632

 
CP-547632 is a potent inhibitor of the VEGFR2 and FGF2 kinases with IC50s of 11 and 9 nM, respectively.

 Names

Name
3-[(4-bromo-2,6-difluorophenyl)methoxy]-5-(4-pyrrolidin-1-ylbutylcarbamoylamino)-1,2-thiazole-4-carboxamide
Synonym
More Synonyms

 CP-547632 Biological Activity

Description
CP-547632 is a potent inhibitor of the VEGFR2 and FGF2 kinases with IC50s of 11 and 9 nM, respectively.
Related Catalog
Signaling Pathways >> Protein Tyrosine Kinase/RTK >> VEGFR
Research Areas >> Cancer
Target

IC50: 11 nM (VEGFR2), 9 nM (FGF2)[1]

In Vitro
CP-547632 is an ATP-competitive kinase inhibitor that blocks VEGFR-2 kinase autophosphorylation (IC50=11 nM) and VEGF-induced VEGFR-2 phosphorylation in VEGFR-2-transfected endothelial cells (IC50=6 nM). CP-547632 is approximately equipotent (i.e., <10-fold selective) against VEGFR-2, bFGF receptor, and EGFR/Tie-2 chimera, the receptor for Angiopoietin[1].
In Vivo
CP-547632 inhibits tumor-associated VEGFR-2 phosphorylation resulting in decreased microvascular density and significant tumor growth inhibition in a number of tumor models (EC50=590 ng/mL). CP-547632 is shown to inhibit VEGF-induced angiogenesis in vivo in a dose-responsive fashion[1].
Cell Assay
Porcine aortic endothelial cells stably expressing full-length VEGFR-2 have been used. CP-547632 is added to serum-deprived cells and incubated at 37°C, 5% for 1 h. The cells are then stimulated with 500 ng/mL VEGF. Whole cell lysates are then immunoprecipitated using anti-VEGFR-2, and Western blot analysis is carried out with antibodies recognizing either the protein or PY (A) [1].
Animal Admin
Mice[1] MDA-MB-231 cells are injected s.c into the flank of BALB/c male mice. Animals bearing tumors of 75-150 mm3 each are treated with CP-547632 (6.25-100 mg/kg, p.o., qd) in 5% Gelucire. The tumors are measured with calipers, and the tumor volumes are calculated[1].
References

[1]. Beebe JS, et al. Pharmacological characterization of CP-547,632, a novel vascular endothelial growth factor receptor-2 tyrosine kinase inhibitor for cancer therapy. Cancer Res. 2003 Nov 1;63(21):7301-9.

 Chemical & Physical Properties

Density
1.5±0.1 g/cm3
Boiling Point
548.6±50.0 °C at 760 mmHg
Molecular Formula
C20H24BrF2N5O3S
Molecular Weight
532.402
Flash Point
285.6±30.1 °C
Exact Mass
531.075134
PSA
137.82000
LogP
3.69
Vapour Pressure
0.0±1.5 mmHg at 25°C
Index of Refraction
1.622

 Safety Information

HS Code
2934999090

 Customs

HS Code
2934999090
Summary
2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Synonyms

3-(4-Bromo-phenoxymethyl)-benzoic acid
3-(4-bromo-2,6-difluoro-benzyloxy)-5-[3-(4-pyrrolidin-1-yl-butyl)-ureido]-isothiazole-4-carboxylic acid amide
3-(4-bromo-2,6-difluorobenzyloxy)-5-(3-(4-pyrrolidin-1-ylbutyl)ureido)isothiazole-4-carboxylic acid amide
3-[(4-Bromo-2,6-difluorobenzyl)oxy]-5-({[4-(1-pyrroli

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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