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AZD 2932

AZD 2932 Suppliers list
Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
Email: ivan@atkchemical.com
Products Intro: Product Name:AZD2932
CAS:883986-34-3
Purity:98% HPLC Package:5MG;10MG;50MG;100MG,1G,5G
Company Name: Hubei xin bonus chemical co. LTD
Tel: 86-13657291602
Email: linda@hubeijusheng.com
Products Intro: Product Name:AZD 2932
CAS:883986-34-3
Purity:0.99 Package:5KG;1KG
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354 +1-00000000000
Email: marketing@targetmol.com
Products Intro: Product Name:AZD2932
CAS:883986-34-3
Purity:98.37% Package:1 mL * 10mM (in DMSO);10 mg;100 mg;2 mg;25 mg;5 mg;50 mg 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:AZD 2932
CAS:883986-34-3
Purity:99.9% Package:25kgs/Drum;200kgs/Drum Remarks:FDA GMP CEP Approved Manufacturer
Company Name: Chemia Biotechnology(Shanghai) Co., Ltd
Tel: +8613816753574
Email: info@chemia-pharm.com
Products Intro: Product Name:AZD2932
CAS:883986-34-3
AZD 2932 Basic information
Product Name:AZD 2932
Synonyms:AZD 2932;2-(4-(6,7-dimethoxyquinazolin-4-yloxy)phenyl)-N-(1-isopropyl-1H-pyrazol-4-yl)acetamide;2-(4-((6,7-dimethoxyquinazolin-4-yl)oxy)phenyl)-N-(1-isopropyl-1H-pyrazol-4-yl)acetamide AZD2932;AZD 2932 USP/EP/BP;AZD 2932; AZD-2932; AGN-PC-00AQ5T;AZD2932;AGN-PC-00AQ5T;CS-1792;Benzeneacetamide, 4-[(6,7-dimethoxy-4-quinazolinyl)oxy]-N-[1-(1-methylethyl)-1H-pyrazol-4-yl]-
CAS:883986-34-3
MF:C24H25N5O4
MW:447.49
EINECS:
Product Categories:Inhibitors
Mol File:883986-34-3.mol
AZD 2932 Structure
AZD 2932 Chemical Properties
storage temp. Store at -20°C
solubility Soluble in DMSO
form crystalline solid
color Light yellow to yellow
Safety Information
MSDS Information
AZD 2932 Usage And Synthesis
UsesAZD2932 is a potent and multi-targeted protein tyrosine kinase inhibitor of VEFGR-2 and PDGFR.
Biological Activityazd2932 is a potent inhibitor for multiple protein tyrosine kinases (ic50 = 8 nm, 4 nm, 7 nm, and 9 nm for vegfr-2, pdgfrβ, flt-3, and c-kit, respectively.) [1]vegfr are receptors for vascular endothelial growth factor and belong to receptor tyrosine kinases. it mediates in various cellular functions, including endothelial proliferation, migration, survival, tubular morphogenesis and sprouting. pdgfr are platelet-derived growth factor receptors that exhibit intracellular tyrosine kinase activity. it involves in embryonic development, angiogenesis, proliferation and differentiation etc.azd2932 has a potent and balanced profile against pdgfr, vegfr-2, flt-3 and c-kit (ic50: 0.009). it also has a good fraction unbound between 3.3% free in human and 7.0% in dog sera and has no activity against herg. [1]in female nude mice bearing c6 tumors, azd2932 treatment at 3–50 mg/kg b.i.d. 10 h apart give 60–80% inhibition of both p-vegfr-2 and p-pdgfrb in a 1:1 ratio. [1]
references1. plé pa, jung f, ashton s, hennequin l et al. discovery of azd2932, a new quinazoline ether inhibitor with high affinity for vegfr-2 and pdgfr tyrosine kinases. bioorg med chem lett. 2012 jan 1;22(1):262-6.
AZD 2932 Preparation Products And Raw materials
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