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Home > Products >  CP 373420

CP 373420 CAS NO.183321-86-0

  • Min.Order: 1 Gram
  • Payment Terms: T/T
  • Product Details

Keywords

  • CP 373420 183321-86-0
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Quick Details

  • ProName: CP 373420
  • CasNo: 183321-86-0
  • Molecular Formula: C21H21N3O4
  • Application: API
  • DeliveryTime: 2 weeks
  • PackAge: according to the request of customer
  • Port: Ji nan;
  • ProductionCapacity: 1 Kilogram/Month
  • Purity: 99%
  • Storage: Low temperature dry and shady
  • Transportation: according to the request of customer
  • LimitNum: 1 Gram

Superiority

We have been providing over 1000 products including molecular targeted anticancer drugs, cell signaling pathway inhibitors,

 

pharmaceutical intermediates, and heterocyclic compounds, and quality services including custom synthesis, transfer of new

 

drug patent and technology, technical cooperation, and process optimization.

 

 

Jinan Trio PharmaTech was founded by a core group of top overseas pharmaceutical chemists, Medical scientists and

 

business management experts, and is an enterprise of science and technology supported by the "Attracting High-Level

 

Talent Scheme" of Jinan government.

 

Details

Jinan Trio PharmaTech Co., Ltd. 

 

Year Establishment: 2008

 

Location: We are located at one of the largest National Technical Integrated Drug Discovery Platforms in the High-Tech Zone of Jinan City

 

Our company was founded by a core group of top overseas pharmaceutical chemists, medical scientists business

management experts

 

We have built up solid cooperation with over twenty oversea companies over one hundred domestic companies

since the foundation

 

 

 

 

 

 

 

 

Specifications:

 

 

Name  CP 373420
 

 

Synonyms  2-[[4-[(3-Ethynylphenyl)amino]-7-(2-methoxyethoxy)-6-quinazolinyl]oxy]ethanol
 
 

Molecular Formula  C21H21N3O4

 


Molecular Weight  379.41

 


CAS Registry Number  183321-86-0
  
 


 

Applications:

 

 

OSI-420 (Desmethyl Erlotinib,CP-473420) is an active metabolite of erlotinib which is anally active EGFR tyrosin kinase inhibitwith IC50 of 2 20 nM fthe inhibition of human EGFR EGFR autophosphorylation in tumcells.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

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