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Home > Products >  Crenolanib

Crenolanib CAS NO.670220-88-9

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

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Quick Details

  • ProName: Crenolanib
  • CasNo: 670220-88-9
  • Molecular Formula: C26H29N5O2
  • 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  Crenolanib

 


Synonyms  ARO 002; CP 868596; [1-[2-[5-(3-Methyloxetan-3-ylmethoxy)benzimidazol-1-yl]quinolin-8-yl]piperidin-4-yl]amine
 

 

Molecular Formula  C26H29N5O2

 


Molecular Weight  443.54

 


CAS Registry Number  670220-88-9
 


 

Applications:

 

Crenolanib (CP-868569) is a highly selective and potent PDGFR-α inhibitor with IC50 of 0.9 and 1.8 nM against

PDGFRα and PDGFRβ, respectively.



 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

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