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927880-90-8,MFCD16659061
Catalog No.:AA00GU3A

927880-90-8 | RAF265

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
98%
in stock  
$33.00   $23.00
- +
5mg
98%
in stock  
$82.00   $57.00
- +
25mg
98%
in stock  
$210.00   $147.00
- +
50mg
98%
in stock  
$341.00   $239.00
- +
  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA00GU3A
Chemical Name:
RAF265
CAS Number:
927880-90-8
Molecular Formula:
C24H16F6N6O
Molecular Weight:
518.4139
MDL Number:
MFCD16659061
SMILES:
Cn1c(Nc2ccc(cc2)C(F)(F)F)nc2c1ccc(c2)Oc1ccnc(c1)c1ncc([nH]1)C(F)(F)F
Properties
Computed Properties
 
Complexity:
763  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
37  
Hydrogen Bond Acceptor Count:
11  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
5  
XLogP3:
5.4  

Literature

Title: Identification of potent Yes1 kinase inhibitors using a library screening approach.

Journal: Bioorganic & medicinal chemistry letters 20130801

Title: Comprehensive analysis of kinase inhibitor selectivity.

Journal: Nature biotechnology 20111030

Title: Synergistic action of a RAF inhibitor and a dual PI3K/mTOR inhibitor in thyroid cancer.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research 20111015

Title: Mesenchymal stem cells and carcinoma-associated fibroblasts sensitize breast cancer cells in 3D cultures to kinase inhibitors.

Journal: International journal of oncology 20110901

Title: Discovery, synthesis, and investigation of the antitumor activity of novel piperazinylpyrimidine derivatives.

Journal: European journal of medicinal chemistry 20110601

Title: Exploration of acridine scaffold as a potentially interesting scaffold for discovering novel multi-target VEGFR-2 and Src kinase inhibitors.

Journal: Bioorganic & medicinal chemistry 20110601

Title: The novel Raf inhibitor Raf265 decreases Bcl-2 levels and confers TRAIL-sensitivity to neuroendocrine tumour cells.

Journal: Endocrine-related cancer 20110401

Title: Use of DNA microarray and small animal positron emission tomography in preclinical drug evaluation of RAF265, a novel B-Raf/VEGFR-2 inhibitor.

Journal: Neoplasia (New York, N.Y.) 20110301

Title: Activation state-dependent binding of small molecule kinase inhibitors: structural insights from biochemistry.

Journal: Chemistry & biology 20101124

Title: Dependence on phosphoinositide 3-kinase and RAS-RAF pathways drive the activity of RAF265, a novel RAF/VEGFR2 inhibitor, and RAD001 (Everolimus) in combination.

Journal: Molecular cancer therapeutics 20100201

Title: A quantitative analysis of kinase inhibitor selectivity.

Journal: Nature biotechnology 20080101

Title: Mordant P, et al. Dependence on phosphoinositide 3-kinase and RAS-RAF pathways drive the activity of RAF265, a novel RAF/VEGFR2 inhibitor, and RAD001 (Everolimus) in combination. Mol Cancer Ther. 2010 Feb;9(2):358-68.

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