Home Amines 1213269-23-8
1213269-23-8,MFCD16621244
Catalog No.:AA008177

1213269-23-8 | N-(3-(5-Chloro-2-(2-methoxy-4-(4-methylpiperazin-1-yl)phenylamino)pyrimidin-4-yloxy)phenyl)acrylamide

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5mg
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$7.00   $5.00
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10mg
98+%
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$9.00   $7.00
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50mg
98+%
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$15.00   $11.00
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1g
98%(HPLC)
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5g
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  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA008177
Chemical Name:
N-(3-(5-Chloro-2-(2-methoxy-4-(4-methylpiperazin-1-yl)phenylamino)pyrimidin-4-yloxy)phenyl)acrylamide
CAS Number:
1213269-23-8
Molecular Formula:
C25H27ClN6O3
Molecular Weight:
494.9733
MDL Number:
MFCD16621244
SMILES:
C=CC(=O)Nc1cccc(c1)Oc1nc(ncc1Cl)Nc1ccc(cc1OC)N1CCN(CC1)C
Properties
Computed Properties
 
Complexity:
694  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
35  
Hydrogen Bond Acceptor Count:
8  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
8  
XLogP3:
4.2  

Literature

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

Journal: Bioorganic & medicinal chemistry letters 20130801

Title: Combined therapy with mutant-selective EGFR inhibitor and Met kinase inhibitor for overcoming erlotinib resistance in EGFR-mutant lung cancer.

Journal: Molecular cancer therapeutics 20121001

Title: Irreversible protein kinase inhibitors: balancing the benefits and risks.

Journal: Journal of medicinal chemistry 20120726

Title: NF-κB signaling is activated and confers resistance to apoptosis in three-dimensionally cultured EGFR-mutant lung adenocarcinoma cells.

Journal: Biochemical and biophysical research communications 20120713

Title: Paracrine receptor activation by microenvironment triggers bypass survival signals and ALK inhibitor resistance in EML4-ALK lung cancer cells.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research 20120701

Title: Design, synthesis, and biological evaluation of novel conformationally constrained inhibitors targeting epidermal growth factor receptor threonine⁷⁹⁰ → methionine⁷⁹⁰ mutant.

Journal: Journal of medicinal chemistry 20120322

Title: WZ4002, a third-generation EGFR inhibitor, can overcome anoikis resistance in EGFR-mutant lung adenocarcinomas more efficiently than Src inhibitors.

Journal: Laboratory investigation; a journal of technical methods and pathology 20120301

Title: Novel mutant-selective EGFR kinase inhibitors against EGFR T790M.

Journal: Nature 20091224

Title: Zhou W, et al. Novel mutant-selective EGFR kinase inhibitors against EGFR T790M.Nature. 2009 Dec 24;462(7276):1070-4.

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Tags:1213269-23-8 Molecular Formula|1213269-23-8 MDL|1213269-23-8 SMILES|1213269-23-8 N-(3-(5-Chloro-2-(2-methoxy-4-(4-methylpiperazin-1-yl)phenylamino)pyrimidin-4-yloxy)phenyl)acrylamide