Home Amines 726695-51-8
726695-51-8,MFCD12922523
Catalog No.:AA01DU7S

726695-51-8 | 5-Pyrimidinecarboxamide,2-[(2-aminoethyl)amino]-4-[[3-(trifluoromethyl)phenyl]amino]-

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1mg
≥98%
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$326.00   $228.00
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5mg
≥98%
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$1,360.00   $952.00
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  • Technical Information
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  • Literature
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  • Technical Information
  • Properties
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Technical Information
Catalog Number:
AA01DU7S
Chemical Name:
5-Pyrimidinecarboxamide,2-[(2-aminoethyl)amino]-4-[[3-(trifluoromethyl)phenyl]amino]-
CAS Number:
726695-51-8
Molecular Formula:
C14H15F3N6O
Molecular Weight:
340.3037
MDL Number:
MFCD12922523
SMILES:
NCCNc1ncc(c(n1)Nc1cccc(c1)C(F)(F)F)C(=O)N
Properties
Computed Properties
 
Complexity:
422  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
24  
Hydrogen Bond Acceptor Count:
9  
Hydrogen Bond Donor Count:
4  
Rotatable Bond Count:
6  
XLogP3:
1.8  

Literature

Title: A broad activity screen in support of a chemogenomic map for kinase signalling research and drug discovery.

Journal: The Biochemical journal 20130415

Title: Comprehensive assay of kinase catalytic activity reveals features of kinase inhibitor selectivity.

Journal: Nature biotechnology 20111101

Title: Pharmacophore modeling study based on known spleen tyrosine kinase inhibitors together with virtual screening for identifying novel inhibitors.

Journal: Bioorganic & medicinal chemistry letters 20090401

Title: Discovery and SAR of novel 4-thiazolyl-2-phenylaminopyrimidines as potent inhibitors of spleen tyrosine kinase (SYK).

Journal: Bioorganic & medicinal chemistry letters 20081201

Title: A novel Syk family kinase inhibitor: design, synthesis, and structure-activity relationship of 1,2,4-triazolo[4,3-c]pyrimidine and 1,2,4-triazolo[1,5-c]pyrimidine derivatives.

Journal: Bioorganic & medicinal chemistry 20080801

Title: Synthetic studies on novel Syk inhibitors. Part 1: Synthesis and structure-activity relationships of pyrimidine-5-carboxamide derivatives.

Journal: Bioorganic & medicinal chemistry 20050815

Title: Hiroyuki Hisamichi, et al. Synthetic studies on novel Syk inhibitors. Part 1: Synthesis and structure-activity relationships of pyrimidine-5-carboxamide derivatives. Bioorg Med Chem. 2005 Aug 15;13(16):4936-51.

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Tags:726695-51-8 Molecular Formula|726695-51-8 MDL|726695-51-8 SMILES|726695-51-8 5-Pyrimidinecarboxamide,2-[(2-aminoethyl)amino]-4-[[3-(trifluoromethyl)phenyl]amino]-