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IMPROVED SYNTHESIS OF SUBSTITUTED 2-ARYL-N- [2-(DIMETHYLAMINO)ETHYL]QUINOLIN-4-AMINES AND THEIR ACTIVITY AS ANTAGONISTS OF IMMUNOSTIMULATORY CpG-OLIGODEOXYNUCLEOTIDES
Journal article   Open access   Peer reviewed

IMPROVED SYNTHESIS OF SUBSTITUTED 2-ARYL-N- [2-(DIMETHYLAMINO)ETHYL]QUINOLIN-4-AMINES AND THEIR ACTIVITY AS ANTAGONISTS OF IMMUNOSTIMULATORY CpG-OLIGODEOXYNUCLEOTIDES

Ekaterina Paliakov, Maged Henary, Martial Say, Lubomir Janda, Lori Manzel, Donald E Macfarlane and Lucjan Strekowski
Heterocyclic communications, Vol.13(1), pp.9-12
01/2007
DOI: 10.1515/HC.2007.13.1.9
url
https://doi.org/10.1515/HC.2007.13.1.9View
Published (Version of record) Open Access

Abstract

A general methodology for the synthesis of substituted quinolin-4-amines developed by us previously has been simplified. The synthesized compounds, depending on substituents, show activities in the range from 35 nM to 550 nM as antagonists of immunostimulatory oligodeoxynucleotides containing a CpG motif. A SAR analysis is presented.

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