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American Journal of PharmTech Research

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An Efficient One Pot Synthesis of Biologically Active Quinoline Trifluoro Esters and DNA Studies

Published in October 2017 Issue 5 (Vol. 7, Issue 5, 2017)

An Efficient One Pot Synthesis of Biologically Active Quinoline Trifluoro Esters and DNA Studies - Issue cover

Abstract

We deliver chemistry of multicomponent reaction (MCR) for 2-Benzyl-5-(2-benzyloxycarbonylamino-3-Phenyl-propylamino)-4-(2-chloro-quinoline-3yl)-5-(2,2,2-trifluoro acetoxy)-pentanoic acid methyl ester (6a-g) by flexible Ugi multi-component approach, through commercially available amino acid,  aldehydes, isocyanides and amino acid ester in one pot. Further, the binding activity with CT DNA and nucleus property with pUC 19 DNA were studied by absorption spectra (Kb constant is= 4.2 × 10-4 M-1). The DNA binding results explored that the new molecule bind to DNA through interaction and also an efficient nucleus agent.

Authors (2)

T. Aravinda

Department of Chemistry, Nitte...

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M.S. Raghu1and Srilatha Rao

Department of Chemistry, Nitte...

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Article Information

AJPTR75005

AJPTR-01-000300

2017-10-01

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How to Cite

Aravinda & M.S. Raghu1and Srilatha Rao (2017). An Efficient One Pot Synthesis of Biologically Active Quinoline Trifluoro Esters and DNA Studies. American Journal of PharmTech Research, 7(5), xx-xx. https://ajptr.com/articles/AJPTR75005

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