Modification of the Benzene Moiety in the Quinolone Nucleus of 4-Hydroxy-6,7-Dimethoxy-2-Oxo-N-(Pyridin-3-Ylmethyl)-1,2-Dihydroquinoline-3-Carboxamide as an Attempt to Enhance its Analgesic Activity


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription Access

Abstract

A series of close analogs of 4-hydroxy-6,7-dimethoxy-2-oxo-N-(pyridin-3-ylmethyl)-1,2-dihydroquinoline-3-carboxamide modified in the benzene moiety of the quinolone nucleus were synthesized to identify the structural fragments determining their analgesic effect. Results of pharmacological tests found that these chemical changes had a relatively weak influence on the analgesic activity of the tested compounds, leading to the conclusion that the modified fragment interacted insignificantly with the biological targets.

About the authors

I. V. Ukrainets

National University of Pharmacy

Author for correspondence.
Email: uiv-2@mail.ru
Ukraine, Kharkiv, 61000

E. V. Mospanova

Kyiv National University of Technologies and Design

Email: uiv-2@mail.ru
Ukraine, Kyiv, 01011

N. L. Bereznyakova

National University of Pharmacy

Email: uiv-2@mail.ru
Ukraine, Kharkiv, 61000

A. A. Davidenko

N. I. Pirogov Vinnitsa National Medical University

Email: uiv-2@mail.ru
Ukraine, Vinnytsya, 21000


Copyright (c) 2019 Springer Science+Business Media, LLC, part of Springer Nature

This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies