Synthesis and Analgesic Activity of [b]-Annelated 4-Quinolones


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Resumo

Considering the side effects of existing drugs used for pain relief, the search for new analgesics with high efficacy and safety remains relevant. Aseries of imidazopyrrolo[3,4-b]quinoline-5,11-diones and pyrimidopyrrolo[3,4-b]quinoline-6,12-diones II were synthesized, whose analgesic activity at a dose of 0.05 mmol/kg was studied in the hotplate test in rats after i.p. administration. One compound was found with analgesic activity comparable to that of reference compound diclofenac sodium. Compounds II were less toxic than diclofenac sodium.

Sobre autores

A. Boteva

Science Education Center for Applied Chemical and Biological Research, Perm National Research Polytechnical University

Autor responsável pela correspondência
Email: aboteva@pstu.ru
Rússia, 29 Komsomolskii Prospekt, Perm, Perm District, 614990

I. Fefilova

Science Education Center for Applied Chemical and Biological Research, Perm National Research Polytechnical University

Email: aboteva@pstu.ru
Rússia, 29 Komsomolskii Prospekt, Perm, Perm District, 614990

G. Triandafilova

Science Education Center for Applied Chemical and Biological Research, Perm National Research Polytechnical University

Email: aboteva@pstu.ru
Rússia, 29 Komsomolskii Prospekt, Perm, Perm District, 614990

V. Maslova

Science Education Center for Applied Chemical and Biological Research, Perm National Research Polytechnical University

Email: aboteva@pstu.ru
Rússia, 29 Komsomolskii Prospekt, Perm, Perm District, 614990

S. Solodnikov

Science Education Center for Applied Chemical and Biological Research, Perm National Research Polytechnical University

Email: aboteva@pstu.ru
Rússia, 29 Komsomolskii Prospekt, Perm, Perm District, 614990

O. Krasnykh

Science Education Center for Applied Chemical and Biological Research, Perm National Research Polytechnical University

Email: aboteva@pstu.ru
Rússia, 29 Komsomolskii Prospekt, Perm, Perm District, 614990


Declaração de direitos autorais © Springer Science+Business Media, LLC, part of Springer Nature, 2019

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