Synthesis and Neurotropic Activity of Piperazino-Derivatives of Pyrano[3,4-c]Pyridines


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Аннотация

Methods were developed for synthesizing new substituted piperazine derivatives from chloropyrano- [3,4-c]pyridines. Pharmacological screening of the synthesized compounds used the well-known corazole antagonism and open field tests. The rotating rod test was used to evaluate the neurotoxicity of the compounds. The tested compounds displayed neurotropic activity. Several compounds of this series exhibited pronounced anticonvulsant and anxiolytic activity.

Об авторах

S. Sirakanyan

A. I. Mnjoyan Institute of Fine Organic Chemistry, Scientific Technological Center of Organic and Pharmaceutical Chemistry, National Academy of Sciences of Armenia

Автор, ответственный за переписку.
Email: shnnr@mail.ru
Армения, 0014, Yerevan, 375014

É. Akopyan

A. I. Mnjoyan Institute of Fine Organic Chemistry, Scientific Technological Center of Organic and Pharmaceutical Chemistry, National Academy of Sciences of Armenia

Email: shnnr@mail.ru
Армения, 0014, Yerevan, 375014

R. Paronikyan

A. I. Mnjoyan Institute of Fine Organic Chemistry, Scientific Technological Center of Organic and Pharmaceutical Chemistry, National Academy of Sciences of Armenia

Email: shnnr@mail.ru
Армения, 0014, Yerevan, 375014

I. Nazaryan

A. I. Mnjoyan Institute of Fine Organic Chemistry, Scientific Technological Center of Organic and Pharmaceutical Chemistry, National Academy of Sciences of Armenia

Email: shnnr@mail.ru
Армения, 0014, Yerevan, 375014

A. Akopyan

A. I. Mnjoyan Institute of Fine Organic Chemistry, Scientific Technological Center of Organic and Pharmaceutical Chemistry, National Academy of Sciences of Armenia

Email: shnnr@mail.ru
Армения, 0014, Yerevan, 375014

A. Ovakimyan

A. I. Mnjoyan Institute of Fine Organic Chemistry, Scientific Technological Center of Organic and Pharmaceutical Chemistry, National Academy of Sciences of Armenia

Email: shnnr@mail.ru
Армения, 0014, Yerevan, 375014


© Springer Science+Business Media, LLC, part of Springer Nature, 2019

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