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Synthesis and analgesic activity of new heterocyclic cyanothioacetamide derivatives

The reaction of cyanothioacetamide with aromatic aldehydes and 1,3-dicarbonyl compounds followed by aminomethylation or S-alkylation gave a series of heterocyclic derivatives with a 1,2,3,4-tetrahydropyridine or 1,4,5,6,7,8-hexahydroquinoline fragment. The resulting compounds were tested for analges...

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主要な著者: Dotsenko, V. V., Доценко, В. В., Aksenov, N. A., Аксенов, Н. А., Aksenova, I. V., Аксенова, И. В., Shcherbakov, S. V., Щербаков, С. В., Ovcharov, S. N., Овчаров, С. Н.
フォーマット: Статья
言語:English
出版事項: Pleiades journals 2021
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オンライン・アクセス:https://dspace.ncfu.ru/handle/20.500.12258/15557
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spelling ir-20.500.12258-155572021-06-04T14:06:04Z Synthesis and analgesic activity of new heterocyclic cyanothioacetamide derivatives Dotsenko, V. V. Доценко, В. В. Aksenov, N. A. Аксенов, Н. А. Aksenova, I. V. Аксенова, И. В. Shcherbakov, S. V. Щербаков, С. В. Ovcharov, S. N. Овчаров, С. Н. 2-oxo-3-cyano-1,4,5,6-tetrahydropyridine-2-thiolates Analgesics Cyanothioacetamide Mannich reaction Pyrido[2,1-b][1,3,5]thiadiazines The reaction of cyanothioacetamide with aromatic aldehydes and 1,3-dicarbonyl compounds followed by aminomethylation or S-alkylation gave a series of heterocyclic derivatives with a 1,2,3,4-tetrahydropyridine or 1,4,5,6,7,8-hexahydroquinoline fragment. The resulting compounds were tested for analgesic activity in vivo. Some of the prepared compounds showed an antinociceptive effect superior to that of ketorolac in dynamics 2021-03-23T12:27:24Z 2021-03-23T12:27:24Z 2021 Статья Bibik, I.V., Bibik, E.Y., Dotsenko, V.V., Frolov, K.A., Krivokolysko, S.G., Aksenov, N.A., Aksenova, I.V., Shcherbakov, S.V., Ovcharov, S.N. Synthesis and analgesic activity of new heterocyclic cyanothioacetamide derivatives // Russian Journal of General Chemistry. - 2021. - Volume 91. - Issue 2. - Pages 154-166 http://hdl.handle.net/20.500.12258/15557 en Russian Journal of General Chemistry application/pdf application/pdf Pleiades journals
institution СКФУ
collection Репозиторий
language English
topic 2-oxo-3-cyano-1,4,5,6-tetrahydropyridine-2-thiolates
Analgesics
Cyanothioacetamide
Mannich reaction
Pyrido[2,1-b][1,3,5]thiadiazines
spellingShingle 2-oxo-3-cyano-1,4,5,6-tetrahydropyridine-2-thiolates
Analgesics
Cyanothioacetamide
Mannich reaction
Pyrido[2,1-b][1,3,5]thiadiazines
Dotsenko, V. V.
Доценко, В. В.
Aksenov, N. A.
Аксенов, Н. А.
Aksenova, I. V.
Аксенова, И. В.
Shcherbakov, S. V.
Щербаков, С. В.
Ovcharov, S. N.
Овчаров, С. Н.
Synthesis and analgesic activity of new heterocyclic cyanothioacetamide derivatives
description The reaction of cyanothioacetamide with aromatic aldehydes and 1,3-dicarbonyl compounds followed by aminomethylation or S-alkylation gave a series of heterocyclic derivatives with a 1,2,3,4-tetrahydropyridine or 1,4,5,6,7,8-hexahydroquinoline fragment. The resulting compounds were tested for analgesic activity in vivo. Some of the prepared compounds showed an antinociceptive effect superior to that of ketorolac in dynamics
format Статья
author Dotsenko, V. V.
Доценко, В. В.
Aksenov, N. A.
Аксенов, Н. А.
Aksenova, I. V.
Аксенова, И. В.
Shcherbakov, S. V.
Щербаков, С. В.
Ovcharov, S. N.
Овчаров, С. Н.
author_facet Dotsenko, V. V.
Доценко, В. В.
Aksenov, N. A.
Аксенов, Н. А.
Aksenova, I. V.
Аксенова, И. В.
Shcherbakov, S. V.
Щербаков, С. В.
Ovcharov, S. N.
Овчаров, С. Н.
author_sort Dotsenko, V. V.
title Synthesis and analgesic activity of new heterocyclic cyanothioacetamide derivatives
title_short Synthesis and analgesic activity of new heterocyclic cyanothioacetamide derivatives
title_full Synthesis and analgesic activity of new heterocyclic cyanothioacetamide derivatives
title_fullStr Synthesis and analgesic activity of new heterocyclic cyanothioacetamide derivatives
title_full_unstemmed Synthesis and analgesic activity of new heterocyclic cyanothioacetamide derivatives
title_sort synthesis and analgesic activity of new heterocyclic cyanothioacetamide derivatives
publisher Pleiades journals
publishDate 2021
url https://dspace.ncfu.ru/handle/20.500.12258/15557
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