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Synthetic Transformations of Higher Terpenoids. 39.∗ Synthesis and Analgesic Activity of Isopimaric Acid Derivatives Научная публикация

Журнал Chemistry of Natural Compounds
ISSN: 0009-3130 , E-ISSN: 1573-8388
Вых. Данные Год: 2021, Том: 57, Страницы: 474–481 Страниц : DOI: 10.1007/s10600-021-03391-1
Ключевые слова amides; analgesic activity; diterpenoids; esters; isopimaric acid
Авторы Gromova M.A. 1 , Kharitonov Y.V. 1 , Borisov S.A. 1 , Baev D.S. 1 , Tolstikova T.G. 1 , Shul’ts E.E. 1
Организации
1 N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry Siberian Branch, Russian Academy of Sciences, 9 Prosp. Lavrent’eva, Novosibirsk, 630090, Russian Federation

Реферат: New derivatives of isopimaric acid at the carboxylic acid were prepared. Their analgesic activity was studied in models of visceral and thermal pain. Isopimaric acid amides with aminoethanol and (2R)-(hydroxymethyl)pyrrolidine groups exhibited statistically significant analgesic activity in acetic acid-induced writhing (5 and 25 mg/kg doses) and hot-plate tests (25 mg/kg dose) that was comparable to that of diclofenac sodium (10 mg/kg dose). The new agents were characterized by low (LD50 > 1250 mg/kg) in vivo toxicity. Molecular modeling of possible interaction of the most active compounds with transmembrane G-protein-binding cannabinoid receptor CB2 was performed. © 2021, Springer Science+Business Media, LLC, part of Springer Nature.
Библиографическая ссылка: Gromova M.A. , Kharitonov Y.V. , Borisov S.A. , Baev D.S. , Tolstikova T.G. , Shul’ts E.E.
Synthetic Transformations of Higher Terpenoids. 39.∗ Synthesis and Analgesic Activity of Isopimaric Acid Derivatives
Chemistry of Natural Compounds. 2021. V.57. P.474–481. DOI: 10.1007/s10600-021-03391-1 WOS Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 мая 2021 г.
Опубликована online: 28 мая 2021 г.
Идентификаторы БД:
Web of science: WOS:000655545100001
Scopus: 2-s2.0-85106699876
РИНЦ: 46777062
OpenAlex: W3167519125
Цитирование в БД:
БД Цитирований
Scopus 3
Web of science 3
РИНЦ 2
OpenAlex 4
Альметрики: