The Decisive Role of Mutual Arrangement of Hydroxy and Methoxy Groups in (3(4)-hydroxy-4(3)-methoxyphenyl)-4,7-dimethyl-3,4,4a,5,8,8a-hexahydro-2H-chromene-4,8-diols in their Biological Activity Научная публикация
Журнал |
Letters in Drug Design and Discovery
ISSN: 1570-1808 , E-ISSN: 1875-628X |
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Вых. Данные | Год: 2017, Том: 14, Номер: 5, Страницы: 508-514 Страниц : 7 DOI: 10.2174/1570180813666161102142642 | ||||
Ключевые слова | Analgesia; monoterpenoids; CB1 receptors; opioid receptors; adrenergic system; dopaminergic system | ||||
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Реферат:
Background: The positional effects of the methoxy-and hydroxyl substituents in the phenyl ring were examined in vivo for distinct receptor classes in order to gain an insight into the mechanism by which isomeric compounds (2S, 4R, 4aR, 8R, 8aR)-2-(3(4)-hydroxy-4(3)-methoxyphenyl)-4,7-dimethyl3,4,4a, 5,8, 8a-hexahydro-2H-chromene-4,8-diols 1 and 2 exhibit their pharmacological activity. Conclusion: Our findings suggest a strong structure-function relationship between the substitution pattern and the mechanism of biological activity of compound. The methoxy substituent at C-4 and the hydroxyl substituent at C-3 (compound 1) seem to employ the cannabinoid and adrenergic systems, whereas compound 2 with the methoxy substituent at C3 and the hydroxyl substituent at C4 possibly targets the opioid and dopaminergic mechanisms.
Библиографическая ссылка:
Pavlova A.
, Patrusheva O.
, Il'ina I.
, Volcho K.
, Tolstikova T.
, Salakhutdinov N.
The Decisive Role of Mutual Arrangement of Hydroxy and Methoxy Groups in (3(4)-hydroxy-4(3)-methoxyphenyl)-4,7-dimethyl-3,4,4a,5,8,8a-hexahydro-2H-chromene-4,8-diols in their Biological Activity
Letters in Drug Design and Discovery. 2017. V.14. N5. P.508-514. DOI: 10.2174/1570180813666161102142642 WOS Scopus
The Decisive Role of Mutual Arrangement of Hydroxy and Methoxy Groups in (3(4)-hydroxy-4(3)-methoxyphenyl)-4,7-dimethyl-3,4,4a,5,8,8a-hexahydro-2H-chromene-4,8-diols in their Biological Activity
Letters in Drug Design and Discovery. 2017. V.14. N5. P.508-514. DOI: 10.2174/1570180813666161102142642 WOS Scopus
Даты:
Опубликована в печати: | 6 апр. 2017 г. |
Идентификаторы:
Web of science | WOS:000399449900001 |
Scopus | 2-s2.0-85019731394 |
OpenAlex | W2607080871 |