Bioorganic & medicinal chemistry · 2012
Alstiphyllanines I-O, ajmaline type alkaloids from Alstonia macrophylla showing vasorelaxant activity.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Arai Hiroko, Zaima Kazumasa, Mitsuta Erika, Tamamoto Haruka, Saito Aiko, Hirasawa Yusuke, Rahman Abdul, Kusumawati Idha, Zaini Noor Cholies, Morita Hiroshi
Аннотация
Seven new ajmaline type alkaloids, alstiphyllanines I-O (1-7) were isolated from the leaves of Alstonia macrophylla together with six related alkaloids (8-13). Structures and stereochemistry of 1-7 were fully elucidated and characterized by 2D NMR analysis. A series of alstiphyllanines I-O (1-7) as well as the known ajmaline type alkaloids (8-13) showed that they relaxed phenylephrine (PE)-induced contractions against rat aortic ring. Among them, vincamedine (10) showed potent vasorelaxant activity, which may be mediated through inhibition of Ca(2+) influx through voltage-dependent Ca(2+) channels (VDCs) and/or receptor-operated Ca(2+) channels (ROCs) as well as partially mediated the NO release from endothelial cells. The presence of substituents at both N-1 and C-17 may be important to show vasorelaxation activity.
Предметные рубрики MeSH
AjmalineAlstoniaAnimalsAortaCalciumCalcium Channel BlockersCalcium ChannelsDose-Response Relationship, DrugDrug Evaluation, PreclinicalEndothelial CellsIn Vitro TechniquesMagnetic Resonance SpectroscopyMaleMolecular StructureNitric OxidePhenylephrineRatsRats, WistarSecologanin Tryptamine AlkaloidsStructure-Activity RelationshipVasodilationVasodilator Agents