大戟科
阿比坦
二萜
抗细菌
植物化学
大戟
立体化学
传统医学
化学
生物
结核分枝杆菌
植物
肺结核
医学
病理
作者
Roseana Meireles,Lucas Silva Abreu,Joanda Silva,Andreza Barbosa Silva Cavalcanti,Renata Priscila Barros de Menezes,Gabriela Zimmermann Prado Rodrigues,Valnês S. Rodrigues-Junior,José Melo,Massuo J. Kato,Vicente Casals Costa,Marcus Tullius Scotti,Josean Fechine Tavares
出处
期刊:Química Nova
[Sociedade Brasileira de Quimica (SBQ)]
日期:2022-01-01
标识
DOI:10.21577/0100-4042.20170932
摘要
ENT-ABIETANE DITERPENES FROM Euphorbia phosphorea (EUPHORBIACEAE). Phytochemical study of the roots of Euphorbia phosphorea Mart. (Euphorbiaceae) was carried out through chromatographic techniques, resulting in the isolation of a new ent-abietane diterpene named 11β,12β-dihydroxy-ent-abieta-8(14),13(15)-dien-16,12α-olide (1), and of nine known ent-abietane diterpenes jolkinolide A (2), jolkinolide E (3), euphorin H (4), euphopilolide (5) jolkinolide F (6), ent-12-hydroxy-12[R]-abieta8(14),13(15)-dien-16,12-olide (7), ent-11α-hydroxyabieta-8(14),13(15)-dien-16,12α-olide (8), 17-hydroxyjolkinolide B (9) and caudicifolin (10). The structures of all compounds were established using spectroscopic techniques such as 1D and 2D NMR, and the structure of the compound 1 was established also with MS, IR and ECD. All compounds were submitted to an in silico study through of a predictive model and then submitted to in vitro tests against Mycobacterium tuberculosis and M. smegmatis for evaluation of their antimycobacterial activity. Compounds 5 and 9 showed mycobacterial growth inhibition with MIC values of 62.5 μM against M. tuberculosis and M. smegmatis, respectively.
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