Química Nova (Dec 2022)

DITERPENOS ENT-ABIETANOS DE Euphorbia phosphorea (EUPHORBIACEAE)

  • Roseana A. R. Meireles,
  • Lucas S. Abreu,
  • Joanda Paolla R. e Silva,
  • Andreza B. S. Cavalcanti,
  • Renata Priscila B. de Menezes,
  • Gabriela Cristina S. Rodrigues,
  • Valnês S. Rodrigues Junior,
  • José Iranildo M. de Melo,
  • Massuo Jorge Kato,
  • Vicente Carlos de O. Costa,
  • Marcus Tullius Scotti,
  • Josean F. Tavares

DOI
https://doi.org/10.21577/0100-4042.20170932
Journal volume & issue
Vol. 45, no. 9
pp. 1092 – 1097

Abstract

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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]-abieta-8(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.