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Guaianolide Sesquiterpene Lactones from Centaurothamnus maximus.
Hussien, Taha A; Mohamed, Tarik A; Elshamy, Abdelsamed I; Moustafa, Mahmoud F; El-Seedi, Hesham R; Pare, Paul W; Hegazy, Mohamed-Elamir F.
Afiliação
  • Hussien TA; Pharmacognosy Department, Faculty of Pharmacy, Sphinx University, New Assiut City, Assiut 10, Egypt.
  • Mohamed TA; National Research Centre, Chemistry of Medicinal Plants Department, 33 El-Bohouth St., Dokki, Giza 12622, Egypt.
  • Elshamy AI; National Research Centre, Department of Natural Compounds Chemistry, 33 El-Bohouth St., Dokki, Giza 12622, Egypt.
  • Moustafa MF; Department of Biology, College of Science, King Khalid University, Abha 61421, Saudi Arabia.
  • El-Seedi HR; Department of Botany & Microbiology, Faculty of Science, South Valley University, Qena 83523, Egypt.
  • Pare PW; Department of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University, S-106 91 Stockholm, Sweden.
  • Hegazy MF; International Research Center for Food Nutrition and Safety, Jiangsu University, Zhenjiang 212013, China.
Molecules ; 26(7)2021 Apr 03.
Article em En | MEDLINE | ID: mdl-33916714
Centaurothamnus maximus (family Asteraceae), is a leafy shrub indigenous to the southwestern Arabian Peninsula. With a paucity of phytochemical data on this species, we set out to chemically characterize the plant. From the aerial parts, two newly identified guaianolides were isolated: 3ß-hydroxy-4α(acetoxy)-4ß(hydroxymethyl)-8α-(4-hydroxy methacrylate)-1αH,5αH, 6αH-gual-10(14),11(13)-dien-6,12-olide (1) and 15-descarboxy picrolide A (2). Seven previously reported compounds were also isolated: 3ß, 4α, 8α-trihydroxy-4-(hydroxymethyl)-lαH, 5αH, 6ßH, 7αH-guai-10(14),11(13)-dien-6,12-olide (3), chlorohyssopifolin B (4), cynaropikrin (5), hydroxyjanerin (6), chlorojanerin (7), isorhamnetin (8), and quercetagetin-3,6-dimethyl ether-4'-O-ß-d-pyranoglucoside (9). Chemical structures were elucidated using spectroscopic techniques, including High Resolution Fast Atom Bombardment Mass Spectrometry (HR-FAB-MS), 1D NMR; 1H, 13C NMR, Distortionless Enhancement by Polarization Transfer (DEPT), and 2D NMR (1H-1H COSY, HMQC, HMBC) analyses. In addition, a biosynthetic pathway for compounds 1-9 is proposed. The chemotaxonomic significance of the reported sesquiterpenoids and flavonoids considering reports from other Centaurea species is examined.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Asteraceae / Sesquiterpenos de Guaiano / Lactonas Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Asteraceae / Sesquiterpenos de Guaiano / Lactonas Idioma: En Ano de publicação: 2021 Tipo de documento: Article