Cargando…
Guaianolide Sesquiterpene Lactones from Centaurothamnus maximus
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: 3β-hydroxy-4α...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8038342/ https://www.ncbi.nlm.nih.gov/pubmed/33916714 http://dx.doi.org/10.3390/molecules26072055 |
_version_ | 1783677353138847744 |
---|---|
author | Hussien, Taha A. Mohamed, Tarik A. Elshamy, Abdelsamed I. Moustafa, Mahmoud F. El-Seedi, Hesham R. Pare, Paul W. Hegazy, Mohamed-Elamir F. |
author_facet | Hussien, Taha A. Mohamed, Tarik A. Elshamy, Abdelsamed I. Moustafa, Mahmoud F. El-Seedi, Hesham R. Pare, Paul W. Hegazy, Mohamed-Elamir F. |
author_sort | Hussien, Taha A. |
collection | PubMed |
description | 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: 3β-hydroxy-4α(acetoxy)-4β(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: 3β, 4α, 8α-trihydroxy-4-(hydroxymethyl)-lαH, 5αH, 6βH, 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-β-d-pyranoglucoside (9). Chemical structures were elucidated using spectroscopic techniques, including High Resolution Fast Atom Bombardment Mass Spectrometry (HR-FAB-MS), 1D NMR; (1)H, (13)C NMR, Distortionless Enhancement by Polarization Transfer (DEPT), and 2D NMR ((1)H-(1)H 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. |
format | Online Article Text |
id | pubmed-8038342 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80383422021-04-12 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. Molecules Article 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: 3β-hydroxy-4α(acetoxy)-4β(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: 3β, 4α, 8α-trihydroxy-4-(hydroxymethyl)-lαH, 5αH, 6βH, 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-β-d-pyranoglucoside (9). Chemical structures were elucidated using spectroscopic techniques, including High Resolution Fast Atom Bombardment Mass Spectrometry (HR-FAB-MS), 1D NMR; (1)H, (13)C NMR, Distortionless Enhancement by Polarization Transfer (DEPT), and 2D NMR ((1)H-(1)H 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. MDPI 2021-04-03 /pmc/articles/PMC8038342/ /pubmed/33916714 http://dx.doi.org/10.3390/molecules26072055 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Hussien, Taha A. Mohamed, Tarik A. Elshamy, Abdelsamed I. Moustafa, Mahmoud F. El-Seedi, Hesham R. Pare, Paul W. Hegazy, Mohamed-Elamir F. Guaianolide Sesquiterpene Lactones from Centaurothamnus maximus |
title | Guaianolide Sesquiterpene Lactones from Centaurothamnus maximus |
title_full | Guaianolide Sesquiterpene Lactones from Centaurothamnus maximus |
title_fullStr | Guaianolide Sesquiterpene Lactones from Centaurothamnus maximus |
title_full_unstemmed | Guaianolide Sesquiterpene Lactones from Centaurothamnus maximus |
title_short | Guaianolide Sesquiterpene Lactones from Centaurothamnus maximus |
title_sort | guaianolide sesquiterpene lactones from centaurothamnus maximus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8038342/ https://www.ncbi.nlm.nih.gov/pubmed/33916714 http://dx.doi.org/10.3390/molecules26072055 |
work_keys_str_mv | AT hussientahaa guaianolidesesquiterpenelactonesfromcentaurothamnusmaximus AT mohamedtarika guaianolidesesquiterpenelactonesfromcentaurothamnusmaximus AT elshamyabdelsamedi guaianolidesesquiterpenelactonesfromcentaurothamnusmaximus AT moustafamahmoudf guaianolidesesquiterpenelactonesfromcentaurothamnusmaximus AT elseediheshamr guaianolidesesquiterpenelactonesfromcentaurothamnusmaximus AT parepaulw guaianolidesesquiterpenelactonesfromcentaurothamnusmaximus AT hegazymohamedelamirf guaianolidesesquiterpenelactonesfromcentaurothamnusmaximus |