Publication Cover
Natural Product Research
Formerly Natural Product Letters
Volume 34, 2020 - Issue 20
179
Views
9
CrossRef citations to date
0
Altmetric
Research Articles

Machaerinic acid 3-O-β-D-glucuronopyranoside from Calendula officinalis

ORCID Icon &
Pages 2938-2944 | Received 17 Feb 2019, Accepted 20 Mar 2019, Published online: 10 Apr 2019

References

  • Ahmed B, Khan RA, Al-Howiriny TA, Al-Rehaily AJ. 2010. Osteosaponins 1 and 2: two new saponin glycosides from Osteospermum vaillantii. Nat Prod Res. 24(13):1258–1267.
  • Arora D, Rani A, Sharma A. 2013. A review on phytochemistry and ethnopharmacological aspects of genus Calendula. Pharmacogn Rev. 7(14):179–187.
  • Basch E, Bent S, Foppa I, Haskmi S, Kroll D, Mele M, Szapary P, Ulbricht C, Vora M, Yong S, et al. 2006. Marigold (Calendula officinalis L.): an evidence-based systematic review by the Natural Standard Research Collaboration. J Herb Pharmacother. 6(3–4):135–159.
  • D’Ambrosio M, Ciocarlan A, Colombo E, et al. 2015. Structure and cytotoxic activity of sesquiterpene glycoside esters from Calendula officinalis L.: studies on the conformation of viridiflorol. Phytochemistry. 117:1–9.
  • Dall’Acqua S, Cervellati R, Loi MC, et al. 2008. Evaluation of in vitro antioxidant properties of some traditional Sardinian medicinal plants: investigation of the high antioxidant capacity of Rubus ulmifolius. Food Chem. 106:745–749.
  • Hamburger M, Adler S, Baumann D, Förg A, Weinreich B. 2003. Preparative purification of the major anti-inflammatory triterpenoid esters from Marigold (Calendula officinalis). Fitoterapia. 74(4):328–338.
  • Lehbili M, Alabdul Magid A, Kabouche A, Voutquenne-Nazabadioko L, Abedini A, Morjani H, Sarazin T, Gangloff SC, Kabouche Z. 2017. Oleanane-type triterpene saponins from Calendula stellata. Phytochemistry. 144:33–42.
  • Markowski M, Długosz M, Szakiel A, Durli M, Poinsignon S, Bouguet-Bonnet S, Vernex-Loset L, Krier G, Henry M. 2018. Increased synthesis of a new oleanane-type saponin in hairy roots of marigold (Calendula officinalis) after treatment with jasmonic acid. Nat Prod Res.
  • Michl G, Abebe D, Bucar F, Debella A, Kunert O, Schmid MG, Mulatu E, Haslinger E. 2000. New triterpenoid saponins from Achyrantes aspera Linn. Helv Chim Acta. 83(2):359–363.
  • Nielsen NJ, Nielsen J, Staerk D. 2010. New resistance-correlated saponins from the insect-resistant crucifer Barbarea vulgaris. J Agric Food Chem. 58(9):5509–5514.
  • Penders A, Delaude C. 1994. Triterpenoid saponins from Melanthera scandens. Phytochemistry. 37(3):821–825.
  • Pizza C, Zhong-Liang Z, de Tommasi N. 1987. Plant metabolites. Triterpenoid saponins from Calendula arvensis. J Nat Prod. 50(5):927–931.
  • Szakiel A, Ruszkowski D, Grudniak A, Kurek A, Wolska K, Doligalska M, Janiszowska W. 2008. Antibacterial and antiparasitic activity of oleanolic acid and its glycosides isolated from marigold (Calendula officinalis). Planta Med. 74(14):1709.
  • Tanaka T, Matsuo Y, Kouno I. 2009. Chemistry of secondary polyphenols produced during processing of tea and selected foods. IJMS. 11(1):14–40.
  • Ukiya M, Akihisa T, Yasukawa K, Tokuda H, Suzuki T, Kimura Y. 2006. Anti-inflammatory, anti-tumor-promoting, and cytotoxic activities of constituents of marigold (Calendula officinalis) flowers. J Nat Prod. 69(12):1692–1696.
  • Vecherko LP, Sviridov AF, Zinkevich ÉP, Kogan LM. 1974. Structures of calendulosides G and H from the roots of Calendula officinalis. Chem Nat Compd. 10(4):548–549.
  • Vidal-Ollivier E, Babadjamian A, Faure R, Chemli R, Boukef K, Balansard G, Vincent EJ. 1989. Two-Dimensional NMR Studies of Triterpenoid Glycosides. II)-1 H NMR Assignment of Arvensoside A and B, Calenduloside C and D. Spectrosc Lett. 22(5):579–584.
  • Yoshikawa M, Murakami T, Kishi A, Kageura T, Matsuda H. 2001. Medicinal flowers. III. Marigold. (1): hypoglycemic, gastric emptying inhibitory, and gastroprotective principles and new oleanane-type triterpene oligoglycosides, calendasaponins A, B, C, and D, from Egyptian Calendula officinalis. Chem Pharm Bull. 49(7):863–870.
  • Zaki A, Ashour A, Mira A, Kishikawa A, Nakagawa T, Zhu Q, Shimizu K. 2016. Biological activities of oleanolic acid derivatives from Calendula officinalis seeds. Phytother Res. 30(5):835–841.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.