lnu.sePublications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Sesquiterpene coumarins
Linnaeus University, Faculty of Science and Engineering, School of Natural Sciences.
Linnaeus University, Faculty of Science and Engineering, School of Natural Sciences.ORCID iD: 0000-0001-8899-5046
2012 (English)In: Phytochemistry Reviews, ISSN 1568-7767, E-ISSN 1572-980X, Vol. 11, no 1, p. 77-96Article in journal (Refereed) Published
Abstract [en]

Plants have a long history as therapeutic tools in the treatment of human diseases and have been used as a source of medicines for ages. In search of new biologically active natural products, many plants and herbs used in traditional medicine are screened for natural products with pharmacological activity. In this paper, we present a group of natural products, the sesquiterpene coumarins isolated from plants, and describe their wide range of biological activity. Sesquiterpene coumarins are found in some plants of the families Apiaceae (Umbelliferae), Asteraceae (Compositae) and Rutaceae. The coumarin moiety is often umbelliferone (7-hydroxycoumarin) but scopo- letin (7-hydroxy-6-methoxycoumarin) and isofraxidin (7-hydroxy-6,8-dimethoxycoumarin) are also found. These coumarins are linked to a C15 terpene moiety through an ether linkage. Another group of sesquiter- pene coumarins is the prenylated 4-hydroxycoumarins where the link between the coumarin and the C15 terpene moiety is a C–C-bond at carbon 3 of the coumarin moiety. Finally, the prenylfurocoumarin-type sesquiterpenoids are a separate group of sesquiterpene coumarins based on the suggested biosynthetic pathway. Our relatively limited knowledge on the biosynthesis of sesquiterpene coumarins is reviewed.

Place, publisher, year, edition, pages
2012. Vol. 11, no 1, p. 77-96
Keywords [en]
Farnesyldiphosphate; 4-Hydroxycoumarin; Isofraxidin; Prenylated coumarins; Prenyl-furocoumarin sesquiterpenenes; Scopoletin; Sesquiterpene coumarins; Umbelliferone
National Category
Biochemistry Molecular Biology
Research subject
Chemistry, Biochemistry
Identifiers
URN: urn:nbn:se:lnu:diva-18067DOI: 10.1007/s11101-011-9220-6ISI: 000307386900004Scopus ID: 2-s2.0-84861233635OAI: oai:DiVA.org:lnu-18067DiVA, id: diva2:511119
Available from: 2012-03-20 Created: 2012-03-20 Last updated: 2025-02-20Bibliographically approved

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full textScopushttp://www.springerlink.com/content/e4182134652nt786/

Authority records

Gliszczynska, AnnaBrodelius, Peter E.

Search in DiVA

By author/editor
Gliszczynska, AnnaBrodelius, Peter E.
By organisation
School of Natural Sciences
In the same journal
Phytochemistry Reviews
BiochemistryMolecular Biology

Search outside of DiVA

GoogleGoogle Scholar

doi
urn-nbn

Altmetric score

doi
urn-nbn
Total: 215 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf