Structural and Stereochemical Studies of Laurokamurols A-C, Uncommon Bis-sesquiterpenoids from the Chinese Red Alga Laurencia okamurai Yamada

Xiao Lu Li, T. Kurtán, Jun Chi Hu, Attila Mándi, Jia Li, Xu Wen Li, Yue Wei Guo

Research output: Contribution to journalArticle

15 Citations (Scopus)

Abstract

Three novel heterodimeric laurane-type sesquiterpenoids, laurokamurols A-C (1-3), along with eight known related monomeric ones (4-11) were isolated from the East China Sea red alga Laurencia okamurai Yamada. The absolute configurations of the new bis-sesquitepenoids, especially their axial chirality, were determined by extensive spectroscopic analyses and TDDFT-ECD method. All of the new compounds showed promising PTP1B inhibitory activities with IC50 values comparable to the positive control, indicating them as potential food additives or pharmaceutical drug leads toward obesity or diabetes.

Original languageEnglish
Pages (from-to)1550-1555
Number of pages6
JournalJournal of Agricultural and Food Chemistry
Volume65
Issue number8
DOIs
Publication statusPublished - Mar 1 2017

Fingerprint

Laurencia
Rhodophyta
Algae
sesquiterpenoids
Food additives
drugs
Food Additives
East China Sea
Chirality
food additives
Medical problems
Oceans and Seas
Pharmaceutical Preparations
Inhibitory Concentration 50
inhibitory concentration 50
diabetes
China
obesity
Obesity
methodology

Keywords

  • axial chirality
  • laurane
  • PTP1B
  • red alga
  • sesquiterpenoid

ASJC Scopus subject areas

  • Chemistry(all)
  • Agricultural and Biological Sciences(all)

Cite this

Structural and Stereochemical Studies of Laurokamurols A-C, Uncommon Bis-sesquiterpenoids from the Chinese Red Alga Laurencia okamurai Yamada. / Li, Xiao Lu; Kurtán, T.; Hu, Jun Chi; Mándi, Attila; Li, Jia; Li, Xu Wen; Guo, Yue Wei.

In: Journal of Agricultural and Food Chemistry, Vol. 65, No. 8, 01.03.2017, p. 1550-1555.

Research output: Contribution to journalArticle

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