1. Academic Validation
  2. Sesquiterpenes from the red alga Laurencia tristicha

Sesquiterpenes from the red alga Laurencia tristicha

  • J Nat Prod. 2005 Jun;68(6):915-9. doi: 10.1021/np050096g.
Jie Sun 1 Dayong Shi Ming Ma Shuai Li Sujuan Wang Lijun Han Yongchun Yang Xiao Fan Jiangong Shi Lan He
Affiliations

Affiliation

  • 1 Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing.
Abstract

Seven new Sesquiterpenes (1-7), together with seven known Sesquiterpenes, aplysin (8), aplysinol (9), gossonorol (10), 7,10-epoxy-ar-bisabol-11-ol (11), 10-epi-7,10-epoxy-ar-bisabol-11-ol (12), johnstonol (13), and laurebiphenyl (14), have been isolated from the red alga Laurencia tristicha. The structures of new compounds were established as laur-11-en-2,10-diol (1), laur-11-en-10-ol (2), laur-11-en-1,10-diol (3), 4-bromo-1,10-epoxylaur-11-ene (4), cyclolauren-2-ol (5), laurentristich-4-ol (6), and ar-bisabol-9-en-7,11-diol (7) by means of spectroscopic methods including IR, HRMS, and 1D and 2D NMR techniques. Compound 6 possessed a novel rearranged skeleton. All compounds were tested against several human Cancer cell lines including lung adenocarcinoma (A549), stomach Cancer (BGC-823), hepatoma (Bel 7402), colon Cancer (HCT-8), and HELA cell lines. Laurebiphenyl (14) showed moderate cytotoxicity against all tested cell lines, with IC(50) values of 1.68, 1.22, 1.91, 1.77, and 1.61 microg/mL, respectively. Other compounds were inactive (IC(50) > 10 microg/mL).

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