101. Characterization of terpenoids from the root of Ceriops tagal with antifouling activity.
- Author
-
Chen JD, Yi RZ, Lin YM, Feng DQ, Zhou HC, and Wang ZC
- Subjects
- Animals, Larva drug effects, Magnetic Resonance Spectroscopy, Molecular Conformation, Plant Roots chemistry, Plant Roots metabolism, Rhizophoraceae metabolism, Structure-Activity Relationship, Terpenes isolation & purification, Terpenes pharmacology, Thoracica drug effects, Thoracica growth & development, Rhizophoraceae chemistry, Terpenes chemistry
- Abstract
One new dimeric diterpenoid, 8(14)-enyl-pimar-2'(3')-en-4'(18')-en-15'(16')-endolabr- 16,15,2',3'-oxoan-16-one (1) and five known terpenoids: Tagalsin C (2), Tagalsin I (3), lup-20(29)-ene-3β,28-diol (4), 3-oxolup-20(29)-en-28-oic acid (5) and 28-hydroxylup- 20(29)-en-3-one (6) were isolated from the roots of the mangrove plant Ceriops tagal. Their structures and relative stereochemistry were elucidated by means of extensive NMR, IR and MS analysis. The antifouling activity against larval settlement of the barnacle Balanus albicostatus were evaluated using capsaicin as a positive control. All these terpenoids exhibited antifouling activity against cyprid larvae of the barnacle without significant toxicity. The structure-activity relationship results demonstrated that the order of antifouling activity was diterpenoid (Compound 2) > triterpenoid (Compounds 4, 5 and 6) > dimeric diterpenoid (Compounds 1 and 3). The functional groups on the C-28 position of lupane triterpenoid significantly affect the antifouling activity. The diterpenoid dimmer with two identical diterpenoid subunits might display more potent antifouling activity than one with two different diterpenoid subunits. The stability test showed that Compounds 2, 4, 5 and 6 remained stable over 2-month exposure under filtered seawater.
- Published
- 2011
- Full Text
- View/download PDF