Data On Percentage Coral Reef Cover In Small Islands Bunaken National Park.

This article describes the data on coral reef percent cover small islands (Bunaken Island; Siladen Island; Manado Tua Island; Mantehage Island; Nain Island) in Bunaken National Park, Noth Sulawesi Province, Indonesia. The data of coral percent cover from 20 stations (1000 quadrans), surveys were done by scuba diving along 50 m belt transects established on upper reef slope, mostly with depths ranging from 5 to 10 m. The method Used Underwater Photo Transect (UPT) and Coral Point Count with excel (CPCe) analysis. Percentage of coral cover between 6,27% and 69,20%. Manado Tua Island has a percentage of coral cover 42,02%, Bunaken Island 39,63%, Mantehage Island 29,10%, Siladen Island 27,87%, and Nain Island 25,97%. The average of live coral cover on the five islands is 32.92% with moderate category [2].

Absolute Structures of Wedelolide Derivatives and Structure-Activity Relationships of Protein Tyrosine Phosphatase 1B Inhibitory ent-Kaurene Diterpenes from Aerial Parts of Wedelia spp. Collected in Indonesia and Japan.

Two sesquiterpene lactones with the (9R)-eudesman-9,12-olide framework, wedelolides I and J, have been isolated together with five eudesmanolide sesquiterpenes and twelve ent-kaurene diterpenes from the aerial parts of Indonesian Wedelia prostrata. The absolute configurations of wedelolides I and J, proposed in the previous communication, were proven by comparing their experimental Electronic Circular Dichroism (ECD) spectra with the calculated ECD spectrum of wedelolide I. The phytochemical study on the aerial parts of Okinawan Wedelia chinensis led to the isolation of three other eudesmanolide sesquiterpenes in addition to the three sesquiterpenes and eleven diterpenes isolated from the Indonesian W. prostrata as above. However, the wedelolide derivatives found in the Indonesian plant were not detected. Among these compounds, most of the diterpenes inhibited protein tyrosine phosphatase (PTP) 1B activity, and a structure-activity relationship study revealed that the cinnamoyl group enhanced inhibitory activity. Therefore, two ent-kaurene derivatives with and without a cinnamoyl group were examined for the ability to accumulate phosphorylated-Akt (p-Akt) because PTP1B dephosphorylates signal transduction from the insulin receptor such as phosphorylated Akt, a key downstream effector. However, neither compound enhanced insulin-stimulated p-Akt levels in two human hepatoma cell lines (Huh-7 and HepG2) at non-cytotoxic doses.