Diterpene compound kalihinol and use thereof
A technology for compounds and diterpenes, applied in the field of diterpenoids, can solve the problem of no anti-fouling active diterpenoids and the like, and achieve the effect of obvious anti-fouling activity
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Embodiment 1
[0017] Embodiment 1. prepare diterpenoid kalihinol T of the present invention
[0018] 1. Preparation of Total Extract
[0019] Take the South China Sea sponge A.cavernosa with a wet weight of 5.5 kg, use 10 times the volume of acetone solution to leak and extract, combine the extracts, and recover the solvent under reduced pressure to obtain a crude extract;
[0020] 2. Separation and purification
[0021] The crude extract was dissolved in water, extracted three times with dichloromethane, the extract was dispersed in 60%-90% methanol and extracted three times with petroleum ether and dichloromethane successively, and the solvent was recovered under reduced pressure to obtain the petroleum ether fraction (49g) and Dichloromethane fraction (30g) extract; put the dichloromethane extract on silica gel decompression column chromatography as usual, use petroleum ether-acetone system at 100:1-50:1-30:1-15:1-10: 1-5:1-1:1 for gradient elution, according to the difference in polar...
Embodiment 2
[0027] Embodiment 2: Antifouling activity test of the compound of the present invention
[0028] The most harmful fouling organism barnacle B. amphitrite larvae were selected to establish the anti-fouling activity screening model. Adult barnacles were collected from the intertidal zone of Hong Kong (22°19'N, 114°16'E) and fed on Chaetoceros gracilis, and were cultured from nauplii to Venus larvae in 0.22-μm-filtered seawater stage, the culture temperature is 28°C, and the anti-fouling activity of Venus stage larvae is tested.
[0029] The test compound kalihinol T was dissolved in dimethyl sulfoxide to form a series of concentration gradients (0.5-10 μg / ml), and sterile filtered seawater was used as the control group. Take about 20 barnacle larvae and put them into a 24-well polystyrene plate, add 1ml of test solution to each well, and make 5 replicate samples for each concentration, and place the 24-well cell culture plate in a 30°C incubator for 24 hours. Observe the numbe...
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