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Chia-Chi Peng Chiung-Yao Huang Atallah F. Ahmed Tsong-Long Hwang Jyh-Horng Sheu 《Marine drugs》2020,18(11)
The present investigation on chemical constituents of the soft coral Sarcophyton cherbonnieri resulted in the isolation of seven new cembranoids, cherbonolides F–L (1–7). The chemical structures of 1–7 were determined by spectroscopic methods, including infrared, one- and two-dimensional (1D and 2D) NMR (COSY, HSQC, HMBC, and NOESY), MS experiments, and a chemical reduction of hydroperoxide by triphenylphosphine. The anti-inflammatory activities of 1–7 against neutrophil proinflammatory responses were evaluated by measuring their inhibitory ability toward N-formyl-methionyl-leucyl-phenylalanine/cytochalasin B (fMLF/CB)-induced superoxide anion generation and elastase release in primary human neutrophils. The results showed that all isolates exhibited moderate activities, while cherbonolide G (2) and cherbonolide H (3) displayed a more active effect than others on the inhibition of elastase release (48.2% ± 6.2%) and superoxide anion generation (44.5% ± 4.6%) at 30 µM, respectively. 相似文献
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In order to search for new bioactive substances from marine organisms, we have investigated the acetone extracts of the soft coral Sarcophyton ehrenbergi collected at San-Hsian-Tai, Taitong County, Taiwan. Chromatographic fractionation of the extracts of the octocoral S. ehrenbergi led to the isolation of three new cembranoids, (+)-12-ethoxycarbonyl-11Z-sarcophine (1), ehrenbergol A and B (2 and 3). The structures of these isolated metabolites were elucidated through extensive spectroscopic analyses. Moreover, metabolites 1-3 were evaluated in vitro for their cytotoxicity towards selected cancer cell lines and antiviral activity against human cytomegalovirus (HCMV). 相似文献
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Ahmed Elkhateeb Ahmed A. El-Beih Amira M. Gamal-Eldeen Montaser A. Alhammady Shinji Ohta Paul W. Paré Mohamed-Elamir F. Hegazy 《Marine drugs》2014,12(4):1977-1986
Chemical investigations of the Egyptian soft coral Sarcophyton ehrenbergi have led to the isolation of compounds 1–3 as well as the previously reported marine cembranoid diterpene sarcophine (4). Structures were elucidated by comprehensive NMR and HRMS experimentation. Isolated compounds were in vitro assayed for cytotoxic activity against human hepatocarcinoma (HepG2) and breast adenocarcinoma (MCF-7) cell lines. 相似文献
5.
Active compounds from natural products have been widely studied. The anti-tumor effects of 13-acetoxysarcocrassolide isolated from Formosan soft coral Sarcophyton crassocaule on bladder cancer cells were examined in this study. An MTT assay showed that 13-acetoxysarcocrassolide was cytotoxic to bladder female transitional cancer (BFTC) cells. We determined that the BFTC cells underwent cell death through apoptosis by flow cytometry. Due to the highly-migratory nature of the BFTC cells, the ability of 13-acetoxysarcocrassolide to stop their migration was assessed by a wound healing assay. To determine which proteins were affected in the BFTC cells upon treatment, a comparative proteomic analysis was performed. By LC-MS/MS analysis, we identified that 19 proteins were up-regulated and eight were down-regulated. Seven of the proteins were confirmed by western blotting analysis. This study reveals clues to the potential mechanism of the cytotoxic effects of 13-acetoxysarcocrassolide on BFTC cells. Moreover, it suggests that PPT1 and hnRNP F could be new biomarkers for bladder cancer. The results of this study are also helpful for the diagnosis, progression monitoring and therapeutic strategies of transitional cell tumors. 相似文献
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Zhifang Xi Wei Bie Wei Chen Dong Liu Leen van Ofwegen Peter Proksch Wenhan Lin 《Marine drugs》2013,11(9):3186-3196
Four new cembrane-type diterpenoids, sarcophyolides B–E (1–4), along with 11 known analogues were isolated from the soft coral Sarcophyton elegans. The structures of new compounds 1–4 were established on the basis of spectroscopic analysis and chemical conversion. The new cembranoids sarcophyolides B (1) and lobocrasol were found to exhibit potent inhibition against A2780 human ovarian tumor cells. 相似文献
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Chia-Chi Peng Tzu-Yin Huang Chiung-Yao Huang Tsong-Long Hwang Jyh-Horng Sheu 《Marine drugs》2021,19(5)
Two new isosarcophine derivatives, cherbonolides M (1) and N (2), were further isolated from a Formosan soft coral Sarcophyton cherbonnieri. The planar structure and relative configuration of both compounds were established by the detailed analysis of the IR, MS, and 1D and 2D NMR data. Further, the absolute configuration of both compounds was determined by the comparison of CD spectra with that of isosarcophine (3). Notably, cherbonolide N (2) possesses the unique cembranoidal scaffold of tetrahydrooxepane with the 12,17-ether linkage fusing with a γ-lactone. In addition, the assay for cytotoxicity of both new compounds revealed that they showed to be noncytotoxic toward the proliferation of A549, DLD-1, and HuCCT-1 cell lines. Moreover, the anti-inflammatory activities of both metabolites were carried out by measuring the N-formyl-methionyl-leucyl-phenylalanine/cytochalasin B (fMLF/CB)-induced generation of superoxide anion and elastase release in the primary human neutrophils. Cherbonolide N (2) was found to reduce the generation of superoxide anion (20.6 ± 6.8%) and the elastase release (30.1 ± 3.3%) in the fMLF/CB-induced human neutrophils at a concentration of 30 μM. 相似文献
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Mahmoud A. A. Ibrahim Alaa H. M. Abdelrahman Mohamed A. M. Atia Tarik A. Mohamed Mahmoud F. Moustafa Abdulrahim R. Hakami Shaden A. M. Khalifa Fahad A. Alhumaydhi Faris Alrumaihi Syed Hani Abidi Khaled S. Allemailem Thomas Efferth Mahmoud E. Soliman Paul W. Par Hesham R. El-Seedi Mohamed-Elamir F. Hegazy 《Marine drugs》2021,19(7)
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Tarik A. Mohamed Abdelsamed I. Elshamy Asmaa M. Abdel-Tawab Mona M. AbdelMohsen Shinji Ohta Paul W. Pare Mohamed-Elamir F. Hegazy 《Marine drugs》2021,19(9)
The soft coral genus Sarcophyton contains the enzymatic machinery to synthesize a multitude of cembrene-type diterpenes. Herein, highly oxygenated cembrenoids, sarcoconvolutum A–E (1–5) were purified and characterized from an ethyl acetate extract of the red sea soft coral, Sarcophyton convolutum. Compounds were assemblies according to spectroscopic methods including FTIR, 1D- and 2D-NMR as well as HRMS. Metabolite cytotoxicity was tested against lung adenocarcinoma, cervical cancer, and oral-cavity carcinoma (A549, HeLa and HSC-2, respectively). The most cytotoxic compound, (4) was observed to be active against cell lines A549 and HSC-2 with IC50 values of 49.70 and 53.17 μM, respectively. 相似文献
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Three soft coral cuttings (finger soft coral, Sinularia sp.; black finger soft coral, Cladiella sp. and leather mushroom soft coral, Sarcophyton sp.) were selected to distinguish among the effects of five methods of attachment (adhering, containing, impaling, tethering and a natural attachment method used as a control) in a recirculating seawater system on healing time, time of self‐attachment, development of the cuttings and final survival. Three replicate and 30 cuttings per replicate (n = 30) were used for each treatment and the experimental period was 70 days. The results showed that the cuttings of Sinularia sp., Sarcophyton sp. and Cladiella sp. had already healed the wound area with pigmentation between 7 and 12 days for all the methods of attachment. The shortest time of self‐attachment for the Sinularia sp., Sarcophyton sp., and Cladiella sp. cuttings was obtained in the impaling method, with average values of 8.2 ± 0.9 days, 6.1 ± 0.1 days and 9.00 ± 0.8 days respectively. At the end of the experiment, the highest average final survival values of the Sinularia sp., Sarcophyton sp. and Cladiella sp. cuttings were obtained in the impaling method (86.7 ± 5.7%), the containing method (93.3 ± 5.7%) and the containing method (53.3 ± 5.7%), respectively. It was concluded from the study that the suitable methods of attachment for each soft coral were different and these methods are available for use in targeted propagation farms for restoration purposes. 相似文献