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Chemistry and Selective Tumor Cell Growth Inhibitory Activity of Polyketides from the South China Sea Sponge Plakortis sp.

机译:南海海绵Plakortis sp。的聚酮化合物的化学和选择性肿瘤细胞生长抑制活性。

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摘要

Simplextone E (>1), a new metabolite of polyketide origin, was isolated with eight known analogues (>2–>9) from the South China Sea sponge Plakortis sp. The relative configuration of the new compound was elucidated by a detailed analysis of the spectroscopic data and quantum mechanical calculation of NMR chemical shifts, aided by the newly reported DP4+ approach. Its absolute configuration was determined by the TDDFT/ECD calculation. Simplextone E (>1) is proven to be one of the isomers of simplextone D. The absolute configuration at C-8 in alkyl chain of plakortone Q (>2) was also assigned based on the NMR calculation. In the preliminary in vitro bioassay, compounds >6 and >7 showed a selective growth inhibitory activity against HCT-116 human colon cancer cells with IC50 values of 8.3 ± 2.4 and 8.4 ± 2.3 μM, corresponding to that of the positive control, adriamycin (IC50 4.1 μM). The two compounds also showed selective activities towards MCF-7 human breast cancer and K562 human erythroleukemia cells while compound >3 only displayed weak activity against K562 cells.
机译:从南海中分离出八种已知类似物(> 2 – > 9 )分离出一种新的聚酮化合物代谢物Simplextone E(> 1 )。海绵Plakortis sp。通过对光谱数据的详细分析和NMR化学位移的量子力学计算,借助新报道的DP4 +方法,阐明了新化合物的相对构型。其绝对配置由TDDFT / ECD计算确定。已证明Simplextone E(> 1 )是Simplextone D的异构体之一。还指定了plakortone Q(> 2 )烷基链中C-8的绝对构型。根据NMR计算。在初步的体外生物测定中,化合物> 6 和> 7 显示出对HCT-116人结肠癌细胞的选择性生长抑制活性,IC50值为8.3±2.4和8.4±2.3 μM,对应于阳性对照阿霉素(IC50 4.1μM)。两种化合物还显示出对MCF-7人乳腺癌和K562人红白血病细胞的选择性活性,而化合物> 3 仅表现出对K562细胞的弱活性。

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