首页> 美国卫生研究院文献>Frontiers in Chemistry >(±)-Peniorthoesters A and B Two Pairs of Novel Spiro-Orthoester en-antiomers With an Unusual 146-Trioxaspi-ro4.5decane-7-One Unit From Penicillium minioluteum
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(±)-Peniorthoesters A and B Two Pairs of Novel Spiro-Orthoester en-antiomers With an Unusual 146-Trioxaspi-ro4.5decane-7-One Unit From Penicillium minioluteum

机译:(±)-高级原酸酯A和B两对新的螺-原酸酯对映体具有来自小青霉的146-Trioxaspi-ro 4.5癸烷-7-一个单元

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摘要

(±)-Peniorthoesters A and B (±>1 and ±>2), two pairs of unprecedented spiro-orthoester enantiomers with a 1,4,6-trioxaspiro[4. 5]decane-7-one unit, were obtained from Penicillium minioluteum. Their structures were determined by spectroscopic methods, X-ray diffraction analyses, and ECD calculations. (±)-Peniorthoesters A and B are the first examples of spiro-orthoester enantiomers, and they represent the first spiro-orthoesters originating from fungi. All compounds showed potential inhibitory activities comparable to dexamethasone against NO production with IC50 values ranging from 14.2 to 34.5 μM.
机译:(±)-高级聚酯A和B(±> 1 和±> 2 ),两对前所未有的螺-原酸酯对映体,带有1,4,6-三氧杂螺[4]。 5]癸烷-7-一单位,获自小青霉。通过光谱法,X射线衍射分析和ECD计算确定其结构。 (±)-原酸酯A和B是螺-原酸酯对映体的第一个实例,它们代表源自真菌的首个螺-原酸酯。所有化合物均显示出与地塞米松相当的潜在抑制活性,其NO产生的IC50值为14.2至34.5μM。

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