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Entonalactams A-C: Isoindolinone derivatives from an Australian rainforest fungus belonging to the genus Entonaema

机译:Entonalactams A-C:属于Entonaema属的澳大利亚雨林真菌中的异吲哚啉酮衍生物

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Bioassay-guided fractionation of an antimalarial DCM/MeOH extract derived from the Australian rainforest fungus Entonaema sp. resulted in the isolation of three new isoindolinone derivatives, entonalactams A-C (1-3), along with the known natural products 3-methoxy-5-methylbenzene-1,2-diol (4), daldinal B (5), and ergosta-4,6,8(14),22-tetraen-3-one (6). The chemical structures of the new secondary metabolites were determined following extensive 1D/2D NMR and MS data analysis. A single crystal X-ray structure for entonalactam A (1) confirmed the NMR-based structure assignment. Entonalactams A-C (1-3) were all determined to be racemic based on chiro-optical data. All secondary metabolites were tested in vitro against Plasmodium falciparum malaria parasites, and ergosta-4,6,8(14),22-tetraen-3-one (6) was identified as the most active compound with 66% inhibition at 50 mu M. (C) 2015 Elsevier Ltd. All rights reserved.
机译:源自澳大利亚雨林真菌Entonaema sp。的抗疟疾DCM / MeOH提取物的生物测定指导分馏。导致分离出三种新的异吲哚啉酮衍生物,戊内酰胺AC(1-3)以及已知的天然产物3-甲氧基-5-甲基苯-1,2-二醇(4),Daldinal B(5)和ergosta- 4,6,8(14),22-四烯-3-一(6)。在广泛的1D / 2D NMR和MS数据分析之后,确定了新的次生代谢产物的化学结构。对戊内酰胺A(1)的单晶X射线结构证实了基于NMR的结构归属。根据手性光学数据,确定所有内酰胺A-C(1-3)是外消旋的。所有次生代谢产物均经过体外抗恶性疟原虫疟原虫测试,ergosta-4,6,8(14),22-tetraen-3-one(6)被鉴定为活性最强的化合物,在50μM时抑制率达66% (C)2015 Elsevier Ltd.保留所有权利。

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