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Suggestion of the Relative Configuration of a Red Alga-DerivedPolyether Callicladol Based on the Model Synthesis

机译:基于模型合成的红色藻类衍生的药物呼叫者的相对配置的建议

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Callicladol (1),a marine triterpene polyether isolated from the red algae Laurenciacalliclada by Suzuki et al.in 1993,exhibits potent cytotoxicity against P388 murineleukemia cell.The structural feature of 1 are a bromine-containing THP ring (A ring),adioxabicyclo[4.4.0]decane ring (BC rings),and two THF rings (DE rings).It is also rare for1 to possess a hydroxy group at the C5 position in A ring,which is unprecedented in otherthyrsiferol congeners.
机译:Callicladol(1),由Suzuki等人分离的海洋三萜酰胺聚醚通过Suzuki等人分离出来的P388穆里奈血症细胞的有效细胞毒性。1是含溴的THP环(环),Adioxabicyclo [ 4.4.0]癸烷环(BC环)和两个THF环(DE RINGS)。它也是罕见的FOR1在环中的C5位置中具有羟基的羟基,其在其他替代的替代品中是前所未有的。

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