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首页> 外文期刊>RSC Advances >Jatrocurcadiones A and B: two novel diterpenoids with an unusual 10,11-seco-premyrsinane skeleton from Jatropha curcas
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Jatrocurcadiones A and B: two novel diterpenoids with an unusual 10,11-seco-premyrsinane skeleton from Jatropha curcas

机译:麻风树甲A和麻风树B:两种新的二萜类化合物,具有来自麻风树麻疯树的不寻常的10,11-seco-早稻草烷骨架

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摘要

Two novel diterpenoids, jatrocurcadiones A (1) and B (2), possessing an unusual 10,11-seco-premyrsinane skeleton were isolated from the twigs of Jatropha curcas. Their structures were determined by combined spectroscopic and chemical methods, and the absolute configurations were elucidated by quantumchemical calculations and Rh-2(OCOCF3)(4)-induced CD analysis. Jatrocurcadione A exhibited more potent inhibitory activity (IC50 = 10.0 mu M) than the positive control (curcumin, IC50 = 25.0 mu M) against thioredoxin reductase (TrxR), a potential target for cancer chemotherapy with redox balance and antioxidant functions.
机译:从麻疯树的细枝中分离出两个新颖的二萜类化合物,麻疯树甲A(1)和B(2),它们具有不寻常的10,11-seco-早稻草烷烷骨架。通过光谱和化学方法确定了它们的结构,并通过量子化学计算和Rh-2(OCOCF3)(4)诱导的CD分析阐明了其绝对构型。相对于阳性对照(姜黄素,IC50 = 25.0μM),Jatrocurcadione A对硫氧还蛋白还原酶(TrxR)表现出更强的抑制活性(姜黄素,IC50 = 25.0μM),这是具有氧化还原平衡和抗氧化功能的癌症化疗的潜在靶标。

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