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Oleanane triterpenes as protein tyrosine phosphatase 1B (PTP1B) inhibitors from Camellia japonica

机译:茶油素三萜类化合物作为山茶的蛋白质酪氨酸磷酸酶1B(PTP1B)抑制剂

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Protein tyrosine phosphatase 1B (PTP1B) plays a key role in metabolic signaling, thereby making it an exciting drug target for type 2 diabetes and obesity. Besides, there is substantial evidence that shows its overexpression is involved in breast cancer, which suggests that selective PTP1B inhibition might be effective in breast cancer treatment. As part of our continuous research on PTP1B inhibitors from medicinal plants, four oleanane-type triterpenes were isolated from an EtOAc-soluble extract of fruit peels of Camellia japonica (Theaceae), together with 6 previously known compounds of this class. Their structures were determined on the basis of spectroscopic data analysis (UV, IR, H-1 and (CNMR)-C-13, HMBC, HSQC, NOESY, and MS). All isolates were evaluated for their inhibitory effects on PTP1B, as well as their cytotoxic effects against human breast cancer cell lines MCF7, MCF7/ADR, and MDA-MB-231. Several compounds with OH-3 or/and COOH-28 functionalities showed strong PTP1B inhibitory activity (IC50 values ranging from 3.77 +/- 0.11 to 6.40 +/- 0.81 mu M) as well as significant cytotoxicity (IC50 values ranging from 0.51 +/- 0.05 to 13.55 +/- 1.44 mu M)
机译:蛋白质酪氨酸磷酸酶1B(PTP1B)在代谢信号传导中起关键作用,因此使其成为2型糖尿病和肥胖症的激动人心的药物靶标。此外,有大量证据表明其过度表达与乳腺癌有关,这表明选择性抑制PTP1B可能在乳腺癌治疗中有效。作为我们对药用植物PTP1B抑制剂的持续研究的一部分,从山茶(Theaceae)的果皮的EtOAc可溶性提取物中与4种先前已知的此类化合物分离出了四种齐墩果烷型三萜。根据光谱数据分析(UV,IR,H-1和(CNMR)-C-13,HMBC,HSQC,NOESY和MS)确定其结构。评估了所有分离株对PTP1B的抑制作用以及对人乳腺癌细胞MCF7,MCF7 / ADR和MDA-MB-231的细胞毒性作用。几种具有OH-3或/和COOH-28功能的化合物显示出强大的PTP1B抑制活性(IC50值为3.77 +/- 0.11至6.40 +/- 0.81μM)以及显着的细胞毒性(IC50值为0.51 + / -0.05至13.55 +/- 1.44μM)

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