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首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Synthesis of xanthone derivatives based on α-mangostin and their biological evaluation for anti-cancer agents
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Synthesis of xanthone derivatives based on α-mangostin and their biological evaluation for anti-cancer agents

机译:基于α-Mangostin的黄酮衍生物的合成及其抗癌药的生物学评价

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A xanthone-derived natural product, α-mangostin is isolated from various parts of the mangosteen, Garcinia mangostana L. (Clusiaceae), a well-known tropical fruit. Novel xanthone derivatives based on α-mangostin were synthesized and evaluated as anti-cancer agents by cytotoxicity activity screening using 5 human cancer cell lines. Some of these analogs had potent to moderate inhibitory activities. The structure-activity relationship studies revealed that phenol groups on C3 and C6 are critical to anti-proliferative activity and C4 modification is capable to improve both anti-cancer activity and drug-like properties. Our findings provide new possibilities for further explorations to improve potency.
机译:黄原酮衍生的天然产物α-芒果是从山竹的不同部分中分离出来的,山竹是众所周知的热带水果,即藤黄(Carcinia mangostana L.(Clusiaceae))。合成了基于α-Mangostin的新型黄酮衍生物,并通过使用5种人类癌细胞系的细胞毒性活性筛选将其作为抗癌药进行了评估。这些类似物中的一些具有强至中等的抑制活性。结构-活性关系研究表明,C3和C6上的酚基对抗增殖活性至关重要,而C4修饰能够提高抗癌活性和类药物性能。我们的发现为进一步探索以提高效力提供了新的可能性。

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