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Synthesis and evaluation of asiatic acid derivatives as anti-fibrotic agents: Structure/activity studies

机译:合成和评估积雪草酸衍生物作为抗纤维化剂:结构/活性研究

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Fibrotic diseases are characterized by the over-accumulation of fibrous components in the extracellular matrix and the liver, which can lead to liver cirrhosis. Current treatment options cannot reverse or halt liver fibrosis, motivating a search for newer treatment options. Previously, we showed that asiaticoside, a bioactive triterpene glycoside from Centella asiatica, has anti-fibrotic properties. Here, the aglycone asiatic acid was chemically modified, and these derivatives were evaluated for their potential as anti-fibrotic agents. The data obtained from in vivo testing of these compounds in a rodent CCl4-induced liver injury model are discussed. The information obtained from these studies may be useful in the design of novel anti-fibrotic agents. (C) 2015 Elsevier Inc. All rights reserved.
机译:纤维化疾病的特征在于细胞外基质和肝脏中纤维成分的过度积累,这可能导致肝硬化。当前的治疗选择不能逆转或阻止肝纤维化,从而促使人们寻找新的治疗选择。以前,我们显示积雪草苷(积雪草中的一种生物活性三萜糖苷)具有抗纤维化特性。在这里,糖苷配基去甲酸经过化学修饰,评估了这些衍生物作为抗纤维化剂的潜力。讨论了在啮齿动物CCl4诱导的肝损伤模型中从这些化合物的体内测试中获得的数据。从这些研究中获得的信息可能对新型抗纤维化药物的设计有用。 (C)2015 Elsevier Inc.保留所有权利。

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