Anticancer Potential of Coumarin derivatives: A Review

R. K. K PRASAD, Kavita R. Loksh
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Abstract

Cancer can conquer or feast on nearly all portions of the body. The cumulative illness and high humanity of cancer generate an innumerable claims for the expansion of innovative anticancer drugs. Coumarin (known as 1,2-benzopyrone or o-hydroxycinnamic acid-8-lactone) encompasses a huge class of phenolic offshoots that originate in plants and they are entailed of bonded benzene and a-pyrone rings. Numerous studies have exposed that several substituents on the coumarin essential structure stimulus different biological activities. Coumarin advert a character of pathways in cancer like kinase inhibition, cell cycle annexation, angiogenesis inhibition, telomerase inhibition, antimitotic activity, carbonic anhydrase inhibition, monocarboxylate transporters inhibition, aromatase inhibition, and sulfatase inhibition. Coumarin moiety is a beneficial template for the progress of novel anticancer agents.
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香豆素衍生物的抗癌潜力综述
癌症可以征服或享用身体的几乎所有部分。癌症的累积性疾病和高人道性为创新抗癌药物的扩展提出了无数的要求。香豆素(被称为1,2-苯并吡咯酮或邻羟基肉桂酸-8-内酯)包含了一大类起源于植物的酚类分支,它们由苯和a-吡咯环结合而成。大量研究表明香豆素基本结构上的几种取代基可刺激不同的生物活性。香豆素在癌症中具有激酶抑制、细胞周期兼并、血管生成抑制、端粒酶抑制、抗有丝分裂活性、碳酸酐酶抑制、单羧酸转运体抑制、芳香化酶抑制和硫酸酯酶抑制等途径的特征。香豆素片段是开发新型抗癌药物的有益模板。
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