A'/> Therapeutic potentials of natural compounds acting on cyclic nucleotide phosphodiesterase families
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Therapeutic potentials of natural compounds acting on cyclic nucleotide phosphodiesterase families

机译:作用于循环核苷酸磷酸二酯酶酶酶系列的天然化合物的治疗潜力

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Abstract Intracellular cyclic AMP and/or cyclic GMP are characterized in the 1960th. These second messengers, hydrolysed specifically by cyclic nucleotide phosphodiesterase (PDE), play a major role in intracellular signalling. Natural products have been a rich source of drug discovery, Theophylline and Methylxanthine originated from tea leaves used for asthma treatment, whereas, Papaverine, a natural isoquinolein originated from Papaver somniferum traditionally used in impotency, altogether as caffeine where firstly described as PDE-inhibiting compounds. Since that time, the knowledge in PDE field has been drastically increased, allowing the design and development of new therapeutic drugs acting against different pathologies in the nanomolar range. During this period some natural compounds have been identified as PDE inhibitors and used in that context to investigate their therapeutic potential effects. The aim of this literature review is to point out the reported data and demonstrating the contribution of natural characterized molecules as PDE inhibitors in various pathologies that can open new fields of research for drug discovery, notably in epigenetic regulation. Highlights
机译:<![cdata [ 抽象 细胞内循环AMP和/或循环GMP的特征在于1960年。这些第二信使由循环核苷酸磷酸二酯酶(PDE)特别洗脱,在细胞内信号传导中起主要作用。天然产品一直是药物发现的丰富来源,茶碱和甲基黄嘌呤起源于用于哮喘治疗的茶叶,而罂粟碱,源自西喹啉源于罂粟属Somniferum 传统上用于恒定,首先被描述为抑制PDE抑制化合物的咖啡因。从那时起,PDE领域的知识已经大幅增加,允许在纳米摩尔范围内的不同病理作用的新治疗药物的设计和开发。在此期间,已经将一些天然化合物鉴定为PDE抑制剂,并用于该背景以研究其治疗潜在的效果。该文献综述的目的是指出报告的数据,并证明了各种病理中的PDE抑制剂的自然特征分子的贡献,可以开辟药物发现的新研究领域,特别是在表观遗传调节中。 亮点 < CE:列表项目

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