摘要
L-3,4-二羟基苯丙氨酸[2-氨基-3-(3,4-二羟苯基)丙酸 (L-DOPA)]是从酪氨酸翻译后修饰衍生而来,广泛存在于动植物组织中的天然成分。在代谢过程中,L-DOPA转化为儿茶酚胺神经递质,去甲肾上腺素和肾上腺素,这些物质具有不同的生物活性。帕金森病是一种神经退行性疾病,与纹状体黑质多巴胺能神经元的丢失有关,左旋多巴一直是治疗该病的首选药物。由于人口的逐步老龄化,这些疾病对社会和经济的影响非常大。本文主要研究了左旋多巴的生物效应、左旋多巴衍生物的合成以及它们在中枢神经系统疾病中的应用。其中,含肽L-DOPA(L-DOPA-Pep)具有重要的生物活性和药理作用。例如,L-DOPA类似物的α因子与G蛋白偶联受体模型相互作用、能抑制低密度脂蛋白的氧化、可以改善帕金森病的长期治疗时L-DOPA的吸收并作为皮肤保湿剂中的化学成分。此外,蛋白质中的左旋多巴残留可以作为制备胶粘剂和涂层材料的反应工具。L-DOPA-Pep通常是从简单的氨基酸,由传统的液态或固态途径合成制备。最近,预成形的肽的选择性侧链修饰也被报道用于合成直链和支链肽。本文总结了L-DOPA和多巴肽的合成以及其生物活性和药理作用的研究进展,重点关注预其新的合成方法和生物学机制。
关键词: L-DOPA,帕金森病,肽,生物活性和药理作用,合成。
Current Medicinal Chemistry
Title:Current Advances in L-DOPA and DOPA-Peptidomimetics: Chemistry, Applications and Biological Activity
Volume: 22 Issue: 36
Author(s): Bruno Mattia Bizzarri, Silvia Tortolini, Luca Rotelli, Giorgia Botta and Raffaele Saladino
Affiliation:
关键词: L-DOPA,帕金森病,肽,生物活性和药理作用,合成。
摘要: L-3,4-Dihydroxyphenylalanine [2-amino-3-(3,4-dihydroxyphenyl) propanoic acid (L-DOPA) is a natural constituent of animal and plant tissue derived from post-translational modification of the amino acid tyrosine. L-DOPA is modified during metabolism to catecholamine neurotransmitters, noradrenaline and adrenaline, which are characterized by different biological activities. L-DOPA has been the first drug of choice in the therapy of Parkinson’s disease that is a progressive neurodegenerative disorder involving the loss of dopaminergic neurons of substantia nigra pars compacta. The social and economic impact of these diseases is very high due to the progressive aging of the population. This review focuses on the biological effect of LDOPA, as well as on the synthesis of L-DOPA derivatives and their application in central nervous system diseases. Among them, L-DOPA-containing peptides (L-DOPA-Pep) show important biological and pharmacological activities. For example, L-DOPA analogues of the alpha-factor interact with models of the G proteincoupled receptor, inhibit the oxidation of low-density lipoproteins, and are used for improving L-DOPA absorption in long-term treatment of Parkinson’s disease and as skin moisturizer in cosmetic compositions. Moreover, L-DOPA residues in proteins provide reactive tools for the preparation of adhesives and coatings materials. Usually, L-DOPA-Pep is prepared by traditional liquid or solid state procedures starting from simple amino acids. Recently, selective side-chain modifications of pre-formed peptides have also been reported both for linear and branched peptides. Here, we describe the recent advances in the synthesis of L-DOPA and dopa-peptidomimetics and their biological and pharmacological activities, focusing the attention on new synthetic procedures and biological mechanism of actions.
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Bruno Mattia Bizzarri, Silvia Tortolini, Luca Rotelli, Giorgia Botta and Raffaele Saladino , Current Advances in L-DOPA and DOPA-Peptidomimetics: Chemistry, Applications and Biological Activity, Current Medicinal Chemistry 2015; 22 (36) . https://dx.doi.org/10.2174/0929867322666150625095748
DOI https://dx.doi.org/10.2174/0929867322666150625095748 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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