摘要
寻找新型的基于酶的前体药物的方法旨于改进治疗药物的药理性质,例如溶解性和生物活性。二肽基肽酶IV(DPP IV/CD26,也被称为CD26)的酶活力提供了之前还未发现的一个成功的前体药物策略。本综述包括了许多酶关键步骤有效用于CD26-介导的前体药物设计。这个前体药物的概念验证被提出用于含胺类制剂合成,其通过一个酰胺结合直接将合适的二(或者低聚的)多肽部分链接到非多肽药物一个自由的氨基官能团上,这是DPP IV/CD26特有的水解性质。在设计和合成更加详细的三方前体药物系统尤其需要强调的,为了进一步扩展该策略到含羟基的药物中。应用该技术到主要的例子如抗病毒核苷以提高其水溶性和口服生物活性被着重介绍。
关键词: 含氨基药物,CD26前体药物,二肽基肽酶IV,含羟基药物,口服生物活性,多肽,稳定性,水溶性。
Current Medicinal Chemistry
Title:Dipeptidyl-Peptidase IV (DPP IV/CD26)-Activated Prodrugs: A Successful Strategy for Improving Water Solubility and Oral Bioavailability
Volume: 22 Issue: 8
Author(s): Sonsoles Velazquez, Sonia de Castro, Alberto Diez-Torrubia, Jan Balzarini and María-Jose Camarasa
Affiliation:
关键词: 含氨基药物,CD26前体药物,二肽基肽酶IV,含羟基药物,口服生物活性,多肽,稳定性,水溶性。
摘要: In the search of novel enzyme-based prodrug approaches to improve pharmacological properties of therapeutic drugs such as solubility and bioavailability, dipeptidyl-peptidase IV (DPP IV, also termed as CD26) enzyme activity provides a previously unexplored successful prodrug strategy. This review covers key aspects of the enzyme useful for the design of CD26-directed prodrugs. The proof-of-concept of this prodrug technology is provided for amine-containing agents by directly linking appropriate di- (or oligo)peptide moieties to a free amino group of a non-peptidic drug through an amide bond which is specifically hydrolized by DPP IV/CD26. Special emphasis is also made in discussing the design and synthesis of more elaborated tripartite prodrug systems, for further extension of the strategy to hydroxy-containing drugs. The application of this technology to improve water solubility and oral bioavailability of prominent examples of antiviral nucleosides is highlighted.
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Sonsoles Velazquez, Sonia de Castro, Alberto Diez-Torrubia, Jan Balzarini and María-Jose Camarasa , Dipeptidyl-Peptidase IV (DPP IV/CD26)-Activated Prodrugs: A Successful Strategy for Improving Water Solubility and Oral Bioavailability, Current Medicinal Chemistry 2015; 22 (8) . https://dx.doi.org/10.2174/0929867322666150114163449
DOI https://dx.doi.org/10.2174/0929867322666150114163449 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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