Recent advances in the development of P2Y14R inhibitors: a patent and literature review (2018-present).

IF 5.4 2区 医学 Q1 CHEMISTRY, MEDICINAL
Expert Opinion on Therapeutic Patents Pub Date : 2024-08-01 Epub Date: 2024-06-19 DOI:10.1080/13543776.2024.2369634
Kai Wang, Fen Zhong, Zhou-Dong Zhang, Huan-Qiu Li, Sheng Tian
{"title":"Recent advances in the development of P2Y<sub>14</sub>R inhibitors: a patent and literature review (2018-present).","authors":"Kai Wang, Fen Zhong, Zhou-Dong Zhang, Huan-Qiu Li, Sheng Tian","doi":"10.1080/13543776.2024.2369634","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>The P2Y<sub>14</sub> receptor (P2Y<sub>14</sub>R), a member of the G protein-coupled receptor family, is activated by extracellular nucleotides. Due to its involvement in inflammatory, immunological and other associated processes, P2Y<sub>14</sub>R has emerged as a promising therapeutic target. Despite lacking a determined three-dimensional crystal structure, the homology modeling technique based on closely related P2Y receptors' crystallography has been extensively utilized for developing active compounds targeting P2Y<sub>14</sub>R. Recent discoveries have unveiled numerous highly effective and subtype-specific P2Y<sub>14</sub>R inhibitors. This study presents an overview of the latest advancements in P2Y<sub>14</sub>R inhibitors.</p><p><strong>Areas covered: </strong>This review presents an overview of the advancements in P2Y<sub>14</sub>R inhibitor research over the past five years, encompassing new patents, journal articles, and highlighting the therapeutic prospects inherent in these compounds.</p><p><strong>Expert opinion: </strong>The recent revelation of the vast potential of P2Y<sub>14</sub>R inhibitors has led to the development of novel compounds that exhibit promising capabilities for the treatment of sterile inflammation of the kidney, potentially diabetes, and asthma. Despite being a relatively nascent class of compounds, certain members have already exhibited their capacity to surmount specific challenges posed by conventional P2Y<sub>14</sub>R inhibitors. Targeting P2Y<sub>14</sub>R through small molecules may present a promising therapeutic strategy for effectively managing diverse inflammatory diseases.</p>","PeriodicalId":12314,"journal":{"name":"Expert Opinion on Therapeutic Patents","volume":" ","pages":"611-625"},"PeriodicalIF":5.4000,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Expert Opinion on Therapeutic Patents","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/13543776.2024.2369634","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/6/19 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: The P2Y14 receptor (P2Y14R), a member of the G protein-coupled receptor family, is activated by extracellular nucleotides. Due to its involvement in inflammatory, immunological and other associated processes, P2Y14R has emerged as a promising therapeutic target. Despite lacking a determined three-dimensional crystal structure, the homology modeling technique based on closely related P2Y receptors' crystallography has been extensively utilized for developing active compounds targeting P2Y14R. Recent discoveries have unveiled numerous highly effective and subtype-specific P2Y14R inhibitors. This study presents an overview of the latest advancements in P2Y14R inhibitors.

Areas covered: This review presents an overview of the advancements in P2Y14R inhibitor research over the past five years, encompassing new patents, journal articles, and highlighting the therapeutic prospects inherent in these compounds.

Expert opinion: The recent revelation of the vast potential of P2Y14R inhibitors has led to the development of novel compounds that exhibit promising capabilities for the treatment of sterile inflammation of the kidney, potentially diabetes, and asthma. Despite being a relatively nascent class of compounds, certain members have already exhibited their capacity to surmount specific challenges posed by conventional P2Y14R inhibitors. Targeting P2Y14R through small molecules may present a promising therapeutic strategy for effectively managing diverse inflammatory diseases.

P2Y14R 抑制剂开发的最新进展:专利和文献综述(2018 年至今)。
简介P2Y14 受体(P2Y14R)是 G 蛋白偶联受体家族的成员,由细胞外核苷酸激活。由于参与炎症、免疫和其他相关过程,P2Y14R 已成为一个很有前景的治疗靶点。尽管缺乏确定的三维晶体结构,但基于密切相关的 P2Y 受体晶体学的同源建模技术已被广泛用于开发针对 P2Y14R 的活性化合物。最近的发现揭示了许多高效的亚型特异性 P2Y14R 抑制剂。本研究概述了 P2Y14R 抑制剂的最新进展:本综述概述了过去五年中 P2Y14R 抑制剂研究的进展,包括新专利和期刊论文,并强调了这些化合物固有的治疗前景:最近,P2Y14R 抑制剂的巨大潜力被揭示出来,导致新型化合物的开发,这些化合物在治疗肾脏无菌性炎症、潜在糖尿病和哮喘方面表现出良好的前景。尽管P2Y14R抑制剂是一类相对新兴的化合物,但其某些成员已经显示出了克服传统P2Y14R抑制剂所带来的特定挑战的能力。通过小分子靶向 P2Y14R 可为有效治疗各种炎症性疾病提供一种前景广阔的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
12.10
自引率
1.50%
发文量
50
审稿时长
6-12 weeks
期刊介绍: Expert Opinion on Therapeutic Patents (ISSN 1354-3776 [print], 1744-7674 [electronic]) is a MEDLINE-indexed, peer-reviewed, international journal publishing review articles on recent pharmaceutical patent claims, providing expert opinion the scope for future development, in the context of the scientific literature. The Editors welcome: Reviews covering recent patent claims on compounds or applications with therapeutic potential, including biotherapeutics and small-molecule agents with specific molecular targets; and patenting trends in a particular therapeutic area Patent Evaluations examining the aims and chemical and biological claims of individual patents Perspectives on issues relating to intellectual property The audience consists of scientists, managers and decision-makers in the pharmaceutical industry and others closely involved in R&D Sample our Bioscience journals, sign in here to start your access, Latest two full volumes FREE to you for 14 days.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信