6α-噻唑基carboxamidonaltrexamine衍生物(NTZ)作为一种有效的中枢神经系统渗透性阿片受体调节剂,具有药物样特性,可能治疗阿片使用障碍

IF 4.9 Q1 CHEMISTRY, MEDICINAL
Boshi Huang, Hongguang Ma, Piyusha P. Pagare, Mengchu Li, Rolando E. Mendez, James C. Gillespie, Justin L. Poklis, Matthew S. Halquist, David L. Stevens, William L. Dewey, Dana E. Selley and Yan Zhang*, 
{"title":"6α-噻唑基carboxamidonaltrexamine衍生物(NTZ)作为一种有效的中枢神经系统渗透性阿片受体调节剂,具有药物样特性,可能治疗阿片使用障碍","authors":"Boshi Huang,&nbsp;Hongguang Ma,&nbsp;Piyusha P. Pagare,&nbsp;Mengchu Li,&nbsp;Rolando E. Mendez,&nbsp;James C. Gillespie,&nbsp;Justin L. Poklis,&nbsp;Matthew S. Halquist,&nbsp;David L. Stevens,&nbsp;William L. Dewey,&nbsp;Dana E. Selley and Yan Zhang*,&nbsp;","doi":"10.1021/acsptsci.4c0059310.1021/acsptsci.4c00593","DOIUrl":null,"url":null,"abstract":"<p >The development of highly potent and selective μ opioid receptor (MOR) modulators with favorable drug-like properties has always been a focus in the opioid domain. Our previous efforts led to the discovery of a lead compound designated as NAT, a potent centrally acting MOR modulator. However, the fact that NAT precipitated considerable withdrawal effects at higher doses largely impaired its further development. In the light of the concept of activity cliff and CNS multiparameter optimization algorithm, a nitrogen atom was incorporated into the thiophene ring of NAT, aiming to preserve desirable pharmacological activities and CNS permeability while alleviating withdrawal symptoms. Among all 16 new analogs, compound <b>6</b> (NTZ) exhibited improved opioid receptor selectivity, enhanced <i>in vivo</i> antagonistic effect, and overall fewer withdrawal symptoms compared to NAT. Further assessment of several key drug-like properties suggested a favorable ADMET profile of NTZ. Taken together, NTZ shows promise as a potential lead to treat opioid use disorder.</p>","PeriodicalId":36426,"journal":{"name":"ACS Pharmacology and Translational Science","volume":"7 12","pages":"4165–4182 4165–4182"},"PeriodicalIF":4.9000,"publicationDate":"2024-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/epdf/10.1021/acsptsci.4c00593","citationCount":"0","resultStr":"{\"title\":\"Discovery of 6α-Thiazolylcarboxamidonaltrexamine Derivative (NTZ) as a Potent and Central Nervous System Penetrant Opioid Receptor Modulator with Drug-like Properties for Potential Treatment of Opioid Use Disorder\",\"authors\":\"Boshi Huang,&nbsp;Hongguang Ma,&nbsp;Piyusha P. Pagare,&nbsp;Mengchu Li,&nbsp;Rolando E. Mendez,&nbsp;James C. Gillespie,&nbsp;Justin L. Poklis,&nbsp;Matthew S. Halquist,&nbsp;David L. Stevens,&nbsp;William L. Dewey,&nbsp;Dana E. Selley and Yan Zhang*,&nbsp;\",\"doi\":\"10.1021/acsptsci.4c0059310.1021/acsptsci.4c00593\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The development of highly potent and selective μ opioid receptor (MOR) modulators with favorable drug-like properties has always been a focus in the opioid domain. Our previous efforts led to the discovery of a lead compound designated as NAT, a potent centrally acting MOR modulator. However, the fact that NAT precipitated considerable withdrawal effects at higher doses largely impaired its further development. In the light of the concept of activity cliff and CNS multiparameter optimization algorithm, a nitrogen atom was incorporated into the thiophene ring of NAT, aiming to preserve desirable pharmacological activities and CNS permeability while alleviating withdrawal symptoms. Among all 16 new analogs, compound <b>6</b> (NTZ) exhibited improved opioid receptor selectivity, enhanced <i>in vivo</i> antagonistic effect, and overall fewer withdrawal symptoms compared to NAT. Further assessment of several key drug-like properties suggested a favorable ADMET profile of NTZ. Taken together, NTZ shows promise as a potential lead to treat opioid use disorder.</p>\",\"PeriodicalId\":36426,\"journal\":{\"name\":\"ACS Pharmacology and Translational Science\",\"volume\":\"7 12\",\"pages\":\"4165–4182 4165–4182\"},\"PeriodicalIF\":4.9000,\"publicationDate\":\"2024-12-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.acs.org/doi/epdf/10.1021/acsptsci.4c00593\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Pharmacology and Translational Science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acsptsci.4c00593\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Pharmacology and Translational Science","FirstCategoryId":"1085","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsptsci.4c00593","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

摘要

具有良好类药物特性的高效选择性μ阿片受体调节剂的开发一直是阿片领域的研究热点。我们之前的努力导致了一个先导化合物的发现,指定为NAT,一个有效的中央作用MOR调节剂。然而,在较高剂量下,NAT会产生相当大的戒断效应,这一事实在很大程度上损害了它的进一步发展。根据活性悬崖概念和CNS多参数优化算法,在NAT的噻吩环中加入一个氮原子,以在减轻戒断症状的同时保持理想的药理活性和CNS通透性。在所有16种新的类似物中,化合物6 (NTZ)与NAT相比,表现出更好的阿片受体选择性,增强的体内拮抗作用,总体上较少的戒断症状。进一步评估几个关键的药物样特性表明NTZ具有良好的ADMET特征。综上所述,NTZ有望成为治疗阿片类药物使用障碍的潜在线索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Discovery of 6α-Thiazolylcarboxamidonaltrexamine Derivative (NTZ) as a Potent and Central Nervous System Penetrant Opioid Receptor Modulator with Drug-like Properties for Potential Treatment of Opioid Use Disorder

The development of highly potent and selective μ opioid receptor (MOR) modulators with favorable drug-like properties has always been a focus in the opioid domain. Our previous efforts led to the discovery of a lead compound designated as NAT, a potent centrally acting MOR modulator. However, the fact that NAT precipitated considerable withdrawal effects at higher doses largely impaired its further development. In the light of the concept of activity cliff and CNS multiparameter optimization algorithm, a nitrogen atom was incorporated into the thiophene ring of NAT, aiming to preserve desirable pharmacological activities and CNS permeability while alleviating withdrawal symptoms. Among all 16 new analogs, compound 6 (NTZ) exhibited improved opioid receptor selectivity, enhanced in vivo antagonistic effect, and overall fewer withdrawal symptoms compared to NAT. Further assessment of several key drug-like properties suggested a favorable ADMET profile of NTZ. Taken together, NTZ shows promise as a potential lead to treat opioid use disorder.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
ACS Pharmacology and Translational Science
ACS Pharmacology and Translational Science Medicine-Pharmacology (medical)
CiteScore
10.00
自引率
3.30%
发文量
133
期刊介绍: ACS Pharmacology & Translational Science publishes high quality, innovative, and impactful research across the broad spectrum of biological sciences, covering basic and molecular sciences through to translational preclinical studies. Clinical studies that address novel mechanisms of action, and methodological papers that provide innovation, and advance translation, will also be considered. We give priority to studies that fully integrate basic pharmacological and/or biochemical findings into physiological processes that have translational potential in a broad range of biomedical disciplines. Therefore, studies that employ a complementary blend of in vitro and in vivo systems are of particular interest to the journal. Nonetheless, all innovative and impactful research that has an articulated translational relevance will be considered. ACS Pharmacology & Translational Science does not publish research on biological extracts that have unknown concentration or unknown chemical composition. Authors are encouraged to use the pre-submission inquiry mechanism to ensure relevance and appropriateness of research.
×
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