• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Design of Next-Generation DGAT2 Inhibitor PF-07202954 with Longer Predicted Half-Life.具有更长预测半衰期的下一代二酰甘油酰基转移酶2(DGAT2)抑制剂PF-07202954的设计
ACS Med Chem Lett. 2023 Oct 2;14(10):1427-1433. doi: 10.1021/acsmedchemlett.3c00330. eCollection 2023 Oct 12.
2
Discovery of Ervogastat (PF-06865571): A Potent and Selective Inhibitor of Diacylglycerol Acyltransferase 2 for the Treatment of Non-alcoholic Steatohepatitis.Ervogastat(PF-06865571)的发现:一种用于治疗非酒精性脂肪性肝炎的强效和选择性二酰基甘油酰基转移酶 2 抑制剂。
J Med Chem. 2022 Nov 24;65(22):15000-15013. doi: 10.1021/acs.jmedchem.2c01200. Epub 2022 Nov 2.
3
Inhibition of Diacylglycerol Acyltransferase 2 Versus Diacylglycerol Acyltransferase 1: Potential Therapeutic Implications of Pharmacology.二酰基甘油酰基转移酶2与二酰基甘油酰基转移酶1的抑制作用:药理学的潜在治疗意义
Clin Ther. 2023 Jan;45(1):55-70. doi: 10.1016/j.clinthera.2022.12.008. Epub 2023 Jan 21.
4
An RNAi therapeutic targeting hepatic DGAT2 in a genetically obese mouse model of nonalcoholic steatohepatitis.一种针对非酒精性脂肪性肝炎的遗传肥胖小鼠模型中肝脏 DGAT2 的 RNAi 治疗药物。
Mol Ther. 2022 Mar 2;30(3):1329-1342. doi: 10.1016/j.ymthe.2021.11.007. Epub 2021 Nov 11.
5
Efficacy and safety of an orally administered DGAT2 inhibitor alone or coadministered with a liver-targeted ACC inhibitor in adults with non-alcoholic steatohepatitis (NASH): rationale and design of the phase II, dose-ranging, dose-finding, randomised, placebo-controlled MIRNA (Metabolic Interventions to Resolve NASH with fibrosis) study.一种 DGAT2 抑制剂单独或与肝靶向 ACC 抑制剂联合用于非酒精性脂肪性肝炎 (NASH) 成人患者的疗效和安全性:具有纤维化的代谢干预解决 NASH 研究(MIRNA)的 II 期、剂量范围、剂量发现、随机、安慰剂对照的原理和设计。
BMJ Open. 2022 Mar 30;12(3):e056159. doi: 10.1136/bmjopen-2021-056159.
6
Targeting diacylglycerol acyltransferase 2 for the treatment of nonalcoholic steatohepatitis.靶向二酰基甘油酰基转移酶 2 治疗非酒精性脂肪性肝炎。
Sci Transl Med. 2019 Nov 27;11(520). doi: 10.1126/scitranslmed.aav9701.
7
Suppression of diacylglycerol acyltransferase-2 (DGAT2), but not DGAT1, with antisense oligonucleotides reverses diet-induced hepatic steatosis and insulin resistance.用反义寡核苷酸抑制二酰甘油酰基转移酶-2(DGAT2)而非DGAT1,可逆转饮食诱导的肝脂肪变性和胰岛素抵抗。
J Biol Chem. 2007 Aug 3;282(31):22678-88. doi: 10.1074/jbc.M704213200. Epub 2007 May 27.
8
Mitigating a Bioactivation Liability with an Azetidine-Based Inhibitor of Diacylglycerol Acyltransferase 2 (DGAT2) En Route to the Discovery of the Clinical Candidate Ervogastat.用基于氮杂环丁烷的二酰基甘油酰基转移酶 2(DGAT2)抑制剂缓解生物活化性风险,进而发现临床候选药物依维莫司。
Chem Res Toxicol. 2023 Jun 19;36(6):934-946. doi: 10.1021/acs.chemrestox.3c00054. Epub 2023 May 6.
9
Role of diacylglycerol O-acyltransferase (DGAT) isoforms in bovine hepatic fatty acid metabolism.二酰甘油 O-酰基转移酶(DGAT)同工酶在牛肝脏脂肪酸代谢中的作用。
J Dairy Sci. 2022 Apr;105(4):3588-3600. doi: 10.3168/jds.2021-21140. Epub 2022 Feb 16.
10
DGAT2 inhibition blocks SREBP-1 cleavage and improves hepatic steatosis by increasing phosphatidylethanolamine in the ER.DGAT2 抑制通过增加内质网中的磷脂酰乙醇胺来阻断 SREBP-1 的切割并改善肝脂肪变性。
Cell Metab. 2024 Mar 5;36(3):617-629.e7. doi: 10.1016/j.cmet.2024.01.011. Epub 2024 Feb 9.

引用本文的文献

1
The translational potential of miR-26 in atherosclerosis and development of agents for its target genes ACC1/2, COL1A1, CPT1A, FBP1, DGAT2, and SMAD7.miR-26 在动脉粥样硬化中的转译潜力及其靶基因 ACC1/2、COL1A1、CPT1A、FBP1、DGAT2 和 SMAD7 相关药物的研发。
Cardiovasc Diabetol. 2024 Jan 9;23(1):21. doi: 10.1186/s12933-024-02119-z.

本文引用的文献

1
Inhibition of Diacylglycerol Acyltransferase 2 Versus Diacylglycerol Acyltransferase 1: Potential Therapeutic Implications of Pharmacology.二酰基甘油酰基转移酶2与二酰基甘油酰基转移酶1的抑制作用:药理学的潜在治疗意义
Clin Ther. 2023 Jan;45(1):55-70. doi: 10.1016/j.clinthera.2022.12.008. Epub 2023 Jan 21.
2
Discovery of Ervogastat (PF-06865571): A Potent and Selective Inhibitor of Diacylglycerol Acyltransferase 2 for the Treatment of Non-alcoholic Steatohepatitis.Ervogastat(PF-06865571)的发现:一种用于治疗非酒精性脂肪性肝炎的强效和选择性二酰基甘油酰基转移酶 2 抑制剂。
J Med Chem. 2022 Nov 24;65(22):15000-15013. doi: 10.1021/acs.jmedchem.2c01200. Epub 2022 Nov 2.
3
Therapeutic pipeline in nonalcoholic steatohepatitis.非酒精性脂肪性肝炎的治疗药物研发管线。
Nat Rev Gastroenterol Hepatol. 2021 Jun;18(6):373-392. doi: 10.1038/s41575-020-00408-y. Epub 2021 Feb 10.
4
Corrigendum: Understanding the Conformational Behavior of Fluorinated Piperidines: The Origin of the Axial-F Preference.勘误:理解氟化哌啶的构象行为:轴向氟偏好的起源。
Chemistry. 2020 Nov 2;26(61):14018-14019. doi: 10.1002/chem.202004224. Epub 2020 Oct 19.
5
Mechanistic insights on clearance and inhibition discordance between liver microsomes and hepatocytes when clearance in liver microsomes is higher than in hepatocytes.当肝微粒体中的清除率高于肝细胞中的清除率时,关于肝微粒体与肝细胞之间清除率和抑制作用不一致的机制性见解。
Eur J Pharm Sci. 2020 Dec 1;155:105541. doi: 10.1016/j.ejps.2020.105541. Epub 2020 Sep 12.
6
Novel antisense inhibition of diacylglycerol O-acyltransferase 2 for treatment of non-alcoholic fatty liver disease: a multicentre, double-blind, randomised, placebo-controlled phase 2 trial.新型二酰基甘油 O-酰基转移酶 2 反义抑制物治疗非酒精性脂肪性肝病:一项多中心、双盲、随机、安慰剂对照的 2 期临床试验。
Lancet Gastroenterol Hepatol. 2020 Sep;5(9):829-838. doi: 10.1016/S2468-1253(20)30186-2. Epub 2020 Jun 15.
7
Understanding the Conformational Behavior of Fluorinated Piperidines: The Origin of the Axial-F Preference.理解氟化哌啶的构象行为:轴向优先的起源。
Chemistry. 2020 May 15;26(28):6141-6146. doi: 10.1002/chem.202001355. Epub 2020 May 12.
8
Targeting diacylglycerol acyltransferase 2 for the treatment of nonalcoholic steatohepatitis.靶向二酰基甘油酰基转移酶 2 治疗非酒精性脂肪性肝炎。
Sci Transl Med. 2019 Nov 27;11(520). doi: 10.1126/scitranslmed.aav9701.
9
Small structural changes of the imidazopyridine diacylglycerol acyltransferase 2 (DGAT2) inhibitors produce an improved safety profile.咪唑并吡啶二酰基甘油酰基转移酶2(DGAT2)抑制剂的微小结构变化可产生更好的安全性。
Medchemcomm. 2016 Nov 22;8(4):771-779. doi: 10.1039/c6md00564k. eCollection 2017 Apr 1.
10
Strategy for Extending Half-life in Drug Design and Its Significance.药物设计中延长半衰期的策略及其意义。
ACS Med Chem Lett. 2018 Apr 2;9(6):528-533. doi: 10.1021/acsmedchemlett.8b00018. eCollection 2018 Jun 14.

具有更长预测半衰期的下一代二酰甘油酰基转移酶2(DGAT2)抑制剂PF-07202954的设计

Design of Next-Generation DGAT2 Inhibitor PF-07202954 with Longer Predicted Half-Life.

作者信息

Filipski Kevin J, Edmonds David J, Garnsey Michelle R, Smaltz Daniel J, Coffman Karen, Futatsugi Kentaro, Lee Jack, O'Neil Steven V, Wright Ann, Nason Deane, Gosset James R, Orozco Christine C, Blackler Dan, Fakhoury Guila, Gutierrez Jemy A, Perez Sylvie, Ross Trenton, Stock Ingrid, Tesz Gregory, Dullea Robert

机构信息

Pfizer Research & Development, 1 Portland Street, Cambridge, Massachusetts 02139, United States.

Pfizer Research & Development, 558 Eastern Point Road, Groton, Connecticut 06340, United States.

出版信息

ACS Med Chem Lett. 2023 Oct 2;14(10):1427-1433. doi: 10.1021/acsmedchemlett.3c00330. eCollection 2023 Oct 12.

DOI:10.1021/acsmedchemlett.3c00330
PMID:37849537
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10577701/
Abstract

Diacylglycerol O-acyltransferase 2 (DGAT2) inhibitors have been shown to lower liver triglyceride content and are being explored clinically as a treatment for non-alcoholic steatohepatitis (NASH). This work details efforts to find an extended-half-life DGAT2 inhibitor. A basic moiety was added to a known inhibitor template, and the basicity and lipophilicity were fine-tuned by the addition of electrophilic fluorines. A weakly basic profile was required to find an appropriate balance of potency, clearance, and permeability. This work culminated in the discovery of PF-07202954 (), a weakly basic DGAT2 inhibitor that has advanced to clinical studies. This molecule displays a higher volume of distribution and longer half-life in preclinical species, in keeping with its physicochemical profile, and lowers liver triglyceride content in a Western-diet-fed rat model.

摘要

二酰甘油O-酰基转移酶2(DGAT2)抑制剂已被证明可降低肝脏甘油三酯含量,目前正在临床研究中作为非酒精性脂肪性肝炎(NASH)的一种治疗方法进行探索。这项工作详细介绍了寻找半衰期延长的DGAT2抑制剂的努力。在已知抑制剂模板上添加了一个碱性基团,并通过添加亲电氟原子对碱性和亲脂性进行微调。需要一个弱碱性特征来在效力、清除率和渗透性之间找到适当的平衡。这项工作最终发现了PF-07202954(),一种弱碱性DGAT2抑制剂,已进入临床研究阶段。该分子在临床前物种中显示出更高的分布容积和更长的半衰期,与其理化性质相符,并且在西方饮食喂养的大鼠模型中降低了肝脏甘油三酯含量。