• 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

从活性分子到先导化合物:活性分子验证与评估

Hit-to-Lead: Hit Validation and Assessment.

作者信息

Hevener Kirk E, Pesavento Russell, Ren JinHong, Lee Hyun, Ratia Kiira, Johnson Michael E

机构信息

Department of Pharmaceutical Sciences, University of Tennessee Health Science Center, Memphis, TN, United States.

Center for Biomolecular Sciences, University of Illinois at Chicago, Chicago, IL, United States; College of Dentistry, University of Illinois at Chicago, Chicago, IL, United States.

出版信息

Methods Enzymol. 2018;610:265-309. doi: 10.1016/bs.mie.2018.09.022. Epub 2018 Oct 25.

DOI:10.1016/bs.mie.2018.09.022
PMID:30390802
Abstract

High-throughput screening assays have become nearly ubiquitous in the search for small compounds or peptides that can modulate biological processes for therapeutic purposes. While many assays have become quite robust, with well-established protocols, the subsequent steps of validating the hits and choosing the best ones to take forward into leads for further chemical development are less established. In this chapter, we describe a variety of approaches, including chemical assessment, the use of various computational approaches, a variety of counter-screens, and "orthogonal" biophysical assays using nuclear magnetic resonance, surface plasmon resonance, isothermal titration calorimetry or thermal shift assays as methods for validating and assessing the quality of hits.

摘要

高通量筛选分析在寻找可调节生物过程以用于治疗目的的小分子化合物或肽的过程中几乎无处不在。虽然许多分析已经相当成熟,有完善的方案,但后续验证筛选出的活性物质并选择最佳的物质以推进到先导物进行进一步化学开发的步骤却不太成熟。在本章中,我们描述了多种方法,包括化学评估、使用各种计算方法、各种反筛选,以及使用核磁共振、表面等离子体共振、等温滴定量热法或热位移分析等“正交”生物物理分析作为验证和评估筛选出的活性物质质量的方法。

相似文献

1
Hit-to-Lead: Hit Validation and Assessment.从活性分子到先导化合物:活性分子验证与评估
Methods Enzymol. 2018;610:265-309. doi: 10.1016/bs.mie.2018.09.022. Epub 2018 Oct 25.
2
A Guide to Run Affinity Screens Using Differential Scanning Fluorimetry and Surface Plasmon Resonance Assays.使用差示扫描荧光法和表面等离子体共振测定法进行亲和筛选的指南。
Methods Enzymol. 2018;610:135-165. doi: 10.1016/bs.mie.2018.09.015. Epub 2018 Oct 26.
3
Applications of Biophysics in High-Throughput Screening Hit Validation.生物物理学在高通量筛选命中验证中的应用。
J Biomol Screen. 2014 Jun;19(5):707-14. doi: 10.1177/1087057114529462. Epub 2014 Apr 2.
4
Hot-Spotting with Thermal Scanning: A Ligand- and Structure-Independent Assessment of Target Ligandability.热点探测的热扫描:配体和结构独立评估靶标可成药性。
J Med Chem. 2017 Jun 22;60(12):4923-4931. doi: 10.1021/acs.jmedchem.7b00208. Epub 2017 Jun 2.
5
Creating a more strategic small molecule biophysical hit characterization workflow.创建更具战略性的小分子生物物理命中特征描述工作流程。
SLAS Discov. 2024 Jun;29(4):100159. doi: 10.1016/j.slasd.2024.100159. Epub 2024 May 7.
6
Biophysics in drug discovery: impact, challenges and opportunities.药物发现中的生物物理学:影响、挑战与机遇。
Nat Rev Drug Discov. 2016 Oct;15(10):679-98. doi: 10.1038/nrd.2016.123. Epub 2016 Aug 12.
7
Mass spectrometry for fragment screening.质谱法用于片段筛选。
Essays Biochem. 2017 Nov 8;61(5):465-473. doi: 10.1042/EBC20170071.
8
Target immobilization as a strategy for NMR-based fragment screening: comparison of TINS, STD, and SPR for fragment hit identification.基于核磁共振的片段筛选策略——靶点固定:用于片段命中识别的TINS、STD和SPR方法比较
J Biomol Screen. 2010 Sep;15(8):978-89. doi: 10.1177/1087057110375614.
9
Biophysical screening for the discovery of small-molecule ligands.用于发现小分子配体的生物物理筛选
Methods Mol Biol. 2013;1008:357-88. doi: 10.1007/978-1-62703-398-5_13.
10
Affinity-based screening techniques: their impact and benefit to increase the number of high quality leads.基于亲和力的筛选技术:其对增加高质量先导化合物数量的影响和益处。
Expert Opin Drug Discov. 2010 Nov;5(11):1095-107. doi: 10.1517/17460441.2010.524641. Epub 2010 Oct 7.

引用本文的文献

1
A Review on Perception of Binding Kinetics in Affinity Biosensors: Challenges and Opportunities.亲和生物传感器中结合动力学感知的综述:挑战与机遇
ACS Omega. 2025 Jan 27;10(5):4197-4216. doi: 10.1021/acsomega.4c10040. eCollection 2025 Feb 11.
2
Machine Learning Assisted Hit Prioritization for High Throughput Screening in Drug Discovery.机器学习辅助药物发现高通量筛选中的活性化合物优先级排序
ACS Cent Sci. 2024 Mar 15;10(4):823-832. doi: 10.1021/acscentsci.3c01517. eCollection 2024 Apr 24.
3
Optimizing drug discovery for snakebite envenoming via a high-throughput phospholipase A2 screening platform.
通过高通量磷脂酶A2筛选平台优化蛇咬伤中毒的药物研发。
Front Pharmacol. 2024 Jan 11;14:1331224. doi: 10.3389/fphar.2023.1331224. eCollection 2023.
4
Machine-Learning- and Structure-Based Virtual Screening for Selecting Cinnamic Acid Derivatives as DHFR-TS Inhibitors.基于机器学习和结构的虚拟筛选,选择肉桂酸衍生物作为 DHFR-TS 抑制剂。
Molecules. 2023 Dec 28;29(1):179. doi: 10.3390/molecules29010179.
5
Pathogen-associated gene discovery workflows for novel antivirulence therapeutic development.病原体相关基因发现工作流程用于新型抗病毒治疗药物的开发。
EBioMedicine. 2023 Feb;88:104429. doi: 10.1016/j.ebiom.2022.104429. Epub 2023 Jan 9.
6
Natural Compounds as Non-Nucleoside Inhibitors of Zika Virus Polymerase through Integration of In Silico and In Vitro Approaches.通过整合计算机模拟和体外实验方法,将天然化合物作为寨卡病毒聚合酶的非核苷抑制剂
Pharmaceuticals (Basel). 2022 Nov 30;15(12):1493. doi: 10.3390/ph15121493.
7
A Liquid Chromatography-Mass Spectrometry Method to Study the Interaction between Membrane Proteins and Low-Molecular-Weight Compound Mixtures.一种液相色谱-质谱联用方法研究膜蛋白与低分子量化合物混合物的相互作用。
Molecules. 2022 Jul 30;27(15):4889. doi: 10.3390/molecules27154889.
8
Homology Modeling, Design of Ligands, and Molecular Docking Identify Potential Inhibitors of 24-Sterol Methyltransferase.同源建模、配体设计和分子对接鉴定 24-固醇甲基转移酶的潜在抑制剂。
Front Cell Infect Microbiol. 2022 Jun 2;12:859981. doi: 10.3389/fcimb.2022.859981. eCollection 2022.
9
Angiotensin II receptor blockers (ARBs) and manufacturing contamination: A retrospective National Register Study into suspected associated adverse drug reactions.血管紧张素 II 受体阻滞剂 (ARB) 和生产污染:一项疑似相关不良药物反应的全国登记回顾性研究。
Br J Clin Pharmacol. 2022 Nov;88(11):4812-4827. doi: 10.1111/bcp.15411. Epub 2022 Jun 8.
10
Adsorption to the Surface of Hemozoin Crystals: Structure-Based Design and Synthesis of Amino-Phenoxazine β-Hematin Inhibitors.血晶蛋白晶体表面的吸附:基于结构的氨基吩嗪 β-血红素抑制剂的设计与合成。
ChemMedChem. 2022 May 18;17(10):e202200139. doi: 10.1002/cmdc.202200139. Epub 2022 Apr 26.