Related Experiment Video
Updated: Sep 2, 2026

Covalent Fragment Screening Using the Quantitative Irreversible Tethering Assay
Published on: February 28, 2025
A Perspective on Covalent Hit Identification and Validation in the European Pharmaceutical Industry
Oliver Schadt1, Sebastian Essig2, Giambattista Testolin3
1Medicinal Chemistry, Merck Healthcare KGaA, Darmstadt, Germany.
Abstract:
This article is an initiative of the Chemical Biology in Industry Working Group of the "European Federation for Medicinal Chemistry and Chemical Biology (EFMC)" connecting discipline experts from several organizations across Europe. In the second half of 2025, we surveyed scientists from the listed organizations to collect precompetitive information on covalent hit identification and validation practices in the pharmaceutical industry. The questionnaire contained 33 questions and covered a broad spectrum of important aspects in covalent drug discovery, including target selection, library characteristics, hit identification, hit validation, and technical limitations. The results are shared and discussed in this article with the goal of generating best practices and providing insights into library design, hit identification, validation, and optimization in covalent drug discovery.
Related Concept Videos
Drug Discovery: Overview
Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches
Non-controlled studies, commonly employed for initial exploration, lack a control group, rendering them susceptible to biases and external influences. In contrast, controlled...
Clinically Relevant Drug Product Specifications: Methods of Establishment
Pharmacovigilance
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
Biopharmaceutical Factors Influencing Drug Product Design: Overview
In Vitro Drug Release Testing: Overview, Development and Validation

