Kinase Degraders, Activators, and Inhibitors: Highlights and Synthesis Routes to the Chemical Probes on opnMe.com, Part 1

Author:

Gollner Andreas1ORCID,Heine Claudia2,Hofbauer Karin S.1

Affiliation:

1. Department of Medicinal Chemistry Boehringer Ingelheim RCV GmbH & Co. KG Boehringer-Gasse Wien, 5–11 1121 Vienna Austria

2. Department of Medicinal Chemistry Boehringer Ingelheim RCV GmbH & Co. KG 88400 Biberach Germany

Abstract

AbstractKinases are among the most important and successful drug targets. Chemical probe compounds have played a critical role in elucidating the role of kinases in many biological pathways. There are currently twelve well‐validated chemical probes that target kinases available free‐of‐cost via the Molecules to Order (M2O) arm of Boehringer Ingelheim's open innovation platform, opnMe.com. Here we present a summary of the key data for each of these probe compounds and the synthesis routes to all twelve compounds. We hope this will aid researchers who use or plan to use these compounds in their research.

Publisher

Wiley

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics,Molecular Medicine,Drug Discovery,Biochemistry,Pharmacology

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