Гетероциклізація або реакції каплінгу: випадок ДНК-кодованих бібліотек

• Datum: 2023
• Hauptverfasser: Oksiuta, Oleksandr V., Pashenko, Alexander E., Smalii, Radomyr V., Volochnyuk, Dmitry M., Ryabukhin, Serhii V.
• Format: Artikel
• Sprache: English
• Veröffentlicht: National University of Pharmacy 2023
• Schlagworte: технологія ДНК-кодованих бібліотек; ортогональні функціональні групи; реакції каплінгу; поліфункціональні білдинг-блоки; гетероциклізації; хемоінформатика; разноманітність молекулярних каркасів
• Online Zugang: https://ophcj.nuph.edu.ua/article/view/275133
• Назва журналу: Journal of Organic and Pharmaceutical Chemistry

Aim. DNA-encoded libraries technologies (DELT) are gradually becoming an important part of standard drug discovery toolbox. DELT is looking to find its place between classic low-molecular-weight drug candidates on the one hand, and high-molecular-weight antibodies and peptides on the other hand. On its natural path to overcoming the “childhood diseases” typical for every novel technology, DELT has reached a point where the chemical diversity of DNA-encoded libraries (DELs) becomes an important factor to look out for. In this paper, we aim to take a closer look at the chemical diversity of DELs in their present state and find the ways to improve it.Results and discussion. We have identified the DEL-viable building blocks from the Enamine Ltd. stock collection, as well as from Chemspace Ltd. virtual collection, using the SMARTS set, which takes into account all the necessary structural restrictions. Using modern cheminformatics tools, such as Synt-On, we have analyzed the scaffold diversity of both stock and virtual core bi- and tri-functional building blocks (BBs) suitable for DNA-tolerant reactions. The identification of scaffolds from the most recently published on-DNA heterocyclization reactions and analysis of their inclusion into the existing BBs space have shown that novel DNA-tolerant heterocyclizations are extremely useful for expanding chemical diversity in DEL technologies.Conclusions. The analysis performed allowed us to recognize which functional groups should be prioritized as the most impactful when the new BBs are designed. It is also made clear that the development of new DNA-tolerant reactions, including heterocyclizations, have a significant potential to further expand DEL molecular diversity.