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Discovery and development of CPL207280 as new GPR40/FFA1 agonist.
Mach, Mateusz; Bazydlo-Guzenda, Katarzyna; Buda, Pawel; Matloka, Mikolaj; Dzida, Radoslaw; Stelmach, Filip; Galazka, Kinga; Wasinska-Kalwa, Malgorzata; Smuga, Damian; Holowinska, Dagmara; Dawid, Urszula; Gurba-Bryskiewicz, Lidia; Wisniewski, Krzysztof; Dubiel, Krzysztof; Pieczykolan, Jerzy; Wieczorek, Maciej.
Afiliación
  • Mach M; Celon Pharma S.A., R&D Centre, Marymoncka 15, 05-152, Kazun Nowy, Poland. Electronic address: mateusz.mach@celonpharma.com.
  • Bazydlo-Guzenda K; Celon Pharma S.A., R&D Centre, Marymoncka 15, 05-152, Kazun Nowy, Poland; Postgraduate School of Molecular Medicine, Medical University of Warsaw, 61 Zwirki i Wigury Street, 02-091, Warsaw, Poland.
  • Buda P; Celon Pharma S.A., R&D Centre, Marymoncka 15, 05-152, Kazun Nowy, Poland.
  • Matloka M; Celon Pharma S.A., R&D Centre, Marymoncka 15, 05-152, Kazun Nowy, Poland.
  • Dzida R; Celon Pharma S.A., R&D Centre, Marymoncka 15, 05-152, Kazun Nowy, Poland.
  • Stelmach F; Celon Pharma S.A., R&D Centre, Marymoncka 15, 05-152, Kazun Nowy, Poland.
  • Galazka K; Celon Pharma S.A., R&D Centre, Marymoncka 15, 05-152, Kazun Nowy, Poland.
  • Wasinska-Kalwa M; Celon Pharma S.A., R&D Centre, Marymoncka 15, 05-152, Kazun Nowy, Poland.
  • Smuga D; Celon Pharma S.A., R&D Centre, Marymoncka 15, 05-152, Kazun Nowy, Poland.
  • Holowinska D; Celon Pharma S.A., R&D Centre, Marymoncka 15, 05-152, Kazun Nowy, Poland.
  • Dawid U; Celon Pharma S.A., R&D Centre, Marymoncka 15, 05-152, Kazun Nowy, Poland.
  • Gurba-Bryskiewicz L; Celon Pharma S.A., R&D Centre, Marymoncka 15, 05-152, Kazun Nowy, Poland.
  • Wisniewski K; Celon Pharma S.A., R&D Centre, Marymoncka 15, 05-152, Kazun Nowy, Poland.
  • Dubiel K; Celon Pharma S.A., R&D Centre, Marymoncka 15, 05-152, Kazun Nowy, Poland.
  • Pieczykolan J; Celon Pharma S.A., R&D Centre, Marymoncka 15, 05-152, Kazun Nowy, Poland.
  • Wieczorek M; Celon Pharma S.A., R&D Centre, Marymoncka 15, 05-152, Kazun Nowy, Poland.
Eur J Med Chem ; 226: 113810, 2021 Dec 15.
Article en En | MEDLINE | ID: mdl-34537444
Due to a unique mechanism that limits the possibility of hypoglycemia, the free fatty acid receptor (FFA1) is an attractive target for the treatment of type 2 diabetes. So far, however, none of the promising agonists have been able to enter the market. The most advanced clinical candidate, TAK-875, was withdrawn from phase III clinical trials due to liver safety issues. In this article, we describe the key aspects leading to the discovery of CPL207280 (13), the design of which focused on long-term safety. The introduction of small, nature-inspired acyclic structural fragments resulted in compounds with retained high potency and a satisfactory pharmacokinetic profile. Optimized synthesis and upscaling provided a stable, solid form of CPL207280-51 (45) with the properties required for the toxicology studies and ongoing clinical trials.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Caproatos / Receptores Acoplados a Proteínas G / Desarrollo de Medicamentos Límite: Animals / Humans Idioma: En Revista: Eur J Med Chem Año: 2021 Tipo del documento: Article Pais de publicación: Francia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Caproatos / Receptores Acoplados a Proteínas G / Desarrollo de Medicamentos Límite: Animals / Humans Idioma: En Revista: Eur J Med Chem Año: 2021 Tipo del documento: Article Pais de publicación: Francia