| Literature DB >> 33160023 |
James M Apgar1, Robert R Wilkening2, Dann L Parker2, Dongfang Meng2, Kenneth J Wildonger2, Donald Sperbeck2, Mark L Greenlee2, James M Balkovec2, Amy M Flattery2, George K Abruzzo2, Andrew M Galgoci2, Robert A Giacobbe2, Charles J Gill2, Ming-Jo Hsu2, Paul Liberator2, Andrew S Misura2, Mary Motyl2, Jennifer Nielsen Kahn2, Maryann Powles2, Fred Racine2, Jasminka Dragovic2, Weiming Fan3, Robin Kirwan3, Shu Lee3, Hao Liu3, Ahmed Mamai3, Kingsley Nelson3, Michael Peel3.
Abstract
We previously reported medicinal chemistry efforts that identified MK-5204, an orally efficacious β-1,3-glucan synthesis inhibitor derived from the natural product enfumafungin. Further extensive optimization of the C2 triazole substituent identified 4-pyridyl as the preferred replacement for the carboxamide of MK-5204, leading to improvements in antifungal activity in the presence of serum, and increased oral exposure. Reoptimizing the aminoether at C3 in the presence of this newly discovered C2 substituent, confirmed that the (R) t-butyl, methyl aminoether of MK-5204 provided the best balance of these two key parameters, culminating in the discovery of ibrexafungerp, which is currently in phase III clinical trials. Ibrexafungerp displayed significantly improved oral efficacy in murine infection models, making it a superior candidate for clinical development as an oral treatment for Candida and Aspergillus infections.Entities:
Keywords: Enfumafungin; Ibrexafungerp; MK-3118; SCY-078; β-1,3-glucan synthesis inhibitor
Year: 2020 PMID: 33160023 DOI: 10.1016/j.bmcl.2020.127661
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823