| Literature DB >> 24900478 |
Mark J Robertson1, Gordana Hadzic1, Joseph Ambrus1, D Yuri Pomè1, Emily Hyde1, Ainslie Whiting2, Anna Mariana2, Lisa von Kleist3, Ngoc Chau2, Volker Haucke3, Phillip J Robinson2, Adam McCluskey1.
Abstract
Six focused rhodanine-based libraries, 60 compounds in total, were synthesized and evaluated as potential dynamin I GTPase inhibitors. Twenty-six were more potent than the lead compound with 13 returning IC50 values ≤10 μM, making the Rhodadyn series among the most active dynamin inhibitors reported. Two analogues were highly effective at blocking receptor-mediated endocytosis: C10 and D10 with IC50(RME) = 7.0 ± 2.2 and 5.9 ± 1.0 μM, respectively. These compounds are equipotent with the best reported in-cell dynamin inhibitors.Entities:
Keywords: Knoevengal condensation; dynamin inhibition; rhodanine
Year: 2012 PMID: 24900478 PMCID: PMC4025782 DOI: 10.1021/ml200284s
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345