ArticleInternational journal of biomedical imaging2013
Hydraphiles: a rigorously studied class of synthetic channel compounds with in vivo activity.
Article in International journal of biomedical imaging, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed.
- Acylated and alkylated benzo(crown-ethers) form ion-dependent ion channels in biological membranes.Biophysical journal · 2022Article
- Re-evaluation of the mechanism of cytotoxicity of dialkylated lariat ether compounds.RSC advances · 2020Article
- Oligonucleotide-Based Systems for Input-Controlled and Non-Covalently Regulated Protein-Binding.Supramolecular chemistry · 2013Article
Corrections and comments
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Authors and funding
5 authors.
Funding
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Abstract
Hydraphiles are a class of synthetic ion channels that now have a twenty-year history of analysis and success. In early studies, these compounds were rigorously validated in a wide range of in vitro assays including liposomal ion flow detected by NMR or ion-selective electrodes, as well as biophysical experiments in planar bilayers. During the past decade, biological activity was observed for these compounds including toxicity to bacteria, yeast, and mammalian cells due to stress caused by the disruption of ion homeostasis. The channel mechanism was verified in cells using membrane polarity sensitive dyes, as well as patch clamping studies. This body of work has provided a solid foundation with which hydraphiles have recently demonstrated acute biological toxicity in the muscle tissue of living mice, as measured by whole animal fluorescence imaging and histological studies. Here we review the critical structure-activity relationships in the hydraphile family of compounds and the in vitro and in cellulo experiments that have validated their channel behavior. This report culminates with a description of recently reported efforts in which these molecules have demonstrated activity in living mice.
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Registered trials
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