Department of Nanopharmaceutical Sciences, Nagoya Institute of Technology, Gokiso, Showa-Ku, Nagoya 466-8555, Japan.
Department of Organic Chemistry, University of Valencia, Pharmacy Faculty, Burjassot, Valencia 46100, Spain.
J Am Chem Soc. 2024 Sep 25;146(38):26435-26441. doi: 10.1021/jacs.4c09389. Epub 2024 Sep 4.
Ice formation is a critical challenge across multiple fields, from industrial applications to biological preservation. Inspired by natural antifreeze proteins, we designed and synthesized a new class of small-molecule antifreezes based on α-helical -terphenyl scaffolds with guanidine side chains. These -terphenyl guanidines , among the smallest molecules that mimic α-helical structures, exhibit potent ice recrystallization inhibition (IRI) activity, similar to that of existing large α-helical antifreeze compounds. The most effective compound, , with four C1-carbon guanidine moieties, demonstrated a superior IRI activity of 0.46 (1 mg/mL). Using molecular dynamics simulations with density-functional theory and separate p calculations, we elucidated the mechanisms underlying their antifreeze properties.
冰的形成是一个跨多个领域的关键挑战,从工业应用到生物保存。受天然抗冻蛋白的启发,我们设计并合成了一类基于 α-螺旋 -三联苯支架和胍侧链的新型小分子抗冻剂。这些 -三联苯胍,作为模拟 α-螺旋结构的最小分子之一,表现出有效的冰晶再结晶抑制(IRI)活性,类似于现有的大型 α-螺旋抗冻化合物。最有效的化合物 ,具有四个 C1-碳胍部分,表现出 0.46(1mg/mL)的优异 IRI 活性。通过使用密度泛函理论和单独的 p 计算的分子动力学模拟,我们阐明了它们抗冻特性的机制。