Institute for Quantitative Biosciences, the University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-0032, Japan.
Institute for Quantitative Biosciences, the University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-0032, Japan; Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University, 2-3-10 Kanda-Surugadai, Chiyoda-ku, Tokyo 101-0062, Japan.
Bioorg Med Chem. 2020 Feb 15;28(4):115310. doi: 10.1016/j.bmc.2020.115310. Epub 2020 Jan 9.
Increasing structural options in medicinal chemistry is important for the development of novel and distinctive drug candidates. In this study, we focused on phosphorus-containing functionalities. We designed and synthesized a series of phosphinophenol derivatives and determined their physicochemical properties, including hydrophobicity parameter LogP, and their biological activity toward estrogen receptor (ER). Notably, the phosphine borane derivatives (9 and 14) exhibited potent ER-antagonistic activity, exceeding the potency of the corresponding alkane (15) and silane (16) derivatives, despite having a less hydrophobic nature. The determined physicochemical parameters will be helpful for the rational design of phosphorus-containing biologically active compounds. Our results indicate that phosphine boranes are a promising new chemical entry in the range of structural options for drug discovery.
增加药物化学中的结构选择对于开发新型独特的药物候选物非常重要。在这项研究中,我们专注于含磷官能团。我们设计并合成了一系列膦酚衍生物,并确定了它们的物理化学性质,包括疏水性参数 LogP,以及它们对雌激素受体 (ER) 的生物活性。值得注意的是,尽管磷硼烷衍生物 (9 和 14) 的疏水性较低,但它们表现出很强的 ER 拮抗活性,超过了相应的烷 (15) 和硅烷 (16) 衍生物的活性。所确定的物理化学参数将有助于含磷生物活性化合物的合理设计。我们的结果表明,磷硼烷是药物发现中结构选择范围的一种很有前途的新型化学物质。