Asano Akiko, Yamada Takeshi, Doi Mitsunobu
Osaka University of Pharmaceutical Sciences, 4-20-1, Nasahara, Takatsuki, Osaka, 569-1094, Japan.
J Pept Sci. 2014 Oct;20(10):794-802. doi: 10.1002/psc.2668. Epub 2014 Jul 1.
We designed four fluorinated Phe-incorporated ascidiacyclamide ([Phe]ASC) analogs, (cyclo(-Xxx1-oxazoline2-D-Val3-thiazole4-Ile5-oxazoline6-D-Val7-thiazole8-)), [(4-F)Phe]ASC (Xxx1: 4-fluorophenylalanine), [(3,5-F₂)Phe]ASC (Xxx1: 3,5-difluorophenylalanine), [(3,4,5-F₃)Phe]ASC (Xxx1: 3,4,5-trifluorophenylalanine) and [(F₅)Phe]ASC (Xxx1: pentafluorophenylalanine), to modulate the π-electron density of the aromatic ring of the Phe residue. X-ray diffraction analysis, ¹H NMR and CD spectra all suggested that the interactions between the benzene ring of the Xxx1 residue and the alkyl groups of oxazoline2 contribute to the stability of the folded structure of these analogs. Substituting fluorines for the hydrogens progressively weakened those interactions through reducing the π-electron density, thereby mediating transformation from the folded to square structure. As a result, [(F₅)Phe]ASC preferred the square form more than the other analogs did. Also contributing to the preference for the square form may be the hindrance of the rotation around the Cα-Cβ bond by the two ortho-fluoro substituents of [(F₅)Phe]ASC. These findings demonstrate that the structure of ASC can be modulated by using fluorine as an electron-withdrawing group.
我们设计了四种含氟苯丙氨酸的海鞘环肽([Phe]ASC)类似物,(环(-Xxx1-恶唑啉2-D-缬氨酸3-噻唑4-异亮氨酸5-恶唑啉6-D-缬氨酸7-噻唑8-)),[(4-F)Phe]ASC(Xxx1:4-氟苯丙氨酸),[(3,5-F₂)Phe]ASC(Xxx1:3,5-二氟苯丙氨酸),[(3,4,5-F₃)Phe]ASC(Xxx1:3,4,5-三氟苯丙氨酸)和[(F₅)Phe]ASC(Xxx1:五氟苯丙氨酸),以调节苯丙氨酸残基芳香环的π电子密度。X射线衍射分析、¹H NMR和CD光谱均表明,Xxx1残基的苯环与恶唑啉2的烷基之间的相互作用有助于这些类似物折叠结构的稳定性。用氟取代氢通过降低π电子密度逐渐削弱了这些相互作用,从而介导了从折叠结构到方形结构的转变。结果,[(F₅)Phe]ASC比其他类似物更倾向于方形结构。[(F₅)Phe]ASC的两个邻位氟取代基对Cα-Cβ键旋转的阻碍也可能导致其对方形结构的偏好。这些发现表明,使用氟作为吸电子基团可以调节海鞘环肽的结构。