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他达拉非与丙酮和甲乙酮的单溶剂化物的晶体结构及去溶剂化行为

Crystal Structure and Desolvation Behaviour of the Tadalafil Monosolvates with Acetone and Methyl Ethyl Ketone.

作者信息

Miclaus Maria O, Kacso Irina E, Martin Flavia A, David Leontin, Pop Mihaela M, Filip Claudiu, Filip Xenia

机构信息

Molecular and Biomolecular Physics Department, National Institute for R&D of Isotopic and Molecular Technologies, Cluj-Napoca 400293, Romania; Faculty of Physics, Babes-Bolyai University, Cluj-Napoca 400084, Romania.

Molecular and Biomolecular Physics Department, National Institute for R&D of Isotopic and Molecular Technologies, Cluj-Napoca 400293, Romania.

出版信息

J Pharm Sci. 2015 Nov;104(11):3782-3788. doi: 10.1002/jps.24597. Epub 2015 Jul 24.

Abstract

Crystal structures of Tadalafil (TDF) monosolvated forms with acetone (ACE) and methyl ethyl ketone (MEK) were determined by single-crystal X-ray diffraction in which same persistent chains of TDF molecules are present as in the reported structures. The solvates crystallize in a higher orthorhombic symmetry than the known forms with monoclinic structures. Weak interactions between TDF and solvent molecules are present in both solvates, leading to slight conformational distortions of TDF molecules. The MEK solvate showed slightly higher stability than the ACE solvate, regardless of their highly similar molecular conformations and crystal packing. Desolvation into anhydrous TDF was achieved by heating, exposure to temperature and relative humidity and by mechanical stress. The high solubility of TDF in ACE and MEK solvents combined with the ease of desolvation of the resulting solvated forms indicates the viability of the solvates use as intermediates in the TDF crystallization process.

摘要

通过单晶X射线衍射确定了他达拉非(TDF)与丙酮(ACE)和甲乙酮(MEK)的单溶剂化物形式的晶体结构,其中存在与报道结构中相同的TDF分子持久链。这些溶剂化物结晶时的正交对称性高于已知的单斜结构形式。两种溶剂化物中均存在TDF与溶剂分子之间的弱相互作用,导致TDF分子出现轻微的构象扭曲。尽管MEK溶剂化物和ACE溶剂化物的分子构象和晶体堆积高度相似,但MEK溶剂化物显示出略高于ACE溶剂化物的稳定性。通过加热、暴露于温度和相对湿度以及机械应力实现了向无水TDF的去溶剂化。TDF在ACE和MEK溶剂中的高溶解度以及所得溶剂化物形式易于去溶剂化,表明溶剂化物用作TDF结晶过程中间体的可行性。

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