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首页> 外文期刊>Journal of Molecular Structure >A 1:1 pharmaceutical cocrystal of myricetin in combination with uncommon piracetam conformer: X-ray single crystal analysis and mechanochemical synthesis
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A 1:1 pharmaceutical cocrystal of myricetin in combination with uncommon piracetam conformer: X-ray single crystal analysis and mechanochemical synthesis

机译:杨梅素的1:1药物共晶体与罕见的吡乙酰胺构象剂结合:X射线单晶分析和机械化学合成

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摘要

Combination of two Active Pharmaceutical Ingredients, myricetin and piracetam, yields a 1:1 cocrystal characterized by X-ray single-crystal and powder diffraction, Raman spectroscopy, ~1H NMR, thermal analysis (DSC and TG-DTA) methods. Constituents of the cocrystalline phase were also investigated in terms of Hirshfeld surfaces. Compounds in their neutral forms cocrystallize in the Pna 2_1 space group of orthorhombic system. Notably, piracetam adopts an uncommon conformation, not encountered in its cocrystals previously described. In the crystal lattice, a three-dimensional hydrogen-bonded network is observed, including formation of a 2D molecular scaffolding motif. A scale-up procedure is readily available with use of solvent-drop grinding method, in which application of a variety of common solvents leads to formation of the cocrystal, as confirmed by XRPD and Raman spectroscopy.
机译:杨梅素和吡拉西坦这两种活性药物成分的组合产生了1:1共晶,其特征在于X射线单晶和粉末衍射,拉曼光谱,〜1H NMR,热分析(DSC和TG-DTA)方法。还根据赫希菲尔德表面研究了共晶相的成分。中性形式的化合物在正交晶系的Pna 2_1空间群中共结晶。值得注意的是,吡乙酰胺具有罕见的构象,这在前述共晶中没有遇到。在晶格中,观察到三维氢键网络,包括2D分子支架基序的形成。如通过XRPD和拉曼光谱法所证实的那样,使用溶剂滴磨法可以容易地进行按比例放大程序,其中多种常用溶剂的应用导致共晶的形成。

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