Noguchi Shuji, Miura Keiko, Fujiki Sadahiro, Iwao Yasunori, Itai Shigeru
Graduate School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka 422-8526, Japan.
Acta Crystallogr C. 2012 Feb;68(Pt 2):o41-4. doi: 10.1107/S0108270111054230. Epub 2012 Jan 6.
The structure of the metastable form I polymorph of the macrolide antibiotic clarithromycin, C(38)H(69)NO(13), was determined by a powder diffraction method using synchrotron radiation. The space group of form I is P2(1)2(1)2. The initial model was determined by a molecular replacement method using the structure of clarithromycin form 0 as a search model, and the final structure was obtained through Rietveld refinements. In the form I crystal structure, the clarithromycin molecules are aligned parallel along the a axis in a head-to-tail manner with intermolecular hydrogen bonds between the hydroxy O atoms. The dimethylamine groups of the clarithromycin molecule interdigitate between neighbouring head-to-tail clarithromycin alignments. The novel crystal packing found in form I provides a mechanism that describes the transformation of form 0 to form I.
通过使用同步辐射的粉末衍射方法确定了大环内酯类抗生素克拉霉素(C₃₈H₆₉NO₁₃)亚稳晶型I的结构。晶型I的空间群为P2(1)2(1)2。初始模型通过使用克拉霉素晶型0的结构作为搜索模型的分子置换法确定,最终结构通过Rietveld精修获得。在晶型I晶体结构中,克拉霉素分子沿a轴以头对头的方式平行排列,羟基O原子之间存在分子间氢键。克拉霉素分子的二甲胺基团在相邻的头对头克拉霉素排列之间相互交错。在晶型I中发现的新型晶体堆积提供了一种描述晶型0向晶型I转变的机制。