用核磁共振晶体学重新研究利托那韦多晶型I和II的晶体结构。

IF 3.6 4区 医学 Q2 CHEMISTRY, MEDICINAL
ChemMedChem Pub Date : 2024-11-29 DOI:10.1002/cmdc.202400709
Łukasz Szeleszczuk, Tomasz Gubica, Dariusz Maciej Pisklak
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引用次数: 0

摘要

利托那韦(Ritonavir)是一种蛋白酶抑制剂,品牌名为Norvir®,是一种有效靶向人类免疫缺陷病毒(HIV)的抗病毒药物。利托那韦可能是制药领域最重要和最著名的晶体多态性例子,在过去的30年里,人们对它进行了广泛的研究,最终在2023年发现了它的新多态性——形式III。到目前为止,在CCDC数据库中沉积了利托那韦形式I和形式II两种晶体结构。本研究的目的是重新审视这些晶体结构,利用核磁共振晶体学,通过记录13C CP/MAS核磁共振光谱和用CASTEP进行GIPAW核磁共振计算。得到的结果揭示了核磁共振化学位移计算值与实验值之间的主要差异。这些差异可以在分子水平上解释,因为实验确定的和dft优化的一些原子的位置存在差异,主要是那些形成苯基和噻唑环的原子。这项工作是核磁共振晶体学如何用于验证和改进已经发表的晶体结构的一个例子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Crystal Structure of Ritonavir Polymorphs I and II Revisited with the Application of NMR Crystallography.

Ritonavir, a protease inhibitor sold under the brand name Norvir®, is an antiviral medication that effectively targets the human immunodeficiency virus (HIV). Being probably the most important and best-known example of the crystal polymorphism in the field of pharmaceutics, ritonavir has been extensively studied in the last 30 years, which eventually led to the discovery of its new polymorph, Form III, in 2023. So far, two crystal structures of both Forms I and II of ritonavir were deposited in CCDC database. The aim of this study was to revisit those crystal structures, using NMR crystallography by recording the 13C CP/MAS NMR spectra and performing GIPAW NMR calculations with CASTEP. The obtained results revealed the major discrepancies between the calculated and experimental NMR chemical shift values. Those differences were explained at the molecular level, as resulting from the differences in the experimentally determined and DFT-optimized positions of some atoms, mostly those forming phenyl and thiazole rings. This work is an example of how NMR crystallography can be used to verify and improve the already published crystal structures.

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来源期刊
ChemMedChem
ChemMedChem 医学-药学
CiteScore
6.70
自引率
2.90%
发文量
280
审稿时长
1 months
期刊介绍: Quality research. Outstanding publications. With an impact factor of 3.124 (2019), ChemMedChem is a top journal for research at the interface of chemistry, biology and medicine. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies. ChemMedChem publishes primary as well as critical secondary and tertiary information from authors across and for the world. Its mission is to integrate the wide and flourishing field of medicinal and pharmaceutical sciences, ranging from drug design and discovery to drug development and delivery, from molecular modeling to combinatorial chemistry, from target validation to lead generation and ADMET studies. ChemMedChem typically covers topics on small molecules, therapeutic macromolecules, peptides, peptidomimetics, and aptamers, protein-drug conjugates, nucleic acid therapies, and beginning 2017, nanomedicine, particularly 1) targeted nanodelivery, 2) theranostic nanoparticles, and 3) nanodrugs. Contents ChemMedChem publishes an attractive mixture of: Full Papers and Communications Reviews and Minireviews Patent Reviews Highlights and Concepts Book and Multimedia Reviews.
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