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类药物天然产物空间的核磁共振指纹图谱鉴定出iotrochotazine A:一种用于研究帕金森病的化学探针。

NMR fingerprints of the drug-like natural-product space identify iotrochotazine A: a chemical probe to study Parkinson's disease.

作者信息

Grkovic Tanja, Pouwer Rebecca H, Vial Marie-Laure, Gambini Luca, Noël Alba, Hooper John N A, Wood Stephen A, Mellick George D, Quinn Ronald J

机构信息

Eskitis Institute for Drug Discovery, Griffith University, Brisbane, QLD, 4111 (Australia).

出版信息

Angew Chem Int Ed Engl. 2014 Jun 10;53(24):6070-4. doi: 10.1002/anie.201402239. Epub 2014 Apr 15.

Abstract

The NMR spectrum of a mixture of small molecules is a fingerprint of all of its components. Herein, we present an NMR fingerprint method that takes advantage of the fact that fractions contain simplified NMR profiles, with minimal signal overlap, to allow the identification of unique spectral patterns. The approach is exemplified in the identification of a novel natural product, iotrochotazine A (1), sourced from an Australian marine sponge Iotrochota sp. Compound 1 was used as a chemical probe in a phenotypic assay panel based on human olfactory neurosphere-derived cells (hONS) from idiopathic Parkinson's disease patients. Compound 1 at 1 μM was not cytotoxic but specifically affected the morphology and cellular distribution of lysosomes and early endosomes.

摘要

小分子混合物的核磁共振谱是其所有组分的指纹图谱。在此,我们提出一种核磁共振指纹方法,该方法利用了馏分具有简化的核磁共振谱图且信号重叠最小这一事实,以实现独特光谱模式的识别。该方法在鉴定一种源自澳大利亚海洋海绵Iotrochota sp.的新型天然产物iotrochotazine A(1)中得到了例证。化合物1在基于特发性帕金森病患者的人类嗅觉神经球衍生细胞(hONS)的表型分析组中用作化学探针。1 μM的化合物1没有细胞毒性,但特异性地影响了溶酶体和早期内体的形态和细胞分布。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f1c/4298794/b1943a938b51/anie0053-6070-f1.jpg

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