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Screening of natural product samples for novel therapeutic compounds such using capillary electrophoresis

机译:使用毛细管电泳筛选天然产物样品中的新型治疗化合物

摘要

(57) Abstract The chemical compound which is connected to the specific molecule which you observe strongly is disclosed, the method where from the natural sample component simultaneously it is divided and is sorted and. This way the ligand which is separated anew comes latently for remedy or the chemical compound for diagnosis well and becomes candidacy. The natural sample to be connected the latent target molecule first, then it is introduced into capillary cataphoresis (CE). Can modify that usual shifting field with CE, or the electric charge which exists in the natural sample which is connected to the target molecule which is added the chemical compound which is done (or neuter) by changing the electric charge anti- mass ratio, peak form or the territory cause change makes. To detect by watching the movement of the target molecule simply it is possible compound form, to the period of cataphoresis. Every new ligand which is connected to the target molecule comes, for remedy or the chemical compound for diagnosis well and becomes candidacy. Generally exists the ligand which weak connection disturbs is not detected inside the crude extract. The minute natural ligand same as the ligand which electric charge is done, can be identified at the time of connection comparison experimenting of the competitive molecule which known electric charge is done.
机译:(57)<摘要>公开了一种与强烈观察到的特定分子连接的化合物,同时从天然样品成分中进行分选的方法。这样,重新分离的配体就可能潜伏于治疗或良好地诊断化合物而成为候选国。首先将要连接潜在靶分子的天然样品,然后将其引入毛细管电泳(CE)。可以通过改变电荷的反质量比,峰值来改变CE或与连接到目标分子的天然样品中存在的电荷的自然位移场,该目标分子中加入了已完成的化合物(或中性的)形式或地区引起变化。为了通过观察靶分子的运动来检测,可以简单地以化合物形式存在于电泳期。每个与靶分子连接的新配体都会用于治疗或很好地诊断化合物,从而成为候选药物。通常在粗提物中没有检测到弱连接干扰的配体。与完成电荷的配体相同的微小天然配体,可以在进行了已知电荷的竞争分子的连接比较实验时确定。

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