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Neuroinhibitory ketamine and norketamine compounds, their derivatives and methods

机译:神经抑制酮酮和瘤醇类化合物,它们的衍生物和方法

摘要

The present invention is directed to novel neuro-attentuating norketamine (NANKET) compounds according to any one of formulas (I - shown below), (I-A) and (I-B), or any of the compounds described in Tables A-D, or in any of the Examples provided herein, and pharmaceutically acceptable salts thereof, novel pharmaceutical formulations and novel methods of uses thereof. The present invention also features novel oral neuro-attenuating ketamine (NAKET) and neuro-attenuating norketamine (NANKET) modified-release pharmaceutical formulations, and novel methods of administration thereof, which ensure the steady release of a therapeutically effective amount of ketamine, norketamine, or derivatives thereof from the oral modified-release pharmaceutical formulations without neurologically toxic spikes in plasma concentration of the ketamine, norketamine, or derivatives during the release periods.
机译:本发明涉及根据根据任何一种(下文所示),(Ia)和(Ib)的新型神经关注的Norketamine(nanket)化合物,或表AD中描述的任何化合物,或者在任何一种中本文提供的实施例,其药学上可接受的盐,新药制剂及其新用途方法。本发明还具有新型口腔神经衰减氯胺酮(Naket)和神经衰减的瘤型(NANKET)改性 - 释放药物制剂,以及其新的给药方法,确保治疗有效量的氯胺酮,Norketamine的稳定释放,或其衍生物来自口腔修饰的药物制剂,没有神经学报释放期间氯胺酮,无瘤或衍生物的血浆浓度的神经学毒性尖峰。

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