首页> 外国专利> NOVEL 3-CHLORO-5-SUBSTITUTED-QUINOXALINE-2-AMINE DERIVATIVES AND PHARMACEUTICALLY ACCEPTABLE SALT THEREOF, METHOD FOR PREPARATION, THERAPEUTIC AGENT FOR ANTIINFLAMMATORY DISEASE INDUCED BY SPC ACTIVITY CONTAINING 3-CHLORO-5-SUBSTITUTED-QUINOXALINE-2-AMINE DERIVATIVES AS AN EFFECTIVE INGREDIENT

NOVEL 3-CHLORO-5-SUBSTITUTED-QUINOXALINE-2-AMINE DERIVATIVES AND PHARMACEUTICALLY ACCEPTABLE SALT THEREOF, METHOD FOR PREPARATION, THERAPEUTIC AGENT FOR ANTIINFLAMMATORY DISEASE INDUCED BY SPC ACTIVITY CONTAINING 3-CHLORO-5-SUBSTITUTED-QUINOXALINE-2-AMINE DERIVATIVES AS AN EFFECTIVE INGREDIENT

机译:新型3-氯5-取代的喹诺啉2-胺衍生物及其药学可接受的盐,其制备方法,包含3-氯5-取代的喹诺酮类药物的SPC活性引起的抗炎性疾病的治疗剂。有效成分

摘要

Provided are a 3-chloro-5-substiuted-quinoxalin-2-amine derivative represented by the following Chemical Formula 1, a pharmaceutically acceptable salt thereof, a method for preparation thereof, and a use thereof as an effective ingredient in a therapeutic agent for inflammatory disease induced by activity of sphingosyl phosphorylcholine (SPC) receptor. The 3-chloro-5-substiuted-quinoxalin-2-amine derivative of the present invention has been confirmed to have superior inhibition activity against SPC receptor in an animal experiment using human-derived endothelial cells and mice. Thus, a therapeutic agent for inflammatory disease containing the 3- chloro-5-substiuted-quinoxalin-2-amine derivative or a pharmaceutically acceptable salt thereof as an effective ingredient may be useful for treating inflammation, itching or skin infection associated with atopic dermatitis or other disease induced by activity of SPC receptor.
机译:提供由以下化学式1表示的3-氯-5-取代的喹喔啉-2-胺衍生物,其药学上可接受的盐,其制备方法及其在治疗剂中作为有效成分的用途。鞘氨醇磷酸胆碱(SPC)受体的活性诱导的炎症性疾病。在使用人源性内皮细胞和小鼠的动物实验中,已经证实本发明的3-氯-5-取代的喹喔啉-2-胺衍生物具有对SPC受体的优异抑制活性。因此,包含3-氯-5-取代的喹喔啉-2-胺衍生物或其药学上可接受的盐作为有效成分的炎性疾病的治疗剂可用于治疗与特应性皮炎或皮肤炎相关的发炎,瘙痒或皮肤感染。 SPC受体活性诱发的其他疾病。

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