
Indeloxazine - Wikipedia
Indeloxazine (Elen, Noin) is an antidepressant and cerebral activator [1] [2] that was marketed in Japan and South Korea by Yamanouchi Pharmaceutical Co., Ltd for the treatment of …
Indeloxazine | C14H17NO2 | CID 3704 - PubChem
Indeloxazine | C14H17NO2 | CID 3704 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity …
茚洛秦 - 百度百科
1.具有复活大脑皮质自发脑波的作用,因而可改善记忆和脑震荡所致的行动障碍,以及延长缺氧环境下的生存时间。 还具有抗抑郁作用,因对 5-羟色胺 、组胺受体有弱的亲和力。 2.口 …
Pharmacological effects of indeloxazine, a new cerebral …
2020年12月9日 · Indeloxazine enhanced passive learned behaviour in rats and ameliorated cerebral ischemia-induced learned disturbances in gerbils. Reserpine-induced hypothermia in …
Pharmacological effects of indeloxazine, a new cerebral …
1989年12月1日 · In biochemical studies, indeloxazine increased the extracellular concentration of acetylcholine in the frontal cortex of mature rats. These results suggest that indeloxazine …
Comparison of the effects of bifemelane hydrochloride, idebenone …
Bifemelane hydrochloride (bifemelane), idebenone and indeloxazine hydrochloride (indeloxazine) are used clinically to reduce apathy and other emotional disturbances in patients with …
茚洛秦_茚洛秦说明书_茚洛秦的作用_茚洛秦副作用_茚洛秦是什么_A…
茚洛秦 (Indeloxazine),商品名 茚氯嗪、茚罗西生、茚洛西亚。 本药品被归类到 心律失常 等药品分类。 A+医学百科茚洛秦条目介绍茚洛秦的功效作用,茚洛秦的副作用和服用方法等。 茚 …
盐酸茚洛秦(Indeloxazine hydrochloride) - 药物靶点:NET x SERT_ …
盐酸茚洛秦: 一种SERT抑制剂、SLC6A2 modulators药物,由Astellas Pharma, Inc. (Astellas Pharma, Inc.)公司最早进行研发,目前全球最高研发状态为撤市,作用机制: SERT抑制剂 (5-羟 …
NCATS Inxight Drugs — INDELOXAZINE
Indeloxazine is a neuroleptic, originally developed and marketed in Japan. It is indicated to allay autonomic hyperactivity following cerebral infarction, cerebral haemorrhage or atherosclerosis. …
盐酸茚洛秦_Indeloxazine hydrochloride-靶点: MAO_适应症-临床_ …
盐酸茚洛秦是由默克和安斯泰来制药集团研发的一种小分子药物,是一种MAO抑制剂。 目前该药物最高研发阶段为撤市,用于治疗抑郁。
- 某些结果已被删除