化学
赫尔格
催化
药理学
阿扑吗啡
利培酮
非定型抗精神病薬
抗精神病药
多巴胺受体D2
多巴胺
亲缘关系
立体化学
兴奋剂
受体
心理学
神经科学
内科学
生物化学
氟哌啶醇
精神分裂症(面向对象编程)
精神科
钾通道
医学
作者
Lanchang Gao,Chao Hao,Jiali Chen,Ru Ma,Lu Zheng,Qingkun Wu,Xin Liu,Bi‐Feng Liu,Guisen Zhang,Yin Chen,Jian Jin
标识
DOI:10.1016/j.bmcl.2021.127909
摘要
A series of benzoisoxazoleylpiperidine derivatives were synthesized by using the multi-target strategies and their potent affinities for dopamine (DA), serotonin (5-HT) and human histamine H3 receptors have been evaluated. Of these compounds, the promising candidate 4w displayed high affinities for D2, D3, 5-HT1A, 5-HT2A and H3, a moderate affinity for 5-HT6, negligible effects on the human ether-a-go-go-related gene (hERG) channel, low affinities for off-target receptors (5-HT2C, adrenergic α1 and H1). In addition, the animal behavioral study revealed that, compared to risperidone, compound 4w significantly inhibited apomorphine-induced climbing and MK-801-induced movement behaviors with a high threshold for catalepsy and low liabilities for weight gain and hyperprolactinemia. Results from the conditioned avoidance response test and novel object recognition task demonstrated that 4w had pro-cognitive effects. Thus, the antipsychotic drug-like activities of 4w indicate that it may be a potential polypharmacological antipsychotic candidate drug.
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