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7-[3-(1-哌啶基)丙氧基]色原酮作为潜在的非典型抗精神病药物。2. 7-[3-[4-(6-氟-1,2-苯并异恶唑-3-基)-哌啶-1-基]丙氧基]-3-(羟甲基)色原酮-4-酮(阿巴哌隆,FI-8602)的药理学特征

7-[3-(1-piperidinyl)propoxy]chromenones as potential atypical antipsychotics. 2. Pharmacological profile of 7-[3-[4-(6-fluoro-1, 2-benzisoxazol-3-yl)-piperidin-1-yl]propoxy]-3-(hydroxymeth yl)chromen -4-one (abaperidone, FI-8602).

作者信息

Bolós J, Anglada L, Gubert S, Planas J M, Agut J, Príncep M, De la Fuente N, Sacristán A, Ortiz J A

机构信息

Departments of Medicinal Chemistry, Pharmacology, and Biochemistry, Centro de Investigación Grupo Ferrer, Juan de Sada, 32, 08028-Barcelona, Spain.

出版信息

J Med Chem. 1998 Dec 31;41(27):5402-9. doi: 10.1021/jm9810396.

Abstract

A series of novel 7-[3-(1-piperidinyl)propoxy]chromenones was synthesized and tested as potential antipsychotics in several in vitro and in vivo assays. The compounds possessed good affinity for D2 receptors, together with a greater affinity for 5-HT2 receptors, a profile which has been proposed as a model for atypical antipsychotics. Several agents also displayed a high potency in the climbing mice assay on oral administration, suggesting a potent antipsychotic effect as compared to reference standards. Compound 23 was selected for further pharmacological evaluation. Induction of catalepsy and inhibition of stereotypies weaker than standards, along with a lower increase in serum prolactin levels, were indicative of a potential atypical profile for this compound. From these results, 7-[3-[4-(6-fluoro-1, 2-benzisoxazol-3-yl)piperidin-1-yl]propoxy]-3-(hydroxymethyl )chromen- 4-one (23, abaperidone) has been proposed for clinical evaluation in humans as a potential atypical antipsychotic.

摘要

合成了一系列新型的7-[3-(1-哌啶基)丙氧基]色原酮,并在多种体外和体内试验中作为潜在的抗精神病药物进行了测试。这些化合物对D2受体具有良好的亲和力,同时对5-HT2受体具有更高的亲和力,这种特性已被提议作为非典型抗精神病药物的模型。几种药物在口服给药的攀爬小鼠试验中也显示出高效能,表明与参考标准相比具有强效的抗精神病作用。选择化合物23进行进一步的药理学评估。与标准药物相比,其致僵作用的诱导和刻板行为的抑制较弱,同时血清催乳素水平的升高较低,这表明该化合物具有潜在的非典型特征。基于这些结果,7-[3-[4-(6-氟-1,2-苯并异恶唑-3-基)哌啶-1-基]丙氧基]-3-(羟甲基)色原酮-4-酮(23,阿巴哌利酮)已被提议作为一种潜在的非典型抗精神病药物进行人体临床评估。

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