Obniska Jolanta, Chlebek Iwona, Pichór Joanna, Kopytko Maciej, Kamiński Krzysztof
Department of Medicinal Chemistry, Jagiellonian University Medical College, 9 Medyczna St. 30-688 Kraków, Poland.
Acta Pol Pharm. 2009 Nov-Dec;66(6):639-47.
The series of N-[(4-arylpiperazin-1-yl)-alkyl]-3-phenyl- and 3-(3-methylphenyl)-pyrrolidine-2,5-diones [VIII-XXV] were synthesized and evaluated for anticonvulsant and neurotoxic properties. Initial anticonvulsant screening was performed in mice, using intraperitoneal (ip) maximal electroshock-induced seizures (MES) and subcutaneous pentylenetetrazole-induced (scPTZ) seizure threshold tests. The neurotoxicity was determined applying the rotorod screen. Compounds VIII-XXV revealed protection only in the electrically induced seizures or were inactive. The most active were Mannich bases of 3-(3-methylphenyl)-pyrrolidine-2,5-dione with electron-withdrawing substituents at position-3 of 4-arylpiperazine fragment [XVII, XVIII], as well as compounds with ethylene or propylene spacer between imide and 4-arylpiperazine nitrogen atoms [XX-XXII, XXV]. All these compounds showed anti-MES protection in mice at doses of 100 mg/kg. Additionally, when given orally, compound XVIII was also active in rats MES screen at a dose of 30 mg/kg.
合成了一系列N-[(4-芳基哌嗪-1-基)-烷基]-3-苯基-和3-(3-甲基苯基)-吡咯烷-2,5-二酮[VIII-XXV],并对其抗惊厥和神经毒性特性进行了评估。最初的抗惊厥筛选在小鼠中进行,采用腹腔注射(ip)最大电休克诱导惊厥(MES)和皮下注射戊四氮诱导(scPTZ)惊厥阈值试验。通过旋转棒试验确定神经毒性。化合物VIII-XXV仅在电诱导惊厥中显示出保护作用或无活性。活性最高的是3-(3-甲基苯基)-吡咯烷-2,5-二酮的曼尼希碱,其4-芳基哌嗪片段的3位带有吸电子取代基[XVII, XVIII],以及在酰亚胺和4-芳基哌嗪氮原子之间带有乙烯或丙烯间隔基的化合物[XX-XXII, XXV]。所有这些化合物在100 mg/kg剂量下对小鼠显示出抗MES保护作用。此外,口服时,化合物XVIII在大鼠MES筛选中以30 mg/kg的剂量也具有活性。