Abram Michał, Zagaja Mirosław, Mogilski Szczepan, Andres-Mach Marta, Latacz Gniewomir, Baś Sebastian, Łuszczki Jarogniew J, Kieć-Kononowicz Katarzyna, Kamiński Krzysztof
Department of Medicinal Chemistry, Faculty of Pharmacy, Jagiellonian University Medical College , Medyczna 9, 30-688 Kraków, Poland.
Isobolographic Analysis Laboratory, Institute of Rural Health , Jaczewskiego 2, 20-090 Lublin, Poland.
J Med Chem. 2017 Oct 26;60(20):8565-8579. doi: 10.1021/acs.jmedchem.7b01114. Epub 2017 Oct 4.
The focused set of new pyrrolidine-2,5-diones as potential broad-spectrum hybrid anticonvulsants was described. These derivatives integrate on the common structural scaffold the chemical fragments of well-known antiepileptic drugs such as ethosuximide, levetiracetam, and lacosamide. Such hybrids demonstrated effectiveness in two of the most widely used animal seizure models, namely, the maximal electroshock (MES) test and the psychomotor 6 Hz (32 mA) seizure models. Compound 33 showed the highest anticonvulsant activity in these models (ED MES = 79.5 mg/kg, ED 6 Hz = 22.4 mg/kg). Compound 33 was also found to be effective in pentylenetetrazole-induced seizure model (ED PTZ = 123.2 mg/kg). In addition, 33 demonstrated effectiveness by decreasing pain responses in formalin-induced tonic pain, in capsaicin-induced neurogenic pain, and notably in oxaliplatin-induced neuropathic pain in mice. The pharmacological data of stereoisomers of compound 33 revealed greater anticonvulsant activity by R(+)-33 enantiomer in both MES and 6 Hz seizure models.
描述了一组新的吡咯烷 - 2,5 - 二酮作为潜在的广谱混合抗惊厥药。这些衍生物在共同的结构支架上整合了知名抗癫痫药物(如乙琥胺、左乙拉西坦和拉科酰胺)的化学片段。此类杂合物在两种最广泛使用的动物癫痫模型中显示出有效性,即最大电休克(MES)试验和精神运动性6Hz(32mA)癫痫模型。化合物33在这些模型中表现出最高的抗惊厥活性(MES的ED = 79.5mg/kg,6Hz的ED = 22.4mg/kg)。还发现化合物33在戊四氮诱导的癫痫模型中有效(PTZ的ED = 123.2mg/kg)。此外,33通过降低小鼠福尔马林诱导的强直性疼痛、辣椒素诱导的神经性疼痛,特别是奥沙利铂诱导的神经性疼痛中的疼痛反应而显示出有效性。化合物33立体异构体的药理学数据表明,在MES和6Hz癫痫模型中,R(+)-33对映体具有更高的抗惊厥活性。