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炔基喹唑啉酮衍生物的合成及其抗惊厥活性

Synthesis and anticonvulsant activity of acetylenic quinazolinone derivatives.

作者信息

Usifoh C O, Scriba G K

机构信息

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Benin, Nigeria.

出版信息

Arch Pharm (Weinheim). 2000 Aug;333(8):261-6.

Abstract

Acetylenic derivatives of quinazolinones and quinazolinediones were synthesized and evaluated for their anticonvulsant activity. Most compounds displayed seizure-antagonizing activity in the maximal electroschock test (MES test) in most cases associated with little or no acute neurotoxicity determined in the rotorod test. Only three compounds exhibited significant activity in the seizure threshold test with subcutaneous pentylenetetrazole (scMet test). Based on the ED50 in the MES test, 1,3-bis-(prop-2-ynyl)-quinazoline-2,4-(1H,3H)-dione(9a) was about ten-fold less active than phenytoin or carbamazepine but about as active as mesuximide.

摘要

合成了喹唑啉酮和喹唑啉二酮的乙炔衍生物,并对其抗惊厥活性进行了评估。大多数化合物在最大电休克试验(MES试验)中表现出抗惊厥活性,在大多数情况下,与旋转棒试验中确定的很少或没有急性神经毒性有关。只有三种化合物在皮下注射戊四氮惊厥阈值试验(scMet试验)中表现出显著活性。根据MES试验中的半数有效剂量(ED50),1,3-双(丙-2-炔基)喹唑啉-2,4-(1H,3H)-二酮(9a)的活性比苯妥英或卡马西平低约10倍,但与甲琥胺活性相当。

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