- Synthesis and anticonvulsant activity of some new thiazolo[3,2-a][1,3] diazepine, benzo[d]thiazolo[5,2-a][12,6]diazepine and benzo[d]oxazolo[5,2-a][12, 6]diazepine analogues
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A new series of 6,7-dihydro-thiazolo[3,2-a][1,3]diazepines (9-12), benzo[d]thiazolo[5,2-a][12,6]diazepines (19-21) and benzo[d]oxazolo[5,2-a][12,6] diazepine (24) analogues were synthesized and evaluated for their anticonvulsant activity. Compounds (E)-2-bromo-6,7-dihydro-thiazolo[3,2-a][1,3]diazepine-8(5H) -thione (12), 3-chloro-benzo[d]thiazolo[5,2-a][12,6]diazepin-10-one (20), and 4-chloro-benzo[d]oxazolo[5,2-a][12,6] diazepin-10-one (24) showed 100% protection against PTZ- and bicuculline-induced seizures; 70%, 33%, 70% protection against MES-induced tonic extension; and 70%, 66%, 100% protection against picrotoxin-induced convulsions, respectively. Compounds 12, 20, and 24 proved to act as GABAA receptor agonists, with ED50 values of 252, 380, 251 mg/kg; TD50 values of 398, 417, 355 mg/kg; PI values of 1.58, 1.09, 1.41; LD50 values of 380, 617, 537 mg/kg and TI values of 1.51, 1.62, 2.14, respectively.
- El-Subbagh, Hussein I.,Hassan, Ghada S.,El-Azab, Adel S.,Abdel-Aziz, Alaa A.-M.,Kadi, Adnan A.,Al-Obaid, Abdulrahman M.,Al-Shabanah, Othman A.,Sayed-Ahmed, Mohamed M.
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experimental part
p. 5567 - 5572
(2012/01/30)
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- Syntheses of Some 2-Pyrrolidones Carrying N-Heterocycles as Substituents
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Cyclisations of 2-(4-chlorobutyrylamino)thiazoles or 2,5-bis(4-chlorobutyrylamino)-1,3,4-thiadiazole in the presence of piperidine or ammonia lead to 1--2-pyrrolidones and 2,5-bis(2-oxopyrrolidino)-1,3,4-thiadiazole, in analogy to the synthes
- Paul, Heinz,Richter, Ulrich,Huschert, Guenter
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