Record number :
1302951
Title of article :
Synthesis of some newer derivatives of substituted quinazolinonyl-2-oxo/thiobarbituric acid as potent anticonvulsant agents Original Research Article
Author/Authors :
Archana، نويسنده , , V.K. Srivastava، نويسنده , , Ashok Kumar، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2004
Pages :
8
From page :
1257
To page :
1264
Abstract :
5-{1′-[3″-Aminoacetyl-2″-methyl-6″,8″-dihalosubstitutedquinazolin-4″(3″H)-onyl]-thiosemicarbazido}-2-oxo/thiobarbituric acids 3a–3h and 5-{2′-amino-5′-[3″-aminomethylene-2″-methyl-6″,8″-dihalosubstitutedquinazolin-4″(3″H)-onyl]-1′,3′,4′-thiadiazol-2′-yl}-2-oxo/thiobarbituric acid 5a–5h were prepared by incorporating 1-[3′-aminoacetyl-2′-methyl-6″,8″-dihalosubstituted-quinazolin-4′(3′H)-onyl]-thiosemicarbazides 2a–2d and 2-amino-5-[3′-aminomethylene-2′-methyl-6′,8′-dihalosubstituted-quinazolin-4′(3′H)-onyl]-1,3,4-thiadiazoles 4a-4 h respectively at 5th position of 2-oxo/thiobarbituric acids (via Mannich reaction). All the newly synthesized compounds were screened for their anti-convulsant activity in MES and PTZ models and were compared with standard drugs phenytoin sodium and sodium valproate. Interestingly, these compounds were found to be devoid of sedative and hypnotic activities when tested. Out of the compounds studied, the most active compound 5h, that is 5-{2′-amino-5′-[3″-aminomethylene-2″-methyl-6″,8″-dibromoquinazolin-4″(3″H)-onyl]-1′,3′,4′-thiadiazol-2′-yl}-2-thiobarbituric acid showed activity (90%) more potent than the standard drug.
Journal title :
Bioorganic and Medicinal Chemistry
Serial Year :
2004
Link To Document :
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