Abstract
A series of 2-substituted-3H-quinazolin-4-one derivatives were designed and synthesized
from anthranilic acid. All these compounds were characterized by IR, 1HNMR, mass
spectroscopy and elemental analysis. The newly synthesized compounds were screened
for their anti-inflammatory and antifungal activities. Anti-inflammatory activity was
assessed by using carrageenan induced rat paw oedema method and antifungal activity
against Candida albicans. by cup plate method.
Publisher
AMG Transcend Association
Subject
Molecular Biology,Molecular Medicine,Biochemistry,Biotechnology
Cited by
7 articles.
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