Synthesis and antifungal activity of 1, 3-bis morpholinomethyl) – 2 – imidazolidone and 1, 3-bis (morpholinomethyl) – imidazolidine – 2-thione compounds
Substituted cyclic ureas and thioureas having aliphatic homocyclic and heterocyclic rings were synthesized. They were screened for their antifugal activity against Cladosporium herbarum and Fusarium oxysporum.1,3 – Bis (morpholinomethyl) – imidazolidine 2- thione (MMIT) and COCl2.MMIT showed total inhibition to C.herbarum at 250, 500 and 1000 ppm concentrations, whereas 1,3-bis (morpholinomethyl)-2-imidazolidone (MMIZ) and ZnCl2.MMIZ showed total inhibition at 1000 ppm concentration towards C.herbarum. Against Fusarium oxysporum only ZnCl2.MMIT showed total inhibition at 1000 ppm concentration. Biosorption of metals on the mycelium of F. oxysporum were decreased in the other cases tried.
KEYWORDS:1,3-bis (morpholinomethyl) -2-imidazolidone (MMIZ), 1,3-bis (morpholinomethyl) imidazolidine – 2
Accepted on: September 29, 2007





