Rakowitz D, Gmeiner A, Matuszczak B
Institute of Pharmacy, Leopold-Franzens University of Innsbruck, Austria.
Pharmazie. 2007 Aug;62(8):636-7. doi: 10.1002/chin.200748146.
Novel N-substituted tetrahydro-2,4-dioxoquinazolin-1-yl acetic acids characterized by formal replacement of the substituted benzyl moiety by cyclohexylmethyl and n-heptyl residues, respectively, were synthesized and evaluated as aldose reductase inhibitors.