Several new 6-oxiranyl-, 6-methyloxiranyluracils, and pyrimidinone derivatives, synthesized by the lithiation-alkylation sequence of 1,3,6-trimethyluracil, 1,3-dimethyl-6-chloromethyluracil, and 2-alkoxy-6-methyl-4(3H)-pyrimidinones, showed a potent and selective antiviral activity against the parainfluenza 1(Sendai) virus replication.

Saladino, R., Danti, M.C., Mincione, E., Crestini, C., Palamara, A.T., Savini, P., et al. (1998). A potent and selective inhibition of parainfluenza 1 (Sendai) virus by new 6-oxiranyl-, 6-methyloxiranyluracils, and 4(3H)-pyrimidinone derivatives. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 8(14), 1833-1838 [10.1016/S0960-894X(98)00314-X].

A potent and selective inhibition of parainfluenza 1 (Sendai) virus by new 6-oxiranyl-, 6-methyloxiranyluracils, and 4(3H)-pyrimidinone derivatives

Botta, Maurizio
1998-01-01

Abstract

Several new 6-oxiranyl-, 6-methyloxiranyluracils, and pyrimidinone derivatives, synthesized by the lithiation-alkylation sequence of 1,3,6-trimethyluracil, 1,3-dimethyl-6-chloromethyluracil, and 2-alkoxy-6-methyl-4(3H)-pyrimidinones, showed a potent and selective antiviral activity against the parainfluenza 1(Sendai) virus replication.
1998
Saladino, R., Danti, M.C., Mincione, E., Crestini, C., Palamara, A.T., Savini, P., et al. (1998). A potent and selective inhibition of parainfluenza 1 (Sendai) virus by new 6-oxiranyl-, 6-methyloxiranyluracils, and 4(3H)-pyrimidinone derivatives. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 8(14), 1833-1838 [10.1016/S0960-894X(98)00314-X].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11365/2738
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