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Merck

Synthesis, antiviral activity and cytotoxicity evaluation of Schiff bases of some 2-phenyl quinazoline-4(3)H-ones.

European journal of medicinal chemistry (2010-08-21)
Krishnan Suresh Kumar, Swastika Ganguly, Ravichandran Veerasamy, Erik De Clercq
RESUMEN

A new series of 3-(benzylideneamino)-2-phenylquinazoline-4(3H)-ones were prepared through Schiff base formation of 3-amino-2-phenyl quinazoline-4(3)H-one with various substituted carbonyl compounds. Their chemical structures were elucidated by spectral studies. Cytotoxicity and antiviral activity were evaluated against herpes simplex virus-1 (KOS), herpes simplex virus-2 (G), vaccinia virus, vesicular stomatitis virus, herpes simplex virus-1 TK- KOS ACVr, para influenza-3 virus, reovirus-1, Sindbis virus, Coxsackie virus B4, Punta Toro virus, feline corona virus (FIPV), feline herpes virus, respiratory syncytial virus, influenza A H1N1 subtype, influenza A H3N2 subtype, and influenza B virus. Compound 2a showed better antiviral activity against the entire tested virus.

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Sigma-Aldrich
L-arginina, from non-animal source, meets EP, USP testing specifications, suitable for cell culture, 98.5-101.0%
SAFC
L-arginina
Sigma-Aldrich
L-arginina, reagent grade, ≥98%
Sigma-Aldrich
L-arginina, 99%, FCC, FG
Sigma-Aldrich
L-arginina, BioUltra, ≥99.5% (NT)