PURINE DERIVATIVES THEIR TAUTOMERS AND SALTS THEREOF AND INTERFERON SECRETION INDUCERS, ANTIVIRAL AGENTS AND ANTICANCER DRUGS CONTAINING THE SAME

A purine derivative represented by the following general formula (I): wherein R is a hydrogen atom or a hydrocarbon group containing at most 14 carbon atoms; any -CH2- group in said hydrocarbon group may be replaced with a carbonyl group, a sulfonyl group, -O- or -S- when said -CH2- group is not dir...

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Bibliographic Details
Main Authors HIROTA, KOHSAKU, TAKAKU, HARUO, OGITA, HARUHISA, CHIBA, NOBUYOSHI, MATSUI, HIROYUKI, ISOBE YOSHIAKI
Format Patent
LanguageEnglish
Published 29.04.1999
Edition6
Subjects
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Summary:A purine derivative represented by the following general formula (I): wherein R is a hydrogen atom or a hydrocarbon group containing at most 14 carbon atoms; any -CH2- group in said hydrocarbon group may be replaced with a carbonyl group, a sulfonyl group, -O- or -S- when said -CH2- group is not directly attached to the purine ring or is in -CH3 group not directly attached to the purine ring; any =CH2 group may be replaced with =O or =S; C-H group in said hydrocarbon group may be replaced with N, a C-halogen group or a C-CN group when said C-H group is in -CH2-group not directly attached to the purine ring, in -CH3 group not directly attached to the purine ring, in >CH-group not directly attached to the purine ring, in =CH-group not directly attached to the purine ring or in =CH2 group; R is a hydroxyl group, an amino group or an amino group mono- or di-substituted with a hydrocarbon group containing at most 10 carbon atoms; R is a hydroxyl group, a mercapto group, an acyloxy group containing at most 18 carbon atoms or an oxycarbonyloxy group substituted with a hydrocarbon group containing at most 19 carbon atoms; R is a hydrocarbon group containing at most 14 carbon atoms; any -CH2- group in said R may be replaced with a carbonyl group, a sulfonyl group, -O- or -S- when said -CH2- group is not directly attached to the purine ring or is in -CH3 group not directly attached to the purine ring; any =CH2 group may be replaced with =O or =S; C-H group in said R may be replaced with N, a C-halogen group or a C-CN group when said C-H group is in -CH2-group not directly attached to the purine ring, in -CH3 group not directly attached to the purine ring, in >CH-group not directly attached to the purine ring, in =CH-group not directly attached to the purine ring, in =CH2 group or in IDENTICAL CH group; or its tautomer or pharmaceutically acceptable salts thereof, and an interferon inducer, an anti-virus agent or an anti-cancer agent which comprises said purine derivative or pharmaceutically acceptable salts thereof as an active ingredient.
Bibliography:Application Number: NZ19970329798