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filingDate 1976-02-06^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1977-12-06^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8354e0e37d9d9d26c9048d746ddb6ed8
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publicationDate 1977-12-06^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4061753-A
titleOfInvention Treating psoriasis with transient pro-drug forms of xanthine derivatives
abstract Compounds of the formula: <IMAGE> wherein R, which may be the same or different, represents a member selected from the group consisting of -CH3, -C2H5, -C3H7, iso-C3H7, -C4H9, iso-C4H9, pentyl, benzyl, allyl, 2-hydroxyethyl, cyclohexyl, 2-isobutenyl, hydroxymethyl, 2-phenylethyl and -CH2O-R2, wherein R2 is defined infra; wherein R1 represents a member selected from the group consisting of H, C1-C7 straight or branched alkyl, CCl3, CBr3, CI3, <IMAGE> CH3O-CH2-, (CH3)2NCH2-, <IMAGE> +TR <IMAGE> wherein R3 represents a member selected from the group consisting of -OH, halogen (Cl, Br, I), -OCH3, -COOCH3, -NO2 and -OCOCH3; wherein <IMAGE> and wherein R2 represents a member selected from the group consisting of <IMAGE> wherein R4 is a member selected from the group consisting of C2-C20 straight or branched alkyl (C3-C7 preferred), -[-(CH2)m-], wherein m represents an integer of from 0 to 10, <IMAGE> wherein R3 is defined as above, <IMAGE> +TR <IMAGE> the residue of any naturally occurring amino acid, the residue of any N- substituted amino acid, wherein said substituent is any amino acid protective group cleavable via hydrogenolysis or hydrolysis (e.g., formyl, benzyloxy, carbonyl, t-butyloxycarbonyl), the residue of an N,N-C1-C5-dialkyl or cycloalkylamino acid, <IMAGE> +TR <IMAGE> wherein n represents an integer of from 1-5 and R5 and R6 which may be the same or different represent C1-C5 alkyl or together form a heterocyclic ring with the N atom to which they are attached (e.g., pyrolidine, piperidine, morpholine, piperazine, imidazoline, thiazolidine, isoxazolidine), imidazolyl, O-C1-C8 alkyl, O-benzyl, O-phenyl and <IMAGE>R5R6,+RE wherein n, R5 and R6 are defined as above; and wherein R2 further represents a member selected from the group consisting of straight or branched C1-C20 alkyl, <IMAGE> wherein n, R5 and R6 are defined as above, phenyl, tolyl, xylyl, and -SO2-R7, wherein R7 is a straight or branched C1-C20 alkyl useful in treating psoriasis in warm-blooded animals are provided.
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