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filingDate 2003-05-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2007-05-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6ee79a5777fb1ecaa3a47c0003dd9241
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publicationDate 2007-05-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-7214668-B2
titleOfInvention Phosphonic acid based prodrugs of PMEA and its analogues
abstract Prodrugs of Formula I, their uses, their intermediates, and their method of manufacture are described: n n n n n n n n n n n n wherein: n M and V are cis to one another and MPO 3 H 2 is a phosphonic acid selected from the group consisting of 9-(2-phosphonylmethoxyethyl)adenine, (R)-9-(2-phosphonylmethoxy propyl)adenine, 9-(2-phosphonylmethoxyethyl)guanine, 9-(2-phosphonylmethoxy ethyloxy)adenine, 9-(2-phosphonylmethoxyethyl)-2,6-diaminopurine, (S)-1-(3-hydroxy-2-phosphonylmethoxypropyl)cytosine, (S)-9-(3-hydroxy-2-phosphonylmethoxypropyl)adenine, 9-(3-hydroxy-2-phosphonylmethoxypropyl)guanine, and (S)-9-(3-fluoro-2-phosphonyl methoxypropyl)adenine; n V is selected from a group consisting of phenyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, 2-furanyl, 3-furanyl, 2-thienyl, and 3-thienyl, all optionally substituted with 1-3 substituents selected from a group consisting of F, Cl, Br, C1-C3 alkyl, CF 3 and OR 6 ; n R 6 is selected from the group consisting of C1-C3 alkyl, and CF 3 ; n and pharmaceutically acceptable salts thereof.
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Total number of triples: 1186.