http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-101213198-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1c539db959cc0106cab1662303f94fce
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D493-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D493-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-513
filingDate 2006-07-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6812721391c4bffce90258719256019f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cf7aa835818d7e9633be1604efaadc34
publicationDate 2008-07-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-101213198-A
titleOfInvention 1-[2',3'-dideoxy-3'C-(hydroxymethyl)-beta-D-erythro-pentofuranosyl] cytosine derivatives as HIV inhibitors
abstract The invention relates to a compound of formula (I) and a salt acceptable by pharmacy, with the utility of curing or preventing HIV, in particular reverse transcriptase mutants which allow an obligate chain terminating nucleoside-or nucleotide phosphate to be excised from the nascent DNA strand by ATP-or pyrophosphate-mediated excision. Wherein, R<1> is independently H1-OR<3>, NHR<4> and C1-C4 alkyl; or, when n is 2, the adjacent R<1> together forms alkyl and R<2> is H; or when gem R<1> is C1-C4 alkyl, R<2> can also be C1-C4 alkyl; or when gem R<1>is -OR<3>, R<2> can also be -C(=O)OH or the acceptable ester in pharmacy; R<3> is dependently H or the acceptable ester in pharmacy; R<4> is dependently H or the acceptable acid amide acceptable in pharmacy; R<5> and R<6> are H or the medicine part before amine; n is 1, 2 and 3.
priorityDate 2005-07-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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