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filingDate 1983-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f50dd35984ee4a833015ad1f19fffb2f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d978f08937ad10974d8ad1eb60526a0c
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publicationDate 1985-06-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S60112799-A
titleOfInvention 2-carbamoyl or thiocarbamoly-6-substituted oxypurine nucleotide and its preparation
abstract NEW MATERIAL:A compound shown by the formula I (R 1 is alkyl, or aralkyl; R 2 is O, or S; X, Y, and Z are H, or protecting group). n EXAMPLE: 2-Carbamoyl- 6-methoxy- 2',3',5'-tri-O-acetylinosine[ 2-carbamoyl- 6-methoxy-9-(1-β-D-2,3,5-tri-O-acetylribofuranosyl)purine]. n USE: An antiviral agent, and an antitumor agent. Useful as a reagent for study in nucleic acid chemistry. n PREPARATION: A 2-cyano-6-substituted oxypurine nucleotide (e.g., 2-cyano-6-methoxy-2',3',5'-tri-O-acetylinosine, etc.) shown by the formula II is hydrolyzed with water or treated with hydrogen sulfide. n COPYRIGHT: (C)1985,JPO&Japio
priorityDate 1983-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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