http://rdf.ncbi.nlm.nih.gov/pubchem/patent/TW-200302822-A

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filingDate 2002-10-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ce62053c7d6a07205e286143b2c2c974
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a5121d93decd2caa11a89c61f2b889ce
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d16e3aa6578894d8171f91d87e256135
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7430b06baca38291985a7a4b9102f856
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_766ac301443142574b400f034060f7d4
publicationDate 2003-08-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TW-200302822-A
titleOfInvention 4-(5-membered)-heteroaryl acyl pyrrolidine derivatives as HCV inhibitors
abstract Novel anti-viral agents of formula, wherein: A represents OR1, NR1R2, or R1 wherein R1 and R2 are hydrogen. C1-6alkyl, aryl, heteroaryl, arylalkyl, or heteroarylalkyl; or R1 and R2 together with the nitrogen atom to which they are attached form a 5 or 6 membered saturated cyclic group; B represents C(O)R3 wherein R3 is C1-6alkyl, aryl, heteroaryl, arylalkyl, or heteroarylalkyl; C represents C1-6alkyl, aryl, heteroaryl or heterocyclyl; D represents a saturated or unsaturated optionally substituted 5-membered heterocyclic ring; E represents hydrogen or C1-6alkyl; and F represents hydrogen, C1-6alkyl, aryl or heteroary; and G represents hydrogen, C1-6alkyl, heterocyclylalkyl, arylalkyl or heteroarylalkyl; and salts and solvates thereof, processes for their preparation and methods of using them in HCV treatment are provided.
priorityDate 2001-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7765
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID448924032
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21531290
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID11089
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID420207534
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID453538532
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ993M1
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424624196
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID11103
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414806589
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID154453846
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18373917
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394903
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID423390781
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID3868
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21916431
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394727
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6860482
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415783918
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419506254
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458392451
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID136085
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394984
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ9QAZ8
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID54675821
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11502
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415784596
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID31268
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID409125596
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1049
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450152145
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450328012
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID410500925
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415755187
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP27738
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18767498
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID148408
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412630842
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9195
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID241608

Total number of triples: 339.