http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2327544-T3

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filingDate 2005-02-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2009-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_25dcbbc3ba6c1827a4d364e7427cf734
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1e5fbacd60d83aa94dec9fdc24a50f4d
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publicationDate 2009-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2327544-T3
titleOfInvention NEW COMPOUNDS AS INHIBITORS OF SERINA PROTEASA NS3 DE VIRUS DE HEPETITIS C.
abstract A compound, or enantiomers, stereoisomers, rotamers, tautomers or racemates of said compound, or a pharmaceutically acceptable salt, solvate or ester of said compound, wherein said compound has the general structure shown in Formula I: ** see formula ** in which: R 1 is H, OR 8, NR 9 R 10 or CHR 9 R 10, where R 8, R 9 and R 10 can be the same or different, each independently selected from the group consisting of H, alkyl- , alkenyl-, alkynyl-, aryl-, heteroalkyl-, heteroaryl-, cycloalkyl-, heterocyclyl-, arylalkyl- and heteroarylalkyl; A and M may be the same or different, each independently being selected from R, OR, NHR, NRR '', SR, SO2R and halo; or A and M are connected to each other so that the rest: ** see formula ** shown above in Formula I forms a three, four, six, seven or eight membered cycloalkyl, a four to eight membered heterocyclyl, a six to ten member aryl or a five to ten member heteroaryl; E is C (H) or C (R); L is C (H), C (R), CH2C (R) or C (R) CH2; R, R '', R 2, and R 3 may be the same or different, each independently being selected from the group consisting of H, alkyl-, alkenyl-, alkynyl-, cycloalkyl-, heteroalkyl-, heterocyclyl-, aryl- , heteroaryl-, (cycloalkyl) alkyl-, (heterocyclyl) alkyl-, aryl-alkyl- and heteroaryl-alkyl-; or alternatively R and R "in NRR" are connected to each other such that NRR "forms a four to eight membered heterocyclyl; and Y is selected from the following residues: ** see formula ** where G is NH or O; and R 15 R 16, R 17 R 18, and R 19 may be the same or different, each independently being selected from the group consisting of H, alkyl, heteroalkyl, alkenyl, heteroalkenyl, alkynyl, heteroalkynyl, cycloalkyl, heterocyclyl, aryl, arylalkyl, heteroaryl and heteroarylalkyl, or alternatively, (i) R 15 and R 16 are connected to each other to form a four to eight member cyclic structure, or R 15 and R 19 are connected to each other to form a cyclic four structure to eight members, and (ii) similarly; independently, R 17 and R 18 connect to each other to form a three to eight membered cycloalkyl or heterocyclyl; wherein each of said alkyl, aryl, heteroaryl, cycloalkyl or heterocyclyl may be unsubstituted or optionally substituted independently with one or more moieties selected from the group consisting of: hydroxy, alkoxy, aryloxy, thio, alkylthio, arylthio, amino, amido , alkylamino, arylamino, alkylsulfonyl, arylsulfonyl, sulfonamido, alkylsulfonamido, arylsulfonamido, alkyl, aryl, heteroaryl, keto, carboxy, carbalkoxy, carboxamido, alkoxycarbonylamino, alkoxycarbonyloxy, alkylureido, arylureido, halo, cyano and nitro.
priorityDate 2004-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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