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filingDate 2000-01-19^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cd0d65deaf4995e73795d954e8681e43
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a047ef78284566b15beed5f13c133cec
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_157174cc084829e7487d08f05547545d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b54532deaab92f46ce38fe6f04edb9fb
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publicationDate 2001-10-10^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1140981-A1
titleOfInvention Tripeptide compounds useful as selective inhibitors of aminopeptidase a and corresponding pharmaceutical compositions
abstract The invention concerns a compound of general formula (I) wherein: R1 represents an alkyl, alkenyl or alkynyl chain, or a cycloalkyl, or (cycloalkyl)alkyl group substituted by at least a COOH, SO3H, PO3H2 or tetrazolyl group; R2 represents an alkyl chain, or an aryl, arylalkyl, cycloalkyl, (cycloalkyl)alkyl, (heteroaryl)alkyl group substituted or not by at least a OH, OR, SR', NH2, NHR', guanidinyl, COOH, CONH2 group, or a halogen atom; R3 represents a hydrogen atom or a methyl group; R4 represents a) an alkyl chain, an aryl, alrylalkyl, cycloalkyl, (cycloalkyl)alkyl, (heteroalkyl)alkyl, heterocycloalkyl or (heterocycloalkyl)alkyl group substituted by at least a CONH2, SO3H, SO2NH2, PO3H2 or tetrazolyl group, (b) C2-C6 alkyl chain, an aryl, arylakyl, cycloalkyl, (cycloalkyl)alkyl, (heteroaryl)alkyl, heterocycloalkyl, (heterocycloalkyl)alkyl group substituted by at least a CO2H group capable of being protected as described above; or c) R3 and R4 can together form a heterocyclic compound, with 5 to 6 links, substituted by at least a CO2H, CONH2, SO3H, SO2NH2 or PO3H2 group; X represents a CONH or CH2NH; and Z represents a OH, OCH2-C6H5 or NR''R''' group.
priorityDate 1999-01-20^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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