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filingDate 2003-02-17^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2b410edfc96d25fc79656aa5f2eabfaf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1493b8caedbf37d6fc58ecfa3c22f50c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_230883e8fe89d2074751514cd6e0358d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bb1f5ce2e5ad027c8a9451970c67c528
publicationDate 2003-08-28^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2474785-A1
titleOfInvention Novel amino acid derivatives, method for production thereof and pharmaceutical compositions comprising said derivative
abstract Compound of formula (I): in which: R1 represents an aryl group, heteroaryl, optionally substituted alkyl, or a group of formula -(CO) -CR6R7NR8R9 in which R6, R7, R8 and R9 are as defined in description, R2 represents a hydrogen atom or an alkyl group, R3 represents a hydrogen atom or an alkyl group optionally substituted, R4 represents a hydrogen atom or an alkyl group optionally substituted, or else R3 and R4 form together, with the atom of carbon carrying them, a mono-, bi- or tricyclic, saturated or unsaturated, from 3 to 18 links, possibly including one or more heteroatoms chosen from O, S and N, and optionally substituted, n represents zero, 1 or 2, Ar represents an aryl or heteroaryl group, R5 represents an amino, guanidino, cyano or amidino group optionally substituted, its optical isomers as well as its addition salts with an acid pharmaceutically acceptable.
priorityDate 2002-02-21^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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