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filingDate 2003-02-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_230883e8fe89d2074751514cd6e0358d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1493b8caedbf37d6fc58ecfa3c22f50c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2b410edfc96d25fc79656aa5f2eabfaf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bb1f5ce2e5ad027c8a9451970c67c528
publicationDate 2005-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EA-006389-B1
titleOfInvention NEW COMPOUNDS OF AMINO ACID, METHOD OF THEIR PRODUCTION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
abstract The compound of formula (I) in which R represents aryl group, heteroaryl group or alkyl group, optionally substituted, or a group of formula - (CO) -CRRNRR, in which R, R, R and R take the values specified in the description, R represents a hydrogen atom or an alkyl group, R represents a hydrogen atom or an optionally substituted alkyl group, R represents a saturated or unsaturated, 7 to 15-membered bicyclic system or an optionally substituted alkyl group, or R and R together with the carbon atom carrying them, forming t is saturated or unsaturated, a 3-18 membered mono-, bi- or tricyclic system, optionally containing one or more heteroatoms selected from O, S, and N, and optionally substituted, n is 0, 1, or 2, Ar is an aryl or heteroaryl group, an R group represents an amino group, a guanidino group, a cyano group and an amidino group of the group which is optionally substituted, its optical isomers, as well as its addition salts with a pharmaceutically acceptable acid. Medicines.
priorityDate 2002-02-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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