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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-00
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K5-06078
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P7-02
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-113
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filingDate 1992-08-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_25383cdc13b0e43051ea5236db4b440a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_31911735b301efc467f72b38508c7878
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8de2dc729104757376ee5905b2f32c49
publicationDate 1994-08-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CZ-38094-A3
titleOfInvention Novel isosteric peptides
abstract The invention relates to new competitive inhibitors of thrombin, their synthesis, pharmaceutical compositions containing the compounds as active ingredients, and the use of the compounds as anticoagulants for prophylaxis and treatment of thromboembolic diseases, according to the formula <CHEM> wherein: A represents -CH2-, -CH=CH-, -CH2-CH2- or -CH2-CH2-CH2- ; R<1> and R<2> are the same or different and each represents H or X-B-, where B is a straight or branched alkylene group having 1-3 carbon atoms and X is H, methyl, ethyl, a cycloalkyl group having 3-6 carbon atoms or R min CO-, where R min is OH, a straight or branched alkoxy group having 1-4 carbon atoms, NH2 or NHR sec , where R sec is a straight or branched alkyl group having 1-4 carbon atoms, or X is a carboxylic acid mimic, known per se, selected from -PO(OR sec min )2, -SO3H and 5-(1H)-tetrazolyl, and R sec min is H, methyl or ethyl, or B is -SO2- and X is methyl or ethyl; m is 0, 1 or 2, R<3> represents a cyclohexyl group and R<3A> represents H: or m is 1 and R<3> represents a cyclohexyl or phenyl group and R<3A> forms an ethylene bridge together with R<1> ; Y represents O or S(O)p, where p is 0, 1 or 2; R<4> represents H; a straight or branched alkyl or a cycloalkyl having 1 to 6 carbon atoms unsubstituted or substituted with one or more fluoro atoms and/or substituted with a phenyl group: a substituted or unsubstituted aromatic ring selected from phenyl, 4-methoxy-phenyl, 4-tertiary-butyl-phenyl, 4-methyl-phenyl, 2-, 3- or 4-trifluoro-methyl-phenyl, phenyl substituted with 1-5 fluoro atoms: or -CH(CF3)-phenyl, either as such or in the form of a physiologically acceptable salt and including stereoisomers.
priorityDate 1991-08-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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