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filingDate 1994-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2002-01-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_51854da139fc60183a36a39a720dbdf9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_daa94c5f928d7506290b1ff7f8c98b54
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d4a0ab98b88e67419bde0492984ce6ca
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4e58f737c96fadff398790a3968e8f61
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1af95d94c56b90783f3ba89463ef4501
publicationDate 2002-01-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TW-472042-B
titleOfInvention Acetic acid derivatives and pharmaceutical composition containing the same
abstract Acetic acid derivatives of the formula, wherein L is a group of formula L1 to L5: in which a carbonyl group present in the L group and/or between the L and M groups which is not bonded in the form of an amide can also be present as an oxime, A is a group of formula A1 to A4, E1 and E2 are H, lower-alkyl, OH, lower-alkoxy, lower-alkoxy-lower-alkyl, carboxy-lower-alkyl, P(O)(O-lower-alkyl)2, C(O)OR1, OC(O)R1 or C(O)OR1 or C(O)SR1, provided that at least one of E1 and E2 is H, or E1 and E2 together with the N atoms to which they are attached are a (5,5-dimethyl or 5-oxo)-4,-5-dihydro-1,2,4-oxadizol-3-yl group, R1 is lower-alkoxy-lower-alkyl, lower-alkyl, lower-alkyl substituted by OH, lower-alkoxycarbonyl, lower-alkanoyloxy, lower-alkenoyloxy, lower-alkyl-CONH, or by benzoyloxy which is optionally substituted by lower-alkanoyloxy; or phenyl which is optionally substituted by lower-alkoxy or halogen, or cycloalkyl optionally interrupted by O, one of X and Y is CH and the other is CH, C-lower-alkoxy or N, D is a group (CH2)s or (CH2)tO, s is 1 to 4, m and n are 0 to 5 and t is 0 to 3 but m+n are 1 to 5 and each of m+t and n+t is at last 1, p and q are 0 to 5, but p+q is 2 to 5, W1 is CH2, alkyl-CH, lower-alkyl-OC(O)CH, NH, lower-alkyl-N or lower-alkoxy-lower-alkyl-N, W2 is O, G is H or the characterized group of an Α-aminocarboxylic acid selected from lower-alkyl optionally substituted by lower-alkylthio, -Ora, -NH-Rc, by phenyl or by phenyl substituted with -Orb, Ra is H, lower-alkyl or lower-alkanoyl; Rb is H, lower-alkyl, lower-alkoxy-lower-alkyl, lower-alkoxycarbonyl, lower alkanoyl, furoyl, benzolyl or benzoyl substituted by -O-lower-alkanoyl or NH2; Rc is lower-alkoxycarbonyl, lower-alkylaminocarbonxyl or benzoyl; M is 1,4-piperidinylene bonded via the N atom to the keto group or 1,4-phenylene optionally substituted by OCH2COO-lower-alkyl, Q is O, CH2, NH, acyl-N or lower-alkyl OC(O)N, T is NH-lower-alkyl (COOH or COO-lower-alkyl), lower-alkoxy or lower-alkenylowy substituted by lower-alkoxy or lower-alkyl-COO, or a group OT, T is H, lower-alkyl, pheny or pyridyl optionally bonded via lower-alkylene or cycloalkyl optionally bonded via lower-alkylene and optionally interrupted by O, NH or NCOO-lower-alkyl, with the provisos that (a) T is different from H, lower-alkyl and phenyl-lower-alkyl where L is a group of the formula A is a group of the formula one of E1 and E2 is hydrogen and the other is hydrogen, tertbutoxycarbonyl or benzyloxycarbonyl, one of X and Y is CH and the other is CH or N and W1 is NH, lower-alkyl-N or lower-alkoxy-lower-alkyl-N, G has the above significance, M is 1,4-piperidinylene bonded via the N atom to the keto group and Q is O, and (b) T is different from H, lower-alkyl, phenyl and phenyl-lower-alkyl where L is group of formula L11, L31, or L41, A is a group of the formula, one of E1 an E2 is hydrogen and the other is hydrogen, tertbutoxycarbonyl or benzyloxycarbonyl, one of X and Y is CH and other is CH, C-lower-alkyl, C-lower-alkoxy or N, R DEG and G DEG are H or lower-alkyl, W4 is C=0 or C=NOH, M is 1,4-phenylene optionally substituted by lower-alkyl, lower-alkoxy, OCH2COOH or OCH2COO-lower-alkyl and Q is O, CH2 or NH, (c) A can only be a group of formula A3 when L is a group of formula L1 and M is 1,4-phenylene, and (d) G is not H when L is a group of formula L1 and A is a group of formula A3 or A4, the term ""lower"" denoting straight -chain or branched groups with 1 to 6C atoms, as well as physiologically usable salts thereof, can be used for the treatment or prophylaxis of illnesses which are caused by the binding of adhesive proteins to blood platelets and by blood platelet aggregation and cell-cell adhesion. They are manufactured by cleaving protecting groups in the corresponding protected compounds or by converting the cyano group into the amidino group in corresponding nitriles.
priorityDate 1993-12-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5961
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID69523
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415710673
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID410473849
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7478
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID66747
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID411626879
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID280909
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID100399036
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID453912263
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414870548
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422519765
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID454397067
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID24715
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9321
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425231868
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10953655
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7918
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414663768
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5459844
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419548960
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393112
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559593
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414562033
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415714256
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID165292
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393653
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2733084
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23437676
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11172847
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID94433
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID67649541
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID423994089
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID429536066
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCF6W228
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559581
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414582156
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID87456319
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424483792
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID152317
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID30318
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8038
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ6DLS0
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419558865
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID58717357
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID87885
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415989339
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID26873
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID574299
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID451712188
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18424405
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID432467336
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9794
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID295974
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID164649
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID94429
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID453784485
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419531073

Total number of triples: 631.