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公开(公告)号:AT204763T
公开(公告)日:2001-09-15
申请号:AT95901432
申请日:1994-11-25
Applicant: BASF AG
Inventor: SCHWEDEN JUERGEN , ECKES PETER , HORNBERGER WILFRIED , SUBKOWSKI THOMAS
Abstract: PCT No. PCT/EP94/03901 Sec. 371 Date May 31, 1996 Sec. 102(e) Date May 31, 1996 PCT Filed Nov. 25, 1994 PCT Pub. No. WO95/15183 PCT Pub. Date Jun. 8, 1995The invention relates to novel hirudin conjugates formed from a hirudin and one or more lipophilic compounds, where the lipophilic compound has an octanol/water partition coefficient of more than 1.8 and is chemically linked to the hirudin, to the preparation thereof and to the use thereof.
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公开(公告)号:PL181405B1
公开(公告)日:2001-07-31
申请号:PL31798995
申请日:1995-06-06
Applicant: BASF AG
Inventor: BOEHM HANS-JOACHIM , KOSER STEFAN , MACK HELMUT , PFEIFFER THOMAS , SEITZ WERNER , HOEFFKEN HANS W , HORNBERGER WILFRIED
IPC: A61K31/40 , A61K38/00 , A61K38/05 , A61K38/55 , A61K47/48 , A61P7/02 , C07C279/00 , C07D205/04 , C07D207/06 , C07D207/16 , C07D207/48 , C07D211/60 , C07K5/06 , C07K5/065 , C07K5/072 , C07K5/078
Abstract: Compounds of the formula and the salts thereof with physiologically tolerated acids and the stereoisomers thereof, in which the substituents have the meanings stated in the description, are described. Also disclosed are intermediates for their preparation. The compounds are suitable for controlling diseases.
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公开(公告)号:DE19962998A1
公开(公告)日:2001-07-12
申请号:DE19962998
申请日:1999-12-24
Applicant: BASF AG
Inventor: ZECHEL JOHANN-CHRISTIAN , KLING ANDREAS , GENESTE HERVE , LANGE UDO , LAUTERBACH ARNULF , GRAEF CLAUDIA ISABELLA , SUBKOWSKI THOMAS , SADOWSKI JENS , HORNBERGER WILFRIED
IPC: A61K45/06 , C07C403/14 , C07D239/34 , C07D401/04 , C07D401/12 , C07D401/14 , C07D403/12 , C07D403/14 , C07D405/04 , C07D405/14 , C07D409/14 , C07D417/12 , C07D417/14 , C07D403/02 , A61K31/415 , A61K31/505 , C07D239/36 , C07D401/02 , C07D409/02 , C07D417/02
Abstract: Integrin receptor ligands (I), their salts, prodrugs, their enantiomers or diastereomers and tautomeres are new. Integrin receptor ligands of formula (I), their salts, prodrugs, their enantiomers or diastereomers and tautomeres are new. L = U-T; T = COOH or a group hydrolyzable to COOH; U = (CRL1RL2)a-(VL)b-(CRL3RL4)c-(WL)d-(CRL5RL6)e-(XL)f(CRL7RL8)g; a, c, e, g = 0-3; b, d, f = 0 or 1; RL1-RL8 = e.g. H, halo or OH; (CH2)w-(YL)y-RL9; 3-7C cycloalkyl, aryl, arylalkyl, hetaryl or hetarylalkyl (all optionally substituted); or RL1+RL2, RL3+RL4, RL5+RL6, RL7+RL8 = 3-7-membered ring optionally substituted and optionally saturated carbo- or heterocyclyl, which may contain up to 3 N, O or S; w = 0- 4, YL = CO, CON(RY1), N(RY1)CO, N(RY1)-C(O)N(RY1 asterisk ), N(RY1)-COO, O, S, SO2, SO2N(RY1), SO2O, COO, OCO, OCON(RY1), N(RY1) or N(RY1')SO2; RY1, RY1 asterisk = e.g. H, optionally substituted 1-6C alkyl or SO2-1-6C alkyl or optionally substituted, CO-aryl, SO2-ary-, hetaryl, CO-hetaryl or SO2-alkylene-aryl; RL9 = e.g. H, OH, CN, halo,optionally substituted 1-6C alkyl, Cl substituted 1-4C-alkyl or aryl substituted alkynyl or alkenyl, optionally substituted 6-12C-bicycloalkyl; or RL9+RY1, RL9+RY1 asterisk = optionally unsaturated 3-7-heterocyclyl optionally containing up to 3 O, S or N; WL = optionally substituted 4-11-membered mono- or polycyclic aliphatic or aromatic hydrocarbyl, having up to 6 double bonds and up to 6 N, O, S; VL, XL = CO, CONRL10, NRL10CO, SO, SO2, SO2NRL10, NRL10SO2, CS, CSNRL10, NRL10CS, CSO, OCS, COO, OCO, O, ethynylene, CHRL11OCHRL12, C(=CRLI1RL12), CRL11=CRL12, CRL11(ORL13)-CHRL12, CHRL11-CRL12(ORL13), CH(NRL14SO2RL15) , -CH(NRL14CORL15), CH(NRL14COORL16), CH(NRL14CONRL14'CRL15), CH(CORL15), CH(COORL16) or CH(CONRL14RL15); RL10 = e.g. H, optionally substituted 1-6C-alkyl, 1-6C-alkoxyalkyl, 2-6C alkenyl, 3-12C alkynyl; or RL10 and RL1, RL 2, RL 3, RL 4, RL5, RL6, RL7 or RL8 together form an optionally substituted 4-8 membered heterocyclyl, containing up to 5 O, N or S; RL11, RL12 = e.g. H, OH, 1-6C alkyl or alkylene-cycloalkyl or optionally substituted 3-7C cycloalkyl, aryl, arylalkyl, hetaryl or hetarylalkyl; RL13 = e.g. H, optionally substituted 1-6C alkyl or alkylene-cycloalkyl or optionally substituted 3-7C-cycloalkyl or hetarylalkyl; RL14, RL14' = e.g. H, optionally substituted 1-6C alkyl, 1-6C alkoxyalkyl, 2-6C alkenyl, 3-12C alkynyl, CO-1-6C alkyl, CO-O-1-6C-alkyl-, 1-6C-alkylene-3-7C-cycloalkyl or SO2-1-6C-alkyl or optionally substituted 3-7C cycloalkyl; RL15 = optionally substituted 1-6C-alkyl, alkoxyalkyl, 1-6C-alkylene-3-7C-cycloalkyl, 6-12C-bicycloalkyl, 1-6C-alkylene-6-12C-bicycloalkyl, 7-20C tricycloalkyl or 1-6C alkylene-7-20C tricycloalkyl, up to 3 substituted 3-7C cycloalkyl, aryl, arylalkyl, hetarylalkyl or 3-8-membered optionally saturated or aromatic heterocyclyl; or RL15+RL14, RL15+RL14 asterisk = an optionally saturated 3-7C heterocyclyl, optionally containing up to 2 O, S or N; RL16 = optionally substituted 1-6C-alkyl, alkoxyalkyl or 1-6C-alkylene-3-7C cycloalkyl or optionally substituted 3-7C cycloalkyl, aryl, arylalkyl, hetaryl or hetarylalkyl, G = a group of formula (a); the incorporation of G can be any of the 2 orientations; ZG = O, S or NRG3; RG1, RG2 = H, CN, NO2, halo, optionally substituted 1-6C alkyl, 2-6C alkenyl or 2-6C alkynyl, optionally substituted 1-4C alkylene-ORG4, 1-4C-alkylene-CO-ORG4, 1-4C-alkylene-CO-RG4, 1-4C-alkylene-SO2-NRG5RG6, 1-4C -alkylene-CO-NRG5RG6, 1-4C-alkylene-NRG5RG6 or 1-4C-alkylene-SRG4, optionally substituted 3-7C-cycloalkyl, 1-4C-alkylene-3-7C cycloalkyl, 1-4C alkylene-3-7C-heterocycloalkyl or 1-4C-alkylene-3-7C heterocycloalkenyl, optionally substituted aryl, arylalkyl, hetaryl or hetarylalkyl, SRG4, ORG4, SORG4, SO2-RG4, COORG4, OCORG4, O-CO-NRG5RG6, SO2NRG5RG6, CONRG5RG6, NRG5RG6 or CORG4; or RG1+RG2 = optionally substituted optionally saturated or aromatic 3-9-membered carbocyclyl, carbopolycyclyl, heterocyclyl or heteropolycyclyl, containing up to 4 O, N or S; RG3 = H, OH, CN, optionally substituted 1-6C alkyl or 1-4C-alkoxy or optionally substituted 3-7C-cycloalkyl, O-3-7C-cycloalkyl, aryl, -O-aryl, arylalkyl-or O-alkylene-aryl; RG4 = e.g. H, optionally substituted 1-8C alkyl or optionally substituted aryl or heterocycloalkyl; RG5, RG6 = e.g. H, optionally substituted 1-8C alkyl or SO2RG4, COORG4, CONRG4RG4 asterisk or CORG4; RG4 asterisk = as for RG4; B = a structural element containing at least one atom which can act as a hydrogen acceptor under physiological conditions, where at least one hydrogen acceptor atom along the shortest possible path on the structural element frame is at a distance of 4-13 atomic bonds to the structural element G. The full definitions are given in the DEFINITIONS (Full Definitions) Field. Independent claims are also included for the following: (1) use of structural elements of formula -G-L for the preparation of compounds which bind to integrin receptors; (2) pharmaceuticals containing -G-L; (3) use of (I) in the manufacture of medicaments for treating diseases, especially diseases involving excessive or reduced interaction between integrins (particularly alpha v beta 3-integrin) and their natural ligands; (4) pharmaceutical composition containing (I), optionally auxiliary substances and at least a further compound selected from other active substances, and the use of these compositions for treating specific diseases.
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24.
公开(公告)号:HU0100082A2
公开(公告)日:2001-06-28
申请号:HU0100082
申请日:1999-01-23
Applicant: BASF AG
Inventor: BAUCKE DORIT , HORNBERGER WILFRIED , HOEFFKEN HANS WOLFGANG , LANGE UDO , MACK HELMUT , SEITZ WERNER
IPC: A61K38/00 , A61P1/18 , A61P7/02 , A61P11/06 , A61P17/04 , A61P19/02 , A61P27/16 , A61P29/00 , C07K5/06 , C07K5/065
Abstract: Novel five-membered heterocyclic amidines, their preparation and use as competitive inhibitors of trypsin-like serine proteases, especially thrombin and kininogenases such as kallikrein. Pharmaceutical compositions which contain the compounds as active ingredients, and use of the compounds as thrombin inhibitors, anticoagulants and antiinflammatory agents.
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公开(公告)号:DE19936780A1
公开(公告)日:2001-02-15
申请号:DE19936780
申请日:1999-08-09
Applicant: BASF AG
Inventor: KLING ANDREAS , GENESTE HERVE , LANGE UDO , LAUTERBACH ARNULF , GRAEF CLAUDIA ISABELLA , SUBKOWSKI THOMAS , HOLZENKAMP UTA , MACK HELMUT , SADOWSKI JENS , HORNBERGER WILFRIED , LAUX VOLKER
IPC: A61K31/4402 , A61K31/55 , A61K31/5513 , A61P3/14 , A61P5/18 , A61P7/02 , A61P9/00 , A61P9/08 , A61P9/10 , A61P9/12 , A61P9/14 , A61P13/12 , A61P17/02 , A61P17/06 , A61P19/00 , A61P19/08 , A61P19/10 , A61P29/00 , A61P31/04 , A61P31/12 , A61P33/00 , A61P35/00 , A61P35/04 , A61P43/00 , C07D213/74 , C07D223/20 , C07D243/38 , C07D401/06 , C07D401/12 , C07D401/14 , C07D403/12 , C07D403/14 , C07D409/12 , C07D409/14 , C07D417/06 , C07D417/12 , C07D417/14 , C07D471/04 , C07D495/04 , C07D495/14 , C07D487/04
Abstract: The invention relates to novel compounds binding to integrin receptors, to the production thereof and to their use as medicaments.
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公开(公告)号:AU3659200A
公开(公告)日:2000-11-14
申请号:AU3659200
申请日:2000-04-05
Applicant: BASF AG
Inventor: BAUCKE DORIT , MACK HELMUT , SEITZ WERNER , HORNBERGER WILFRIED , BACKFISCH GISELA , DELZER JURGEN
IPC: C12N9/99 , A61K38/00 , A61K38/55 , A61K47/48 , A61P7/02 , A61P43/00 , C07B43/00 , C07D401/12 , C07K5/062 , C07K5/065 , A61K31/4427
Abstract: The present invention relates to prodrugs of general formula (I). The meaning of said formula is given in the description. Disclosed are the prodrugs of pharmaceutically active, heterocyclic amidines. In vivo compounds which are competitive inhibitors of trypsin-like serine proteases, especially thrombin, are produced from the amidines. The invention also relates to the production and use of the prodrugs as medicaments.
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公开(公告)号:DE59702414D1
公开(公告)日:2000-11-02
申请号:DE59702414
申请日:1997-07-29
Applicant: BASF AG
Inventor: BAUCKE DORIT , LANGE UDO , MACK HELMUT , PFEIFFER THOMAS , SEITZ WERNER , ZIERKE THOMAS , HOEFFKEN WOLFGANG , HORNBERGER WILFRIED
IPC: A61K31/40 , A61K31/44 , A61K38/00 , A61K38/05 , A61P1/18 , A61P7/02 , A61P11/02 , A61P11/06 , A61P17/00 , A61P19/02 , A61P29/00 , A61P43/00 , C07D207/22 , C07D211/78 , C07K5/00 , C07K5/02 , C07K5/083
Abstract: Compounds of the formula Iwhere R, R1, R2, R3, R4, R5 and R6, and l, m and n have the meanings stated in the description, and their preparation are described. The novel compounds are suitable for controlling diseases.
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公开(公告)号:CZ20000057A3
公开(公告)日:2000-05-17
申请号:CZ20000057
申请日:1998-06-23
Applicant: BASF AG
Inventor: SUBKOWSKI THOMAS , HORNBERGER WILFRIED
IPC: A61K38/00 , A61K39/395 , A61P7/02 , A61P7/04 , A61P39/02 , C07K16/00 , C07K16/40 , C12N5/10 , C12N15/02 , C12P21/08 , G01N33/573
CPC classification number: G01N33/573 , A61K38/00 , C07K16/40 , G01N2333/96433
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公开(公告)号:NO20000079A
公开(公告)日:2000-03-07
申请号:NO20000079
申请日:2000-01-07
Applicant: BASF AG
Inventor: SUBKOWSKI THOMAS , HORNBERGER WILFRIED
IPC: A61K38/00 , A61K39/395 , A61P7/02 , A61P7/04 , A61P39/02 , C07K16/00 , C07K16/40 , C12N5/10 , C12N15/02 , C12P21/08 , G01N33/573 , C07K
CPC classification number: G01N33/573 , A61K38/00 , C07K16/40 , G01N2333/96433
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公开(公告)号:NZ333679A
公开(公告)日:1999-09-29
申请号:NZ33367997
申请日:1997-07-29
Applicant: BASF AG
Inventor: BAUCKE DORIT , LANGE UDO , MACK HELMUT , SEITZ WERNER , ZIERKE THOMAS , HOFFKEN HANS WOLFGANG , HORNBERGER WILFRIED
IPC: A61K38/00 , A61K38/05 , A61P7/02 , A61P29/00 , A61P35/00 , A61P35/04 , C07K5/06 , C07K5/062 , C07K5/065 , C07D417/12 , C07D409/12 , C07D413/12 , C07D407/12 , C07D401/12
Abstract: PCT No. PCT/EP97/04104 Sec. 371 Date Feb. 10, 1999 Sec. 102(e) Date Feb. 10, 1999 PCT Filed Jul. 29, 1997 PCT Pub. No. WO98/06741 PCT Pub. Date Feb. 19, 1998Compounds of the formula where A, B, E and D have the meanings indicated in the description, and their preparation are described. The substances are suitable for controlling diseases.
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