公开(公告)号：EA002767B1

公开(公告)日：2002-08-29

申请号：EA199700155

申请日：1996-02-06

Applicant: BASF AG

Inventor： SEITZ WERNER ,  MACK HELMUT ,  ZIERKE THOMAS ,  BOHM HANS-JOACHIM ,  HOFFKEN HANS WOLFGANG ,  KOSER STEFAN ,  PFEIFFER THOMAS ,  HORNBERGER WILFRIED

IPC: A61K38/55 ,  A61K38/00 ,  A61P7/02 ,  C07K5/06 ,  C07K5/065 ,  C07K5/072 ,  C07K5/087

Abstract: Описываютсяингибиторытромбинаформулы (I)где R, А, Ви D имеютуказанныев п.1 формулыизобретениязначения,иихстереоизомерыи ихсолис физиологическипереносимымикислотами, вкоторыхамидиноваяфункцияможетиметьсяв моно- илибис-защищеннойформе. Данныесоединениямогутприменятьсядлялеченияи профилактикиразличногородатромбинзависящихсобытий. Дополнительнымиобъектамиизобретенияявляютсясоединенияформул (VII) и (VIII)где R, А, Ви D имеютуказанноев п.1 формулыизобретениязначение, ив формуле (VII) амидиноваяфункцияможетиметьсяв моно- илибис-защищеннойформе,которыепредставляютсобойпромежуточныепродуктыдляполучениясоединенийформулы (I). Крометого, онипредставляютсобойценныевеществадлясинтезаингибиторовсеринпротеазы. Дальнейшимобъектомизобретенияявляетсяструктурныйфрагментформулы (IX)которыйпредставляетсобойценныйкомпонентингибиторовсеринпротеазы, ив частностиингибиторовтромбина.

公开(公告)号：BG105978A

公开(公告)日：2002-07-31

申请号：BG10597801

申请日：2001-10-04

Applicant: BASF AG

Inventor： HILLEN HEINZ ,  SCHMIDT MARTIN ,  MACK HELMUT ,  SEITZ WERNER ,  HAUPT ANDREAS ,  ZEICHEL JOHANN-CHRISTIA ,  KLING ANDREAS

IPC: C12N9/99 ,  A61K38/00 ,  A61K38/55 ,  A61P1/04 ,  A61P1/18 ,  A61P5/14 ,  A61P7/02 ,  A61P9/00 ,  A61P9/10 ,  A61P11/00 ,  A61P11/06 ,  A61P13/12 ,  A61P15/00 ,  A61P17/02 ,  A61P19/02 ,  A61P21/04 ,  A61P25/00 ,  A61P25/28 ,  A61P29/00 ,  A61P37/02 ,  C07B43/00 ,  C07D401/12 ,  C07D409/12 ,  C07K5/06 ,  C07K5/062 ,  C07K5/065 ,  C07K5/068 ,  C07K5/072 ,  C07K5/078

Abstract: The invention relates to peptidic substances, to the production of said substances and to their use as complement inhibitors. In particular, the invention relates to substances with a guanadine or amidine radical as the terminal group, especially inhibitors of the complement proteases C1s and C1r. 8 claims

公开(公告)号：DE10028575A1

公开(公告)日：2002-03-14

申请号：DE10028575

申请日：2000-06-14

Applicant: BASF AG

Inventor： GENESTE HERVE ,  KLING ANDREAS ,  LANGE UDO ,  LAUTERBACH ARNULF ,  SEITZ WERNER ,  GRAEF CLAUDIA ISABELLA ,  SUBKOWSKI THOMAS ,  HORNBERGER WILFRIED

IPC: A61K45/06 ,  A61P9/00 ,  C07D403/04 ,  C07D401/04 ,  C07D409/04 ,  C07D417/04 ,  C07D471/04 ,  C07D487/04 ,  C07D495/04 ,  A61K31/55

Abstract: The invention relates to novel compounds which bind to integrin receptors, their use as ligands of integrin receptors, in particular as ligands of the αv&bgr;3 integrin receptor, and pharmaceutical preparations comprising these compounds.

公开(公告)号：BR0009678A

公开(公告)日：2002-01-22

申请号：BR0009678

申请日：2000-03-28

Applicant: BASF AG

Inventor： HILLEN HEINZ ,  SCHMIDT MARTIN ,  MACK HELMUT ,  SEITZ WERNER ,  HAUPT ANDREAS ,  ZECHEL JOHANN-CHRISTIAN ,  KLING ANDREAS

IPC: C12N9/99 ,  A61K38/00 ,  A61K38/55 ,  A61P1/04 ,  A61P1/18 ,  A61P5/14 ,  A61P7/02 ,  A61P9/00 ,  A61P9/10 ,  A61P11/00 ,  A61P11/06 ,  A61P13/12 ,  A61P15/00 ,  A61P17/02 ,  A61P19/02 ,  A61P21/04 ,  A61P25/00 ,  A61P25/28 ,  A61P29/00 ,  A61P37/02 ,  C07B43/00 ,  C07D401/12 ,  C07D409/12 ,  C07K5/06 ,  C07K5/062 ,  C07K5/065 ,  C07K5/068 ,  C07K5/072 ,  C07K5/078

Abstract: Peptide substances, their preparation and their use as complement inhibitors are described. These are in particular substances having a guanidine or amidine radical as a terminal group. In particular, inhibitors of the complement proteases C1s and C1r are described.

公开(公告)号：NO20014876L

公开(公告)日：2001-12-04

申请号：NO20014876

申请日：2001-10-08

Applicant: BASF AG

Inventor： HILLEN HEINZ ,  SCHMIDT MARTIN ,  MACK HELMUT ,  SEITZ WERNER ,  HAUPT ANDREAS ,  ZECHEL JOHANN-CHRISTIAN ,  KLING ANDREAS

IPC: A61K38/00 ,  A61K38/55 ,  C12N9/99 ,  A61P1/04 ,  A61P1/18 ,  A61P5/14 ,  A61P7/02 ,  A61P9/00 ,  A61P9/10 ,  A61P11/00 ,  A61P11/06 ,  A61P13/12 ,  A61P15/00 ,  A61P17/02 ,  A61P19/02 ,  A61P21/04 ,  A61P25/00 ,  A61P25/28 ,  A61P29/00 ,  A61P37/02 ,  C07B43/00 ,  C07D401/12 ,  C07D409/12 ,  C07K5/06 ,  C07K5/062 ,  C07K5/065 ,  C07K5/068 ,  C07K5/072 ,  C07K5/078 ,  A61K38/05

Abstract: Peptide substances, their preparation and their use as complement inhibitors are described. These are in particular substances having a guanidine or amidine radical as a terminal group. In particular, inhibitors of the complement proteases C1s and C1r are described.

公开(公告)号：NO20014875A

公开(公告)日：2001-11-13

申请号：NO20014875

申请日：2001-10-08

Applicant: BASF AG

Inventor： BAUCKE DORIT ,  MACK HELMUT ,  SEITZ WERNER ,  HORNBERGER WILFRIED ,  BACKFISH GISELA ,  DELZER JUERGEN

IPC: C12N9/99 ,  A61K38/00 ,  A61K38/55 ,  A61P7/02 ,  A61P9/06 ,  A61P9/10 ,  A61P25/00 ,  A61P25/28 ,  A61P29/00 ,  A61P35/00 ,  A61P35/04 ,  A61P43/00 ,  C07B43/00 ,  C07K5/02 ,  C07K5/062 ,  C07K5/065 ,  A61K38/05

CPC classification number: C07K5/06078 ,  A61K38/00 ,  C07B43/00 ,  C07K5/0222

公开(公告)号：ES2151741T3

公开(公告)日：2001-01-01

申请号：ES97934552

申请日：1997-07-29

Applicant: BASF AG

Inventor： BAUCKE DORIT ,  LANGE UDO ,  MACK HELMUT ,  PFEIFFER THOMAS ,  SEITZ WERNER ,  ZIERKE THOMAS

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.

公开(公告)号：CZ20002463A3

公开(公告)日：2000-10-11

申请号：CZ20002463

申请日：1999-01-23

Applicant: BASF AG

Inventor： BAUCKE DORIT ,  LANGE UDO ,  MACK HELMUT ,  SEITZ WERNER ,  HOEFFKEN HANS WOLFGANG ,  HORNBERGER WILFRIED

IPC: A61K38/05 ,  A61P7/02 ,  A61P19/02 ,  C07K5/065

公开(公告)号：PT808302E

公开(公告)日：2000-09-29

申请号：PT96901746

申请日：1996-01-20

Applicant: BASF AG

Inventor： KARL ULRICH ,  SEITZ WERNER

IPC: C07B57/00 ,  C07C253/34 ,  C07C255/43

Abstract: PCT No. PCT/EP96/00236 Sec. 371 Date Jul. 7, 1997 Sec. 102(e) Date Jul. 7, 1997 PCT Filed Jan. 20, 1996 PCT Pub. No. WO96/23764 PCT Pub. Date Aug. 8, 1996A process for resolving the racemates of phenylacetonitriles of the formula I I where R1, R2, R3 and m have the meanings stated in the description is described. The process comprises dissolving the racemates I in a polar solvent, adding from 0.5 to 1.0 mol of optically active camphorsulfonic acid per mol of compound I, heating to 40 DEG -100 DEG C., allowing to cool and liberating the optically active phenylacetonitrile I from the salt obtained in this way.

公开(公告)号：GR3033164T3

公开(公告)日：2000-08-31

申请号：GR20000400732

申请日：2000-04-06

Applicant: BASF AG

Inventor： KARL ULRICH ,  SEITZ WERNER

IPC: C07B57/00 ,  C07C253/34 ,  C07C255/43

Abstract: PCT No. PCT/EP96/00236 Sec. 371 Date Jul. 7, 1997 Sec. 102(e) Date Jul. 7, 1997 PCT Filed Jan. 20, 1996 PCT Pub. No. WO96/23764 PCT Pub. Date Aug. 8, 1996A process for resolving the racemates of phenylacetonitriles of the formula I I where R1, R2, R3 and m have the meanings stated in the description is described. The process comprises dissolving the racemates I in a polar solvent, adding from 0.5 to 1.0 mol of optically active camphorsulfonic acid per mol of compound I, heating to 40 DEG -100 DEG C., allowing to cool and liberating the optically active phenylacetonitrile I from the salt obtained in this way.