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公开(公告)号:JPH1077279A
公开(公告)日:1998-03-24
申请号:JP20757497
申请日:1997-08-01
Applicant: HOECHST AG
Inventor: BOSSLET KLAUS , CZECH JOERG , VASELLA ANDREA , HOOS ROLAND
IPC: C07D309/28 , A61K31/35 , A61K31/351 , A61P29/00 , A61P35/00 , A61P43/00 , C07D211/74 , C07D211/78 , C07D309/30 , C07D335/02 , C07F9/59 , C07F9/655 , C07F9/6553
Abstract: PROBLEM TO BE SOLVED: To obtain a compound which is useful as a β-gluculonidase inhibitor which inhibit tumors from growing and metastasizing. SOLUTION: This compound is represented by formula I [Y is -COOH, -PO3 H2 , -P(O)(OR )(OH); R is a 1-4 alkyl; X is NH, O, S; R is H, -C(O)NHC6 (R )5 ; R is H, OH, a halogen] and formula II (R -R is H, OH a halogen, -COOH, -PO3 H2 ), typically (Z)-O-(D-glucopyranuronosilidene)amino-N- phenyl carbamate. The formulation of the compound of formula I and formula II affords a medicine effective for treatment of postoperative carcinomatous diseases or the inhibition of tumor metastasis and treatment of inflammatory diseases. The compounds of formulas I and II can be prepared by a known process. The does is
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公开(公告)号:ES2166031T3
公开(公告)日:2002-04-01
申请号:ES97112940
申请日:1997-07-28
Applicant: HOECHST AG
Inventor: BOSSLET KLAUS , CZECH JOERG , VASELLA ANDREA , HOOS ROLAND
IPC: A61K31/35 , A61K31/351 , A61P29/00 , A61P35/00 , A61P43/00 , C07D211/74 , C07D309/28 , C07D211/78 , C07D309/30 , C07D335/02 , C07F9/59 , C07F9/655 , C07F9/6553
Abstract: Trihydroxyheterocyclylamino compounds of formula (I) and their salts are new. Y = COOH, PO3H2, P(O)(OR6)(OH), P(O)R6(OH), tetrazole or SO3H; R6 = 1-4C alkyl; X = NH, O or S; R = H or CONH-C6(R7)5; and R7 = H, OH, halo, COOH, PO3H2 or SO3H.
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公开(公告)号:AT207067T
公开(公告)日:2001-11-15
申请号:AT97112940
申请日:1997-07-28
Applicant: HOECHST AG
Inventor: BOSSLET KLAUS , CZECH JOERG , VASELLA ANDREA , HOOS ROLAND
IPC: C07D309/28 , A61K31/35 , A61K31/351 , A61P29/00 , A61P35/00 , A61P43/00 , C07D211/74 , C07D211/78 , C07D309/30 , C07D335/02 , C07F9/59 , C07F9/655 , C07F9/6553
Abstract: Trihydroxyheterocyclylamino compounds of formula (I) and their salts are new. Y = COOH, PO3H2, P(O)(OR6)(OH), P(O)R6(OH), tetrazole or SO3H; R6 = 1-4C alkyl; X = NH, O or S; R = H or CONH-C6(R7)5; and R7 = H, OH, halo, COOH, PO3H2 or SO3H.
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公开(公告)号:PT642799E
公开(公告)日:2002-04-29
申请号:PT94113388
申请日:1994-08-26
Applicant: HOECHST AG , HOECHST HOUDE S A LAB
Inventor: MONNERET CLAUDE , FLORENT JEAN-CLAUDE , GESSON JEAN-PIERRE , JACQUESY JEAN-CLAUDE , KOCH MICHEL , TILLEQUIN FRANCOIS , BOSSLET KLAUS , AZOULAY MICHEL , JORG CZECH DR , VASELLA ANDREA , DIETER HOFFMANN DR , HOOS ROLAND
IPC: C07H15/203 , A61K31/70 , A61K31/7028 , A61K31/7034 , A61K31/704 , A61K47/48 , A61P35/00 , A61P43/00 , C07H15/244
Abstract: Enzymatically cleavable prodrugs with reduced Michaelis-Menten constant (Km) are described.
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公开(公告)号:PT822192E
公开(公告)日:2002-03-28
申请号:PT97112940
申请日:1997-07-28
Applicant: HOECHST AG
Inventor: BOSSLET KLAUS , CZECH JOERG , VASELLA ANDREA , HOOS ROLAND
IPC: A61K31/35 , A61K31/351 , A61P29/00 , A61P35/00 , A61P43/00 , C07D211/74 , C07D309/28 , C07D211/78 , C07D309/30 , C07D335/02 , C07F9/59 , C07F9/655 , C07F9/6553
Abstract: Trihydroxyheterocyclylamino compounds of formula (I) and their salts are new. Y = COOH, PO3H2, P(O)(OR6)(OH), P(O)R6(OH), tetrazole or SO3H; R6 = 1-4C alkyl; X = NH, O or S; R = H or CONH-C6(R7)5; and R7 = H, OH, halo, COOH, PO3H2 or SO3H.
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公开(公告)号:DK0822192T3
公开(公告)日:2002-02-11
申请号:DK97112940
申请日:1997-07-28
Applicant: HOECHST AG
Inventor: HOOS ROLAND , CZECH JOERG , BOSSLET KLAUS , VASELLA ANDREA
IPC: C07D309/28 , A61K31/35 , A61K31/351 , A61P29/00 , A61P35/00 , A61P43/00 , C07D211/74 , C07D211/78 , C07D309/30 , C07D335/02 , C07F9/59 , C07F9/655 , C07F9/6553
Abstract: Trihydroxyheterocyclylamino compounds of formula (I) and their salts are new. Y = COOH, PO3H2, P(O)(OR6)(OH), P(O)R6(OH), tetrazole or SO3H; R6 = 1-4C alkyl; X = NH, O or S; R = H or CONH-C6(R7)5; and R7 = H, OH, halo, COOH, PO3H2 or SO3H.
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公开(公告)号:DE59704940D1
公开(公告)日:2001-11-22
申请号:DE59704940
申请日:1997-07-28
Applicant: HOECHST AG
Inventor: BOSSLET KLAUS , CZECH JOERG , VASELLA ANDREA , HOOS ROLAND
IPC: C07D309/28 , A61K31/35 , A61K31/351 , A61P29/00 , A61P35/00 , A61P43/00 , C07D211/74 , C07D211/78 , C07D309/30 , C07D335/02 , C07F9/59 , C07F9/655 , C07F9/6553
Abstract: Trihydroxyheterocyclylamino compounds of formula (I) and their salts are new. Y = COOH, PO3H2, P(O)(OR6)(OH), P(O)R6(OH), tetrazole or SO3H; R6 = 1-4C alkyl; X = NH, O or S; R = H or CONH-C6(R7)5; and R7 = H, OH, halo, COOH, PO3H2 or SO3H.
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公开(公告)号:AU717219B2
公开(公告)日:2000-03-23
申请号:AU3241997
申请日:1997-07-31
Applicant: HOECHST AG
Inventor: BOSSLET KLAUS , CZECH JOERG , VASELLA ANDREA , HOOS ROLAND
IPC: C07D309/28 , A61K31/35 , A61K31/351 , A61P29/00 , A61P35/00 , A61P43/00 , C07D211/74 , C07D211/78 , C07D309/30 , C07D335/02 , C07F9/59 , C07F9/655 , C07F9/6553
Abstract: Trihydroxyheterocyclylamino compounds of formula (I) and their salts are new. Y = COOH, PO3H2, P(O)(OR6)(OH), P(O)R6(OH), tetrazole or SO3H; R6 = 1-4C alkyl; X = NH, O or S; R = H or CONH-C6(R7)5; and R7 = H, OH, halo, COOH, PO3H2 or SO3H.
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公开(公告)号:AU3241997A
公开(公告)日:1998-02-12
申请号:AU3241997
申请日:1997-07-31
Applicant: HOECHST AG
Inventor: BOSSLET KLAUS , CZECH JOERG , VASELLA ANDREA , HOOS ROLAND
IPC: C07D309/28 , A61K31/35 , A61K31/351 , A61P29/00 , A61P35/00 , A61P43/00 , C07D211/74 , C07D211/78 , C07D309/30 , C07D335/02 , C07F9/59 , C07F9/655 , C07F9/6553
Abstract: Trihydroxyheterocyclylamino compounds of formula (I) and their salts are new. Y = COOH, PO3H2, P(O)(OR6)(OH), P(O)R6(OH), tetrazole or SO3H; R6 = 1-4C alkyl; X = NH, O or S; R = H or CONH-C6(R7)5; and R7 = H, OH, halo, COOH, PO3H2 or SO3H.
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公开(公告)号:CA2212200C
公开(公告)日:2007-05-22
申请号:CA2212200
申请日:1997-08-01
Applicant: HOECHST AG
Inventor: CZECH JORG , BOSSLET KLAUS , HOOS ROLAND , VASELLA ANDREA
IPC: C07D309/28 , C07H5/10 , A61K31/35 , A61K31/351 , A61K31/38 , A61K31/445 , A61K31/66 , A61K31/70 , A61P29/00 , A61P35/00 , A61P43/00 , C07D211/72 , C07D211/74 , C07D211/78 , C07D309/30 , C07D335/02 , C07D401/04 , C07D409/04 , C07F9/59 , C07F9/655 , C07F9/6553 , C07H5/06 , C07H7/033 , C07H13/12
Abstract: Novel inhibitors of .beta.-glucuronidase Compounds of the formulae I and II are suitable for the suppression of tumor growth and of tumor metastasis.
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