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公开(公告)号:JP2002226479A
公开(公告)日:2002-08-14
申请号:JP2001384280
申请日:2001-12-18
Applicant: SERVIER LAB
Inventor: DE NANTEUIL GUILLAUME , BENOIST ALAIN , PASTOUREAU PHILIPPE , SABATINI MASSIMO , HICKMAN JOHN , PIERRE ALAIN , TUCKER GORDON
IPC: C07D491/048 , A61K31/4433 , A61K31/444 , A61K31/541 , A61P9/10 , A61P19/02 , A61P29/00 , A61P35/00 , A61P43/00 , C07D405/14 , C07D417/14 , C07D491/04
Abstract: PROBLEM TO BE SOLVED: To provide a novel metalloprotease inhibitor that is useful for treating rheumatoid arthritis and the like, a method of producing the same and medicinal composition containing the same. SOLUTION: This invention relates to a novel compound represented by formula (I) [wherein R1 is H or the like; X is O or the like; A represents the compound represented by formula A (wherein Ra is H or the like) or the like], an isomer thereof, an N-oxide thereof and a pharmaceutically acceptable adduct salt.
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公开(公告)号:CA2364864C
公开(公告)日:2006-07-18
申请号:CA2364864
申请日:2001-12-20
Applicant: SERVIER LAB
Inventor: PIERRE ALAIN , TUCKER GORDON , DE NANTEUIL GUILLAUME , BENOIST ALAIN , SABATINI MASSIMO , HICKMAN JOHN , PASTOUREAU PHILIPPE
IPC: C07D491/048 , A61K31/4355 , A61K31/4433 , A61K31/444 , A61K31/4523 , A61K31/4525 , A61K31/541 , A61P9/10 , A61P19/02 , A61P29/00 , A61P35/00 , A61P43/00 , C07D405/14 , C07D417/14 , C07D491/04
Abstract: -25- L'invention concerne de nouveaux composés répondant à la formule (I) (Voir formule I) dans laquelle R1 représente un atome d'hydrogène ou d'halogène, un groupemen t alkyle ou alkoxy; X représente un atome d'oxygène ou de soufre, ou un groupement NR da ns lequel R représente un atome d'hydrogène ou un groupement alkyle; A représente l'un quelconque des groupements suivants: (Voir formule II) dans lequel R a représente un atome d'hydrogène ou d'halogène, ou un groupement alkyle ou alkoxy, (Voir formule III) dans lequel R b et R c, identiques ou différents, représentent un atome d'hydrogène ou un groupement alkyle, n représente 0, 1 ou 2, (Voir formule IV) L'invention vise également les isomères des composés de formule (I), ainsi q ue leurs sels d'addition à un acide ou à une base pharmaceutiquement acceptable. Les composés selon l'invention sont utiles comme inhibiteurs de métalloprotéases.
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公开(公告)号:ES2227096T3
公开(公告)日:2005-04-01
申请号:ES01403333
申请日:2001-12-21
Applicant: SERVIER LAB
Inventor: DE NANTEUIL GUILLAUME , BENOIST ALAIN , PASTOUREAU PHILIPPE , SABATINI MASSIMO , HICKMAN JOHN , PIERRE ALAIN
IPC: C07D491/048 , A61K31/4433 , A61K31/444 , A61K31/541 , A61P9/10 , A61P19/02 , A61P29/00 , A61P35/00 , A61P43/00 , C07D405/14 , C07D417/14 , C07D491/04
Abstract: Compuestos de Fórmula (I): **(Fórmula)** en la cual: - R1 representa un átomo de hidrógeno, de halógeno, un grupo alquilo de 1 a 6 carbonos lineal o ramificado o un grupo alcoxi de 1 a 6 carbonos lineal o ramificado, - X representa un átomo de oxígeno, de azufre o un grupo NR donde R es un átomo de hidrógeno o un grupo alquilo de 1 a 6 carbonos lineal o ramificado, - A representa uno cualquiera de los grupos siguientes: **(Fórmula)** donde Ra es un átomo de hidrógeno, de halógeno, un grupo alquilo de 1 a 6 carbonos lineal o ramificado o alcoxi de 1 a 6 carbonos lineal o ramificado **(Fórmula)** donde Rb, Rc, idénticos o diferentes, representan un átomo de hidrógeno o un grupo alquilo de 1 a 6 carbonos lineal o ramificado, n es 0, 1 ó 2 **(Fórmula)** sus isómeros, N-óxidos, así como sus sales de adición de un ácido o de una base farmacéuticamente aceptables.
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公开(公告)号:PT1217002E
公开(公告)日:2004-11-30
申请号:PT01403333
申请日:2001-12-21
Applicant: SERVIER LAB
Inventor: NANTEUIL GUILLAUME DE , PIERRE ALAIN , PASTOUREAU PHILIPPE , TUCKER GORDON , SABATINI MASSIMO , BENOIST ALAIN , HICKMAN JOHN
IPC: C07D491/048 , A61K31/4433 , A61K31/444 , A61K31/541 , A61P9/10 , A61P19/02 , A61P29/00 , A61P35/00 , A61P43/00 , C07D405/14 , C07D417/14 , C07D491/04
Abstract: 5-Sulfonyl-2-(4-pyridinyl)-benzofuran, benzothiophene or indole derivatives (I), containing a hydroxamic acid function, are new. Benzofuran, benzothiophene or indole derivatives of formula (I) and their isomers, N-oxides and acid or base addition salts are new. R1 = H, halo, 1-6C alkyl or 1-6C alkoxy; X = O, S or NR; R = H or 1-6C alkyl; A = N-hydroxy-carboxamido-substituted tetrahydrofuropyridine, thiomorpholine or tetrahydropyranylmethyl group of formula (i)-(iii); Ra = H, halo, 1-6C alkyl or 1-6C alkoxy; Rb, Rc = H or 1-6C alkyl; and n = 0-2. An Independent claim is also included for the preparation of (I).
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公开(公告)号:DK1065209T3
公开(公告)日:2003-08-25
申请号:DK00401864
申请日:2000-06-30
Applicant: SERVIER LAB
Inventor: DE NANTEUIL GUILLAUME , BENOIST ALAIN , BONNET JACQUELINE , SABATINI MASSIMO , ATASSI GHANEM , PIERRE ALAIN
IPC: C07D307/77 , A61K31/4355 , A61K31/4406 , A61K31/4409 , A61K31/4453 , A61K31/506 , A61K31/5377 , A61P9/10 , A61P19/02 , A61P29/00 , A61P35/00 , A61P43/00 , C07D491/04 , C07D491/048
Abstract: N-Arylsulfonyl tetrahydrofuropyridine carboxylic acid derivatives (I), their isomers and acid and base addition salts, their preparation and compositions containing them. N-Arylsulfonyl tetrahydrofuropyridine carboxylic acid derivatives of formula (I), their isomers and acid and base addition salts, their preparation and compositions containing them: R1 = H, halogen, 1-6C alkyl or alkoxy; R2 = OH, 1-6C alkoxy, or NHOH; Ar1 = phenylene or biphenylene; X = O, S, NR, -OC- or a bond; R = H, or 1-6C alkyl; n = 0-6; Ar2 = phenyl substituted by heteroaryl, biphenyl substituted by heteroaryl, pyridinyl substituted by heteroaryl, or a heterocycle
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公开(公告)号:FR2818643B1
公开(公告)日:2003-02-07
申请号:FR0016826
申请日:2000-12-22
Applicant: SERVIER LAB
Inventor: DE NANTEUIL GUILLAUME , BENOIST ALAIN , PASTOUREAU PHILIPPE , SABATINI MASSIMO , KICKMANN JOHN , PIERRE ALAIN , TUCKER GORDON
IPC: C07D491/048 , A61K31/4433 , A61K31/444 , A61K31/541 , A61P9/10 , A61P19/02 , A61P29/00 , A61P35/00 , A61P43/00 , C07D405/14 , C07D417/14 , C07D491/04 , C07D498/04
Abstract: 5-Sulfonyl-2-(4-pyridinyl)-benzofuran, benzothiophene or indole derivatives (I), containing a hydroxamic acid function, are new. Benzofuran, benzothiophene or indole derivatives of formula (I) and their isomers, N-oxides and acid or base addition salts are new. R1 = H, halo, 1-6C alkyl or 1-6C alkoxy; X = O, S or NR; R = H or 1-6C alkyl; A = N-hydroxy-carboxamido-substituted tetrahydrofuropyridine, thiomorpholine or tetrahydropyranylmethyl group of formula (i)-(iii); Ra = H, halo, 1-6C alkyl or 1-6C alkoxy; Rb, Rc = H or 1-6C alkyl; and n = 0-2. An Independent claim is also included for the preparation of (I).
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公开(公告)号:DE69803648T2
公开(公告)日:2002-10-31
申请号:DE69803648
申请日:1998-11-13
Applicant: SERVIER LAB
Inventor: DE NANTEUIL GUILLAUME , REMOND GEORGES , PALADINO JOSEPH , ATASSI GHANEM , PIERRE ALAIN , TUCKER GORDON , BONNET JACQUELINE , SABATINI MASSIMO
IPC: A61K31/00 , A61K31/435 , A61K31/4353 , A61K31/437 , A61P9/00 , A61P9/10 , A61P29/00 , A61P35/00 , A61P43/00 , C07D471/04 , A61K31/44
Abstract: Tetrahydro carboline derivatives of formula (I) and their preparation from D-tryptophan derivatives. Tetrahydrocarboline derivatives of formula (I) their isomers and their salts m = 1, 2,3, or 4; n and p = 0, 1, 2, 3, or 4; X = O, S, or a simple bond; R1 = H, halogen, 1-6C alkyl or trihaloalkyl, OH, 1-6C alkoxy or trihaloalkoxy; R2, R3, and R4 = H or 1-6C alkyl; R5 = H, halogen,1-6C alkoxy, aryloxy or heteroaryloxy; R6, R7, and R8 = H, 1-6C alkyl, or R6 with N and R7 or R8 form a heterocycle; R9 = -SO3H, -COOR10, -CO-NR11R12, or -NR13R14; R10 = H or 1-6C alkyl; R11 and R12 = H or 1-6C alkyl or form an optionally substituted heterocycle with the N atom; R13 and R14 = H or 1-6C alkyl or form an optionally substituted heterocycle with the N atom
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公开(公告)号:HU0105410A2
公开(公告)日:2002-08-28
申请号:HU0105410
申请日:2001-12-21
Applicant: SERVIER LAB
Inventor: BENOIST ALAIN , HICKMANN JOHN , DE NANTEUIL GUILLAUME , PASTOUREAU PHILIPPE , PIERRE ALAIN , SABATINI MASSIMO , TUCKER GORDON
IPC: C07D491/048 , A61K31/4433 , A61K31/444 , A61K31/541 , A61P9/10 , A61P19/02 , A61P29/00 , A61P35/00 , A61P43/00 , C07D405/14 , C07D417/14 , C07D491/04 , C07D411/14
Abstract: 5-Sulfonyl-2-(4-pyridinyl)-benzofuran, benzothiophene or indole derivatives (I), containing a hydroxamic acid function, are new. Benzofuran, benzothiophene or indole derivatives of formula (I) and their isomers, N-oxides and acid or base addition salts are new. R1 = H, halo, 1-6C alkyl or 1-6C alkoxy; X = O, S or NR; R = H or 1-6C alkyl; A = N-hydroxy-carboxamido-substituted tetrahydrofuropyridine, thiomorpholine or tetrahydropyranylmethyl group of formula (i)-(iii); Ra = H, halo, 1-6C alkyl or 1-6C alkoxy; Rb, Rc = H or 1-6C alkyl; and n = 0-2. An Independent claim is also included for the preparation of (I).
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公开(公告)号:PL351301A1
公开(公告)日:2002-07-01
申请号:PL35130101
申请日:2001-12-20
Applicant: SERVIER LAB
Inventor: DE NANTEUIL GUILLAUME , BENOIST ALAIN , PASTOUREAU PHILIPPE , SABATINI MASSIMO , HICKMAN JOHN , PIERRE ALAIN , TUCKER GORDON
IPC: C07D491/048 , A61K31/4433 , A61K31/444 , A61K31/541 , A61P9/10 , A61P19/02 , A61P29/00 , A61P35/00 , A61P43/00 , C07D405/14 , C07D417/14 , C07D491/04 , C07D403/14 , C07D407/14 , C07D409/14 , A61K31/44
Abstract: 5-Sulfonyl-2-(4-pyridinyl)-benzofuran, benzothiophene or indole derivatives (I), containing a hydroxamic acid function, are new. Benzofuran, benzothiophene or indole derivatives of formula (I) and their isomers, N-oxides and acid or base addition salts are new. R1 = H, halo, 1-6C alkyl or 1-6C alkoxy; X = O, S or NR; R = H or 1-6C alkyl; A = N-hydroxy-carboxamido-substituted tetrahydrofuropyridine, thiomorpholine or tetrahydropyranylmethyl group of formula (i)-(iii); Ra = H, halo, 1-6C alkyl or 1-6C alkoxy; Rb, Rc = H or 1-6C alkyl; and n = 0-2. An Independent claim is also included for the preparation of (I).
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公开(公告)号:CA2364864A1
公开(公告)日:2002-06-22
申请号:CA2364864
申请日:2001-12-20
Applicant: SERVIER LAB
Inventor: PIERRE ALAIN , TUCKER GORDON , HICKMAN JOHN , SABATINI MASSIMO , PASTOUREAU PHILIPPE , BENOIST ALAIN , DE NANTEUIL GUILLAUME
IPC: C07D491/048 , A61K31/4433 , A61K31/444 , A61K31/541 , A61P9/10 , A61P19/02 , A61P29/00 , A61P35/00 , A61P43/00 , C07D405/14 , C07D417/14 , C07D491/04 , A61K31/4355 , A61K31/4523 , A61K31/4525
Abstract: -25- L'invention concerne de nouveaux composés répondant à la formule (I) (Voir formule I) dans laquelle R1 représente un atome d'hydrogène ou d'halogène, un groupemen t alkyle ou alkoxy; X représente un atome d'oxygène ou de soufre, ou un groupement NR da ns lequel R représente un atome d'hydrogène ou un groupement alkyle; A représente l'un quelconque des groupements suivants: (Voir formule II) dans lequel R a représente un atome d'hydrogène ou d'halogène, ou un groupement alkyle ou alkoxy, (Voir formule III) dans lequel R b et R c, identiques ou différents, représentent un atome d'hydrogène ou un groupement alkyle, n représente 0, 1 ou 2, (Voir formule IV) L'invention vise également les isomères des composés de formule (I), ainsi q ue leurs sels d'addition à un acide ou à une base pharmaceutiquement acceptable. Les composés selon l'invention sont utiles comme inhibiteurs de métalloprotéases.
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