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1. 发明申请

US20100168065A1 QUINOLINONE DERIVATIVES AS PARP AND TANK INHIBITORS 有权
标题翻译：喹诺酮衍生物作为PARP和油墨抑制剂
公开(公告)号：US20100168065A1
公开(公告)日：2010-07-01
申请号：US12529142
申请日：2008-03-07
申请人： Jorge Eduardo Vialard , Patrick René Angibaud , Laurence Anne Mevellec , Christophe Meyer , Eddy Jean Edgard Freyne , Isabelle Noëlle Pilatte , Bruno Roux , Elisabeth Thérèse Jeanne Pasquier , Xavier Marc Bourdrez , Christophe Denis Adelinet , Laurence Francoise Bernadette Marconnet-Decrane , Jacqueline Anne Macritchie , James Edward Stewart Duffy , Andrew Pate Owens , Pierre-Henri Storck , Virginie Sophie Poncelet
发明人： Jorge Eduardo Vialard , Patrick René Angibaud , Laurence Anne Mevellec , Christophe Meyer , Eddy Jean Edgard Freyne , Isabelle Noëlle Pilatte , Bruno Roux , Elisabeth Thérèse Jeanne Pasquier , Xavier Marc Bourdrez , Christophe Denis Adelinet , Laurence Francoise Bernadette Marconnet-Decrane , Jacqueline Anne Macritchie , James Edward Stewart Duffy , Andrew Pate Owens , Pierre-Henri Storck , Virginie Sophie Poncelet
IPC分类号： A61K31/675 , C07D215/227 , A61K31/4704 , C07D413/12 , A61K31/5377 , C07D401/12 , A61K31/496 , A61K31/506 , C07F9/38 , A61K31/502 , A61K31/498 , C07D471/04 , A61K31/437 , A61P35/00
CPC分类号： C07D215/227 , C07D401/06 , C07D401/12 , C07D405/06 , C07D409/06 , C07D413/06 , C07D417/06
摘要： The present invention provides compounds of formula (I), their use as PARP inhibitors as well as pharmaceutical compositions comprising said compounds of formula (I) wherein R1, R2, R3, R4, R5, R6, R7, n, m and X have defined meanings.
摘要翻译：本发明提供式（I）化合物，它们作为PARP抑制剂的用途以及包含所述式（I）化合物的药物组合物，其中R1，R2，R3，R4，R5，R6，R7，n，m和X具有定义含义。

2. 发明授权

US08299256B2 Quinolinone derivatives as PARP and TANK inhibitors 有权
标题翻译：喹啉酮衍生物作为PARP和TANK抑制剂
公开(公告)号：US08299256B2
公开(公告)日：2012-10-30
申请号：US12529142
申请日：2008-03-07
申请人： Jorge Eduardo Vialard , Patrick René Angibaud , Laurence Anne Mevellec , Christophe Meyer , Eddy Jean Edgard Freyne , Isabelle Noëlle Constance Pilatte , Bruno Roux , Elisabeth Thérèse Jeanne Pasquier , Xavier Marc Bourdrez , Christophe Denis Adelinet , Laurence Françoise Bernadette Marconnet-Decrane , Jacqueline Anne Macritchie , James Edward Stewart Duffy , Andrew Pate Owens , Pierre-Henri Storck , Virginie Sophie Poncelet
发明人： Jorge Eduardo Vialard , Patrick René Angibaud , Laurence Anne Mevellec , Christophe Meyer , Eddy Jean Edgard Freyne , Isabelle Noëlle Constance Pilatte , Bruno Roux , Elisabeth Thérèse Jeanne Pasquier , Xavier Marc Bourdrez , Christophe Denis Adelinet , Laurence Françoise Bernadette Marconnet-Decrane , Jacqueline Anne Macritchie , James Edward Stewart Duffy , Andrew Pate Owens , Pierre-Henri Storck , Virginie Sophie Poncelet
IPC分类号： C07D215/38
CPC分类号： C07D215/227 , C07D401/06 , C07D401/12 , C07D405/06 , C07D409/06 , C07D413/06 , C07D417/06
摘要： The present invention provides compounds of formula (I), their use as PARP inhibitors as well as pharmaceutical compositions comprising said compounds of formula (I) wherein R1, R2, R3, R4, R5, R6, R7, n, m and X have defined meanings.
摘要翻译：本发明提供式（I）化合物，它们作为PARP抑制剂的用途以及包含所述式（I）化合物的药物组合物，其中R1，R2，R3，R4，R5，R6，R7，n，m和X具有定义含义。

3. 发明授权

US08778966B2 Quinolinone derivatives as PARP and tank inhibitors 有权
标题翻译：喹啉酮衍生物作为PARP和罐抑制剂
公开(公告)号：US08778966B2
公开(公告)日：2014-07-15
申请号：US13617686
申请日：2012-09-14
申请人： Jorge Eduardo Vialard , Patrick René Angibaud , Laurence Anne Mevellec , Christophe Meyer , Eddy Jean Edgard Freyne , Isabelle Noëlle Constance Pilatte , Bruno Roux , Elisabeth Thèrése Jeanne Pasquier , Xavier Marc Bourdrez , Christophe Denis Adelinet , Laurence Françoise Bernadette Marconnet-Decrane , Jacqueline Anne Macritchie , James Edward Stewart Duffy , Andrew Pate Owens , Pierre-Henri Storck , Virginie Sophie Poncelet
发明人： Jorge Eduardo Vialard , Patrick René Angibaud , Laurence Anne Mevellec , Christophe Meyer , Eddy Jean Edgard Freyne , Isabelle Noëlle Constance Pilatte , Bruno Roux , Elisabeth Thèrése Jeanne Pasquier , Xavier Marc Bourdrez , Christophe Denis Adelinet , Laurence Françoise Bernadette Marconnet-Decrane , Jacqueline Anne Macritchie , James Edward Stewart Duffy , Andrew Pate Owens , Pierre-Henri Storck , Virginie Sophie Poncelet
IPC分类号： A61K31/04 , C07D413/06 , C07D401/06 , C07D401/12 , C07D405/06 , C07D409/06 , C07D215/227 , C07D417/06
CPC分类号： C07D215/227 , C07D401/06 , C07D401/12 , C07D405/06 , C07D409/06 , C07D413/06 , C07D417/06
摘要： The present invention provides compounds of formula (I), their use as PARP inhibitors as well as pharmaceutical compositions comprising said compounds of formula (I) wherein R1, R2, R3, R4, R5, R6, R7, n, m and X have defined meanings.
摘要翻译：本发明提供式（I）化合物，它们作为PARP抑制剂的用途以及包含所述式（I）化合物的药物组合物，其中R1，R2，R3，R4，R5，R6，R7，n，m和X具有定义含义。

4. 发明授权

US06936626B2 Retinoic acid mimetic anilides 有权
公开(公告)号：US06936626B2
公开(公告)日：2005-08-30
申请号：US09962551
申请日：2001-09-25
申请人： Dominique Mabire , Christophe Denis Adelinet , Imré Christian Csoka , Marc Gaston Venet
发明人： Dominique Mabire , Christophe Denis Adelinet , Imré Christian Csoka , Marc Gaston Venet
IPC分类号： A61K31/4164 , A61K31/4196 , A61K31/427 , A61K31/4402 , A61K31/4406 , A61K31/4409 , A61K31/4418 , A61K31/4427 , A61K31/443 , A61K31/4433 , A61K31/4439 , A61K31/454 , A61K31/4709 , A61K31/496 , A61P17/00 , A61P43/00 , C07D207/335 , C07D207/337 , C07D213/40 , C07D233/56 , C07D233/61 , C07D249/08 , C07D257/04 , C07D401/12 , C07D403/12 , C07D405/12 , C07D409/12 , C07D417/12 , C07D521/00 , C07D213/02 , A61K31/44
CPC分类号： C07D231/12 , C07D233/56 , C07D233/61 , C07D249/08 , C07D401/12 , C07D403/12 , C07D405/12 , C07D409/12 , C07D413/12 , C07D417/12
摘要： The present invention is concerned with compounds of formula the N-oxides, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof, wherein X represents O, S or NR3; R1 represents hydrogen, hydroxy, C1-6alkyl or aryl; R2 represents hydrogen; optionally substituted C1-12alkyl; C3-7cycloalkyl; C2-8alkenyl; aryl; Het1; or R1 and R2 taken together may form a bivalent radical of formula —(CH2)n— wherein n is 2, 3, 4, 5 or 6; R3 represents hydrogen, optionally substituted C1-6alkyl, aryl, Het1; R4 represents hydrogen; hydroxy; mercapto; C1-6alkyloxy; C1-6alkylthio; aryloxy; arylthio; Het1-oxy; Het1-thio; optionally substituted C1-12alkyl; optionally substituted C2-8alkenyl; optionally substituted C2-8alkynyl; optionally substituted C3-7cycloalkyl; optionally substituted C5-7cycloalkenyl; aryl; Het1; or -Alk—NR3R5 (i) or —NR3R5 (ii) wherein Alk represents C1-6alkanediyl; and R5 represents hydrogen, C1-6alkyl, aryl, Het1, (aryl or Het1)C1-6alkyl, (aryl or Het1)carbonyl or (aryl or Het1)C1-6alkyloxycarbonyl; aryl represents optionally substituted indanyl, indenyl, naphtyl, 5,6,7,8-tetrahydro-2-naphtalenyl or phenyl; Het represents an optionally substituted unsaturated heterocycle; and Het1 represents an optionally substituted monocyclic or bicyclic heterocycle; having retinoic mimetic activity; their preparation, compositions containing them and their use as a medicine.

5. 发明授权

US06319939B1 Retinoic acid mimetic anlides 有权
标题翻译：视黄酸模拟物
公开(公告)号：US06319939B1
公开(公告)日：2001-11-20
申请号：US09555775
申请日：2000-06-01
申请人： Dominique Mabire , Christophe Denis Adelinet , Imré Christian Csoka , Marc Gaston Venet
发明人： Dominique Mabire , Christophe Denis Adelinet , Imré Christian Csoka , Marc Gaston Venet
IPC分类号： C07D22354
CPC分类号： C07D231/12 , C07D233/56 , C07D233/61 , C07D249/08 , C07D401/12 , C07D403/12 , C07D405/12 , C07D409/12 , C07D413/12 , C07D417/12
摘要： The present invention is concerned with compounds of formula the N-oxides, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof, wherein X represents O, S or NR3; R1 represents hydrogen, hydroxy, C1-6alkyl or aryl; R2 represents hydrogen; optionally substituted C1-12alkyl; C3-7cycloalkyl; C2-8alkenyl; aryl; Het1; or R1 and R2 taken together may form a bivalent radical of formula —(CH2)n— wherein n is 2, 3, 4, 5 or 6; R3 represents hydrogen, optionally substituted C1-6alkyl, aryl, Het1; R4 represents hydrogen; hydroxy; mercapto; C1-6alkyloxy; C1-6alkylthio; aryloxy; arylthio; Het1-oxy; Het1-thio; optionally substituted C1-12alkyl; optionally substituted C2-8alkenyl; optionally substituted C2-8alkynyl; optionally substituted C3-7cycloalkyl; optionally substituted C5-7cycloalkenyl; aryl; Het1; or -Alk-NR3R5 (i) or —NR3R5 (ii) wherein Alk represents C1-6alkanediyl; and R5 represents hydrogen, C1-6alkyl, aryl, Het1, (aryl or Het1)C1-6alkyl, (aryl or Het1)carbonyl or (aryl or Het1)C1-6alkyloxycarbonyl; aryl represents optionally substituted indanyl, indenyl, naphtyl, 5,6,7,8-tetrahydro-2-naphtalenyl or phenyl; Het represents an optionally substituted unsaturated heterocycle; and Het1 represents an optionally substituted monocyclic or bicyclic heterocycle; having retinoic mimetic activity; their preparation, compositions containing them and their use as a medicine.
摘要翻译：本发明涉及配制N-氧化物的化合物，其药学上可接受的加成盐和立体化学异构形式，其中X表示O，S或NR 3; R 1表示氢，羟基，C 1-6烷基或芳基; R2表示氢; 任选取代的C 1-12烷基; C 3-7环烷基; C2-8烯基; 芳基; Het1; 或者R 1和R 2一起形成式 - （CH 2）n - 的二价基团，其中n为2,3,4,5或6; R 3表示氢，任选取代的C 1-6烷基，芳基，Het 1; R4代表氢; 羟基; 巯基 C 1-6烷氧基; C 1-6烷硫基; 芳氧基芳硫基 Het1-oxy; Het1-硫代任选取代的C 1-12烷基; 任选取代的C 2-8烯基; 任选取代的C 2-8炔基; 任选取代的C 3-7环烷基; 任选取代的C 5-7环烯基; 芳基; Het1; 或-Alk-NR 3 R 5（i）或-NR 3 R 5（ii）其中Alk表示C 1-6烷二基; 并且R 5表示氢，C 1-6烷基，芳基，Het 1，（芳基或Het 1）C 1-6烷基，（芳基或Het 1）羰基或（芳基或Het 1）C 1-6烷氧基羰基; 芳基表示任选取代的茚满基，茚基，萘基，5,6,7,8-四氢-2-萘基或苯基; Het表示任选取代的不饱和杂环; 且Het1表示任选取代的单环或双环杂环; 具有视黄酸模拟活性; 其制剂，含有它们的组合物及其作为药物的用途。

6. 发明申请

US20130018017A1 QUINOLINONE DERIVATIVES AS PARP AND TANK INHIBITORS 有权
标题翻译：喹诺酮衍生物作为PARP和油墨抑制剂
公开(公告)号：US20130018017A1
公开(公告)日：2013-01-17
申请号：US13617686
申请日：2012-09-14
申请人： Jorge Eduardo VIALARD , Patrick René ANGIBAUD , Laurence Anne MEVELLEC , Christophe MEYER , Eddy Jean Edgard FREYNE , Isabelle Noëlle Constance PILATTE , Bruno ROUX , Elizabeth Thérèse Jeanne PASQUIER , Xavier Marc BOURDREZ , Christophe Denis ADELINET , Laurence Françoise Bernadette MARCONNET-DECRANE , Jacqueline Anne MACRITCHIE , James Edward Stewart DUFFY , Andrew Pate OWENS , Pierre-Henri STORCK , Virginie Sophie PONCELET
发明人： Jorge Eduardo VIALARD , Patrick René ANGIBAUD , Laurence Anne MEVELLEC , Christophe MEYER , Eddy Jean Edgard FREYNE , Isabelle Noëlle Constance PILATTE , Bruno ROUX , Elizabeth Thérèse Jeanne PASQUIER , Xavier Marc BOURDREZ , Christophe Denis ADELINET , Laurence Françoise Bernadette MARCONNET-DECRANE , Jacqueline Anne MACRITCHIE , James Edward Stewart DUFFY , Andrew Pate OWENS , Pierre-Henri STORCK , Virginie Sophie PONCELET
IPC分类号： A61K31/4704 , A61K31/5377 , A61K31/496 , A61K31/506 , A61K31/675 , A61K31/4709 , A61K31/501 , A61K31/475 , A61P25/00 , A61P25/28 , A61P9/00 , A61P21/00 , A61P29/00 , A61P19/06 , A61P19/02 , A61P9/10 , A61P37/00 , A61P35/00 , A61P1/00 , A61P19/10 , A61P3/10 , A61P13/12 , A61K31/695
CPC分类号： C07D215/227 , C07D401/06 , C07D401/12 , C07D405/06 , C07D409/06 , C07D413/06 , C07D417/06
摘要： The present invention provides compounds of formula (I), their use as PARP inhibitors as well as pharmaceutical compositions comprising said compounds of formula (I) wherein R1, R2, R3, R4, R5, R6, R7, n, m and X have defined meanings.
摘要翻译：本发明提供式（I）化合物，它们作为PARP抑制剂的用途以及包含所述式（I）化合物的药物组合物，其中R1，R2，R3，R4，R5，R6，R7，n，m和X具有定义含义。

7. 发明授权

US07579352B2 Retinoic acid mimetic anilides 有权
标题翻译：视黄酸模拟苯胺
公开(公告)号：US07579352B2
公开(公告)日：2009-08-25
申请号：US11926699
申请日：2007-10-29
申请人： Dominique Mabire , Christophe Denis Adelinet , Imré Christian Csoka , Marc Gaston Venet
发明人： Dominique Mabire , Christophe Denis Adelinet , Imré Christian Csoka , Marc Gaston Venet
IPC分类号： A61K31/496 , A61K31/454 , A61K31/4439 , A61K31/4196 , C07D403/02 , C07D401/06 , C07D401/02 , C07D249/08
CPC分类号： C07D231/12 , C07D233/56 , C07D233/61 , C07D249/08 , C07D401/12 , C07D403/12 , C07D405/12 , C07D409/12 , C07D413/12 , C07D417/12
摘要： The present invention is concerned with compounds of formula the N-oxides, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof, wherein X represents O, S or NR3; R1 represents hydrogen, hydroxy, C1-6alkyl or aryl; R2 represents hydrogen; optionally substituted C1-12alkyl; C3-7cycloalkyl; C2-8alkenyl; aryl; Het1; R3 represents hydrogen, optionally substituted C1-6alkyl, aryl, Het1; R4 represents hydrogen; hydroxy; mercapto; C1-6alkyloxy; C1-6alkylthio; aryloxy; arylthio; Het1-oxy; Het1-thio; optionally substituted C1-12alkyl; optionally substituted C2-8alkenyl; optionally substituted C2-8alkynyl; optionally substituted C3-7cycloalkyl; optionally substituted C5-7cycloalkenyl; aryl; Het1; or -Alk-NR3R5 (i) or —NR3R5 (ii) wherein Alk represents C1-6alkanediyl; and R5 represents hydrogen, C1-6alkyl, aryl, Het1, (aryl or Het1)C1-6alkyl, (aryl or Het1)carbonyl or (aryl or Het1)C1-6alkyloxycarbonyl; aryl represents optionally substituted indanyl, indenyl, naphtyl, 5,6,7,8-tetrahydro-2-naphtalenyl or phenyl; Het is triazolyl; and Het1 represents an optionally substituted monocyclic or bicyclic heterocycle; having retinoic mimetic activity; their preparation, compositions containing them and their use as a medicine.
摘要翻译：本发明涉及式I化合物的N-氧化物，其药学上可接受的加成盐和立体化学异构形式，其中X代表O，S或NR 3; R 1表示氢，羟基，C 1-6烷基或芳基; R2表示氢; 任选取代的C 1-12烷基; C 3-7环烷基; C2-8烯基; 芳基; Het1; R 3表示氢，任选取代的C 1-6烷基，芳基，Het 1; R4代表氢; 羟基; 巯基 C 1-6烷氧基; C 1-6烷硫基; 芳氧基芳硫基; Het1-oxy; Het1-硫代任选取代的C 1-12烷基; 任选取代的C 2-8烯基; 任选取代的C 2-8炔基; 任选取代的C 3-7环烷基; 任选取代的C 5-7环烯基; 芳基; Het1; 或-Alk-NR 3 R 5（i）或-NR 3 R 5（ii）其中Alk表示C 1-6烷二基; 并且R 5表示氢，C 1-6烷基，芳基，Het 1，（芳基或Het 1）C 1-6烷基，（芳基或Het 1）羰基或（芳基或Het 1）C 1-6烷氧基羰基; 芳基表示任选取代的茚满基，茚基，萘基，5,6,7,8-四氢-2-萘基或苯基; Het是三唑基; 且Het1表示任选取代的单环或双环杂环; 具有视黄酸模拟活性; 其制剂，含有它们的组合物及其作为药物的用途。

8. 发明授权

US07179825B2 Retinoic acid mimetic anilides 有权
公开(公告)号：US07179825B2
公开(公告)日：2007-02-20
申请号：US11081393
申请日：2005-03-16
申请人： Dominique Mabire , Christophe Denis Adelinet , Imré Christian Csoka , Marc Gaston Venet
发明人： Dominique Mabire , Christophe Denis Adelinet , Imré Christian Csoka , Marc Gaston Venet
IPC分类号： C07D213/02 , A61K31/44
CPC分类号： C07D231/12 , C07D233/56 , C07D233/61 , C07D249/08 , C07D401/12 , C07D403/12 , C07D405/12 , C07D409/12 , C07D413/12 , C07D417/12
摘要： The present invention is concerned with compounds of formula the N-oxides, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof, wherein X represents O, S or NR3; R1 represents hydrogen, hydroxy, C1-6alkyl or aryl; R2 represents hydrogen; optionally substituted C1-12alkyl; C3-7cycloalkyl; C2-8alkenyl; aryl; Het1; or R1 and R2 taken together may form a bivalent radical of formula —(CH2)n— wherein n is 2, 3, 4, 5 or 6; R3 represents hydrogen, optionally substituted C1-6alkyl, aryl, Het1; R4 represents hydrogen; hydroxy; mercapto; C1-6alkyloxy; C1-6alkylthio; aryloxy; arylthio; Het1-oxy; Het1-thio; optionally substituted C1-12alkyl; optionally substituted C2-8alkenyl; optionally substituted C2-8alkynyl; optionally substituted C3-7cycloalkyl; optionally substituted C5-7cycloalkenyl; aryl; Het1; or -Alk-NR3R5 (i) or —NR3R5 (ii) wherein Alk represents C1-6alkanediyl; and R5 represents hydrogen, C1-6alkyl, aryl, Het1, (aryl or Het1)C1-6alkyl, (aryl or Het1)carbonyl or (aryl or Het1)C1-6alkyloxycarbonyl; aryl represents optionally substituted indanyl, indenyl, naphtyl, 5,6,7,8-tetrahydro-2-naphtalenyl or phenyl; Het represents an optionally substituted unsaturated heterocycle; and Het1 represents an optionally substituted monocyclic or bicyclic heterocycle; having retinoic mimetic activity; their preparation, compositions containing them and their use as a medicine.

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