-
![Imidazo[1,5-a]pyridine derivatives, method for preparing same and pharmaceutical compositions containing same](/abs-image/US/2014/01/21/US08633216B2/abs.jpg.150x150.jpg)
1.发明授权Imidazo[1,5-a]pyridine derivatives, method for preparing same and pharmaceutical compositions containing same 有权咪唑并[1,5-a]吡啶衍生物，其制备方法和含有其的药物组合物公开(公告)号：US08633216B2
公开(公告)日：2014-01-21
申请号：US13020883
申请日：2011-02-04
CPC分类号： C07D471/04
摘要： The invention concerns compounds of formula I, a method for preparing said compounds, pharmaceutical compositions containing same and the therapeutic uses thereof.
摘要翻译： 本发明涉及式I化合物，制备所述化合物的方法，含有该化合物的药物组合物及其治疗用途。
-
![Imidazo[1,5-a] pyridine derivatives, method for preparing same and pharmaceutical compositions containing same](/abs-image/US/2011/08/30/US08008321B2/abs.jpg.150x150.jpg)
2.发明授权Imidazo[1,5-a] pyridine derivatives, method for preparing same and pharmaceutical compositions containing same 有权咪唑并[1,5-a]吡啶衍生物，其制备方法和含有其的药物组合物公开(公告)号：US08008321B2
公开(公告)日：2011-08-30
申请号：US11855549
申请日：2007-09-14
IPC分类号： A61K31/4375 , C07D471/04 , A61P43/00 , A61P35/00 , A61P9/00 , A61P37/00 , A61P19/02
CPC分类号： C07D471/04
摘要： The invention concerns compounds of formula I, a method for preparing said compounds, pharmaceutical compositions containing same and the therapeutic uses thereof.
摘要翻译： 本发明涉及式I化合物，制备所述化合物的方法，含有该化合物的药物组合物及其治疗用途。
-
3.发明授权Indolizine derivatives, process for the preparation thereof and therapeutic use thereof 有权中氮茚衍生物，其制备方法及其治疗用途公开(公告)号：US08859544B2
公开(公告)日：2014-10-14
申请号：US13808483
申请日：2011-07-04
IPC分类号： C07D471/04 , A61K45/06 , A61K31/5377 , A61K31/517 , A61K31/4709 , A61K9/20 , C07D207/32 , C07D207/36 , C07D211/82
CPC分类号： C07D471/04 , A61K9/2018 , A61K9/2054 , A61K9/2059 , A61K31/4709 , A61K31/517 , A61K31/5377 , A61K45/06 , C07D207/32 , C07D207/36 , C07D211/82
摘要： The invention relates to compounds corresponding to formula (I): in which R3 and R4 together form, with the carbon atoms of the phenyl nucleus to which they are attached, a 6-membered nitrogenous heterocycle corresponding to one of formula (A), (B) or (C) below: in which the wavy lines represent the phenyl nucleus to which R3 and R4 are attached. Preparation process and therapeutic use.
摘要翻译： 本发明涉及对应于式（I）的化合物：其中R 3和R 4与它们所连接的苯环的碳原子一起形成对应于式（A），（A）中的一个的6-元含氮杂环， B）或（C）：其中波浪线表示R3和R4连接的苯基核。 制备过程和治疗用途。
-
4.发明授权Substituted indolizine 1,2,3,6,7,8 derivatives, FGFs inhibitors, a method for the preparation thereof and pharmaceutical compositions containing said derivatives 有权取代的中氮茚1,2,3,6,7,8衍生物，FGF抑制剂，其制备方法和含有所述衍生物的药物组合物公开(公告)号：US07553845B2
公开(公告)日：2009-06-30
申请号：US11378972
申请日：2006-03-17
申请人： Chantal Alcouffe , Alain Badorc , Francoise Bono , Marie-Francoise Bordes , Nathalie Guillo , Jean-Marc Herbert
发明人： Chantal Alcouffe , Alain Badorc , Francoise Bono , Marie-Francoise Bordes , Nathalie Guillo , Jean-Marc Herbert
IPC分类号： A61K31/437 , C07D471/04
CPC分类号： C07D471/04
摘要： The invention is directed to a compound of formula I, wherein R, R1, R2, R3 and R4 are as defined herein, or a pharmaceutically acceptable salt thereof, and its pharmaceutically composition, preparation and uses as an inhibitor of FGFs (fibroblast growth factors).
摘要翻译： 本发明涉及式I化合物，其中R，R 1，R 2，R 3和R 4如本文所定义，或其药学上可接受的盐及其作为FGF抑制剂的药物组合物，制备和用途（成纤维细胞生长因子 ）。
-
5.发明授权Imidazopyridine derivatives, process for preparation thereof and therapeutic use thereof 有权咪唑并吡啶衍生物，其制备方法及其治疗用途公开(公告)号：US08759344B2
公开(公告)日：2014-06-24
申请号：US13808503
申请日：2011-07-04
IPC分类号： A61K31/53 , C07D401/00 , C07D413/00 , A61K31/517 , A61K9/20 , C07D211/82 , C07D471/04 , C07D233/88 , C07D211/90 , C07D233/64 , A61K45/06 , A61K31/5377 , C07D233/90
CPC分类号： A61K31/517 , A61K9/2018 , A61K9/2054 , A61K9/2059 , A61K31/437 , A61K31/5377 , A61K45/06 , C07D211/82 , C07D211/90 , C07D233/64 , C07D233/88 , C07D233/90 , C07D471/04
摘要： The invention relates to compounds corresponding to formula (I): in which R2 and R3 together form, with the carbon atoms of the phenyl nucleus to which they are attached, a 6-membered nitrogenous heterocycle corresponding to one of formula (A), (B) or (C) below: in which the wavy lines represent the phenyl nucleus to which R2 and R3 are attached. Preparation process and therapeutic use.
摘要翻译： 本发明涉及对应于式（I）的化合物：其中R 2和R 3一起与它们所连接的苯基的碳原子一起形成对应于式（A），（A）中的一个的6-元含氮杂环， B）或（C）：其中波浪线表示R2和R3所连接的苯基核。 制备过程和治疗用途。
-
6.发明申请IMIDAZOPYRIDINE DERIVATIVES, PROCESS FOR PREPARATION THEREOF AND THERAPEUTIC USE THEREOF 有权咪唑吡啶衍生物，其制备方法及其治疗用途公开(公告)号：US20130116250A1
公开(公告)日：2013-05-09
申请号：US13808503
申请日：2011-07-04
IPC分类号： A61K31/5377 , A61K31/517 , A61K45/06 , C07D471/04
CPC分类号： A61K31/517 , A61K9/2018 , A61K9/2054 , A61K9/2059 , A61K31/437 , A61K31/5377 , A61K45/06 , C07D211/82 , C07D211/90 , C07D233/64 , C07D233/88 , C07D233/90 , C07D471/04
摘要： The invention relates to compounds corresponding to formula (I): in which R2 and R3 together form, with the carbon atoms of the phenyl nucleus to which they are attached, a 6-membered nitrogenous heterocycle corresponding to one of formula (A), (B) or (C) below: in which the wavy lines represent the phenyl nucleus to which R2 and R3 are attached.Preparation process and therapeutic use.
摘要翻译： 本发明涉及对应于式（I）的化合物：其中R 2和R 3一起与它们所连接的苯基的碳原子一起形成对应于式（A），（A）中的一个的6-元含氮杂环， B）或（C）：其中波浪线表示R2和R3所连接的苯基核。 制备过程和治疗用途。
-
7.发明申请公开(公告)号：US20130116249A1
公开(公告)日：2013-05-09
申请号：US13808483
申请日：2011-07-04
IPC分类号： C07D471/04 , A61K45/06 , A61K31/5377 , A61K31/517 , A61K31/4709
CPC分类号： C07D471/04 , A61K9/2018 , A61K9/2054 , A61K9/2059 , A61K31/4709 , A61K31/517 , A61K31/5377 , A61K45/06 , C07D207/32 , C07D207/36 , C07D211/82
摘要： The invention relates to compounds corresponding to formula (I): in which R3 and R4 together form, with the carbon atoms of the phenyl nucleus to which they are attached, a 6-membered nitrogenous heterocycle corresponding to one of formula (A), (B) or (C) below: in which the wavy lines represent the phenyl nucleus to which R3 and R4 are attached.Preparation process and therapeutic use.
摘要翻译： 本发明涉及对应于式（I）的化合物：其中R 3和R 4与它们所连接的苯环的碳原子一起形成对应于式（A），（A）中的一个的6-元含氮杂环， B）或（C）：其中波浪线表示R3和R4连接的苯基核。 制备过程和治疗用途。
-
![Novel imidazo[1,5-a]pyridine derivatives, method for preparing same and pharmaceutical compositions containing same](/abs-image/US/2011/06/09/US20110136856A1/abs.jpg.150x150.jpg)
8.发明申请Novel imidazo[1,5-a]pyridine derivatives, method for preparing same and pharmaceutical compositions containing same 有权新的咪唑并[1,5-a]吡啶衍生物，其制备方法和含有它们的药物组合物公开(公告)号：US20110136856A1
公开(公告)日：2011-06-09
申请号：US13020883
申请日：2011-02-04
IPC分类号： A61K31/437 , A61K31/444 , A61P35/00 , A61P27/02 , A61P9/00 , A61P9/10 , A61P29/00 , A61P19/00 , A61P3/04
CPC分类号： C07D471/04
摘要： The invention concerns compounds of formula I, a method for preparing said compounds, pharmaceutical compositions containing same and the theraprutic uses thereof.
摘要翻译： 本发明涉及式I化合物，制备所述化合物的方法，含有该化合物的药物组合物及其治疗用途。
-
![Novel imidazo[1,5-a] pyridine derivatives, method for preparing same and pharmaceutical compositions containing same](/abs-image/US/2008/05/08/US20080108648A1/abs.jpg.150x150.jpg)
9.发明申请Novel imidazo[1,5-a] pyridine derivatives, method for preparing same and pharmaceutical compositions containing same 有权新的咪唑并[1,5-a]吡啶衍生物，其制备方法和含有它们的药物组合物公开(公告)号：US20080108648A1
公开(公告)日：2008-05-08
申请号：US11855549
申请日：2007-09-14
IPC分类号： A61K31/4375 , C07D471/04 , A61P43/00 , A61P35/00 , A61P9/00 , A61P37/00 , A61P19/02
CPC分类号： C07D471/04
摘要： The invention concerns compounds of formula I, a method for preparing said compounds, pharmaceutical compositions containing same and the therapeutic uses thereof.
摘要翻译： 本发明涉及式I化合物，制备所述化合物的方法，含有该化合物的药物组合物及其治疗用途。
-
10.发明申请Substituted indolizine 1,2,3,6,7,8 derivatives, FGFs inhibitors, a method for the preparation thereof and pharmaceutical compositions containing said derivatives 有权取代的中氮茚1,2,3,6,7,8衍生物，FGF抑制剂，其制备方法和含有所述衍生物的药物组合物公开(公告)号：US20060199962A1
公开(公告)日：2006-09-07
申请号：US11378972
申请日：2006-03-17
申请人： Chantal Alcouffe , Alain Badorc , Francoise Bono , Marie-Francoise Bordes , Nathalie Guillo , Jean-Marc Herbert
发明人： Chantal Alcouffe , Alain Badorc , Francoise Bono , Marie-Francoise Bordes , Nathalie Guillo , Jean-Marc Herbert
IPC分类号： C07D455/02
CPC分类号： C07D471/04
摘要： The invention is directed to a compound of formula I, wherein R, R1, R2, R3 and R4 are as defined herein, or a pharmaceutically acceptable salt thereof, and its pharmaceutically composition, preparation and uses as an inhibitor of FGFs (fibroblast growth factors).
摘要翻译： 本发明涉及式I化合物，其中R 1，R 2，R 2，R 3和R 4， / SUB>如本文所定义，或其药学上可接受的盐及其作为FGF抑制剂（成纤维细胞生长因子）的药学组合物，制备和用途。
-
-
-
-
-
-
-
-
-
搜索结果
10 条记录 (耗时 0.022 秒)
