-
公开(公告)号:US08471005B2
公开(公告)日:2013-06-25
申请号:US13160890
申请日:2011-06-15
申请人: Henry J. Breslin , Sankar Chatterjee , James L. Diebold , Bruce D. Dorsey , Derek D. Dunn , Diane E. Gingrich , Greg A. Hostetler , Robert L. Hudkins , Rachael Hunter , Kurt A. Josef , Joseph Lisko , Eugen F. Mesaros , Karen L. Milkiewicz , Gregory R. Ott , Babu G. Sundar , Jay P. Theroff , Tho Thieu , Rabindranath Tripathy , Theodore L. Underiner , Linda Weinberg , Gregory J. Wells , Craig A. Zificsak
发明人: Henry J. Breslin , Sankar Chatterjee , James L. Diebold , Bruce D. Dorsey , Derek D. Dunn , Diane E. Gingrich , Greg A. Hostetler , Robert L. Hudkins , Rachael Hunter , Kurt A. Josef , Joseph Lisko , Eugen F. Mesaros , Karen L. Milkiewicz , Gregory R. Ott , Babu G. Sundar , Jay P. Theroff , Tho Thieu , Rabindranath Tripathy , Theodore L. Underiner , Linda Weinberg , Gregory J. Wells , Craig A. Zificsak
IPC分类号: C07D487/04 , C07D403/12 , A61K31/53 , A61K31/5377 , A61P35/00
CPC分类号: C07D487/04
摘要: The present invention provides a compound of formula I or a salt form thereof, wherein Q1, Q2, Q3, and Q4 are as defined herein. The compound of formula I has ALK and/or JAK2 inhibitory activity, and may be used to treat proliferative disorders.
摘要翻译: 本发明提供式I化合物或其盐形式,其中Q 1,Q 2,Q 3和Q 4如本文所定义。 式I化合物具有ALK和/或JAK2抑制活性,可用于治疗增殖性疾病。
-
公开(公告)号:US20120028919A1
公开(公告)日:2012-02-02
申请号:US13160890
申请日:2011-06-15
申请人: Henry J. Breslin , Sankar Chatterjee , James L. Diebold , Bruce D. Dorsey , Derek D. Dunn , Diane E. Gingrich , Greg A. Hostetler , Robert L. Hudkins , Rachael Hunter , Kurt A. Josef , Joseph Lisko , Eugen F. Mesaros , Karen L. Milkiewicz , Gregory R. Ott , Babu G. Sundar , Jay P. Theroff , Tho Thieu , Rabindranath Tripathy , Theodore L. Underiner , Linda Weinberg , Gregory J. Wells , Craig A. Zificsak
发明人: Henry J. Breslin , Sankar Chatterjee , James L. Diebold , Bruce D. Dorsey , Derek D. Dunn , Diane E. Gingrich , Greg A. Hostetler , Robert L. Hudkins , Rachael Hunter , Kurt A. Josef , Joseph Lisko , Eugen F. Mesaros , Karen L. Milkiewicz , Gregory R. Ott , Babu G. Sundar , Jay P. Theroff , Tho Thieu , Rabindranath Tripathy , Theodore L. Underiner , Linda Weinberg , Gregory J. Wells , Craig A. Zificsak
IPC分类号: A61K31/5377 , C07D223/16 , A61P35/00 , A61K31/53 , A61K31/695 , C07D487/04 , A61K31/55
CPC分类号: C07D487/04
摘要: The present invention provides a compound of formula I or a salt form thereof, wherein Q1, Q2, Q3, and Q4 are as defined herein. The compound of formula I has ALK and/or JAK2 inhibitory activity, and may be used to treat proliferative disorders.
摘要翻译: 本发明提供式I化合物或其盐形式,其中Q 1,Q 2,Q 3和Q 4如本文所定义。 式I化合物具有ALK和/或JAK2抑制活性,可用于治疗增殖性疾病。
-
3.Substituted Phenoxypropylcycloamine Derivatives as Histamine-3 (H3) Receptor Ligands 失效
标题翻译: 作为组胺-3(H3)受体配体的取代苯氧基丙基环胺衍生物公开(公告)号:US20120238551A1
公开(公告)日:2012-09-20
申请号:US13334311
申请日:2011-12-22
申请人: Edward R. Bacon , Thomas R. Bailey , Sankar Chatterjee , Derek D. Dunn , Greg A. Hostetler , Robert L. Hudkins , Brigitte Lesur , Babu G. Sundar , Allizon L. Zulli , Christophe Yue
发明人: Edward R. Bacon , Thomas R. Bailey , Sankar Chatterjee , Derek D. Dunn , Greg A. Hostetler , Robert L. Hudkins , Brigitte Lesur , Babu G. Sundar , Allizon L. Zulli , Christophe Yue
IPC分类号: A61K31/5377 , C07D403/12 , A61K31/496 , C07D401/12 , A61K31/4545 , A61K31/4025 , A61K31/4725 , A61K31/454 , A61K31/541 , C07D487/04 , A61K31/55 , A61K31/506 , A61P25/28 , A61P25/18 , A61P29/00 , A61P25/06 , A61P9/10 , A61P11/00 , A61P25/08 , A61P25/24 , A61P25/22 , A61P3/04 , A61P25/00 , C07D413/12
CPC分类号: C07D403/12 , C07C217/54 , C07D207/06 , C07D207/08 , C07D207/10 , C07D207/27 , C07D209/44 , C07D211/14 , C07D211/22 , C07D211/38 , C07D211/46 , C07D215/02 , C07D215/06 , C07D217/04 , C07D241/08 , C07D295/108 , C07D295/185 , C07D401/12 , C07D407/12 , C07D409/12 , C07D413/12 , C07D471/04 , C07D487/04
摘要: The present invention provides compounds of formula I: their use as H3 antagonists/inverse agonists, processes for their preparation, and pharmaceutical compositions thereof.
摘要翻译: 本发明提供式I化合物:它们用作H3拮抗剂/反向激动剂,其制备方法及其药物组合物。
-
4.Substituted phenoxypropylcycloamine derivatives as histamine-3 (H3) receptor ligands 失效
标题翻译: 取代的苯氧基丙胺环胺衍生物作为组胺-3(H3)受体配体公开(公告)号:US08648067B2
公开(公告)日:2014-02-11
申请号:US13334311
申请日:2011-12-22
申请人: Edward R. Bacon , Thomas R. Bailey , Sankar Chatterjee , Derek D. Dunn , Greg A. Hostetler , Robert L. Hudkins , Brigitte Lesur , Babu G. Sundar , Allison L. Zulli , Christophe Yue
发明人: Edward R. Bacon , Thomas R. Bailey , Sankar Chatterjee , Derek D. Dunn , Greg A. Hostetler , Robert L. Hudkins , Brigitte Lesur , Babu G. Sundar , Allison L. Zulli , Christophe Yue
IPC分类号: A61K31/55 , A61K31/54 , A61K31/45 , A61K31/535 , A61K31/497 , A61K31/545 , A61K31/445 , A01N43/40 , C07D223/18 , C07D279/10 , C07D413/00 , C07D403/00 , C07D401/00 , C07D217/00 , C07D211/00 , C07D405/00 , C07D295/00
CPC分类号: C07D403/12 , C07C217/54 , C07D207/06 , C07D207/08 , C07D207/10 , C07D207/27 , C07D209/44 , C07D211/14 , C07D211/22 , C07D211/38 , C07D211/46 , C07D215/02 , C07D215/06 , C07D217/04 , C07D241/08 , C07D295/108 , C07D295/185 , C07D401/12 , C07D407/12 , C07D409/12 , C07D413/12 , C07D471/04 , C07D487/04
摘要: The present invention provides compounds of formula I: their use as H3 antagonists/inverse agonists, processes for their preparation, and pharmaceutical compositions thereof.
摘要翻译: 本发明提供式I化合物:它们用作H3拮抗剂/反向激动剂,其制备方法及其药物组合物。
-
5.
公开(公告)号:US08765779B2
公开(公告)日:2014-07-01
申请号:US13529378
申请日:2012-06-21
申请人: Edward R. Bacon , Thomas R. Bailey , Derek D. Dunn , Greg A. Hostetler , Robert J. McHugh , George C. Morton , Gerard C. Rosse , Joseph M. Salvino , Babu G. Sundar , Rabindranath Tripathy
发明人: Edward R. Bacon , Thomas R. Bailey , Derek D. Dunn , Greg A. Hostetler , Robert J. McHugh , George C. Morton , Gerard C. Rosse , Joseph M. Salvino , Babu G. Sundar , Rabindranath Tripathy
IPC分类号: A61K31/4355 , C07D491/048
CPC分类号: C07D491/153 , C07D491/048 , C07D491/20 , C07D513/04
摘要: This application relates to tricyclic compounds of Formula I: including all stereoisomers, mixtures of stereoisomers, and salts thereof. This application also relates to compositions comprising compounds of Formula I and uses therefore.
摘要翻译: 本申请涉及式I的三环化合物:包括所有立体异构体,立体异构体的混合物及其盐。 本申请还涉及包含式I化合物的组合物并因此使用。
-
6.
公开(公告)号:US20120295882A1
公开(公告)日:2012-11-22
申请号:US13529378
申请日:2012-06-21
申请人: Edward R. Bacon , Thomas R. Bailey , Derek D. Dunn , Greg A. Hostetler , Robert J. McHugh , George C. Morton , Gerard C. Rosse , Joseph M. Salvino , Babu G. Sundar , Rabindranath Tripathy
发明人: Edward R. Bacon , Thomas R. Bailey , Derek D. Dunn , Greg A. Hostetler , Robert J. McHugh , George C. Morton , Gerard C. Rosse , Joseph M. Salvino , Babu G. Sundar , Rabindranath Tripathy
IPC分类号: A61K31/4355 , C07D491/20 , A61K31/438 , A61K31/444 , A61K31/506 , C07D495/20 , A61K31/497 , A61K31/4709 , A61K31/5377 , C07D491/22 , C07D513/04 , A61K31/4725 , A61K31/496 , A61P25/22 , A61P25/08 , A61P25/24 , A61P25/18 , A61P25/28 , A61P25/16 , A61P25/20 , A61P25/30 , A61P3/04 , A61P25/00 , C07D491/048
CPC分类号: C07D491/153 , C07D491/048 , C07D491/20 , C07D513/04
摘要: This application relates to tricyclic compounds of Formula I: including all stereoisomers, mixtures of stereoisomers, and salts thereof. This application also relates to compositions comprising compounds of Formula I and uses therefore.
摘要翻译: 本申请涉及式I的三环化合物:包括所有立体异构体,立体异构体的混合物及其盐。 本申请还涉及包含式I化合物的组合物并因此使用。
-
7.SUBSTITUTED PHENOXYPROPYLCYCLOAMINE DERIVATIVES AS HISTAMINE-3 (H3) RECEPTOR LIGANDS 审中-公开
标题翻译: 作为HISTAMINE-3(H3)受体配体的取代的羟基丙烯酰胺衍生物公开(公告)号:US20140296212A1
公开(公告)日:2014-10-02
申请号:US14177046
申请日:2014-02-10
申请人: Edward R. Bacon , Thomas R. Bailey , Sankar Chatterjee , Derek Dunn , Greg A. Hostetler , Robert L. Hudkins , Allison L. Zulli , Brigitte Lesur , Babu G. Sundar , Christophe Yue
发明人: Edward R. Bacon , Thomas R. Bailey , Sankar Chatterjee , Derek Dunn , Greg A. Hostetler , Robert L. Hudkins , Allison L. Zulli , Brigitte Lesur , Babu G. Sundar , Christophe Yue
IPC分类号: C07D403/12 , C07C217/54 , C07D211/22 , C07D209/44 , C07D215/02 , C07D207/08 , C07D217/04
CPC分类号: C07D403/12 , C07C217/54 , C07D207/06 , C07D207/08 , C07D207/10 , C07D207/27 , C07D209/44 , C07D211/14 , C07D211/22 , C07D211/38 , C07D211/46 , C07D215/02 , C07D215/06 , C07D217/04 , C07D241/08 , C07D295/108 , C07D295/185 , C07D401/12 , C07D407/12 , C07D409/12 , C07D413/12 , C07D471/04 , C07D487/04
摘要: The present invention provides compounds of formula I: their use as H3 antagonists/inverse agonists, processes for their preparation, and pharmaceutical compositions thereof.
摘要翻译: 本发明提供式I化合物:它们用作H3拮抗剂/反向激动剂,其制备方法及其药物组合物。
-
8.Substituted Pyridazinone Derivatives as Histamine-3 (H3) Receptor Ligands 审中-公开
标题翻译: 作为组胺-3(H3)受体配体的取代哒嗪酮衍生物公开(公告)号:US20110098269A1
公开(公告)日:2011-04-28
申请号:US12948496
申请日:2010-11-17
申请人: Nadine C. Becknell , Reddeppa reddy Dandu , Derek D. Dunn , Robert L. Hudkins , Kurt A. Josef , Babu G. Sundar , Allison L. Zulli
发明人: Nadine C. Becknell , Reddeppa reddy Dandu , Derek D. Dunn , Robert L. Hudkins , Kurt A. Josef , Babu G. Sundar , Allison L. Zulli
IPC分类号: A61K31/501 , C07D403/10 , C07D401/14 , C07D403/14 , C07D237/14 , C07D401/10 , C07D413/10 , A61K31/55 , A61K31/4985 , A61K31/5377 , A61P3/00 , A61P3/04 , A61P25/00 , A61P25/20 , A61P25/28 , A61P25/18 , A61P25/22 , A61P25/06 , A61P25/04 , A61P25/24 , A61P25/08 , A61P29/00 , A61P9/10 , A61P1/00 , A61P11/00
CPC分类号: C07D403/04 , C07D237/14 , C07D401/14 , C07D403/10 , C07D403/12 , C07D487/04
摘要: The present invention provides compounds according to Formulas I, II, III, IV, V, VI, VII or VIII: their use as H3 antagonists/inverse agonists, processes for their preparation, and pharmaceutical compositions thereof.
摘要翻译: 本发明提供了根据式I,II,III,IV,V,VI,VII或VIII的化合物:它们用作H3拮抗剂/反向激动剂,其制备方法及其药物组合物。
-
公开(公告)号:US20120004231A1
公开(公告)日:2012-01-05
申请号:US13231293
申请日:2011-09-13
申请人: Robert L. Hudkins , Lars J.S. Knutsen , Catherine P. Prouty , Babu G. Sundar , Kevin J. Wells-Knecht
发明人: Robert L. Hudkins , Lars J.S. Knutsen , Catherine P. Prouty , Babu G. Sundar , Kevin J. Wells-Knecht
IPC分类号: A61K31/501 , A61P25/28 , A61P25/00 , A61P3/00 , A61K31/5377 , A61K31/502
CPC分类号: C07D237/12 , C07D237/08 , C07D237/14 , C07D237/18 , C07D237/20 , C07D401/12 , C07D403/04 , C07D405/04 , C07D409/04
摘要: The present invention is directed to compounds having histamine H3 antagonist activity, as well as methods of their use and preparation.
摘要翻译: 本发明涉及具有组胺H3拮抗剂活性的化合物及其使用和制备方法。
-
公开(公告)号:US20100311752A1
公开(公告)日:2010-12-09
申请号:US12846112
申请日:2010-07-29
申请人: Robert L. Hudkins , Lars J.S. Knutsen , Catherine P. Prouty , Babu G. Sundar , Kevin J. Wells-Knecht
发明人: Robert L. Hudkins , Lars J.S. Knutsen , Catherine P. Prouty , Babu G. Sundar , Kevin J. Wells-Knecht
IPC分类号: A61K31/5377 , C07D403/12 , A61K31/501 , C07D413/14 , A61P25/28 , A61P25/18 , A61P25/24 , A61P9/10 , A61P3/04 , A61P25/06 , A61P11/00 , A61P29/00 , A61P25/20 , A61P25/00
CPC分类号: C07D237/12 , C07D237/08 , C07D237/14 , C07D237/18 , C07D237/20 , C07D401/12 , C07D403/04 , C07D405/04 , C07D409/04
摘要: The present invention is directed to compounds having histamine H3 antagonist activity, as well as methods of their use and preparation.
摘要翻译: 本发明涉及具有组胺H3拮抗剂活性的化合物及其使用和制备方法。
-
-
-
-
-
-
-
-
-