JP2008540547A5 - - Google Patents

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Publication number
JP2008540547A5
JP2008540547A5 JP2008511281A JP2008511281A JP2008540547A5 JP 2008540547 A5 JP2008540547 A5 JP 2008540547A5 JP 2008511281 A JP2008511281 A JP 2008511281A JP 2008511281 A JP2008511281 A JP 2008511281A JP 2008540547 A5 JP2008540547 A5 JP 2008540547A5
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JP
Japan
Prior art keywords
alkyl
heteroaryl
aryl
cycloalkyl
heterocyclo
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JP2008511281A
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English (en)
Japanese (ja)
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JP2008540547A (ja
JP5047164B2 (ja
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Priority claimed from US11/430,215 external-priority patent/US7737279B2/en
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Publication of JP2008540547A publication Critical patent/JP2008540547A/ja
Publication of JP2008540547A5 publication Critical patent/JP2008540547A5/ja
Application granted granted Critical
Publication of JP5047164B2 publication Critical patent/JP5047164B2/ja
Expired - Fee Related legal-status Critical Current
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JP2008511281A 2005-05-10 2006-05-09 IKK酵素活性の阻害剤としての1,6−ジヒドロ−1,3,5,6−テトラアザ−as−インダセンをベースとした三環式化合物およびそれを含む医薬組成物 Expired - Fee Related JP5047164B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US67969205P 2005-05-10 2005-05-10
US60/679,692 2005-05-10
US11/430,215 US7737279B2 (en) 2005-05-10 2006-05-08 1,6-dihydro-1,3,5,6-tetraaza-as-indacene based tricyclic compounds and pharmaceutical compositions comprising same
US11/430,215 2006-05-08
PCT/US2006/017950 WO2006122137A1 (en) 2005-05-10 2006-05-09 1, 6 -dihydro- 1,3, 5, 6-tetraaza-as-indacene based tricyclic compounds and pharmaceutical compositions comprising same as inhibitors of ikk enzyme activity

Publications (3)

Publication Number Publication Date
JP2008540547A JP2008540547A (ja) 2008-11-20
JP2008540547A5 true JP2008540547A5 (cg-RX-API-DMAC7.html) 2009-06-04
JP5047164B2 JP5047164B2 (ja) 2012-10-10

Family

ID=36808856

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008511281A Expired - Fee Related JP5047164B2 (ja) 2005-05-10 2006-05-09 IKK酵素活性の阻害剤としての1,6−ジヒドロ−1,3,5,6−テトラアザ−as−インダセンをベースとした三環式化合物およびそれを含む医薬組成物

Country Status (15)

Country Link
US (2) US7737279B2 (cg-RX-API-DMAC7.html)
EP (1) EP1888584B1 (cg-RX-API-DMAC7.html)
JP (1) JP5047164B2 (cg-RX-API-DMAC7.html)
AR (1) AR053725A1 (cg-RX-API-DMAC7.html)
AT (1) ATE465162T1 (cg-RX-API-DMAC7.html)
CY (1) CY1110419T1 (cg-RX-API-DMAC7.html)
DE (1) DE602006013816D1 (cg-RX-API-DMAC7.html)
DK (1) DK1888584T3 (cg-RX-API-DMAC7.html)
ES (1) ES2342976T3 (cg-RX-API-DMAC7.html)
PE (1) PE20061424A1 (cg-RX-API-DMAC7.html)
PL (1) PL1888584T3 (cg-RX-API-DMAC7.html)
PT (1) PT1888584E (cg-RX-API-DMAC7.html)
SI (1) SI1888584T1 (cg-RX-API-DMAC7.html)
TW (1) TW200718422A (cg-RX-API-DMAC7.html)
WO (1) WO2006122137A1 (cg-RX-API-DMAC7.html)

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NZ599938A (en) 2009-12-01 2014-08-29 Abbvie Inc Novel tricyclic compounds
TWI500620B (zh) * 2009-12-01 2015-09-21 Abbvie Inc 新穎三環化合物
US8461328B2 (en) * 2010-01-12 2013-06-11 Genentech, Inc. Tricyclic heterocyclic compounds, compositions and methods of use thereof
WO2011112687A2 (en) * 2010-03-10 2011-09-15 Kalypsys, Inc. Heterocyclic inhibitors of histamine receptors for the treatment of disease
EA201492223A1 (ru) 2012-06-13 2015-03-31 Ф. Хоффманн-Ля Рош Аг Новые диазаспироциклоалканы и азаспироциклоалканы
PL2900669T3 (pl) 2012-09-25 2020-01-31 F. Hoffmann-La Roche Ag Pochodne heksahydropirolo[3,4-C]pirolu i związki pokrewne jako inhibitory autotaksyny (ATX) oraz inhibitory produkcji kwasu lizofosfatydowego (LPA) do leczenia np. chorób nerek
AR095079A1 (es) 2013-03-12 2015-09-16 Hoffmann La Roche Derivados de octahidro-pirrolo[3,4-c]-pirrol y piridina-fenilo
US9518058B2 (en) 2013-08-29 2016-12-13 Bristol-Myers Squibb Company Process for the preparation of N,N-dicyclopropyl-4-(1,5-dimethyl-1H-pyrazol-3-ylamino)-6-ethyl-1-methyl-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridine-7-carboxamide
EP3061754A4 (en) 2013-10-23 2017-03-22 Takeda Pharmaceutical Company Limited Heterocyclic compound
UA118201C2 (uk) 2013-11-26 2018-12-10 Ф. Хоффманн-Ля Рош Аг НОВИЙ ОКТАГІДРОЦИКЛОБУТА[1,2-c;3,4-c']ДИПІРОЛ-2-ІЛ
SG11201607839UA (en) 2014-03-26 2016-10-28 Hoffmann La Roche Bicyclic compounds as autotaxin (atx) and lysophosphatidic acid (lpa) production inhibitors
CR20160418A (es) 2014-03-26 2016-11-07 Hoffmann La Roche Nuevos compuestos biciclicos de 7 eslabones
MA41898A (fr) 2015-04-10 2018-02-13 Hoffmann La Roche Dérivés de quinazolinone bicyclique
MX387736B (es) 2015-09-04 2025-03-18 Hoffmann La Roche Derivados de fenoximetilo.
AU2016328365B2 (en) 2015-09-24 2020-04-23 F. Hoffmann-La Roche Ag New bicyclic compounds as dual ATX/CA inhibitors
WO2017050732A1 (en) 2015-09-24 2017-03-30 F. Hoffmann-La Roche Ag Bicyclic compounds as atx inhibitors
AU2016328436B2 (en) 2015-09-24 2020-05-14 F. Hoffmann-La Roche Ag New bicyclic compounds as dual ATX/CA inhibitors
MA42919A (fr) 2015-09-24 2018-08-01 Hoffmann La Roche Composés bicycliques utilisés en tant qu'inhibiteurs d'atx
US11365198B2 (en) 2015-10-16 2022-06-21 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
CA3251507A1 (en) 2015-10-16 2025-05-21 Abbvie Inc. Use of a solid dosage form comprising (3s,4r)-3-ethyl-4-(3h-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide for treating rheumatoid arthritis
US11512092B2 (en) 2015-10-16 2022-11-29 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11524964B2 (en) 2015-10-16 2022-12-13 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US12365689B2 (en) 2015-10-16 2025-07-22 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11773106B2 (en) 2015-10-16 2023-10-03 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US10550126B2 (en) 2015-10-16 2020-02-04 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-A]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
CA3033752C (en) * 2016-08-15 2022-05-31 Purdue Research Foundation 4-substituted aminoisoquinoline derivatives
EP4086256A1 (en) 2016-12-16 2022-11-09 Janssen Pharmaceutica NV Small molecule inhibitors of the jak family of kinases
JOP20190144A1 (ar) 2016-12-16 2019-06-16 Janssen Pharmaceutica Nv إيميدازو بيرولو بيريدين كمثبطات لعائلة jak الخاصة بإنزيمات الكيناز
WO2018167113A1 (en) 2017-03-16 2018-09-20 F. Hoffmann-La Roche Ag New bicyclic compounds as atx inhibitors
CR20190423A (es) 2017-03-16 2019-11-01 Hoffmann La Roche Nuevos compuestos biciclícos como inhibidores dobles de atx/ca
TW202016110A (zh) 2018-06-15 2020-05-01 比利時商健生藥品公司 Jak激酶家族之小分子抑制劑
JP2023544678A (ja) * 2020-10-08 2023-10-25 ユニケム ラボラトリーズ リミテッド 置換三環系化合物
CN116507627A (zh) 2020-11-02 2023-07-28 勃林格殷格翰国际有限公司 作为egfr抑制剂的经取代1h-吡唑并[4,3-c]吡啶及衍生物
CA3213134A1 (en) 2021-03-11 2022-09-15 Janssen Pharmaceutica Nv Lorpucitinib for use in the treatment of jak mediated disorders

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US7329668B2 (en) 2003-02-25 2008-02-12 Bristol-Myers Squibb Company Pyrazolopurine-based tricyclic compounds and pharmaceutical compositions comprising same
US7176214B2 (en) 2003-05-21 2007-02-13 Bristol-Myers Squibb Company Imidazo-fused oxazolo[4,5-β]pyridine and imidazo-fused thiazolo[4,5-β]pyridine based tricyclic compounds and pharmaceutical compositions comprising same
US7071333B2 (en) 2003-07-30 2006-07-04 Bristol-Myers Squibb Company Triazolopurine-based tricyclic compounds and pharmaceutical compositions comprising same
AU2004266657B2 (en) * 2003-08-14 2009-07-02 3M Innovative Properties Company Lipid-modified immune response modifiers
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US7737279B2 (en) * 2005-05-10 2010-06-15 Bristol-Myers Squibb Company 1,6-dihydro-1,3,5,6-tetraaza-as-indacene based tricyclic compounds and pharmaceutical compositions comprising same

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