JP2015163632A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2015163632A5 JP2015163632A5 JP2015096257A JP2015096257A JP2015163632A5 JP 2015163632 A5 JP2015163632 A5 JP 2015163632A5 JP 2015096257 A JP2015096257 A JP 2015096257A JP 2015096257 A JP2015096257 A JP 2015096257A JP 2015163632 A5 JP2015163632 A5 JP 2015163632A5
- Authority
- JP
- Japan
- Prior art keywords
- optionally substituted
- alkyl
- heteroaryl
- alkylene
- substituted
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 14
- 125000000623 heterocyclic group Chemical group 0.000 claims 13
- 229910052757 nitrogen Inorganic materials 0.000 claims 10
- 125000006573 (C1-C10) heteroaryl group Chemical group 0.000 claims 8
- -1 —N (R a ) (R b ) Chemical class 0.000 claims 8
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 claims 6
- 229910052739 hydrogen Inorganic materials 0.000 claims 6
- 150000002431 hydrogen Chemical class 0.000 claims 6
- 239000001257 hydrogen Substances 0.000 claims 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 5
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims 5
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims 5
- 125000002993 cycloalkylene group Chemical group 0.000 claims 5
- 229910052805 deuterium Inorganic materials 0.000 claims 5
- 150000001875 compounds Chemical class 0.000 claims 4
- 125000005724 cycloalkenylene group Chemical group 0.000 claims 4
- 229910052736 halogen Inorganic materials 0.000 claims 4
- 150000002367 halogens Chemical class 0.000 claims 4
- 125000006585 (C6-C10) arylene group Chemical group 0.000 claims 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims 3
- 125000005549 heteroarylene group Chemical group 0.000 claims 3
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims 2
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims 2
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims 2
- 125000006590 (C2-C6) alkenylene group Chemical group 0.000 claims 2
- 125000006591 (C2-C6) alkynylene group Chemical group 0.000 claims 2
- 125000006586 (C3-C10) cycloalkylene group Chemical group 0.000 claims 2
- 125000006553 (C3-C8) cycloalkenyl group Chemical group 0.000 claims 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 125000006832 (C1-C10) alkylene group Chemical group 0.000 claims 1
- 125000006694 (C2-C10) heterocyclyl group Chemical group 0.000 claims 1
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 claims 1
- 125000004450 alkenylene group Chemical group 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 125000004419 alkynylene group Chemical group 0.000 claims 1
- 230000000975 bioactive effect Effects 0.000 claims 1
- 239000002207 metabolite Substances 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 125000004430 oxygen atom Chemical group O* 0.000 claims 1
- 229940002612 prodrug Drugs 0.000 claims 1
- 239000000651 prodrug Substances 0.000 claims 1
- 125000003226 pyrazolyl group Chemical group 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
Applications Claiming Priority (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13159908P | 2008-06-10 | 2008-06-10 | |
| US13160208P | 2008-06-10 | 2008-06-10 | |
| US61/131,599 | 2008-06-10 | ||
| US61/131,602 | 2008-06-10 | ||
| US61/190,159 | 2008-08-25 | ||
| US19015908P | 2008-08-26 | 2008-08-26 | |
| US20106408P | 2008-12-05 | 2008-12-05 | |
| US61/201,064 | 2008-12-05 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011513627A Division JP5748659B2 (ja) | 2008-06-10 | 2009-06-09 | 新規な三環式化合物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2015163632A JP2015163632A (ja) | 2015-09-10 |
| JP2015163632A5 true JP2015163632A5 (OSRAM) | 2016-02-18 |
Family
ID=41415363
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011513627A Active JP5748659B2 (ja) | 2008-06-10 | 2009-06-09 | 新規な三環式化合物 |
| JP2015096257A Pending JP2015163632A (ja) | 2008-06-10 | 2015-05-11 | 新規な三環式化合物 |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011513627A Active JP5748659B2 (ja) | 2008-06-10 | 2009-06-09 | 新規な三環式化合物 |
Country Status (36)
| Country | Link |
|---|---|
| US (5) | US8962629B2 (OSRAM) |
| EP (2) | EP3031324A3 (OSRAM) |
| JP (2) | JP5748659B2 (OSRAM) |
| KR (2) | KR101718384B1 (OSRAM) |
| CN (2) | CN102118968A (OSRAM) |
| AR (1) | AR072086A1 (OSRAM) |
| AU (1) | AU2009257602B2 (OSRAM) |
| BR (1) | BRPI0915374B1 (OSRAM) |
| CA (2) | CA2727032C (OSRAM) |
| CL (1) | CL2010001426A1 (OSRAM) |
| CO (1) | CO6382083A2 (OSRAM) |
| CR (1) | CR20160007A (OSRAM) |
| CY (1) | CY1117165T1 (OSRAM) |
| DK (1) | DK2299821T3 (OSRAM) |
| DO (2) | DOP2010000382A (OSRAM) |
| EC (1) | ECSP10010657A (OSRAM) |
| ES (1) | ES2559403T3 (OSRAM) |
| HR (1) | HRP20160098T1 (OSRAM) |
| HU (1) | HUE028347T2 (OSRAM) |
| IL (1) | IL209434A0 (OSRAM) |
| ME (1) | ME02340B (OSRAM) |
| MX (1) | MX2010013557A (OSRAM) |
| MY (1) | MY161369A (OSRAM) |
| NO (1) | NO20101688A1 (OSRAM) |
| NZ (1) | NZ623922A (OSRAM) |
| PE (2) | PE20110223A1 (OSRAM) |
| PL (1) | PL2299821T3 (OSRAM) |
| PT (1) | PT2299821E (OSRAM) |
| RS (1) | RS54560B1 (OSRAM) |
| RU (2) | RU2545023C9 (OSRAM) |
| SI (1) | SI2299821T1 (OSRAM) |
| TW (3) | TW201612182A (OSRAM) |
| UA (1) | UA106045C2 (OSRAM) |
| UY (1) | UY31881A (OSRAM) |
| WO (1) | WO2009152133A1 (OSRAM) |
| ZA (1) | ZA201008562B (OSRAM) |
Families Citing this family (75)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HUE028347T2 (en) * | 2008-06-10 | 2016-12-28 | Abbvie Inc | Tricyclic compounds |
| JPWO2010119875A1 (ja) * | 2009-04-14 | 2012-10-22 | アステラス製薬株式会社 | 縮合ピロロピリジン誘導体 |
| CN102459270B (zh) * | 2009-04-20 | 2015-04-29 | 奥斯拜客斯制药有限公司 | Janus激酶3的哌啶抑制剂 |
| WO2011011594A2 (en) * | 2009-07-23 | 2011-01-27 | Shriners Hospitals For Children | Intracellular toll-like receptors pathways and axonal degeneration |
| US8361962B2 (en) * | 2009-07-27 | 2013-01-29 | Roche Palo Alto Llc | Tricyclic inhibitors of JAK |
| CA2773182A1 (en) | 2009-09-10 | 2011-03-17 | F. Hoffmann-La Roche Ag | Inhibitors of jak |
| EP2480554B1 (en) | 2009-09-21 | 2014-08-06 | F.Hoffmann-La Roche Ag | Macrocyclic inhibitors of jak |
| ES2759949T3 (es) | 2009-10-29 | 2020-05-12 | Bristol Myers Squibb Co | Compuestos heterocíclicos tricíclicos |
| HUE033099T2 (en) * | 2009-12-01 | 2017-11-28 | Abbvie Inc | Novel tricyclic compounds |
| WO2011068899A1 (en) * | 2009-12-01 | 2011-06-09 | Abbott Laboratories | Novel tricyclic compounds |
| US8329705B2 (en) | 2009-12-30 | 2012-12-11 | Arqule, Inc. | Substituted triazolo-pyrazine compounds |
| KR20140015162A (ko) * | 2010-01-12 | 2014-02-06 | 에프. 호프만-라 로슈 아게 | 트라이사이클릭 헤테로사이클릭 화합물, 조성물 및 이의 사용 방법 |
| US8637529B2 (en) | 2010-06-11 | 2014-01-28 | AbbYie Inc. | Pyrazolo[3,4-d]pyrimidine compounds |
| DE102011106849A1 (de) * | 2010-12-15 | 2012-06-21 | Merck Patent Gmbh | Verfahren zur Synthese N-N verknüpfter und um die N-N Bindung rotationsgehinderter bis-N-heterocyclische Carbene und deren Einsatz als Liganden für Metallkomplexe |
| TW201309639A (zh) * | 2011-02-17 | 2013-03-01 | Lg Life Sciences Ltd | 作為ｇｐｒ１１９促效劑之肟衍生物 |
| WO2012127506A1 (en) * | 2011-03-22 | 2012-09-27 | Advinus Therapeutics Limited | Substituted fused tricyclic compounds, compositions and medicinal applications thereof |
| SG194216A1 (en) * | 2011-04-21 | 2013-11-29 | Origenis Gmbh | Heterocyclic compounds as kinase inhibitors |
| US20120330012A1 (en) * | 2011-04-29 | 2012-12-27 | Abbott Laboratories | Novel Tricyclic Compounds |
| AR086113A1 (es) | 2011-04-30 | 2013-11-20 | Abbott Lab | Isoxazolinas como agentes terapeuticos |
| WO2013007768A1 (en) * | 2011-07-13 | 2013-01-17 | F. Hoffmann-La Roche Ag | Tricyclic heterocyclic compounds, compositions and methods of use thereof as jak inhibitors |
| AU2012295802B2 (en) * | 2011-08-12 | 2017-03-30 | Nissan Chemical Industries, Ltd. | Tricyclic heterocyclic compounds and JAK inhibitors |
| CA2881566A1 (en) | 2012-07-19 | 2014-01-23 | Yohei Ikuma | 1-(cycloalkyl-carbonyl)proline derivative |
| KR20150056844A (ko) | 2012-09-17 | 2015-05-27 | 아비에 도이치란트 게엠베하 운트 콤파니 카게 | 포스포디에스테라제 타입 10a의 신규 억제제 화합물 |
| JP2015529242A (ja) * | 2012-09-21 | 2015-10-05 | アドヴィヌス セラピューティクス リミテッドＡｄｖｉｎｕｓ Ｔｈｅｒａｐｅｕｔｉｃｓ Ｌｉｍｉｔｅｄ | 置換された縮合三環式化合物、組成物およびその医薬用途 |
| WO2014060113A1 (en) | 2012-10-19 | 2014-04-24 | Origenis Gmbh | Novel kinase inhibitors |
| CN102961382B (zh) * | 2012-11-28 | 2014-07-16 | 玉林师范学院 | 一种骨肉瘤细胞抑制剂及制备方法 |
| ES2755130T3 (es) | 2013-02-08 | 2020-04-21 | Nissan Chemical Corp | Compuesto de pirrolopiridina tricíclico, e inhibidor de JAK |
| JP2016135742A (ja) * | 2013-03-29 | 2016-07-28 | 日本農薬株式会社 | 縮合複素環化合物又はその塩類及び該化合物を含有する農園芸用殺虫剤並びにその使用方法 |
| WO2014169473A1 (en) * | 2013-04-19 | 2014-10-23 | Abbvie Inc. | 6H-IMIDAZO[1,5-a]PYRROLO[2,3-e]PYRAZINE COMPOUNDS |
| CA2919892C (en) | 2013-08-12 | 2019-06-18 | Pharmaceutical Manufacturing Research Services, Inc. | Extruded immediate release abuse deterrent pill |
| CN103694168B (zh) * | 2013-12-05 | 2015-08-19 | 贵州威顿晶磷电子材料股份有限公司 | 一种6-氯-4-三氟甲基-3-氰基吡啶的制备方法 |
| US9492444B2 (en) | 2013-12-17 | 2016-11-15 | Pharmaceutical Manufacturing Research Services, Inc. | Extruded extended release abuse deterrent pill |
| US10172797B2 (en) | 2013-12-17 | 2019-01-08 | Pharmaceutical Manufacturing Research Services, Inc. | Extruded extended release abuse deterrent pill |
| ES2744213T3 (es) | 2014-05-14 | 2020-02-24 | Nissan Chemical Corp | Compuesto tricíclico e inhibidor de JAK |
| DK3169315T3 (da) | 2014-07-17 | 2020-08-10 | Pharmaceutical Manufacturing Res Services In | Væskefyldt doseringsform til forhindring af misbrug med øjeblikkelig frigivelse |
| CA2957579A1 (en) * | 2014-08-27 | 2016-03-03 | Abbvie Inc. | Topical formulation |
| EP3209282A4 (en) | 2014-10-20 | 2018-05-23 | Pharmaceutical Manufacturing Research Services, Inc. | Extended release abuse deterrent liquid fill dosage form |
| CA2981365A1 (en) | 2015-04-02 | 2016-10-06 | Merck Patent Gmbh | Imidazolonylquinolines and the use thereof as atm kinase inhibitors |
| 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 |
| US11780848B2 (en) | 2015-10-16 | 2023-10-10 | 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 |
| 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 |
| 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 |
| 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 |
| RU2718902C2 (ru) | 2016-02-24 | 2020-04-15 | Пфайзер Инк. | Производные пиразоло[1,5-а]пиразин-4-ила в качестве jak-ингибиторов |
| EP3433615A1 (en) | 2016-03-21 | 2019-01-30 | Institut National de la Sante et de la Recherche Medicale (INSERM) | Methods for diagnosis and treatment of solar lentigo |
| JOP20190060A1 (ar) | 2016-09-26 | 2019-03-26 | Chugai Pharmaceutical Co Ltd | مشتق بيرازولو بيريدين له تأثير مساعد لمستقبل glp-1 |
| JOP20190144A1 (ar) | 2016-12-16 | 2019-06-16 | Janssen Pharmaceutica Nv | إيميدازو بيرولو بيريدين كمثبطات لعائلة jak الخاصة بإنزيمات الكيناز |
| ES2922379T3 (es) | 2016-12-16 | 2022-09-14 | Janssen Pharmaceutica Nv | Compuestos de imidazo[4,5,D]pirrolo[2,3,B]piridina como inhibidores de Janus quinasas |
| WO2018165581A1 (en) | 2017-03-09 | 2018-09-13 | Abbvie Inc. | Methods of treating crohn's disease and ulcerative colitis |
| US11564922B2 (en) | 2017-03-09 | 2023-01-31 | Abbvie Inc. | Methods of treating crohn's disease and ulcerative colitis |
| WO2018167283A1 (en) | 2017-03-17 | 2018-09-20 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for the diagnosis and treatment of pancreatic ductal adenocarcinoma associated neural remodeling |
| EP3668858A1 (en) | 2017-08-14 | 2020-06-24 | Pfizer Inc | Pyrazolo[1,5-a]pyrazin-4-yl and related derivatives |
| NZ763299A (en) | 2017-09-14 | 2025-09-26 | Daiichi Sankyo Co Ltd | Compound having cyclic structure |
| WO2019100008A1 (en) * | 2017-11-20 | 2019-05-23 | Georgetown University | Treatments and methods for controlling hypertension |
| JP7312412B2 (ja) | 2018-01-05 | 2023-07-21 | オタワ ホスピタル リサーチ インスティチュート | 改変オルトポックスウイルスベクター |
| TW201940483A (zh) | 2018-03-12 | 2019-10-16 | 美商艾伯維有限公司 | 酪胺酸激酶２介導的傳訊之抑制劑 |
| CN110294761B (zh) * | 2018-06-08 | 2020-09-08 | 南京雷正医药科技有限公司 | 作为Trk激酶抑制剂的取代的吡唑并[1,5-a]嘧啶化合物 |
| 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 |
| CN110872250B (zh) * | 2018-08-31 | 2023-01-10 | 苏州鹏旭医药科技有限公司 | 两种化合物及其制备方法和在合成乌西替尼中的用途 |
| MX2021004517A (es) | 2018-11-01 | 2021-11-04 | Lynk Pharmaceuticals Co Ltd | Inhibidores de cinasa de janus 1 triciclicos y composiciones y metodos de los mismos. |
| WO2020092015A1 (en) | 2018-11-02 | 2020-05-07 | University Of Rochester | Therapeutic mitigation of epithelial infection |
| CN109369659B (zh) * | 2018-12-06 | 2020-10-27 | 浙江师范大学 | 一种jak抑制剂的合成方法 |
| CN112300180B (zh) * | 2019-07-26 | 2022-04-29 | 珠海宇繁生物科技有限责任公司 | 一种irak4激酶抑制剂及其制备方法 |
| CN110483514B (zh) | 2019-09-16 | 2022-06-14 | 启元生物(杭州)有限公司 | 一种氰基取代的环肼衍生物及其应用 |
| CN113912535B (zh) * | 2020-07-07 | 2023-04-07 | 新发药业有限公司 | 一种6-氯-4-三氟甲基-3-氰基吡啶的制备方法 |
| CA3189037A1 (en) | 2020-07-08 | 2022-01-13 | Crystal Pharmaceutical (Suzhou) Co., Ltd. | Crystal form of upadacitinib, preparation method therefor, and use thereof |
| EP3944859A1 (en) | 2020-07-30 | 2022-02-02 | Assistance Publique Hôpitaux de Paris | Method for treating immune toxicities induced by immune checkpoint inhibitors |
| CN112028888B (zh) * | 2020-09-11 | 2021-08-20 | 中国药科大学 | 一种化合物及其制备方法和用途 |
| WO2022143628A1 (zh) * | 2020-12-29 | 2022-07-07 | 上海岸阔医药科技有限公司 | 预防或治疗抗肿瘤剂相关疾病或病症的方法 |
| AU2022233254A1 (en) | 2021-03-11 | 2023-10-26 | Janssen Pharmaceutica Nv | Lorpucitinib for use in the treatment of jak mediated disorders |
| CN113332298A (zh) * | 2021-05-27 | 2021-09-03 | 成都医学院 | 米诺环素作为酪氨酸激酶抑制剂的新用途 |
| CN113603693B (zh) * | 2021-07-13 | 2022-08-26 | 陕西丽彩药业有限公司 | 一种2-溴-5-对甲苯磺酰基-5H-吡咯并[2,3-b]吡嗪的制备方法 |
| WO2023194842A1 (en) | 2022-04-05 | 2023-10-12 | Unichem Laboratories Limited | Substituted tricyclic compounds and their use in rheumatoid arthritis |
Family Cites Families (71)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1376A (en) * | 1839-10-18 | Wateb-wheel | ||
| GB716327A (en) | 1951-09-05 | 1954-10-06 | Ici Ltd | New heterocyclic compounds |
| US3663559A (en) | 1969-12-03 | 1972-05-16 | Union Carbide Corp | Preparation of oxo-furo-pyridines from furylvinyl isocyanates |
| ZA737247B (en) | 1972-09-29 | 1975-04-30 | Ayerst Mckenna & Harrison | Rapamycin and process of preparation |
| US4053474A (en) * | 1976-04-21 | 1977-10-11 | E. R. Squibb & Sons, Inc. | Pyrazolo[4,3-e][1,2,4]triazolo[4,3-c]pyrimidine |
| US5605690A (en) | 1989-09-05 | 1997-02-25 | Immunex Corporation | Methods of lowering active TNF-α levels in mammals using tumor necrosis factor receptor |
| US5270316A (en) | 1989-10-20 | 1993-12-14 | Kyowa Hakko Kogyo Co., Ltd. | Condensed purine derivatives |
| AU651569B2 (en) | 1990-01-11 | 1994-07-28 | Isis Pharmaceuticals, Inc. | Compositions and methods for detecting and modulating RNA activity and gene expression |
| US6262241B1 (en) | 1990-08-13 | 2001-07-17 | Isis Pharmaceuticals, Inc. | Compound for detecting and modulating RNA activity and gene expression |
| DE69233701T2 (de) | 1991-03-18 | 2008-04-10 | New York University | Monoklonale und chimäre Antikörper spezifisch für menschlichen Tumornekrosefaktor |
| WO1992022552A1 (en) | 1991-06-14 | 1992-12-23 | The Upjohn Company | IMIDAZO[1,5-a]QUINOXALINES |
| US5212310A (en) | 1991-12-19 | 1993-05-18 | Neurogen Corporation | Certain aryl fused imidazopyrimidines; a new class of GABA brain receptor ligands |
| US5266698A (en) | 1992-04-30 | 1993-11-30 | Neurogen Corporation | Certain aryl and cycloalkyl fused imidazopyrazinediones; a new class of GABA brain receptor ligands |
| US5306819A (en) | 1992-08-27 | 1994-04-26 | Neurogen Corporation | Certain aryl a cycloalkyl fused imidazopyrazinols; and new class of GABA brain receptor ligands |
| ES2091684T3 (es) | 1992-11-13 | 1996-11-01 | Idec Pharma Corp | Aplicacion terapeutica de anticuerpos quimericos y radiomarcados contra el antigeno de diferenciacion restringida de los linfocitos b humanos para el tratamiento del linfoma de las celulas b. |
| CA2156918A1 (en) | 1993-02-26 | 1994-09-01 | Deen Tulshian | 2-benzyl-polycyclic guanine derivatives and process for preparing them |
| US5736540A (en) | 1993-07-29 | 1998-04-07 | American Cyanamid Company | Tricyclic diazepine vasopressin antagonists and oxytocin antagonists |
| US5733905A (en) | 1993-07-29 | 1998-03-31 | American Cyanamid Company | Tricyclic diazepine vasopressin antagonists and oxytocin antagonists |
| IL112248A0 (en) | 1994-01-25 | 1995-03-30 | Warner Lambert Co | Tricyclic heteroaromatic compounds and pharmaceutical compositions containing them |
| US5547975A (en) | 1994-09-20 | 1996-08-20 | Talley; John J. | Benzopyranopyrazolyl derivatives for the treatment of inflammation |
| RU2158127C2 (ru) * | 1994-12-23 | 2000-10-27 | Варнер-Ламберт Компани | Способы ингибирования тирозинкиназы рецептора эпидермального фактора роста, азотсодержащие трициклические соединения, фармацевтическая композиция, предназначенная для введения ингибитора тирозинкиназы рецептора эпидермального фактора роста, например, erb-b2, erb-b3 или erb-b4, и противозачаточная композиция |
| US5521173A (en) | 1995-01-17 | 1996-05-28 | American Home Products Corporation | Tricyclic benzazepine vasopressin antagonists |
| US5753648A (en) | 1995-01-17 | 1998-05-19 | American Cyanamid Company | Tricyclic benzazepine vasopressin antagonists |
| US5763137A (en) | 1995-08-04 | 1998-06-09 | Agfa-Gevaert, N.V. | Method for making a lithographic printing plate |
| US6090382A (en) | 1996-02-09 | 2000-07-18 | Basf Aktiengesellschaft | Human antibodies that bind human TNFα |
| WO1999045009A1 (en) * | 1998-03-04 | 1999-09-10 | Bristol-Myers Squibb Company | Heterocyclo-substituted imidazopyrazine protein tyrosine kinase inhibitors |
| IL139197A0 (en) | 1999-10-29 | 2001-11-25 | Pfizer Prod Inc | Use of corticotropin releasing factor antagonists and related compositions |
| TWI271406B (en) | 1999-12-13 | 2007-01-21 | Eisai Co Ltd | Tricyclic condensed heterocyclic compounds, preparation method of the same and pharmaceuticals comprising the same |
| AU2001285401A1 (en) | 2000-08-07 | 2002-02-18 | Neurogen Corporation | Heterocyclic compounds as ligands of the GABAa receptor |
| GB0115393D0 (en) | 2001-06-23 | 2001-08-15 | Aventis Pharma Ltd | Chemical compounds |
| GB0124299D0 (en) | 2001-10-10 | 2001-11-28 | Astrazeneca Ab | Crystal structure of enzyme and uses thereof |
| EP1478357B1 (en) | 2002-02-19 | 2007-01-31 | Pfizer Italia S.r.l. | Tricyclic pyrazole derivatives, process for their preparation and their use as antitumor agents |
| TW200400034A (en) | 2002-05-20 | 2004-01-01 | Bristol Myers Squibb Co | Pyrazolo-pyrimidine aniline compounds useful as kinase inhibitors |
| WO2004065378A1 (en) | 2003-01-17 | 2004-08-05 | Warner-Lambert Company Llc | 2-aminopyridine substituted heterocycles as inhibitors of cellular proliferation |
| US7169926B1 (en) | 2003-08-13 | 2007-01-30 | Takeda Pharmaceutical Company Limited | Dipeptidyl peptidase inhibitors |
| US20060074102A1 (en) | 2004-05-14 | 2006-04-06 | Kevin Cusack | Kinase inhibitors as therapeutic agents |
| AR049300A1 (es) | 2004-06-15 | 2006-07-12 | Schering Corp | Compuestos triciclicos antagonistas de mglur1 como agentes terapeuticos |
| ATE455777T1 (de) | 2004-07-23 | 2010-02-15 | Medicines Co Leipzig Gmbh | Substituierte pyridoä3',2':4,5üthienoä3,2- düpyrimidine und pyridoä3',2':4,5üfuroä3,2-dü- pyrimidine zur verwendung als inhibitoren der pda-4 und/oder tnf-alpha freisetzung |
| ES2345997T3 (es) | 2005-01-14 | 2010-10-07 | Janssen Pharmaceutica Nv | Pirazolopiramidinas como inhibidores de las quinasas del ciclo celular. |
| AU2006205851A1 (en) | 2005-01-14 | 2006-07-20 | Janssen Pharmaceutica N.V. | 5-membered annelated heterocyclic pyrimidines as kinase inhibitors |
| US20060183758A1 (en) | 2005-02-17 | 2006-08-17 | Cb Research And Development, Inc. | Method for synthesis of AZA-annelated pyrroles, thiophenes, and furans |
| EP1863813A2 (en) * | 2005-04-01 | 2007-12-12 | Coley Pharmaceutical Group, Inc. | Pyrazolo[3,4-c]quinolines, pyrazolo[3,4-c]naphthyridines, analogs thereof, and methods |
| 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 |
| US7593820B2 (en) | 2005-05-12 | 2009-09-22 | Cytopia Research Pty Ltd | Crystal structure of human Janus Kinase 2 (JAK2) and uses thereof |
| KR20080026654A (ko) | 2005-07-14 | 2008-03-25 | 아스텔라스세이야쿠 가부시키가이샤 | 헤테로시클릭 야누스 키나제 3 억제제 |
| EP2251341A1 (en) * | 2005-07-14 | 2010-11-17 | Astellas Pharma Inc. | Heterocyclic Janus kinase 3 inhibitors |
| RU2008109908A (ru) * | 2005-08-16 | 2009-09-27 | Айрм Ллк (Bm) | Соединения и композиции в качестве ингибиторов протеинкиназы |
| US20090240055A1 (en) | 2005-09-23 | 2009-09-24 | Krepski Larry R | Method for 1H-Imidazo[4,5-C] Pyridines and Analogs Thereof |
| JP5249772B2 (ja) | 2005-11-22 | 2013-07-31 | メルク・シャープ・アンド・ドーム・コーポレーション | キナーゼの阻害剤として有用な三環式化合物 |
| TW201307354A (zh) | 2005-12-29 | 2013-02-16 | Abbott Lab | 蛋白質激酶抑制劑 |
| JP5386350B2 (ja) | 2006-05-31 | 2014-01-15 | タケダ カリフォルニア インコーポレイテッド | グルコキナーゼ活性剤としての、インダゾールおよびイソインドール誘導体 |
| US8063225B2 (en) | 2006-08-14 | 2011-11-22 | Chembridge Corporation | Tricyclic compound derivatives useful in the treatment of neoplastic diseases, inflammatory disorders and immunomodulatory disorders |
| US7790741B2 (en) | 2006-10-06 | 2010-09-07 | Abbott Laboratories | Imidazothiazoles and imidazoxazoles |
| JP5287253B2 (ja) | 2007-01-12 | 2013-09-11 | アステラス製薬株式会社 | 縮合ピリジン化合物 |
| WO2008094575A2 (en) | 2007-01-30 | 2008-08-07 | Biogen Idec Ma Inc. | 1-h-pyrazolo(3,4b)pyrimidine derivatives and their use as modulators of mitotic kinases |
| WO2008112695A2 (en) | 2007-03-12 | 2008-09-18 | Irm Llc | Pyrazolo [3,4-d] pyrimidines and 1, 2, 5, 6-tetraaza- as- indacenes as protein kinase inhibitors for cancer treatment |
| US7723343B2 (en) | 2007-03-30 | 2010-05-25 | King Pharmaceuticals Research And Development, Inc. | Adenosine A2A receptor antagonists |
| EP2170337A4 (en) | 2007-06-28 | 2013-12-18 | Abbvie Inc | NEW TRIAZOLOPYRIDAZINE |
| CN101939324B (zh) | 2008-02-25 | 2014-10-15 | 霍夫曼-拉罗奇有限公司 | 吡咯并吡嗪激酶抑制剂 |
| PT2250172E (pt) | 2008-02-25 | 2011-11-30 | Hoffmann La Roche | Inibidores de pirrolpirazina-cinase |
| CN101945877B (zh) | 2008-02-25 | 2013-07-03 | 霍夫曼-拉罗奇有限公司 | 吡咯并吡嗪激酶抑制剂 |
| WO2009108827A1 (en) | 2008-02-29 | 2009-09-03 | Wyeth | Fused tricyclic pyrazolo[1, 5-a]pyrimidines, methods for preparation and uses thereof |
| HUE028347T2 (en) | 2008-06-10 | 2016-12-28 | Abbvie Inc | Tricyclic compounds |
| EP2320895A2 (en) | 2008-07-03 | 2011-05-18 | Exelixis, Inc. | Cdk modulators |
| JPWO2010119875A1 (ja) | 2009-04-14 | 2012-10-22 | アステラス製薬株式会社 | 縮合ピロロピリジン誘導体 |
| US8361962B2 (en) | 2009-07-27 | 2013-01-29 | Roche Palo Alto Llc | Tricyclic inhibitors of JAK |
| WO2011068899A1 (en) | 2009-12-01 | 2011-06-09 | Abbott Laboratories | Novel tricyclic compounds |
| HUE033099T2 (en) | 2009-12-01 | 2017-11-28 | Abbvie Inc | Novel tricyclic compounds |
| US8637529B2 (en) | 2010-06-11 | 2014-01-28 | AbbYie Inc. | Pyrazolo[3,4-d]pyrimidine compounds |
| US20120330012A1 (en) | 2011-04-29 | 2012-12-27 | Abbott Laboratories | Novel Tricyclic Compounds |
| WO2013043826A1 (en) | 2011-09-21 | 2013-03-28 | Abbvie Inc. | Tricyclic compounds useful as protein kinase inhibitors |
-
2009
- 2009-06-09 HU HUE09763424A patent/HUE028347T2/en unknown
- 2009-06-09 PE PE2010001126A patent/PE20110223A1/es active IP Right Grant
- 2009-06-09 SI SI200931347T patent/SI2299821T1/sl unknown
- 2009-06-09 KR KR1020167035162A patent/KR101718384B1/ko active Active
- 2009-06-09 ME MEP-2016-72A patent/ME02340B/me unknown
- 2009-06-09 KR KR1020117000497A patent/KR20110017431A/ko not_active Withdrawn
- 2009-06-09 MY MYPI2010005827A patent/MY161369A/en unknown
- 2009-06-09 CA CA2727032A patent/CA2727032C/en active Active
- 2009-06-09 EP EP15192686.2A patent/EP3031324A3/en not_active Withdrawn
- 2009-06-09 AU AU2009257602A patent/AU2009257602B2/en active Active
- 2009-06-09 PE PE2013001090A patent/PE20140407A1/es not_active Application Discontinuation
- 2009-06-09 RU RU2010153582/04A patent/RU2545023C9/ru active
- 2009-06-09 BR BRPI0915374-8A patent/BRPI0915374B1/pt active IP Right Grant
- 2009-06-09 TW TW104143241A patent/TW201612182A/zh unknown
- 2009-06-09 DK DK09763424.0T patent/DK2299821T3/en active
- 2009-06-09 NZ NZ623922A patent/NZ623922A/en unknown
- 2009-06-09 PL PL09763424T patent/PL2299821T3/pl unknown
- 2009-06-09 ES ES09763424.0T patent/ES2559403T3/es active Active
- 2009-06-09 TW TW098119270A patent/TWI449703B/zh active
- 2009-06-09 PT PT97634240T patent/PT2299821E/pt unknown
- 2009-06-09 RU RU2015105591/04A patent/RU2015105591A/ru not_active Application Discontinuation
- 2009-06-09 CN CN2009801311819A patent/CN102118968A/zh active Pending
- 2009-06-09 JP JP2011513627A patent/JP5748659B2/ja active Active
- 2009-06-09 TW TW103118323A patent/TWI527819B/zh active
- 2009-06-09 WO PCT/US2009/046714 patent/WO2009152133A1/en not_active Ceased
- 2009-06-09 UA UAA201100242A patent/UA106045C2/uk unknown
- 2009-06-09 HR HRP20160098TT patent/HRP20160098T1/hr unknown
- 2009-06-09 MX MX2010013557A patent/MX2010013557A/es active IP Right Grant
- 2009-06-09 CN CN201410747767.0A patent/CN104592231A/zh active Pending
- 2009-06-09 CA CA3000973A patent/CA3000973A1/en not_active Abandoned
- 2009-06-09 US US12/481,028 patent/US8962629B2/en active Active
- 2009-06-09 RS RS20160062A patent/RS54560B1/sr unknown
- 2009-06-09 UY UY0001031881A patent/UY31881A/es not_active Application Discontinuation
- 2009-06-09 EP EP09763424.0A patent/EP2299821B1/en active Active
- 2009-06-10 AR ARP090102084A patent/AR072086A1/es active IP Right Grant
-
2010
- 2010-11-18 IL IL209434A patent/IL209434A0/en active IP Right Grant
- 2010-11-29 ZA ZA2010/08562A patent/ZA201008562B/en unknown
- 2010-11-29 CO CO10150402A patent/CO6382083A2/es not_active Application Discontinuation
- 2010-12-02 NO NO20101688A patent/NO20101688A1/no not_active Application Discontinuation
- 2010-12-03 EC EC2010010657A patent/ECSP10010657A/es unknown
- 2010-12-08 DO DO2010000382A patent/DOP2010000382A/es unknown
- 2010-12-10 CL CL2010001426A patent/CL2010001426A1/es unknown
-
2013
- 2013-03-08 DO DO2013000055A patent/DOP2013000055A/es unknown
-
2015
- 2015-01-30 US US14/610,119 patent/US9365579B2/en active Active
- 2015-05-11 JP JP2015096257A patent/JP2015163632A/ja active Pending
-
2016
- 2016-01-06 CR CR20160007A patent/CR20160007A/es unknown
- 2016-01-27 CY CY20161100074T patent/CY1117165T1/el unknown
- 2016-05-12 US US15/152,823 patent/US20160326181A1/en not_active Abandoned
-
2017
- 2017-11-07 US US15/806,104 patent/US20180291029A1/en not_active Abandoned
-
2022
- 2022-01-14 US US17/575,731 patent/US20230082167A1/en not_active Abandoned
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2015163632A5 (OSRAM) | ||
| RU2500680C2 (ru) | Новые замещенные пиридин-2-оны и пиридазин-3-оны | |
| JP2019524883A5 (OSRAM) | ||
| JP2008505194A5 (OSRAM) | ||
| JP2015057390A5 (OSRAM) | ||
| JP2011530500A5 (OSRAM) | ||
| JP2017137291A5 (OSRAM) | ||
| JP2017512779A5 (OSRAM) | ||
| JP2016540742A5 (OSRAM) | ||
| CY1114932T1 (el) | Αντιπαρασιτικοι παραγοντες | |
| JP2015181191A5 (OSRAM) | ||
| JP2015143283A5 (OSRAM) | ||
| MY140528A (en) | Spiroketal derivatives and their use as therapeutic agents for diabetes | |
| JP2015024998A5 (OSRAM) | ||
| JP2015534574A5 (OSRAM) | ||
| JP2016505614A5 (OSRAM) | ||
| JP2017538773A5 (OSRAM) | ||
| JP2013544233A5 (OSRAM) | ||
| NO20084742L (no) | Aziridinyl-epotilonforbindelser | |
| JP2017536416A5 (OSRAM) | ||
| JP2015063518A5 (ja) | 有機化合物 | |
| WO2010053583A3 (en) | Small molecule cd4 mimetics and uses thereof | |
| JP2012087114A5 (ja) | カルバゾール誘導体 | |
| JP2018531218A5 (OSRAM) | ||
| CO2021002768A2 (es) | Compuestos de 2,6-diaminopiridina |