JP2011505356A5 - - Google Patents
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- JP2011505356A5 JP2011505356A5 JP2010535919A JP2010535919A JP2011505356A5 JP 2011505356 A5 JP2011505356 A5 JP 2011505356A5 JP 2010535919 A JP2010535919 A JP 2010535919A JP 2010535919 A JP2010535919 A JP 2010535919A JP 2011505356 A5 JP2011505356 A5 JP 2011505356A5
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- JP
- Japan
- Prior art keywords
- compound
- formula
- pharmaceutically acceptable
- acceptable salt
- disease
- 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.)
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- 150000001875 compounds Chemical class 0.000 claims description 11
- 150000003839 salts Chemical class 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims 3
- 239000002671 adjuvant Substances 0.000 claims 2
- 239000003085 diluting agent Substances 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- 208000011231 Crohn disease Diseases 0.000 claims 1
- 208000022559 Inflammatory bowel disease Diseases 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 125000006239 protecting group Chemical group 0.000 claims 1
- 238000006268 reductive amination reaction Methods 0.000 claims 1
- 206010039073 rheumatoid arthritis Diseases 0.000 claims 1
- 238000002560 therapeutic procedure Methods 0.000 claims 1
- NNJVILVZKWQKPM-UHFFFAOYSA-N Lidocaine Chemical compound CCN(CC)CC(=O)NC1=C(C)C=CC=C1C NNJVILVZKWQKPM-UHFFFAOYSA-N 0.000 description 1
- 229960004194 lidocaine Drugs 0.000 description 1
- 239000003589 local anesthetic agent Substances 0.000 description 1
Description
本発明は、さらに、本発明の化合物、またはその薬学的に許容される塩と、非経腸的または局所的(吸入を含む)に適用する局所麻酔剤、例えばリグノカインまたはその誘導体の組み合わせに関する。
Claims (8)
- 式(Ｉ)
- 請求項１に記載の式(Ｉ)の化合物、またはその薬学的に許容される塩を薬学的に許容されるアジュバント、希釈剤または担体と共に含む、医薬組成物。
- 請求項１に記載の式(Ｉ)の化合物、またはその薬学的に許容される塩と薬学的に許容されるアジュバント、希釈剤または担体を混合することを含む、請求項２に記載の医薬組成物の製造方法。
- 治療に使用するための、請求項１に記載の式(Ｉ)の化合物、またはその薬学的に許容される塩。
- リウマチ性関節炎の処置に使用するための医薬の製造における、請求項１に記載の式(Ｉ)の化合物、またはその薬学的に許容される塩の使用。
- 炎症性腸疾患またはクローン病の処置に使用するための医薬の製造における、請求項１に記載の式(Ｉ)の化合物、またはその薬学的に許容される塩の使用。
- 請求項１に記載の式(Ｉ)の化合物の製造方法であって、式(II)
を還元的アミノ化条件下に反応させ、そして
所望により本化合物の薬学的に許容される塩を形成させることを含む、方法。 - 請求項１に記載の化合物を、それを必要とする対象に投与することを含む、当該化合物により治療し得る疾患の処置方法。
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US99126507P | 2007-11-30 | 2007-11-30 | |
| PCT/SE2008/051370 WO2009070116A1 (en) | 2007-11-30 | 2008-11-28 | A quinoline derivative acting as a p2x7-receptor antagonist |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2011505356A JP2011505356A (ja) | 2011-02-24 |
| JP2011505356A5 true JP2011505356A5 (ja) | 2012-02-02 |
Family
ID=40676391
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010535919A Withdrawn JP2011505356A (ja) | 2007-11-30 | 2008-11-28 | Ｐ２ｘ７受容体アンタゴニストとして作用するキノリン誘導体 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US8106073B2 (ja) |
| EP (1) | EP2225222B1 (ja) |
| JP (1) | JP2011505356A (ja) |
| AR (1) | AR069508A1 (ja) |
| AT (1) | ATE524458T1 (ja) |
| ES (1) | ES2370960T3 (ja) |
| HK (1) | HK1148002A1 (ja) |
| PE (1) | PE20091036A1 (ja) |
| TW (1) | TW200932229A (ja) |
| WO (1) | WO2009070116A1 (ja) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PE20091225A1 (es) * | 2007-03-22 | 2009-09-16 | Astrazeneca Ab | Derivados de quinolina como antagonistas del receptor p2x7 |
| PE20091036A1 (es) | 2007-11-30 | 2009-08-15 | Astrazeneca Ab | Derivado de quinolina como antagonista del receptor p2x7 |
| EA022494B1 (ru) * | 2009-12-17 | 2016-01-29 | Мерк Шарп Энд Домэ Корп. | Соединения хинолинамида в качестве положительных аллостерических модуляторов мускаринового рецептора m1 |
| WO2012110190A1 (en) | 2011-02-17 | 2012-08-23 | Affectis Pharmaceuticals Ag | Novel p2x7r antagonists and their use |
| WO2012163456A1 (en) | 2011-05-27 | 2012-12-06 | Affectis Pharmaceuticals Ag | Novel p2x7r antagonists and their use |
| WO2012163792A1 (en) | 2011-05-27 | 2012-12-06 | Affectis Pharmaceuticals Ag | Novel p2x7r antagonists and their use |
| AR087274A1 (es) | 2011-07-22 | 2014-03-12 | Actelion Pharmaceuticals Ltd | Derivados de amidas heterociclicas como antagonistas de receptores p2x7 |
| SG11201403933UA (en) | 2012-01-20 | 2014-08-28 | Actelion Pharmaceuticals Ltd | Heterocyclic amide derivatives as p2x7 receptor antagonists |
| CA2890886C (en) | 2012-12-12 | 2020-10-27 | Actelion Pharmaceuticals Ltd | Indole carboxamide derivatives as p2x7 receptor antagonists |
| WO2014097140A1 (en) | 2012-12-18 | 2014-06-26 | Actelion Pharmaceuticals Ltd | Indole carboxamide derivatives as p2x7 receptor antagonists |
| EP2956457B1 (en) | 2013-01-22 | 2016-11-23 | Actelion Pharmaceuticals Ltd | Heterocyclic amide derivatives as p2x7 receptor antagonists |
| JP6282016B2 (ja) | 2013-01-22 | 2018-02-21 | イドーシア ファーマシューティカルズ リミテッドＩｄｏｒｓｉａ Ｐｈａｒｍａｃｅｕｔｉｃａｌｓ Ｌｔｄ | Ｐ２ｘ７受容体アンタゴニストとしての複素環アミド誘導体 |
| WO2015187905A1 (en) * | 2014-06-05 | 2015-12-10 | Merck Patent Gmbh | Novel quinoline derivatives and their use in neurodegenerative diseases |
| MA55805A (fr) | 2019-05-03 | 2022-03-09 | Flagship Pioneering Innovations V Inc | Métodes de modulation de l'activité immunitaire |
Family Cites Families (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3352912A (en) | 1963-07-24 | 1967-11-14 | Du Pont | Adamantanes and tricyclo[4. 3. 1. 1 3.8] undecanes |
| US3471491A (en) | 1967-08-28 | 1969-10-07 | Squibb & Sons Inc | Adamantyl-s-triazines |
| US3464998A (en) | 1968-03-04 | 1969-09-02 | Searle & Co | Adamantyl esters and amides of pyridinecarboxylic acids |
| GB1274652A (en) | 1968-08-27 | 1972-05-17 | Lilly Industries Ltd | Adamantanyl-alkylamine derivatives and their preparation |
| IL53441A0 (en) | 1977-11-22 | 1978-01-31 | Teva Pharma | Methyladamantyl hydrazines their preparation and pharmaceutical compositions containing them |
| US4751292A (en) | 1985-07-02 | 1988-06-14 | The Plant Cell Research Institute, Inc. | Adamantyl purines |
| US5643925A (en) | 1991-02-21 | 1997-07-01 | Sankyo Company, Limited | Benzene derivatives having NGF production-promoting activity |
| CA2167154A1 (en) | 1993-08-10 | 1995-02-16 | Sarkis Barret Kalindjian | Gastrin and cck receptor ligands |
| PT940391E (pt) | 1994-05-27 | 2004-12-31 | Glaxosmithkline Spa | Derivados de quinolina como antagonistas do receptor de taquicinina nk3 |
| AR004735A1 (es) | 1995-11-24 | 1999-03-10 | Smithkline Beecham Spa | Quinoleina 4-amido sustituida, un procedimiento para su preparacion, una composicion farmaceutica que los contiene y el uso de los mismos para lapreparacion de un medicamento. |
| BR9709015A (pt) | 1996-05-20 | 1999-08-03 | Darwin Discovery Ltd | Quinolina carboxamidas como inbidores de tnf e como inbidores de pde-iv |
| FR2761358B1 (fr) | 1997-03-27 | 1999-05-07 | Adir | Nouveaux composes de n-aryl piperidine, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| CA2311131A1 (en) | 1997-11-21 | 1999-06-03 | Nps Pharmaceuticals, Inc. | Metabotropic glutamate receptor antagonists for treating central nervous system diseases |
| SE9704544D0 (sv) | 1997-12-05 | 1997-12-05 | Astra Pharma Prod | Novel compounds |
| SE9704545D0 (sv) | 1997-12-05 | 1997-12-05 | Astra Pharma Prod | Novel compounds |
| TR200102911T2 (tr) | 1999-04-09 | 2002-01-21 | Astrazeneca Ab | Adamantan türevleri. |
| CN1361768A (zh) | 1999-06-02 | 2002-07-31 | Nps药物有限公司 | 代谢移变的谷氨酸盐受体拮抗剂和它们治疗中枢神经***疾病的用途 |
| ES2311479T3 (es) | 1999-11-26 | 2009-02-16 | SHIONOGI & CO., LTD. | Antagonistas de npy-y5. |
| GB0013737D0 (en) | 2000-06-07 | 2000-07-26 | Astrazeneca Ab | Novel compounds |
| RU2347570C2 (ru) | 2001-07-02 | 2009-02-27 | Н.В.Органон | Тетрагидрохинолиновые производные |
| WO2003042190A1 (en) | 2001-11-12 | 2003-05-22 | Pfizer Products Inc. | N-alkyl-adamantyl derivatives as p2x7-receptor antagonists |
| SE0103836D0 (sv) | 2001-11-16 | 2001-11-16 | Astrazeneca Ab | Novel compounds |
| AU2002352878B2 (en) | 2001-11-27 | 2007-11-22 | Merck Sharp & Dohme Corp. | 2-Aminoquinoline compounds |
| SE0200920D0 (sv) | 2002-03-25 | 2002-03-25 | Astrazeneca Ab | Novel compounds |
| EP1494997A4 (en) | 2002-04-05 | 2007-04-11 | Merck & Co Inc | SUBSTITUTED ARYLAMID |
| GB0312609D0 (en) | 2003-06-02 | 2003-07-09 | Astrazeneca Ab | Novel compounds |
| SE0302139D0 (sv) | 2003-07-28 | 2003-07-28 | Astrazeneca Ab | Novel compounds |
| SE0402925D0 (sv) | 2004-11-30 | 2004-11-30 | Astrazeneca Ab | Novel Compounds |
| US20080058309A1 (en) | 2006-07-27 | 2008-03-06 | Astrazeneca Ab | Novel Compounds 171 |
| PE20091225A1 (es) * | 2007-03-22 | 2009-09-16 | Astrazeneca Ab | Derivados de quinolina como antagonistas del receptor p2x7 |
| PE20091036A1 (es) | 2007-11-30 | 2009-08-15 | Astrazeneca Ab | Derivado de quinolina como antagonista del receptor p2x7 |
-
2008
- 2008-11-26 PE PE2008001976A patent/PE20091036A1/es not_active Application Discontinuation
- 2008-11-26 US US12/324,397 patent/US8106073B2/en not_active Expired - Fee Related
- 2008-11-28 AR ARP080105220A patent/AR069508A1/es unknown
- 2008-11-28 TW TW097146304A patent/TW200932229A/zh unknown
- 2008-11-28 JP JP2010535919A patent/JP2011505356A/ja not_active Withdrawn
- 2008-11-28 ES ES08855156T patent/ES2370960T3/es active Active
- 2008-11-28 AT AT08855156T patent/ATE524458T1/de not_active IP Right Cessation
- 2008-11-28 EP EP08855156A patent/EP2225222B1/en not_active Not-in-force
- 2008-11-28 WO PCT/SE2008/051370 patent/WO2009070116A1/en active Application Filing
-
2011
- 2011-03-02 HK HK11102084.0A patent/HK1148002A1/xx not_active IP Right Cessation
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