JP2008512380A - Pde4b阻害剤 - Google Patents
Pde4b阻害剤 Download PDFInfo
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- JP2008512380A JP2008512380A JP2007530399A JP2007530399A JP2008512380A JP 2008512380 A JP2008512380 A JP 2008512380A JP 2007530399 A JP2007530399 A JP 2007530399A JP 2007530399 A JP2007530399 A JP 2007530399A JP 2008512380 A JP2008512380 A JP 2008512380A
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- Prior art keywords
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- pde4b
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- 0 CC(C=C=C=C)C(C(I)=C)=C(*=*C)NI Chemical compound CC(C=C=C=C)C(C(I)=C)=C(*=*C)NI 0.000 description 4
- DDWKKQSWFMETDC-UHFFFAOYSA-N CC(C1c2ccc3OCOc3c2)Nc2c1cccn2 Chemical compound CC(C1c2ccc3OCOc3c2)Nc2c1cccn2 DDWKKQSWFMETDC-UHFFFAOYSA-N 0.000 description 1
- CZGHGKQHLOOVRG-UHFFFAOYSA-N CC(c(cc1)ccc1NCN(C1)C2=NCCC=C2C1c(cc1)cc(OC)c1OC)=O Chemical compound CC(c(cc1)ccc1NCN(C1)C2=NCCC=C2C1c(cc1)cc(OC)c1OC)=O CZGHGKQHLOOVRG-UHFFFAOYSA-N 0.000 description 1
- UHNNXWCDTTYLRO-UHFFFAOYSA-P CC1(c(cc(cc2)OC)c2[NH+](C[SH+](C)(CO)c2c3ncc(C)cc3ccc2)C1)c(cc1)cc(OC)c1OC Chemical compound CC1(c(cc(cc2)OC)c2[NH+](C[SH+](C)(CO)c2c3ncc(C)cc3ccc2)C1)c(cc1)cc(OC)c1OC UHNNXWCDTTYLRO-UHFFFAOYSA-P 0.000 description 1
- FAGHKSRUPVRXHD-UHFFFAOYSA-O CCOc1c(C([n]2c3ncccc3c(-c(cc3)ccc3[SH+]C)c2)=O)c(cccc2)c2cc1 Chemical compound CCOc1c(C([n]2c3ncccc3c(-c(cc3)ccc3[SH+]C)c2)=O)c(cccc2)c2cc1 FAGHKSRUPVRXHD-UHFFFAOYSA-O 0.000 description 1
- QPCAOPQFVPATDZ-UHFFFAOYSA-N COc(c(OC)c1)ccc1-c1c[n](C(c(c2c3cccc2)ccc3F)=O)c2ncccc12 Chemical compound COc(c(OC)c1)ccc1-c1c[n](C(c(c2c3cccc2)ccc3F)=O)c2ncccc12 QPCAOPQFVPATDZ-UHFFFAOYSA-N 0.000 description 1
- UOXKILGOKTUXJP-NJXTYKNDSA-N COc(ccc(-c1c[n](C(C(/C=C(/c2cc(I)ccc2)\O)=N)=O)c2c1cccn2)c1)c1OC Chemical compound COc(ccc(-c1c[n](C(C(/C=C(/c2cc(I)ccc2)\O)=N)=O)c2c1cccn2)c1)c1OC UOXKILGOKTUXJP-NJXTYKNDSA-N 0.000 description 1
- RWBGYQGXKODULN-UHFFFAOYSA-N COc(ccc(C(c1c2nccc1)=C[NH+]2[SH+](c(cc1)ccc1Oc1ccccc1)=O)c1)c1OC Chemical compound COc(ccc(C(c1c2nccc1)=C[NH+]2[SH+](c(cc1)ccc1Oc1ccccc1)=O)c1)c1OC RWBGYQGXKODULN-UHFFFAOYSA-N 0.000 description 1
- AVVATIPHESEVMD-UHFFFAOYSA-N COc(ccc(C1c2cccnc2N(CC(CC(C2C=CC=CC2)N)O)C1)c1)c1OC Chemical compound COc(ccc(C1c2cccnc2N(CC(CC(C2C=CC=CC2)N)O)C1)c1)c1OC AVVATIPHESEVMD-UHFFFAOYSA-N 0.000 description 1
- BIEZULAGNRMRTL-UHFFFAOYSA-O COc(nc1)ncc1-c(c1c2nccc1)c[n]2S(Cc1ccccc1)[OH2+] Chemical compound COc(nc1)ncc1-c(c1c2nccc1)c[n]2S(Cc1ccccc1)[OH2+] BIEZULAGNRMRTL-UHFFFAOYSA-O 0.000 description 1
- DJUWHXBZOVSJAA-UHFFFAOYSA-N COc1ccc(C(C2)C3=CC=CNC3N2C(C2=C3NCC=CC3CC=C2)=O)cc1OC Chemical compound COc1ccc(C(C2)C3=CC=CNC3N2C(C2=C3NCC=CC3CC=C2)=O)cc1OC DJUWHXBZOVSJAA-UHFFFAOYSA-N 0.000 description 1
- JLDQUQLTOVTXBJ-UHFFFAOYSA-N COc1ccc(C2c3cccnc3NC2)cc1OC1CCCC1 Chemical compound COc1ccc(C2c3cccnc3NC2)cc1OC1CCCC1 JLDQUQLTOVTXBJ-UHFFFAOYSA-N 0.000 description 1
- MCHJXVJGXMNZJZ-UHFFFAOYSA-N O=S(c1ccccc1)(N(C=CC1=C2)C1=NCC2c1cccc(F)c1)=O Chemical compound O=S(c1ccccc1)(N(C=CC1=C2)C1=NCC2c1cccc(F)c1)=O MCHJXVJGXMNZJZ-UHFFFAOYSA-N 0.000 description 1
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- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
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- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
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- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- Bioinformatics & Cheminformatics (AREA)
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- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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- Spectroscopy & Molecular Physics (AREA)
- Physics & Mathematics (AREA)
- Biomedical Technology (AREA)
- Theoretical Computer Science (AREA)
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Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US60740704P | 2004-09-03 | 2004-09-03 | |
| PCT/US2005/031322 WO2006026754A2 (en) | 2004-09-03 | 2005-09-02 | Bicyclic heteroaryl pde4b inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2008512380A true JP2008512380A (ja) | 2008-04-24 |
| JP2008512380A5 JP2008512380A5 (https=) | 2008-10-23 |
Family
ID=36000749
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007530399A Pending JP2008512380A (ja) | 2004-09-03 | 2005-09-02 | Pde4b阻害剤 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US7605168B2 (https=) |
| EP (1) | EP1786813A2 (https=) |
| JP (1) | JP2008512380A (https=) |
| CN (1) | CN101048407A (https=) |
| AU (1) | AU2005279795A1 (https=) |
| CA (1) | CA2583428A1 (https=) |
| WO (1) | WO2006026754A2 (https=) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008545660A (ja) * | 2005-05-20 | 2008-12-18 | バーテックス ファーマシューティカルズ インコーポレイテッド | プロテインキナーゼ阻害剤として有用なピロロピリジン化合物 |
| JP2014509316A (ja) * | 2011-02-11 | 2014-04-17 | メルク・シャープ・アンド・ドーム・コーポレーション | RORγT阻害薬 |
| JP2014522858A (ja) * | 2011-07-15 | 2014-09-08 | ヴィーブ ヘルスケア ユーケー リミテッド | アザインドール化合物及びhivを治療するための方法 |
| JP2015526441A (ja) * | 2012-08-15 | 2015-09-10 | メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. | RORγT阻害剤としての4−ヘテロアリール置換安息香酸化合物およびその使用 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6663602B2 (en) | 2000-06-16 | 2003-12-16 | Novo Nordisk A/S | Injection device |
| US7686786B2 (en) | 2004-10-21 | 2010-03-30 | Novo Nordiks A/S | Dial-down mechanism for wind-up pen |
| US7579360B2 (en) | 2005-06-09 | 2009-08-25 | Bristol-Myers Squibb Company | Triazolopyridine 11-beta hydroxysteroid dehydrogenase type I inhibitors |
| US7572807B2 (en) | 2005-06-09 | 2009-08-11 | Bristol-Myers Squibb Company | Heteroaryl 11-beta-hydroxysteroid dehydrogenase type I inhibitors |
| KR101468830B1 (ko) | 2005-06-24 | 2014-12-03 | 바이엘 크롭사이언스 엔.브이. | 식물 세포벽의 반응성을 변경하는 방법 |
| DE102006012617A1 (de) * | 2006-03-20 | 2007-09-27 | Merck Patent Gmbh | 4-(Pyrrolopyridinyl)-pyrimidinyl-2-amin-derivate |
| PL2023982T3 (pl) | 2006-05-18 | 2012-11-30 | Novo Nordisk As | Urządzenie wstrzykujące ze środkami blokującymi |
| US8097699B2 (en) | 2006-08-30 | 2012-01-17 | Rsr Limited | Crystal structure of thyroid stimulating hormone receptor |
| WO2008063888A2 (en) | 2006-11-22 | 2008-05-29 | Plexxikon, Inc. | Compounds modulating c-fms and/or c-kit activity and uses therefor |
| GB0702456D0 (en) | 2007-02-08 | 2007-03-21 | Astrazeneca Ab | New combination |
| JP2010533729A (ja) | 2007-07-17 | 2010-10-28 | プレキシコン,インコーポレーテッド | キナーゼ調節のための化合物と方法、及びそのための適応 |
| US8119658B2 (en) | 2007-10-01 | 2012-02-21 | Bristol-Myers Squibb Company | Triazolopyridine 11-beta hydroxysteroid dehydrogenase type I inhibitors |
| WO2009067597A1 (en) * | 2007-11-21 | 2009-05-28 | Decode Genetics Ehf | 4- (or 5-) substituted catechol derivatives |
| MX2010006657A (es) | 2007-12-20 | 2010-10-05 | Astrazeneca Ab | Dispositivo y metodo para desagregar polvo 854. |
| WO2009143018A2 (en) | 2008-05-19 | 2009-11-26 | Plexxikon, Inc. | Compounds and methods for kinase modulation, and indications therefor |
| TW201036957A (en) | 2009-02-20 | 2010-10-16 | Astrazeneca Ab | Novel salt 628 |
| AU2010266754B2 (en) | 2009-07-01 | 2013-12-05 | Astrazeneca Ab | Dispenser and method for entraining powder in an airflow |
| US8673928B2 (en) | 2009-11-18 | 2014-03-18 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| WO2011073662A1 (en) | 2009-12-17 | 2011-06-23 | Astrazeneca Ab | Combination of a benzoxazinone and a further agent for treating respiratory diseases |
| CN102753549A (zh) | 2009-12-23 | 2012-10-24 | 普莱希科公司 | 用于激酶调节的化合物和方法及其适应症 |
| NZ601454A (en) | 2010-02-10 | 2014-06-27 | Astrazeneca Uk Ltd | Process for providing a filled canister for an inhaler |
| TWI619713B (zh) | 2010-04-21 | 2018-04-01 | 普雷辛肯公司 | 用於激酶調節的化合物和方法及其適應症 |
| JO3131B1 (ar) | 2010-04-27 | 2017-09-20 | Glaxosmithkline Llc | مركبات كيميائية |
| CN103140490A (zh) | 2010-07-15 | 2013-06-05 | 百时美施贵宝公司 | 氮杂吲唑化合物 |
| NZ605179A (en) | 2010-07-21 | 2014-08-29 | Astrazeneca Ab | Inhaler |
| MX2013000518A (es) | 2010-07-21 | 2013-02-27 | Aztrazeneca Ab | Inhalador. |
| KR101911972B1 (ko) | 2011-02-07 | 2018-10-25 | 플렉시콘 인코퍼레이티드 | 키나제 조절을 위한 화합물 및 방법, 및 그에 대한 적응증 |
| AU2012255275B2 (en) | 2011-05-17 | 2016-01-28 | Plexxikon Inc. | Kinase modulation and indications therefor |
| GB201115874D0 (en) | 2011-09-14 | 2011-10-26 | Astrazeneca Ab | Inhaler |
| CN103998077B (zh) | 2011-12-29 | 2017-05-31 | 诺沃—诺迪斯克有限公司 | 具有向上拨动/向下拨动定量机构的基于扭力弹簧的卷紧自动注射器笔 |
| US9358235B2 (en) | 2012-03-19 | 2016-06-07 | Plexxikon Inc. | Kinase modulation, and indications therefor |
| CN104379180A (zh) * | 2012-04-10 | 2015-02-25 | 佐治亚州立大学研究基金会公司 | 用cyld抑制剂治疗中耳炎及其它病状的组合物和方法 |
| WO2014026329A1 (en) | 2012-08-15 | 2014-02-20 | Merck Sharp & Dohme Corp. | N-alkylated indole and indazole compounds as rorgammat inhibitors and uses thereof |
| WO2014026330A1 (en) | 2012-08-15 | 2014-02-20 | Merck Sharp & Dohme Corp. | 3-AMINOCYCLOALKYL COMPOUNDS AS RORgammaT INHIBITORS AND USES THEREOF |
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| JP2014522858A (ja) * | 2011-07-15 | 2014-09-08 | ヴィーブ ヘルスケア ユーケー リミテッド | アザインドール化合物及びhivを治療するための方法 |
| JP2015526441A (ja) * | 2012-08-15 | 2015-09-10 | メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. | RORγT阻害剤としての4−ヘテロアリール置換安息香酸化合物およびその使用 |
Also Published As
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|---|---|
| WO2006026754B1 (en) | 2007-02-22 |
| WO2006026754A9 (en) | 2006-04-20 |
| WO2006026754A2 (en) | 2006-03-09 |
| AU2005279795A1 (en) | 2006-03-09 |
| CA2583428A1 (en) | 2006-03-09 |
| US7605168B2 (en) | 2009-10-20 |
| EP1786813A2 (en) | 2007-05-23 |
| CN101048407A (zh) | 2007-10-03 |
| US20060100218A1 (en) | 2006-05-11 |
| WO2006026754A3 (en) | 2007-01-11 |
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