JP5583028B2 - オキサゾリジン及びチアゾリジン選択的サブタイプアルファ2アドレナリン作用薬並びにこれらの使用方法 - Google Patents
オキサゾリジン及びチアゾリジン選択的サブタイプアルファ2アドレナリン作用薬並びにこれらの使用方法 Download PDFInfo
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- JP5583028B2 JP5583028B2 JP2010543198A JP2010543198A JP5583028B2 JP 5583028 B2 JP5583028 B2 JP 5583028B2 JP 2010543198 A JP2010543198 A JP 2010543198A JP 2010543198 A JP2010543198 A JP 2010543198A JP 5583028 B2 JP5583028 B2 JP 5583028B2
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- Prior art keywords
- pyridin
- compound
- alpha
- pain
- compounds
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- 0 C*C(C)(*1CCC*CCCC1)C(C)(C1CCCCC1)N=C(NCC1)I1=C Chemical compound C*C(C)(*1CCC*CCCC1)C(C)(C1CCCCC1)N=C(NCC1)I1=C 0.000 description 30
- CQVVKKZMLUJTNU-OAHLLOKOSA-N C([C@H](c1ccccc1)/N=C1\OCCN1)c1ccncc1 Chemical compound C([C@H](c1ccccc1)/N=C1\OCCN1)c1ccncc1 CQVVKKZMLUJTNU-OAHLLOKOSA-N 0.000 description 2
- OHGVNEKDEMZZMF-UHFFFAOYSA-N C(C(c1ccccc1)N=C1NCCN1)c1ccncc1 Chemical compound C(C(c1ccccc1)N=C1NCCN1)c1ccncc1 OHGVNEKDEMZZMF-UHFFFAOYSA-N 0.000 description 1
- QIFDDUKOVLWNJI-UHFFFAOYSA-N C(CN1)C2[N-]1=C2 Chemical compound C(CN1)C2[N-]1=C2 QIFDDUKOVLWNJI-UHFFFAOYSA-N 0.000 description 1
- GOEXAGPTRFRPAH-UHFFFAOYSA-N C=[Cl]c(cccc1C(Cc2ccncc2)/N=C2\OCCN2)c1Cl Chemical compound C=[Cl]c(cccc1C(Cc2ccncc2)/N=C2\OCCN2)c1Cl GOEXAGPTRFRPAH-UHFFFAOYSA-N 0.000 description 1
- RVXCCOHZORCSMC-OVVQPSECSA-N CC(CCF)C(C)/C(/C)=N/C(Cc1nccnc1)c1ccc(C[IH]C)cc1 Chemical compound CC(CCF)C(C)/C(/C)=N/C(Cc1nccnc1)c1ccc(C[IH]C)cc1 RVXCCOHZORCSMC-OVVQPSECSA-N 0.000 description 1
- ZOZUFUYMTYTCKV-UHFFFAOYSA-N CC1(C=CC=CC1C(Cc1ccncc1)N=C1NCCN1)O Chemical compound CC1(C=CC=CC1C(Cc1ccncc1)N=C1NCCN1)O ZOZUFUYMTYTCKV-UHFFFAOYSA-N 0.000 description 1
- RRMDMTXEZWSQSY-UHFFFAOYSA-N CC1NC=CN=C1CC(c1ccccc1)/N=C(/NCCI)\S Chemical compound CC1NC=CN=C1CC(c1ccccc1)/N=C(/NCCI)\S RRMDMTXEZWSQSY-UHFFFAOYSA-N 0.000 description 1
- XCCBYCFGXLPIKO-UHFFFAOYSA-N Cc1c(C)c(C(CC2=CCNC=C2)/N=C2\OCCN2)ccc1 Chemical compound Cc1c(C)c(C(CC2=CCNC=C2)/N=C2\OCCN2)ccc1 XCCBYCFGXLPIKO-UHFFFAOYSA-N 0.000 description 1
- ZJSZPKKNTMNPMN-UHFFFAOYSA-N Cc1cc(C(Cc2ccncc2)/N=C2\OCCN2)ccc1 Chemical compound Cc1cc(C(Cc2ccncc2)/N=C2\OCCN2)ccc1 ZJSZPKKNTMNPMN-UHFFFAOYSA-N 0.000 description 1
- VQFGSZHALYPKMT-UHFFFAOYSA-N Cc1ccc(C(Cc2nccnc2)N)cc1 Chemical compound Cc1ccc(C(Cc2nccnc2)N)cc1 VQFGSZHALYPKMT-UHFFFAOYSA-N 0.000 description 1
- QBQHNMVODGXZPA-UHFFFAOYSA-N Fc(c(C(Cc1ccncc1)/N=C1\OCCN1)ccc1)c1Cl Chemical compound Fc(c(C(Cc1ccncc1)/N=C1\OCCN1)ccc1)c1Cl QBQHNMVODGXZPA-UHFFFAOYSA-N 0.000 description 1
- MVUXVDLGFFZBQU-UHFFFAOYSA-N Fc1cc(C(Cc2ccncc2)/N=C2\OCCN2)ccc1 Chemical compound Fc1cc(C(Cc2ccncc2)/N=C2\OCCN2)ccc1 MVUXVDLGFFZBQU-UHFFFAOYSA-N 0.000 description 1
- KFQSIODVJQZPKK-UHFFFAOYSA-N N=C(NCC1)N1c1c(CCc2ccncc2)cccc1 Chemical compound N=C(NCC1)N1c1c(CCc2ccncc2)cccc1 KFQSIODVJQZPKK-UHFFFAOYSA-N 0.000 description 1
- ODBMVUDWVBNMQH-UHFFFAOYSA-N NC(CC1=CC=CCN1)c1ccccc1Cl Chemical compound NC(CC1=CC=CCN1)c1ccccc1Cl ODBMVUDWVBNMQH-UHFFFAOYSA-N 0.000 description 1
- VKHLDYOGXPGSKP-UHFFFAOYSA-N NC(Cc1ccncc1)c1cccc(Cl)c1 Chemical compound NC(Cc1ccncc1)c1cccc(Cl)c1 VKHLDYOGXPGSKP-UHFFFAOYSA-N 0.000 description 1
- VXWJRTQGWKFRFR-UHFFFAOYSA-N NC(Cc1ccncc1)c1cccc(F)c1 Chemical compound NC(Cc1ccncc1)c1cccc(F)c1 VXWJRTQGWKFRFR-UHFFFAOYSA-N 0.000 description 1
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- 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
- C07D401/12—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 linked by a chain containing hetero atoms as chain links
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- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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- C07D213/16—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom containing only one pyridine ring
- C07D213/18—Salts thereof
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US2215208P | 2008-01-18 | 2008-01-18 | |
| US61/022,152 | 2008-01-18 | ||
| PCT/US2009/030887 WO2009091760A1 (en) | 2008-01-18 | 2009-01-14 | Oxazolidine and thiazolidine selective subtype alpha 2 adrenergic agents and methods for use thereof |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011510008A JP2011510008A (ja) | 2011-03-31 |
| JP2011510008A5 JP2011510008A5 (https=) | 2012-03-01 |
| JP5583028B2 true JP5583028B2 (ja) | 2014-09-03 |
Family
ID=40345009
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010543198A Expired - Fee Related JP5583028B2 (ja) | 2008-01-18 | 2009-01-14 | オキサゾリジン及びチアゾリジン選択的サブタイプアルファ2アドレナリン作用薬並びにこれらの使用方法 |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US8735399B2 (https=) |
| EP (1) | EP2242753B1 (https=) |
| JP (1) | JP5583028B2 (https=) |
| AU (1) | AU2009205473B8 (https=) |
| BR (1) | BRPI0906875A2 (https=) |
| CA (1) | CA2712190A1 (https=) |
| WO (1) | WO2009091760A1 (https=) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
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| AU2010289703A1 (en) * | 2009-08-26 | 2012-04-12 | Allergan, Inc. | Method of treating compulsive disorders with alpha-2B adrenergic receptor agonists |
| HUE038366T2 (hu) | 2010-08-16 | 2018-10-29 | Allergan Inc | Módszer szabályozó T-sejtek alfa-2B adrenerg receptor agonistákkal való aktiválásához |
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| CN101346374A (zh) * | 2005-12-22 | 2009-01-14 | 巴斯夫欧洲公司 | 农业组合物 |
| US7709507B2 (en) * | 2006-05-17 | 2010-05-04 | Allergan, Inc. | Therapeutic fluoroethyl ureas |
| WO2008123821A1 (en) * | 2007-03-01 | 2008-10-16 | Albireo Ab | 4, 5-dihydro-lh-imidazol-2-amine derivatives for use in the treatment of respiratory, cardiovascular, neurological or gastrointestinal disorders |
| US8809379B2 (en) * | 2008-01-18 | 2014-08-19 | Allergan, Inc. | Selective subtype alpha 2 adrenergic agents and methods for use thereof |
| JP5480819B2 (ja) * | 2008-01-18 | 2014-04-23 | アラーガン インコーポレイテッド | 選択的サブタイプアルファ2アドレナリンアゴニスト及びその使用方法 |
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- 2009-01-14 JP JP2010543198A patent/JP5583028B2/ja not_active Expired - Fee Related
- 2009-01-14 AU AU2009205473A patent/AU2009205473B8/en not_active Ceased
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|---|---|
| WO2009091760A1 (en) | 2009-07-23 |
| JP2011510008A (ja) | 2011-03-31 |
| US20140206701A1 (en) | 2014-07-24 |
| US20110105526A1 (en) | 2011-05-05 |
| CA2712190A1 (en) | 2009-07-23 |
| US8735399B2 (en) | 2014-05-27 |
| AU2009205473A1 (en) | 2009-07-23 |
| EP2242753B1 (en) | 2015-04-08 |
| EP2242753A1 (en) | 2010-10-27 |
| AU2009205473B2 (en) | 2014-05-01 |
| AU2009205473B8 (en) | 2014-09-11 |
| BRPI0906875A2 (pt) | 2015-07-07 |
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