JP4712384B2 - Orl−1受容体介在障害の治療に有用なヒドロキシアルキル置換1,3,8−トリアザスピロ[4.5]デカン−4−オン誘導体 - Google Patents
Orl−1受容体介在障害の治療に有用なヒドロキシアルキル置換1,3,8−トリアザスピロ[4.5]デカン−4−オン誘導体 Download PDFInfo
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- JP4712384B2 JP4712384B2 JP2004534697A JP2004534697A JP4712384B2 JP 4712384 B2 JP4712384 B2 JP 4712384B2 JP 2004534697 A JP2004534697 A JP 2004534697A JP 2004534697 A JP2004534697 A JP 2004534697A JP 4712384 B2 JP4712384 B2 JP 4712384B2
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- Prior art keywords
- methyl
- phenyl
- ethyl
- propyl
- pyrrolidinyl
- 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.)
- Expired - Fee Related
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- 0 CCCC(CN1*)C(CC2)(CCN2I)C1=O Chemical compound CCCC(CN1*)C(CC2)(CCN2I)C1=O 0.000 description 9
- RNUHRLOJTDZIMQ-UHFFFAOYSA-N CC(C)C([C-]=O)NC(OC(C)(C)C)=O Chemical compound CC(C)C([C-]=O)NC(OC(C)(C)C)=O RNUHRLOJTDZIMQ-UHFFFAOYSA-N 0.000 description 2
- HRDWHBMAXHWZBF-UHFFFAOYSA-N CC(C)C(C(C(C)C)=O)N Chemical compound CC(C)C(C(C(C)C)=O)N HRDWHBMAXHWZBF-UHFFFAOYSA-N 0.000 description 1
- LQKJPBCCNFJUCX-UHFFFAOYSA-N CC(C)C(C(C)=O)N Chemical compound CC(C)C(C(C)=O)N LQKJPBCCNFJUCX-UHFFFAOYSA-N 0.000 description 1
- HKKZYTVANOBAPE-LJAQVGFWSA-N CCCCN(C[C@@H](CN(CN(C12CCN(Cc3c(C(F)(F)F)cccc3Cl)CC1)c(cc1)ccc1F)C2=O)O)Cc1ccccc1 Chemical compound CCCCN(C[C@@H](CN(CN(C12CCN(Cc3c(C(F)(F)F)cccc3Cl)CC1)c(cc1)ccc1F)C2=O)O)Cc1ccccc1 HKKZYTVANOBAPE-LJAQVGFWSA-N 0.000 description 1
- UAKFVMQYNYVBPS-NDEPHWFRSA-N CCN(C)C[C@@H](CN(CN(C12CCN(Cc3c(c(C)ccc4)c4ccc3)CC1)c(cc1)ccc1F)C2=O)O Chemical compound CCN(C)C[C@@H](CN(CN(C12CCN(Cc3c(c(C)ccc4)c4ccc3)CC1)c(cc1)ccc1F)C2=O)O UAKFVMQYNYVBPS-NDEPHWFRSA-N 0.000 description 1
- NQNDFTLOVCESQK-XNMGPUDCSA-N CCOC[C@@H](CN(CN(C1(CC2)CCN2[C@H](C2)c3cccc4c3c2ccc4)c(cc2)ccc2F)C1=O)O Chemical compound CCOC[C@@H](CN(CN(C1(CC2)CCN2[C@H](C2)c3cccc4c3c2ccc4)c(cc2)ccc2F)C1=O)O NQNDFTLOVCESQK-XNMGPUDCSA-N 0.000 description 1
- RYAGAIBILJRCGX-IRPSRAIASA-N NC[C@@](CCN(CN(C1(CC2)CCN2[C@H](C2)c3cccc4c3c2ccc4)c(cc2)ccc2F)C1=O)(O)S Chemical compound NC[C@@](CCN(CN(C1(CC2)CCN2[C@H](C2)c3cccc4c3c2ccc4)c(cc2)ccc2F)C1=O)(O)S RYAGAIBILJRCGX-IRPSRAIASA-N 0.000 description 1
- BOGHPEASFJVRRJ-OAQYLSRUSA-N O=C(C12CCN(Cc(cc3)ccc3Cl)CC1)N(C[C@H]1OC1)CN2c(cc1)ccc1F Chemical compound O=C(C12CCN(Cc(cc3)ccc3Cl)CC1)N(C[C@H]1OC1)CN2c(cc1)ccc1F BOGHPEASFJVRRJ-OAQYLSRUSA-N 0.000 description 1
- KTYXKWCNSFLYHL-UHFFFAOYSA-N O=C(C12CCN(Cc(cc3)ccc3Cl)CC1)NCN2c(cc1)ccc1F Chemical compound O=C(C12CCN(Cc(cc3)ccc3Cl)CC1)NCN2c(cc1)ccc1F KTYXKWCNSFLYHL-UHFFFAOYSA-N 0.000 description 1
- LBAWSLFILPJPGL-GOSISDBHSA-N O=C(C12CCN(Cc3c(C(F)(F)F)cccc3Cl)CC1)N(C[C@H]1OC1)CN2c(cc1)ccc1F Chemical compound O=C(C12CCN(Cc3c(C(F)(F)F)cccc3Cl)CC1)N(C[C@H]1OC1)CN2c(cc1)ccc1F LBAWSLFILPJPGL-GOSISDBHSA-N 0.000 description 1
- KLFWDMQZEZYWAE-UHFFFAOYSA-N O=C(C12CCN(Cc3ccc(-c4ccccc4)[s]3)CC1)NCN2c(cc1)ccc1F Chemical compound O=C(C12CCN(Cc3ccc(-c4ccccc4)[s]3)CC1)NCN2c(cc1)ccc1F KLFWDMQZEZYWAE-UHFFFAOYSA-N 0.000 description 1
- NEKSCTHROFVYGS-UHFFFAOYSA-N O=C(C12CCN(Cc3cccc4c3cccc4)CC1)NCN2c(cc1)ccc1F Chemical compound O=C(C12CCN(Cc3cccc4c3cccc4)CC1)NCN2c(cc1)ccc1F NEKSCTHROFVYGS-UHFFFAOYSA-N 0.000 description 1
- QQWBFPIQYBTKKR-KWHHRMCASA-N OCC1CN(C[C@H](CN(CN(C2(CC3)CCN3[C@H](C3)c4cccc5c4c3ccc5)c(cc3)ccc3F)C2=O)O)CCC1 Chemical compound OCC1CN(C[C@H](CN(CN(C2(CC3)CCN3[C@H](C3)c4cccc5c4c3ccc5)c(cc3)ccc3F)C2=O)O)CCC1 QQWBFPIQYBTKKR-KWHHRMCASA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D471/10—Spiro-condensed systems
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- Health & Medical Sciences (AREA)
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- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
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- Urology & Nephrology (AREA)
- Emergency Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US40913402P | 2002-09-09 | 2002-09-09 | |
| US60/409,134 | 2002-09-09 | ||
| PCT/US2003/027956 WO2004022558A2 (en) | 2002-09-09 | 2003-09-05 | Hydroxy alkyl substituted 1,3,8-triazaspiro[4.5]decan-4-one derivatives useful for the treatment of orl-1 receptor mediated disorders |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2006500393A JP2006500393A (ja) | 2006-01-05 |
| JP2006500393A5 JP2006500393A5 (https=) | 2006-10-26 |
| JP4712384B2 true JP4712384B2 (ja) | 2011-06-29 |
Family
ID=31978719
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004534697A Expired - Fee Related JP4712384B2 (ja) | 2002-09-09 | 2003-09-05 | Orl−1受容体介在障害の治療に有用なヒドロキシアルキル置換1,3,8−トリアザスピロ[4.5]デカン−4−オン誘導体 |
Country Status (19)
| Country | Link |
|---|---|
| US (3) | US7081463B2 (https=) |
| EP (1) | EP1601674B1 (https=) |
| JP (1) | JP4712384B2 (https=) |
| KR (1) | KR20050043935A (https=) |
| CN (1) | CN100402529C (https=) |
| AR (1) | AR041205A1 (https=) |
| AU (1) | AU2003268512A1 (https=) |
| BR (1) | BR0306309A (https=) |
| CA (1) | CA2498275C (https=) |
| CL (1) | CL2003001814A1 (https=) |
| EA (1) | EA009369B1 (https=) |
| MX (1) | MXPA05002622A (https=) |
| NO (1) | NO20051743L (https=) |
| NZ (1) | NZ538307A (https=) |
| PL (1) | PL377047A1 (https=) |
| RS (1) | RS20050208A (https=) |
| TW (1) | TWI296627B (https=) |
| WO (1) | WO2004022558A2 (https=) |
| ZA (1) | ZA200502836B (https=) |
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ538307A (en) | 2002-09-09 | 2008-04-30 | Janssen Pharmaceutica Nv | Hydroxy alkyl substituted 1,3,8-triazaspiro[4.5]decan-4-one derivatives useful for the treatment of ORL-1 receptor mediated disorders |
| US20080287478A1 (en) * | 2003-05-23 | 2008-11-20 | Lars Bo Laurenborg Hansen | Nociceptin Analogues and Uses Thereof |
| AR046756A1 (es) | 2003-12-12 | 2005-12-21 | Solvay Pharm Gmbh | Derivados de hidronopol como agonistas de receptores orl-1 humanos. |
| US20060178390A1 (en) * | 2004-08-02 | 2006-08-10 | Alfonzo Jordan | 1,3,8-Triazaspiro[4,5]decan-4-one derivatives useful for the treatment of ORL-1 receptor mediated disorders |
| CN101273046B (zh) | 2005-09-28 | 2011-05-25 | 弗·哈夫曼-拉罗切有限公司 | 作为加压素受体拮抗剂的吲哚-3-基-羰基氮杂螺环衍生物 |
| TW200819457A (en) * | 2006-08-30 | 2008-05-01 | Actelion Pharmaceuticals Ltd | Spiro antibiotic derivatives |
| KR20090087042A (ko) * | 2006-11-28 | 2009-08-14 | 얀센 파마슈티카 엔.브이. | 알콜 남용, 중독 및 의존증 치료방법 |
| CN103202840B (zh) | 2006-11-28 | 2015-02-11 | 詹森药业有限公司 | 3-(3-氨基-2-(r)-羟基-丙基)-1-(4-氟-苯基)-8-(8-甲基-萘-1-基甲基)-1,3,8-三氮杂-螺[4.5]癸烷-4-酮的盐 |
| JP5490677B2 (ja) * | 2007-04-09 | 2014-05-14 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | 不安及び鬱病の処置のためのorl−1受容体リガンドとしての1,3,8−三置換−1,3,8−トリアザ−スピロ[4.5]デカン−4−オン誘導体 |
| US20100076003A1 (en) * | 2008-09-19 | 2010-03-25 | Kathleen Battista | 5-oxazolidin-2-one substituted 1,3,8-triazaspiro[4.5]decan-4-one derivatives useful as orl-1 receptor modulators |
| UA107943C2 (xx) * | 2009-11-16 | 2015-03-10 | Lilly Co Eli | Сполуки спіропіперидину як антагоністи рецептора orl-1 |
| US9611257B2 (en) | 2012-12-21 | 2017-04-04 | Epizyme, Inc. | PRMT5 inhibitors and uses thereof |
| EP3406607A1 (en) | 2012-12-21 | 2018-11-28 | Epizyme, Inc. | Prmt5 inhibitors containing a dihydro- or tetrahydroisoquinoline and uses thereof |
| UA118548C2 (uk) | 2012-12-21 | 2019-02-11 | Епізайм, Інк. | Тетрагідро- та дигідроізохіноліни як інгібітори prmt5 та їх застосування |
| CA2894157A1 (en) | 2012-12-21 | 2014-06-26 | Epizyme, Inc. | Prmt5 inhibitors and uses thereof |
| JP2016505000A (ja) | 2012-12-21 | 2016-02-18 | エピザイム,インコーポレイティド | Prmt5阻害剤およびその使用 |
| TW201607923A (zh) | 2014-07-15 | 2016-03-01 | 歌林達有限公司 | 被取代之氮螺環(4.5)癸烷衍生物 |
| EP3177288A4 (en) | 2014-08-04 | 2018-04-04 | Epizyme, Inc. | Prmt5 inhibitors and uses thereof |
| KR102043337B1 (ko) | 2014-08-28 | 2019-11-11 | 아셰뉴론 에스아 | 글리코시다제 저해제 |
| JP7011596B2 (ja) * | 2015-12-02 | 2022-02-10 | アストライア セラピューティクス, エルエルシー | ピペリジニルノシセプチン受容体化合物 |
| US10112924B2 (en) | 2015-12-02 | 2018-10-30 | Astraea Therapeutics, Inc. | Piperdinyl nociceptin receptor compounds |
| CA3014572C (en) | 2016-02-25 | 2023-10-03 | Asceneuron S.A. | Acid addition salts of piperazine derivatives |
| KR20180132629A (ko) | 2016-02-25 | 2018-12-12 | 아셰뉴론 에스아 | 글리코시다제 저해제 |
| AU2017222964B2 (en) | 2016-02-25 | 2020-01-02 | Asceneuron S. A. | Glycosidase inhibitors |
| US11261183B2 (en) | 2016-02-25 | 2022-03-01 | Asceneuron Sa | Sulfoximine glycosidase inhibitors |
| US11213525B2 (en) | 2017-08-24 | 2022-01-04 | Asceneuron Sa | Linear glycosidase inhibitors |
| MX2020003242A (es) | 2017-09-22 | 2020-09-18 | Jubilant Epipad LLC | Compuestos heterociclicos como inhibidores de pad. |
| AU2018352142B2 (en) | 2017-10-18 | 2022-08-25 | Jubilant Epipad LLC | Imidazo-pyridine compounds as PAD inhibitors |
| KR20200085836A (ko) | 2017-11-06 | 2020-07-15 | 주빌런트 프로델 엘엘씨 | Pd1/pd-l1 활성화 억제제로서의 피리미딘 유도체 |
| BR112020010322A2 (pt) | 2017-11-24 | 2020-11-17 | Jubilant Episcribe Llc | composto da fórmula i; composto da fórmula ia; composto da fórmula ib; processo de preparação de compostos da fórmula i; composição farmacêutica; método para o tratamento e/ou prevenção de várias doenças; uso dos compostos; método para o tratamento de câncer; e método para o tratamento e/ou prevenção de uma afecção mediada por prmt5 ou um distúrbio proliferativo ou câncer |
| SG11202008950PA (en) | 2018-03-13 | 2020-10-29 | Jubilant Prodel LLC | Bicyclic compounds as inhibitors of pd1/pd-l1 interaction/activation |
| WO2020039029A1 (en) * | 2018-08-22 | 2020-02-27 | Asceneuron S. A. | Spiro compounds as glycosidase inhibitors |
| WO2020039027A1 (en) | 2018-08-22 | 2020-02-27 | Asceneuron S. A. | Pyrrolidine glycosidase inhibitors |
| JP7407171B2 (ja) | 2018-08-22 | 2023-12-28 | エースニューロン・ソシエテ・アノニム | グリコシダーゼ阻害剤として有用なピペラジン誘導体のコハク酸付加塩及びフマル酸付加塩 |
| WO2020039028A1 (en) | 2018-08-22 | 2020-02-27 | Asceneuron S. A. | Tetrahydro-benzoazepine glycosidase inhibitors |
Family Cites Families (61)
| Publication number | Priority date | Publication date | Assignee | Title |
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- 2003-09-05 AU AU2003268512A patent/AU2003268512A1/en not_active Abandoned
- 2003-09-05 KR KR1020057003938A patent/KR20050043935A/ko not_active Ceased
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- 2003-09-05 CN CNB038249901A patent/CN100402529C/zh not_active Expired - Fee Related
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Also Published As
| Publication number | Publication date |
|---|---|
| CN1694883A (zh) | 2005-11-09 |
| EP1601674A2 (en) | 2005-12-07 |
| AR041205A1 (es) | 2005-05-11 |
| EA200500331A1 (ru) | 2005-08-25 |
| US20060030577A1 (en) | 2006-02-09 |
| RS20050208A (sr) | 2007-08-03 |
| US20090124614A1 (en) | 2009-05-14 |
| AU2003268512A1 (en) | 2004-03-29 |
| US8778956B2 (en) | 2014-07-15 |
| JP2006500393A (ja) | 2006-01-05 |
| TWI296627B (en) | 2008-05-11 |
| US7081463B2 (en) | 2006-07-25 |
| CN100402529C (zh) | 2008-07-16 |
| NZ538307A (en) | 2008-04-30 |
| TW200418857A (en) | 2004-10-01 |
| US7582649B2 (en) | 2009-09-01 |
| CA2498275C (en) | 2011-07-12 |
| WO2004022558A2 (en) | 2004-03-18 |
| KR20050043935A (ko) | 2005-05-11 |
| MXPA05002622A (es) | 2005-09-08 |
| US20040142955A1 (en) | 2004-07-22 |
| EA009369B1 (ru) | 2007-12-28 |
| EP1601674B1 (en) | 2012-08-08 |
| NO20051743L (no) | 2005-05-18 |
| CA2498275A1 (en) | 2004-03-18 |
| ZA200502836B (en) | 2006-06-28 |
| BR0306309A (pt) | 2004-10-19 |
| PL377047A1 (pl) | 2006-01-23 |
| CL2003001814A1 (es) | 2005-02-11 |
| WO2004022558A3 (en) | 2004-05-21 |
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