MX2009012885A - Nuevo derivado de 1,2,3,4-tetrahidroquinoxalina que tiene, como sustituyente, grupo fenilo que tiene estructura de ester de acido sulfonico o estructura de amida de acido sulfonico introducida en este, y tiene actividad de enlace al receptor de gluco - Google Patents
Nuevo derivado de 1,2,3,4-tetrahidroquinoxalina que tiene, como sustituyente, grupo fenilo que tiene estructura de ester de acido sulfonico o estructura de amida de acido sulfonico introducida en este, y tiene actividad de enlace al receptor de glucoInfo
- Publication number
- MX2009012885A MX2009012885A MX2009012885A MX2009012885A MX2009012885A MX 2009012885 A MX2009012885 A MX 2009012885A MX 2009012885 A MX2009012885 A MX 2009012885A MX 2009012885 A MX2009012885 A MX 2009012885A MX 2009012885 A MX2009012885 A MX 2009012885A
- Authority
- MX
- Mexico
- Prior art keywords
- sulfonic acid
- alkyl group
- lower alkyl
- hydrogen atom
- glucocorticoid receptor
- Prior art date
Links
- 102000003676 Glucocorticoid Receptors Human genes 0.000 title abstract 2
- 108090000079 Glucocorticoid Receptors Proteins 0.000 title abstract 2
- HORKYAIEVBUXGM-UHFFFAOYSA-N 1,2,3,4-tetrahydroquinoxaline Chemical class C1=CC=C2NCCNC2=C1 HORKYAIEVBUXGM-UHFFFAOYSA-N 0.000 title 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 title 1
- 230000027455 binding Effects 0.000 title 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 title 1
- 125000001424 substituent group Chemical group 0.000 title 1
- 125000002130 sulfonic acid ester group Chemical group 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 7
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 3
- 229910052717 sulfur Inorganic materials 0.000 abstract 3
- 125000004434 sulfur atom Chemical group 0.000 abstract 3
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- XSXHWVKGUXMUQE-UHFFFAOYSA-N osmium dioxide Inorganic materials O=[Os]=O XSXHWVKGUXMUQE-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/36—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
- C07D241/38—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
- C07D241/40—Benzopyrazines
- C07D241/44—Benzopyrazines with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the hetero ring
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
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- A61P9/12—Antihypertensives
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- 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
- C07D405/02—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
- C07D405/12—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 linked by a chain containing hetero atoms as chain links
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
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- General Chemical & Material Sciences (AREA)
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- Diabetes (AREA)
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- Hematology (AREA)
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- Neurology (AREA)
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- Psychiatry (AREA)
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- Endocrinology (AREA)
- Cardiology (AREA)
- Pain & Pain Management (AREA)
- Heart & Thoracic Surgery (AREA)
- Rheumatology (AREA)
- Dermatology (AREA)
- Emergency Medicine (AREA)
- Child & Adolescent Psychology (AREA)
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Abstract
Se describe un compuesto representado por la fórmula general (1) o una sal del mismo, que es útil como un modulador para un receptor de glucocorticoides. En la fórmula, R1 representa un grupo alquilo inferior, un grupo cicloalquilo inferior, un grupo arilo o similares; R2 representa un átomo de hidrógeno, un grupo alquilo inferior o similares; R3 representa un átomo de hidrógeno, un grupo alquilo inferior o similares; R4 y R5 representan independientemente un átomo de hidrógeno, un grupo alquilo inferior o similares; R6 representa un átomo de hidrógeno, un grupo alquilo inferior o similares; R7 representa un átomo de hidrógeno, un grupo alquilo inferior, un grupo alquenilo inferior o similares; W representa un átomo de oxigeno, un átomo de azufre, NR8 o similares; R8 representa un átomo de hidrógeno, un grupo alquilo inferior o similares; X representa un átomo de oxígeno o un átomo de azufre; Y representa un grupo alquileno inferior o similares; Z representa un átomo de oxígeno, un átomo de azufre, NR9, OCO u OSO2 y R9 representa un átomo de hidrógeno, un grupo alquilo inferior o similares.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2007141568 | 2007-05-29 | ||
| PCT/JP2008/059866 WO2008146871A1 (ja) | 2007-05-29 | 2008-05-29 | グルココルチコイド受容体結合活性を有する、スルホン酸エステル又はスルホン酸アミド構造を導入したフェニル基を置換基として有する新規1,2,3,4-テトラヒドロキノキサリン誘導体 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2009012885A true MX2009012885A (es) | 2009-12-10 |
Family
ID=40075104
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2009012885A MX2009012885A (es) | 2007-05-29 | 2008-05-29 | Nuevo derivado de 1,2,3,4-tetrahidroquinoxalina que tiene, como sustituyente, grupo fenilo que tiene estructura de ester de acido sulfonico o estructura de amida de acido sulfonico introducida en este, y tiene actividad de enlace al receptor de gluco |
Country Status (14)
| Country | Link |
|---|---|
| US (2) | US8193187B2 (es) |
| EP (1) | EP2151436B1 (es) |
| JP (1) | JP5183302B2 (es) |
| KR (1) | KR20100022456A (es) |
| CN (1) | CN101679317B (es) |
| AU (1) | AU2008255733B8 (es) |
| BR (1) | BRPI0811262A2 (es) |
| CA (1) | CA2687948A1 (es) |
| ES (1) | ES2419239T3 (es) |
| MX (1) | MX2009012885A (es) |
| NZ (1) | NZ581666A (es) |
| PL (1) | PL2151436T3 (es) |
| RU (1) | RU2498980C2 (es) |
| WO (1) | WO2008146871A1 (es) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PT1995242E (pt) | 2006-03-14 | 2012-11-22 | Santen Pharmaceutical Co Ltd | Novos derivados de 1,2,3,4-tetra-hidroquinoxalina tendo actividade de ligação ao receptor de glucocorticóides |
| WO2008146871A1 (ja) * | 2007-05-29 | 2008-12-04 | Santen Pharmaceutical Co., Ltd. | グルココルチコイド受容体結合活性を有する、スルホン酸エステル又はスルホン酸アミド構造を導入したフェニル基を置換基として有する新規1,2,3,4-テトラヒドロキノキサリン誘導体 |
| US20090042936A1 (en) * | 2007-08-10 | 2009-02-12 | Ward Keith W | Compositions and Methods for Treating or Controlling Anterior-Segment Inflammation |
| CA2735417A1 (en) * | 2008-09-12 | 2010-03-18 | Santen Pharmaceutical Co., Ltd. | Glucocorticoid receptor agonist comprising novel 1,2,3,4-tetrahydroquinoxaline derivatives containing phenyl group having sulfonic acid ester structure introduced therein as substituent |
| WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
| US8530413B2 (en) | 2010-06-21 | 2013-09-10 | Sanofi | Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments |
| TW201215387A (en) | 2010-07-05 | 2012-04-16 | Sanofi Aventis | Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament |
| TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
| TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
| JP5993875B2 (ja) | 2011-01-21 | 2016-09-14 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 縮合アミノジヒドロチアジン誘導体の合成に有用な方法および化合物 |
| US20120316199A1 (en) | 2011-06-07 | 2012-12-13 | Ward Keith W | Compositions and methods for treating, controlling, reducing, or ameliorating inflammatory pain |
| WO2013037390A1 (en) | 2011-09-12 | 2013-03-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| EP2760862B1 (en) | 2011-09-27 | 2015-10-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| US20150011518A1 (en) | 2012-01-31 | 2015-01-08 | Santen Pharmaceutical Co., Ltd. | Non-aqueous liquid composition |
| TW201609145A (zh) | 2013-12-25 | 2016-03-16 | 參天製藥股份有限公司 | 注射劑及形成緩釋(depot)之方法 |
| KR20180043329A (ko) * | 2015-08-25 | 2018-04-27 | 산텐 세이야꾸 가부시키가이샤 | [4-(1,3,3-트리메틸-2-옥소-3,4-디히드로-1h-퀴녹살린-7-일)페녹시]에틸옥시 화합물 또는 그의 염 |
| US20200121652A1 (en) | 2017-06-16 | 2020-04-23 | The Doshisha | Compounds having caspase inhibitory activity, pharmaceutical agent containing said compounds and for treating or preventing corneal endothelial symptoms, disorders, or diseases, and application of said pharmaceutical agent |
| CA3067332A1 (en) | 2017-06-16 | 2018-12-20 | The Doshisha | Mtor-inhibitor-containing medicine for treating or preventing ophthalmic symptoms, disorders, or diseases, and application thereof |
| CA3106752A1 (en) | 2018-07-20 | 2020-01-23 | Grunenthal Gmbh | Substituted triazolo quinoxaline derivatives |
| TWI811400B (zh) | 2018-07-20 | 2023-08-11 | 德商歌林達有限公司 | 經進一步取代之三唑并喹噁啉衍生物 |
| WO2025111184A1 (en) | 2023-11-21 | 2025-05-30 | Fmc Corporation | Substituted tetrahydroquinoline and tetrahydroquinoxaline herbicides |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0509398B1 (de) | 1991-04-15 | 2001-09-19 | Aventis Pharma Deutschland GmbH | Chinoxaline, Verfahren zu ihrer Herstellung und ihre Verwendung |
| US6369057B1 (en) * | 1991-04-15 | 2002-04-09 | Aventis Pharma Deutschland Gmbh | Quinoxalines, processes for their preparation and their use |
| EP0784054B1 (en) * | 1994-09-27 | 2001-11-28 | Yamanouchi Pharmaceutical Co. Ltd. | 1,2,3,4-tetrahydroquinoxalinedione derivatives and use as glutamate receptor antagonists |
| WO1997020578A1 (en) | 1995-12-04 | 1997-06-12 | University Of Miami | Non-preserved topical corticosteroid for treatment of dry eye, filamentary keratitis, and delayed tear clearance |
| US6340758B1 (en) | 1997-05-16 | 2002-01-22 | Warner-Lambert Company | Conformationally semi-constrained quinoxaline 2,3-diones as neuroprotective agents |
| EP1201660B1 (en) * | 2000-10-30 | 2005-08-31 | Pfizer Products Inc. | Glucocorticoid receptor modulators |
| WO2004099192A2 (en) | 2003-04-30 | 2004-11-18 | The Institutes Of Pharmaceutical Discovery, Llc | Heterocycle substituted carboxylic acids as inhibitors of protein tyrosine phosphatase-1b |
| US7235662B2 (en) * | 2003-06-11 | 2007-06-26 | Bristol-Myers Squibb Company | Modulators of the glucocorticoid receptor and method |
| WO2005085416A1 (ja) | 2004-03-04 | 2005-09-15 | Riken | 糸状菌特異的抗菌剤のスクリーニング方法及びそのためのキット |
| CN101365696A (zh) * | 2004-07-28 | 2009-02-11 | Irm责任有限公司 | 作为类固醇激素核受体调节剂的化合物和组合物 |
| CN101263119B (zh) | 2005-09-14 | 2014-04-09 | 参天制药株式会社 | 具有糖皮质激素受体结合活性的1,2-二氢喹啉衍生物 |
| PT1995242E (pt) * | 2006-03-14 | 2012-11-22 | Santen Pharmaceutical Co Ltd | Novos derivados de 1,2,3,4-tetra-hidroquinoxalina tendo actividade de ligação ao receptor de glucocorticóides |
| JP5054996B2 (ja) * | 2006-03-14 | 2012-10-24 | 参天製薬株式会社 | グルココルチコイド受容体結合活性を有する新規1,2,3,4−テトラヒドロキノキサリン誘導体 |
| WO2007112347A1 (en) | 2006-03-28 | 2007-10-04 | Takeda Pharmaceutical Company Limited | Dipeptidyl peptidase inhibitors |
| US8008497B2 (en) * | 2006-11-14 | 2011-08-30 | Santen Pharmaceutical Co., Ltd. | 1,2-dihydroquinoline derivative having (substituted phenyl or substituted heterocyclic) carbonyloxy lower alkyl group and ester-introduced phenyl group as substituents |
| JP2008255112A (ja) | 2007-03-13 | 2008-10-23 | Santen Pharmaceut Co Ltd | 2,2,4−トリメチル−6−フェニル−1,2−ジヒドロキノリン誘導体からなるグルココルチコイド受容体アゴニスト |
| WO2008146871A1 (ja) * | 2007-05-29 | 2008-12-04 | Santen Pharmaceutical Co., Ltd. | グルココルチコイド受容体結合活性を有する、スルホン酸エステル又はスルホン酸アミド構造を導入したフェニル基を置換基として有する新規1,2,3,4-テトラヒドロキノキサリン誘導体 |
| WO2009035067A1 (ja) | 2007-09-13 | 2009-03-19 | Santen Pharmaceutical Co., Ltd. | 1,3,3-トリメチル-7-フェニル-3,4-ジヒドロ-1h-キノキサリン-2-オン誘導体からなるグルココルチコイド受容体アゴニスト |
| JP2009084274A (ja) | 2007-09-13 | 2009-04-23 | Santen Pharmaceut Co Ltd | 新規1,3,3−トリメチル−7−フェニル−3,4−ジヒドロ−1h−キノキサリン−2−オン誘導体 |
-
2008
- 2008-05-29 WO PCT/JP2008/059866 patent/WO2008146871A1/ja not_active Ceased
- 2008-05-29 ES ES08764835T patent/ES2419239T3/es active Active
- 2008-05-29 NZ NZ581666A patent/NZ581666A/en not_active IP Right Cessation
- 2008-05-29 KR KR1020097024711A patent/KR20100022456A/ko not_active Ceased
- 2008-05-29 RU RU2009149185/04A patent/RU2498980C2/ru not_active IP Right Cessation
- 2008-05-29 CA CA002687948A patent/CA2687948A1/en not_active Abandoned
- 2008-05-29 JP JP2008140300A patent/JP5183302B2/ja not_active Expired - Fee Related
- 2008-05-29 AU AU2008255733A patent/AU2008255733B8/en not_active Ceased
- 2008-05-29 US US12/451,653 patent/US8193187B2/en not_active Expired - Fee Related
- 2008-05-29 MX MX2009012885A patent/MX2009012885A/es active IP Right Grant
- 2008-05-29 EP EP08764835.8A patent/EP2151436B1/en not_active Not-in-force
- 2008-05-29 CN CN2008800179279A patent/CN101679317B/zh not_active Expired - Fee Related
- 2008-05-29 PL PL08764835T patent/PL2151436T3/pl unknown
- 2008-05-29 BR BRPI0811262-2A2A patent/BRPI0811262A2/pt not_active IP Right Cessation
-
2012
- 2012-02-02 US US13/364,680 patent/US8569493B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| EP2151436A4 (en) | 2011-08-03 |
| RU2009149185A (ru) | 2011-07-10 |
| CA2687948A1 (en) | 2008-12-04 |
| EP2151436A1 (en) | 2010-02-10 |
| NZ581666A (en) | 2011-06-30 |
| US8569493B2 (en) | 2013-10-29 |
| US20100137307A1 (en) | 2010-06-03 |
| AU2008255733A8 (en) | 2013-06-13 |
| AU2008255733B8 (en) | 2013-06-13 |
| JP2009007344A (ja) | 2009-01-15 |
| JP5183302B2 (ja) | 2013-04-17 |
| WO2008146871A1 (ja) | 2008-12-04 |
| CN101679317B (zh) | 2012-10-31 |
| AU2008255733A1 (en) | 2008-12-04 |
| RU2498980C2 (ru) | 2013-11-20 |
| ES2419239T3 (es) | 2013-08-20 |
| US20120129866A1 (en) | 2012-05-24 |
| CN101679317A (zh) | 2010-03-24 |
| AU2008255733B2 (en) | 2013-06-06 |
| BRPI0811262A2 (pt) | 2014-11-04 |
| PL2151436T3 (pl) | 2013-09-30 |
| KR20100022456A (ko) | 2010-03-02 |
| EP2151436B1 (en) | 2013-04-24 |
| US8193187B2 (en) | 2012-06-05 |
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