CR20130178A - COMPUESTOS 3-FENILSULFANILMETIL-BICICLO[3.1.0.]HEXANO 4-SUSTITUIDOS COMO ANTAGONISTAS DE mGluR 2/3 - Google Patents
COMPUESTOS 3-FENILSULFANILMETIL-BICICLO[3.1.0.]HEXANO 4-SUSTITUIDOS COMO ANTAGONISTAS DE mGluR 2/3Info
- Publication number
- CR20130178A CR20130178A CR20130178A CR20130178A CR20130178A CR 20130178 A CR20130178 A CR 20130178A CR 20130178 A CR20130178 A CR 20130178A CR 20130178 A CR20130178 A CR 20130178A CR 20130178 A CR20130178 A CR 20130178A
- Authority
- CR
- Costa Rica
- Prior art keywords
- phenylsulphanylme
- mglur
- antagonists
- hexane
- substituted
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/50—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton
- C07C323/51—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
- C07C323/57—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being further substituted by nitrogen atoms, not being part of nitro or nitroso groups
- C07C323/58—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being further substituted by nitrogen atoms, not being part of nitro or nitroso groups with amino groups bound to the carbon skeleton
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/095—Sulfur, selenium, or tellurium compounds, e.g. thiols
- A61K31/10—Sulfides; Sulfoxides; Sulfones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
- C07C2601/08—Systems containing only non-condensed rings with a five-membered ring the ring being saturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/14—All rings being cycloaliphatic
- C07C2602/18—All rings being cycloaliphatic the ring system containing six carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Epidemiology (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
LA PRESENTE INVENCIÓN SE REFIERE A UN ANTAGONISTA DEL RECEPTOR mGlu2/3 DE LA FÓRMULA, SE DESCRIBEN SUS USOS, Y MÉTODOS PARA SU PREPARACIÓN.-
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US41512110P | 2010-11-18 | 2010-11-18 | |
| PCT/US2011/060730 WO2012068067A1 (en) | 2010-11-18 | 2011-11-15 | 4-substituted-3-phenylsulfanylmethyl-bicyclo[3.1.0]hexane compounds as mglur 2/3 antagonists |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CR20130178A true CR20130178A (es) | 2013-07-09 |
Family
ID=45099188
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CR20130178A CR20130178A (es) | 2010-11-18 | 2013-04-24 | COMPUESTOS 3-FENILSULFANILMETIL-BICICLO[3.1.0.]HEXANO 4-SUSTITUIDOS COMO ANTAGONISTAS DE mGluR 2/3 |
Country Status (36)
| Country | Link |
|---|---|
| US (1) | US8629169B2 (es) |
| EP (1) | EP2640697B1 (es) |
| JP (1) | JP5877847B2 (es) |
| KR (2) | KR20150140876A (es) |
| CN (1) | CN103228625B (es) |
| AR (1) | AR083845A1 (es) |
| AU (1) | AU2011329076B2 (es) |
| BR (1) | BR112013012118A2 (es) |
| CA (1) | CA2818116C (es) |
| CL (1) | CL2013001345A1 (es) |
| CO (1) | CO6761385A2 (es) |
| CR (1) | CR20130178A (es) |
| DK (1) | DK2640697T3 (es) |
| DO (1) | DOP2013000099A (es) |
| EA (1) | EA021724B1 (es) |
| EC (1) | ECSP13012629A (es) |
| ES (1) | ES2650139T3 (es) |
| GT (1) | GT201300126A (es) |
| HR (1) | HRP20171649T1 (es) |
| HU (1) | HUE037457T2 (es) |
| IL (1) | IL225843A (es) |
| LT (1) | LT2640697T (es) |
| MA (1) | MA34663B1 (es) |
| MX (1) | MX339973B (es) |
| NO (1) | NO2640697T3 (es) |
| NZ (1) | NZ609816A (es) |
| PE (1) | PE20140997A1 (es) |
| PL (1) | PL2640697T3 (es) |
| PT (1) | PT2640697T (es) |
| RS (1) | RS56535B1 (es) |
| SG (1) | SG189959A1 (es) |
| SI (1) | SI2640697T1 (es) |
| TW (1) | TWI520935B (es) |
| UA (1) | UA110039C2 (es) |
| WO (1) | WO2012068067A1 (es) |
| ZA (1) | ZA201302918B (es) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR079343A1 (es) * | 2009-12-21 | 2012-01-18 | Lilly Co Eli | Compuesto de acido 2-amino-4-(4h-1,2,4-triazol-3-ilsulfanil)biciclo[3.1.0]hexano-2,6-dicarboxilico, composicion farmaceutica que lo comprende y su uso para preparar un medicamento util para tratar un trastorno psiquiatrico |
| EP3000814A1 (en) | 2014-09-26 | 2016-03-30 | Domain Therapeutics | Substituted pyrazoloquinazolinones and pyrroloquinazolinones as allosteric modulators of group II metabotropic glutamate receptors |
| CA3019097C (en) | 2016-04-18 | 2023-08-29 | Taisho Pharmaceutical Co., Ltd. | Prodrug of amino acid derivative |
| JP2020506895A (ja) | 2017-01-17 | 2020-03-05 | ボード オブ レジェンツ, ザ ユニバーシティ オブ テキサス システムBoard Of Regents, The University Of Texas System | インドールアミン２，３−ジオキシゲナーゼおよび／またはトリプトファンジオキシゲナーゼの阻害剤として有用な化合物 |
| US11046649B2 (en) | 2018-07-17 | 2021-06-29 | Board Of Regents, The University Of Texas System | Compounds useful as inhibitors of indoleamine 2,3-dioxygenase and/or tryptophan dioxygenase |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0669928B2 (ja) | 1987-10-06 | 1994-09-07 | 宇部興産株式会社 | 光重合性歯科材料 |
| JP2589812B2 (ja) | 1989-07-05 | 1997-03-12 | 松下電器産業株式会社 | スチームアイロン |
| ZA969485B (en) | 1995-11-16 | 1998-05-12 | Lilly Co Eli | Excitatory amino acid receptor antagonists. |
| AU703093B2 (en) * | 1995-11-16 | 1999-03-18 | Eli Lilly And Company | Excitatory amino acid receptor antagonists |
| ZA983930B (en) * | 1997-05-14 | 1999-11-08 | Lilly Co Eli | Excitatory amino acid receptor modulators. |
| TR200002671T2 (tr) * | 1998-03-17 | 2000-12-21 | Pfizer Products Inc. | Bisiklo(2.2.1)Heptanlar ve ilgili bileşikler |
| GB9815542D0 (en) | 1998-07-17 | 1998-09-16 | Lilly Co Eli | Bicyclohexane derivatives |
| CH694053A5 (de) | 1998-09-03 | 2004-06-30 | Hoffmann La Roche | Verfahren zur Herstellung von 2-Amino-bicyclo[3.1.0]hexan-2,6-dicarbonsäure-Derivaten. |
| WO2002068380A1 (en) * | 2001-02-22 | 2002-09-06 | Eli Lilly And Company | Synthetic excitatory amino acids |
| KR20090031962A (ko) | 2001-12-27 | 2009-03-30 | 다이쇼 세이야꾸 가부시끼가이샤 | 6-플루오로비시클로[3.1.0]헥산 유도체 |
| BR0311558A (pt) * | 2002-06-11 | 2007-04-27 | Lilly Co Eli | composto ou sal farmaceuticamente aceitável do mesmo, processo para preparar o mesmo, métodos para afetar os receptores de glutamato metabotrópicos ligados a camp, para administrar uma quantidade eficaz de um composto e para tratar um distúrbio neurológico e psiquiátrico em um paciente, e, formulação farmacêutica |
| US7381746B2 (en) * | 2003-06-26 | 2008-06-03 | Taisho Pharmaceutical Co., Ltd. | 2-Aminobicyclo[3.1.0]hexane-2,6-dicarboxylic acid derivative |
| JP2007063129A (ja) | 2003-06-26 | 2007-03-15 | Taisho Pharmaceut Co Ltd | ２−アミノ−３−アルコキシビシクロ［３．１．０］ヘキサン誘導体 |
| WO2005000791A1 (ja) | 2003-06-26 | 2005-01-06 | Taisho Pharmaceutical Co., Ltd. | ２－アミノ－ビシクロ[３．１．０]ヘキサン－２，６－ジカルボン酸エステル誘導体 |
| AR079343A1 (es) * | 2009-12-21 | 2012-01-18 | Lilly Co Eli | Compuesto de acido 2-amino-4-(4h-1,2,4-triazol-3-ilsulfanil)biciclo[3.1.0]hexano-2,6-dicarboxilico, composicion farmaceutica que lo comprende y su uso para preparar un medicamento util para tratar un trastorno psiquiatrico |
-
2011
- 2011-11-11 TW TW100141326A patent/TWI520935B/zh not_active IP Right Cessation
- 2011-11-11 AR ARP110104219A patent/AR083845A1/es unknown
- 2011-11-15 KR KR1020157034547A patent/KR20150140876A/ko not_active Application Discontinuation
- 2011-11-15 EP EP11791692.4A patent/EP2640697B1/en active Active
- 2011-11-15 DK DK11791692.4T patent/DK2640697T3/en active
- 2011-11-15 LT LTEP11791692.4T patent/LT2640697T/lt unknown
- 2011-11-15 RS RS20171082A patent/RS56535B1/sr unknown
- 2011-11-15 NZ NZ609816A patent/NZ609816A/en not_active IP Right Cessation
- 2011-11-15 PE PE2013001215A patent/PE20140997A1/es not_active Application Discontinuation
- 2011-11-15 EA EA201390498A patent/EA021724B1/ru not_active IP Right Cessation
- 2011-11-15 PL PL11791692T patent/PL2640697T3/pl unknown
- 2011-11-15 AU AU2011329076A patent/AU2011329076B2/en not_active Ceased
- 2011-11-15 CN CN201180055263.7A patent/CN103228625B/zh active Active
- 2011-11-15 NO NO11791692A patent/NO2640697T3/no unknown
- 2011-11-15 MX MX2013005622A patent/MX339973B/es active IP Right Grant
- 2011-11-15 PT PT117916924T patent/PT2640697T/pt unknown
- 2011-11-15 SG SG2013030507A patent/SG189959A1/en unknown
- 2011-11-15 HU HUE11791692A patent/HUE037457T2/hu unknown
- 2011-11-15 UA UAA201305835A patent/UA110039C2/ru unknown
- 2011-11-15 US US13/296,384 patent/US8629169B2/en active Active
- 2011-11-15 WO PCT/US2011/060730 patent/WO2012068067A1/en active Application Filing
- 2011-11-15 JP JP2013539938A patent/JP5877847B2/ja active Active
- 2011-11-15 BR BR112013012118A patent/BR112013012118A2/pt not_active IP Right Cessation
- 2011-11-15 ES ES11791692.4T patent/ES2650139T3/es active Active
- 2011-11-15 CA CA2818116A patent/CA2818116C/en active Active
- 2011-11-15 KR KR1020137012697A patent/KR20130101094A/ko active IP Right Grant
- 2011-11-15 SI SI201131304T patent/SI2640697T1/sl unknown
-
2013
- 2013-04-18 IL IL225843A patent/IL225843A/en not_active IP Right Cessation
- 2013-04-22 ZA ZA2013/02918A patent/ZA201302918B/en unknown
- 2013-04-24 CR CR20130178A patent/CR20130178A/es unknown
- 2013-05-08 DO DO2013000099A patent/DOP2013000099A/es unknown
- 2013-05-13 MA MA35898A patent/MA34663B1/fr unknown
- 2013-05-15 CL CL2013001345A patent/CL2013001345A1/es unknown
- 2013-05-15 GT GT201300126A patent/GT201300126A/es unknown
- 2013-05-17 EC ECSP13012629 patent/ECSP13012629A/es unknown
- 2013-05-30 CO CO13133036A patent/CO6761385A2/es unknown
-
2017
- 2017-10-27 HR HRP20171649TT patent/HRP20171649T1/hr unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DOP2012000135A (es) | Compuestos de espiropiperidina como antagonistas del receptor orl-1 | |
| GB201017345D0 (en) | Receptor antagonists | |
| GT201500138A (es) | Novedososo derivados de bencimidazol como antagonistas de ep4 | |
| CU24094B1 (es) | Anticuerpos para el receptor 3 del factor de crecimiento epidérmico(her3) | |
| ECSP12012221A (es) | Anticuerpos anti-cd40 | |
| UY34467A (es) | Procedimiento para la preparación de 5-fluoro-1h-pirazolopiridinas sustituidas | |
| UY34352A (es) | 3-pirimidin-4-il-oxazolidin-2-onas como inhibidores de la idh mutante | |
| MX2014010849A (es) | Formas solidas de un inhibidor de cinasa del receptor del factor de crecimiento epidermico. | |
| UY34572A (es) | Compuestos heterocíclicos agonistas del receptor ip | |
| CR20140306A (es) | Fluormetil -5,6-dihidro-4h-[1,3] oxazinas | |
| CR20130178A (es) | COMPUESTOS 3-FENILSULFANILMETIL-BICICLO[3.1.0.]HEXANO 4-SUSTITUIDOS COMO ANTAGONISTAS DE mGluR 2/3 | |
| BR112013028511A2 (pt) | receptor de sinais de radiofrequência | |
| CO6470820A2 (es) | Espiro-epóxidos como productos intermedios | |
| HK1178902A1 (en) | Disubstituted tetrahydofuranyl compounds as antagonists of the bradykinin b1 receptor b1 | |
| ES2636441T8 (es) | Un procedimiento novedoso para la síntesis de polifenoles | |
| HK1207855A1 (en) | Substituted carbamate compounds and their use as transient receptor potential (trp) channel antagonists (trp) | |
| GT201200328A (es) | Intermedios de agomelatina y método de preparación de éstos | |
| CL2015000038A1 (es) | Métodos para preparar triazolopiridinas sustituidas y compuestos intermediarios. | |
| BR112013012384A2 (pt) | compostos 3-benzilóóxi-biciclo[3.1.0]hexano 4-substituídos como antagonistas receptores de mglu2 e mglu3 | |
| EP3046923A4 (en) | Formulations for cgrp receptor antagonists | |
| MX2013000539A (es) | Nuevas formulaciones de analogos 14-epi de la vitamina d. | |
| HK1208028A1 (en) | Novel acetamide derivatives as trp channel antagonists trp | |
| TN2013000209A1 (en) | 4-substituted-3-phenylsulfanylmethyl-bicyclo[3.1.0]hexane compounds as mglur 2/3 antagonists | |
| UA54879U (ru) | Применение антагониста рецепторов интерлейкина-1 как средства антиоксидантного действия | |
| ES2421810R1 (es) | Intermedios utiles para la sintesis de fexofenadina, procedimientos para su preparacion y para la preparacion de fexofenadina |