ECSP088888A - Antagonistas del receptor de vanilloides del subtipo (vr1) - Google Patents
Antagonistas del receptor de vanilloides del subtipo (vr1)Info
- Publication number
- ECSP088888A ECSP088888A EC2008008888A ECSP088888A ECSP088888A EC SP088888 A ECSP088888 A EC SP088888A EC 2008008888 A EC2008008888 A EC 2008008888A EC SP088888 A ECSP088888 A EC SP088888A EC SP088888 A ECSP088888 A EC SP088888A
- Authority
- EC
- Ecuador
- Prior art keywords
- subtipo
- vanilloid
- receiver antagonists
- antagonists
- receiver
- Prior art date
Links
- 239000005557 antagonist Substances 0.000 title 1
- 208000004454 Hyperalgesia Diseases 0.000 abstract 2
- 208000002193 Pain Diseases 0.000 abstract 2
- 208000035154 Hyperesthesia Diseases 0.000 abstract 1
- 206010061218 Inflammation Diseases 0.000 abstract 1
- 206010046543 Urinary incontinence Diseases 0.000 abstract 1
- 206010053552 allodynia Diseases 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 208000013403 hyperactivity Diseases 0.000 abstract 1
- 208000027866 inflammatory disease Diseases 0.000 abstract 1
- 230000002757 inflammatory effect Effects 0.000 abstract 1
- 230000004054 inflammatory process Effects 0.000 abstract 1
- 208000004296 neuralgia Diseases 0.000 abstract 1
- 208000021722 neuropathic pain Diseases 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/10—Spiro-condensed systems
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4747—Quinolines; Isoquinolines spiro-condensed
-
- 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
- A61K31/33—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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/10—Drugs for disorders of the urinary system of the bladder
-
- 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/12—Antidiuretics, e.g. drugs for diabetes insipidus
-
- 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
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/10—Spiro-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Urology & Nephrology (AREA)
- Neurosurgery (AREA)
- Epidemiology (AREA)
- Pain & Pain Management (AREA)
- Diabetes (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Rheumatology (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
La presente invención se refiere a compuestos de fórmula (I) (I)donde las variables X1, X2, Y, R1a, R1b, R2a, R2b, A1, A2, A3, y A4 son como se definen en la memoria descriptiva, y métodos de uso para tratar dolor, dolor neuropático, alodinia, dolor asociado con inflamación o una enfermedad inflamatoria, hiperalgesia inflamatoria, hiperactividad vesical e incontinencia urinaria.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US79269906P | 2006-04-18 | 2006-04-18 | |
| PCT/US2007/066515 WO2007121299A2 (en) | 2006-04-18 | 2007-04-12 | Antagonists of the vanilloid receptor subtype 1 (vr1) and uses thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ECSP088888A true ECSP088888A (es) | 2008-12-30 |
Family
ID=38610380
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EC2008008888A ECSP088888A (es) | 2006-04-18 | 2008-11-14 | Antagonistas del receptor de vanilloides del subtipo (vr1) |
Country Status (20)
| Country | Link |
|---|---|
| US (2) | US7622493B2 (es) |
| EP (1) | EP2012778A4 (es) |
| JP (1) | JP2009534399A (es) |
| KR (1) | KR20080111144A (es) |
| CN (2) | CN102796086A (es) |
| AU (1) | AU2007238071B2 (es) |
| BR (1) | BRPI0710507A2 (es) |
| CA (1) | CA2647256A1 (es) |
| CR (1) | CR10362A (es) |
| EC (1) | ECSP088888A (es) |
| GT (1) | GT200800227A (es) |
| MX (1) | MX2008013428A (es) |
| MY (1) | MY144307A (es) |
| NO (1) | NO20084729L (es) |
| NZ (1) | NZ571706A (es) |
| RU (1) | RU2450006C2 (es) |
| TW (1) | TWI357904B (es) |
| UA (1) | UA94940C2 (es) |
| WO (1) | WO2007121299A2 (es) |
| ZA (1) | ZA200808691B (es) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009511465A (ja) * | 2005-10-07 | 2009-03-19 | グレンマーク・ファーマシューティカルズ・エスエー | 置換ベンゾ縮合誘導体およびバニロイド受容体リガンドとしてのその使用 |
| EP2012778A4 (en) * | 2006-04-18 | 2011-08-10 | Abbott Lab | VANILLOID RECEPTOR (VR1) SUBType 1 ANTAGONISTS AND USES THEREOF |
| WO2008110863A1 (en) * | 2007-03-15 | 2008-09-18 | Glenmark Pharmaceuticals S.A. | Indazole derivatives and their use as vanilloid receptor ligands |
| WO2009081219A1 (en) * | 2007-12-20 | 2009-07-02 | Glenmark Pharmaceuticals, S.A. | Quinazoline derivatives as vanilloid receptor modulators |
| WO2009095726A1 (en) * | 2008-01-29 | 2009-08-06 | Glenmark Pharmaceuticals, S.A. | Acrylamide derivatives as vanilloid receptor 1 modulators |
| AR073631A1 (es) * | 2008-10-17 | 2010-11-17 | Abbott Lab | Antagonistas del receptor transitorio potencial de vanilloides 1 ( trpv1) utiles para tratar inflamacion y dolor |
| MX2011004090A (es) | 2008-10-17 | 2011-05-31 | Abbott Lab | Antagonistas trpv1. |
| MX2012013197A (es) | 2010-05-12 | 2013-04-03 | Abbvie Inc | Inhibidores de indazol de cinasa. |
| EP2688866A1 (en) | 2011-03-25 | 2014-01-29 | AbbVie Inc. | Trpv1 antagonists |
| US8859584B2 (en) | 2011-12-19 | 2014-10-14 | Abbvie, Inc. | TRPV1 antagonists |
| US8969325B2 (en) | 2011-12-19 | 2015-03-03 | Abbvie Inc. | TRPV1 antagonists |
| US8889730B2 (en) | 2012-04-10 | 2014-11-18 | Pfizer Inc. | Indole and indazole compounds that activate AMPK |
| US8796328B2 (en) | 2012-06-20 | 2014-08-05 | Abbvie Inc. | TRPV1 antagonists |
| EP2970177A1 (en) | 2013-03-15 | 2016-01-20 | Pfizer Inc. | Indole compounds that activate ampk |
| CN112771045B (zh) | 2018-09-30 | 2022-04-19 | 南京明德新药研发有限公司 | 喹啉并吡咯烷-2-酮类衍生物及其应用 |
| RU2755206C1 (ru) | 2020-05-20 | 2021-09-14 | Федеральное государственное бюджетное учреждение науки Тихоокеанский институт биоорганической химии им. Г.Б. Елякова Дальневосточного отделения Российской академии наук (ТИБОХ ДВО РАН) | Средство пролонгированного анальгетического действия и лекарственный препарат на его основе |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2745305A1 (de) * | 1977-10-07 | 1979-04-19 | Bayer Ag | Insektizide und akarizide mittel |
| US5374643A (en) * | 1992-09-11 | 1994-12-20 | E. R. Squibb & Sons, Inc. | Aryl urea (thiourea) and cyanoguanidine derivatives |
| TW475930B (en) * | 1995-04-24 | 2002-02-11 | Novartis Ag | Novel compound, its use and pharmaceutical composition comprising it |
| WO2002020509A2 (de) * | 2000-09-06 | 2002-03-14 | Bayer Aktiengesellschaft | Arzneimittel gegen virale erkrankungen |
| DE10120619A1 (de) * | 2001-04-26 | 2002-10-31 | Merck Patent Gmbh | 2-(5-(4-Fluorphenyl)-3-pyridylmethylaminomethyl-chroman |
| GB0110901D0 (en) * | 2001-05-02 | 2001-06-27 | Smithkline Beecham Plc | Novel Compounds |
| US6821971B2 (en) * | 2001-09-20 | 2004-11-23 | The Procter & Gamble Company | Fused pyrazolone compounds which inhibit the release of inflammatory cytokines |
| CA2476936A1 (en) * | 2002-02-20 | 2003-08-28 | Chih-Hung Lee | Fused azabicyclic compounds that inhibit vanilloid receptor subtype 1 (vr1) receptor |
| WO2003097586A1 (en) | 2002-05-17 | 2003-11-27 | Janssen Pharmaceutica N.V. | Aminotetralin-derived urea modulators of vanilloid vr1 receptor |
| US6933311B2 (en) * | 2003-02-11 | 2005-08-23 | Abbott Laboratories | Fused azabicyclic compounds that inhibit vanilloid receptor subtype 1 (VR1) receptor |
| EP1601665A2 (en) | 2003-03-07 | 2005-12-07 | Glaxo Group Limited | Urea derivatives |
| KR101138216B1 (ko) * | 2003-06-12 | 2012-09-05 | 아보트 러보러터리즈 | 바닐로이드 수용체 아형 1(vr1) 수용체를 억제하는융합 화합물 |
| EP1589015A1 (en) * | 2004-02-03 | 2005-10-26 | Université de Liège | Benzopyran derivatives, method of production and use thereof |
| NZ555318A (en) * | 2004-11-24 | 2011-01-28 | Abbott Lab | Chromanylurea compounds that inhibit vanilloid receptor subtype 1 (VR1) receptor and uses thereof |
| AU2005316739A1 (en) * | 2004-12-13 | 2006-06-22 | Galileo Pharmaceuticals, Inc. | Spiro derivatives as lipoxygenase inhibitors |
| US7615570B2 (en) * | 2004-12-13 | 2009-11-10 | Abbott Laboratories | Antagonists to the vanilloid receptor subtype 1 (VR1) and uses thereof |
| AU2006243987B2 (en) * | 2005-05-11 | 2011-11-24 | Abbott Laboratories | Antagonists of the vanilloid receptor subtype 1 (VR1) and uses thereof |
| CN101321766A (zh) * | 2005-10-07 | 2008-12-10 | 格兰马克药品股份有限公司 | 取代的苯并稠合的衍生物及其作为香草素受体配体的用途 |
| JP2009511465A (ja) * | 2005-10-07 | 2009-03-19 | グレンマーク・ファーマシューティカルズ・エスエー | 置換ベンゾ縮合誘導体およびバニロイド受容体リガンドとしてのその使用 |
| CN101365684A (zh) | 2005-10-28 | 2009-02-11 | 艾博特公司 | 抑制trpv1受体的吲唑衍生物 |
| EP2012778A4 (en) * | 2006-04-18 | 2011-08-10 | Abbott Lab | VANILLOID RECEPTOR (VR1) SUBType 1 ANTAGONISTS AND USES THEREOF |
| PE20081692A1 (es) * | 2007-01-24 | 2008-12-18 | Mochida Pharm Co Ltd | Nuevo derivado de heterocicliden acetamida |
| WO2008110863A1 (en) * | 2007-03-15 | 2008-09-18 | Glenmark Pharmaceuticals S.A. | Indazole derivatives and their use as vanilloid receptor ligands |
-
2007
- 2007-04-12 EP EP07760554A patent/EP2012778A4/en not_active Withdrawn
- 2007-04-12 WO PCT/US2007/066515 patent/WO2007121299A2/en not_active Ceased
- 2007-04-12 BR BRPI0710507-0A patent/BRPI0710507A2/pt not_active IP Right Cessation
- 2007-04-12 RU RU2008145506/04A patent/RU2450006C2/ru not_active IP Right Cessation
- 2007-04-12 UA UAA200813308A patent/UA94940C2/ru unknown
- 2007-04-12 MY MYPI20084102A patent/MY144307A/en unknown
- 2007-04-12 CN CN2012102446499A patent/CN102796086A/zh active Pending
- 2007-04-12 NZ NZ571706A patent/NZ571706A/en not_active IP Right Cessation
- 2007-04-12 KR KR1020087028075A patent/KR20080111144A/ko not_active Ceased
- 2007-04-12 MX MX2008013428A patent/MX2008013428A/es active IP Right Grant
- 2007-04-12 CN CNA2007800136476A patent/CN101426498A/zh active Pending
- 2007-04-12 JP JP2009506693A patent/JP2009534399A/ja active Pending
- 2007-04-12 CA CA002647256A patent/CA2647256A1/en not_active Abandoned
- 2007-04-12 AU AU2007238071A patent/AU2007238071B2/en not_active Ceased
- 2007-04-13 US US11/735,074 patent/US7622493B2/en not_active Expired - Fee Related
- 2007-04-18 TW TW096113670A patent/TWI357904B/zh not_active IP Right Cessation
-
2008
- 2008-10-10 ZA ZA200808691A patent/ZA200808691B/xx unknown
- 2008-10-14 CR CR10362A patent/CR10362A/es not_active Application Discontinuation
- 2008-10-21 GT GT200800227A patent/GT200800227A/es unknown
- 2008-11-10 NO NO20084729A patent/NO20084729L/no not_active Application Discontinuation
- 2008-11-14 EC EC2008008888A patent/ECSP088888A/es unknown
-
2009
- 2009-05-28 US US12/474,035 patent/US8598220B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| TW200808808A (en) | 2008-02-16 |
| KR20080111144A (ko) | 2008-12-22 |
| CR10362A (es) | 2008-12-11 |
| US20090233953A1 (en) | 2009-09-17 |
| ZA200808691B (en) | 2010-03-31 |
| NO20084729L (no) | 2008-11-10 |
| JP2009534399A (ja) | 2009-09-24 |
| AU2007238071B2 (en) | 2012-06-07 |
| UA94940C2 (ru) | 2011-06-25 |
| WO2007121299A3 (en) | 2008-11-13 |
| NZ571706A (en) | 2012-06-29 |
| WO2007121299A2 (en) | 2007-10-25 |
| CA2647256A1 (en) | 2007-10-25 |
| CN102796086A (zh) | 2012-11-28 |
| AU2007238071A1 (en) | 2007-10-25 |
| MX2008013428A (es) | 2008-11-04 |
| US7622493B2 (en) | 2009-11-24 |
| EP2012778A2 (en) | 2009-01-14 |
| RU2450006C2 (ru) | 2012-05-10 |
| US20070249614A1 (en) | 2007-10-25 |
| BRPI0710507A2 (pt) | 2011-08-16 |
| MY144307A (en) | 2011-08-29 |
| TWI357904B (en) | 2012-02-11 |
| GT200800227A (es) | 2009-07-09 |
| US8598220B2 (en) | 2013-12-03 |
| RU2008145506A (ru) | 2010-05-27 |
| CN101426498A (zh) | 2009-05-06 |
| EP2012778A4 (en) | 2011-08-10 |
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