MX2009005023A - Nuevas amidas que actuan sobre los receptores de adenosina. - Google Patents
Nuevas amidas que actuan sobre los receptores de adenosina.Info
- Publication number
- MX2009005023A MX2009005023A MX2009005023A MX2009005023A MX2009005023A MX 2009005023 A MX2009005023 A MX 2009005023A MX 2009005023 A MX2009005023 A MX 2009005023A MX 2009005023 A MX2009005023 A MX 2009005023A MX 2009005023 A MX2009005023 A MX 2009005023A
- Authority
- MX
- Mexico
- Prior art keywords
- amino
- adenosine receptors
- carbon atoms
- compounds
- groups selected
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/14—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
- A61K31/4045—Indole-alkylamines; Amides thereof, e.g. serotonin, melatonin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/05—Dipeptides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/18—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D209/20—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals substituted additionally by nitrogen atoms, e.g. tryptophane
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Rheumatology (AREA)
- Immunology (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Gastroenterology & Hepatology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Indole Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
La presente invención se refiere a compuestos de fórmula (I) en la cual R3 a R8 son independientemente seleccionados a partir de hidrógeno, halógeno, trihaloalquilo, alquilo que tiene 1, 2, 3, 4 ó 5 átomos de carbono, grupos donadores de electrón seleccionados de alcoxi que tiene 1, 2, 3, 4 ó 5 átomos de carbono, trihaloalcoxi, hidroxi o amino, grupos aceptores de electrón seleccionados de ciano, sulfónico, nitro o amida; R1 es un grupo fenilo, bencilo, o ciclohexilo opcionalmente sustituido; R2 se selecciona de grupos amino, amino sustituido o guanidino, Z es una cadena de hidrocarburo C1-5 saturada o insaturada y sales de los mismos. También se describen un proceso para su preparación y composiciones que los contienen. Los compuestos son ya sea agonistas o antagonistas de un receptor de adenosina específico o un número de receptores de adenosina y que tienen utilidad para el tratamiento de inflamación, condiciones artríticas, artritis reumatoide, osteoartritis, trastornos mentales o para inducir regeneración de nerviosa central.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0622826.6A GB0622826D0 (en) | 2006-11-15 | 2006-11-15 | Novel amides acting on the adenosine receptors |
PCT/EP2007/009721 WO2008058679A2 (en) | 2006-11-15 | 2007-11-09 | Novel amides acting on the adenosine receptors |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2009005023A true MX2009005023A (es) | 2009-05-20 |
Family
ID=37605369
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2009005023A MX2009005023A (es) | 2006-11-15 | 2007-11-09 | Nuevas amidas que actuan sobre los receptores de adenosina. |
Country Status (12)
Country | Link |
---|---|
US (1) | US8227502B2 (es) |
EP (1) | EP2099815B1 (es) |
JP (1) | JP5536456B2 (es) |
KR (1) | KR20090091166A (es) |
AU (1) | AU2007321460B2 (es) |
CA (1) | CA2669162C (es) |
ES (1) | ES2389271T3 (es) |
GB (1) | GB0622826D0 (es) |
IL (1) | IL198618A (es) |
MX (1) | MX2009005023A (es) |
NZ (1) | NZ576781A (es) |
WO (1) | WO2008058679A2 (es) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0019357D0 (en) * | 2000-08-07 | 2000-09-27 | Melacure Therapeutics Ab | Novel phenyl guanidines |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5007067A (en) | 1989-09-29 | 1991-04-09 | At&T Bell Laboratories | Diversity coding for transparent self-healing communications networks |
DE10110747A1 (de) * | 2001-03-07 | 2002-09-12 | Bayer Ag | Substituierte 2,6-Diamino-3,5-dicyano-4-aryl-pyridine und ihre Verwendung |
RU2334742C2 (ru) * | 2003-01-13 | 2008-09-27 | Ф.Хоффманн-Ля Рош Аг | Производные бензоксазола и фармацевтическая композиция, обладающая свойствами лигандов рецептора аденозина |
SI1633355T1 (sl) * | 2003-05-30 | 2008-08-31 | Hoffmann La Roche | Derivati benzotiazola in njihova uporaba pri zdravljenju bolezni, povezanih z receptorjem a2a adenozina |
US7217702B2 (en) * | 2004-04-02 | 2007-05-15 | Adenosine Therapeutics, Llc | Selective antagonists of A2A adenosine receptors |
EP1778712B1 (en) * | 2004-08-02 | 2013-01-30 | University Of Virginia Patent Foundation | 2-propynyl adenosine analogs with modified 5'-ribose groups having a2a agonist activity |
US7576069B2 (en) | 2004-08-02 | 2009-08-18 | University Of Virginia Patent Foundation | 2-polycyclic propynyl adenosine analogs having A2A agonist activity |
WO2006091896A2 (en) | 2005-02-25 | 2006-08-31 | Adenosine Therapeutics, Llc | Pyridyl substituted xanthines |
US7579348B2 (en) | 2005-02-25 | 2009-08-25 | Pgxhealth, Llc | Derivatives of 8-substituted xanthines |
US7598379B2 (en) * | 2005-02-25 | 2009-10-06 | Pgx Health, Llc | Methods for the synthesis of unsymmetrical cycloalkyl substituted xanthines |
WO2006091898A2 (en) | 2005-02-25 | 2006-08-31 | Adenosine Therapeutics, Llc | Pyrazolyl substituted xanthines |
-
2006
- 2006-11-15 GB GBGB0622826.6A patent/GB0622826D0/en not_active Ceased
-
2007
- 2007-11-09 EP EP07846549A patent/EP2099815B1/en not_active Not-in-force
- 2007-11-09 JP JP2009536639A patent/JP5536456B2/ja not_active Expired - Fee Related
- 2007-11-09 KR KR1020097012201A patent/KR20090091166A/ko not_active Application Discontinuation
- 2007-11-09 WO PCT/EP2007/009721 patent/WO2008058679A2/en active Application Filing
- 2007-11-09 ES ES07846549T patent/ES2389271T3/es active Active
- 2007-11-09 US US12/514,634 patent/US8227502B2/en not_active Expired - Fee Related
- 2007-11-09 NZ NZ576781A patent/NZ576781A/en unknown
- 2007-11-09 AU AU2007321460A patent/AU2007321460B2/en not_active Ceased
- 2007-11-09 CA CA2669162A patent/CA2669162C/en not_active Expired - Fee Related
- 2007-11-09 MX MX2009005023A patent/MX2009005023A/es active IP Right Grant
-
2009
- 2009-05-07 IL IL198618A patent/IL198618A/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
CA2669162C (en) | 2015-02-10 |
JP5536456B2 (ja) | 2014-07-02 |
JP2010509383A (ja) | 2010-03-25 |
EP2099815B1 (en) | 2012-06-20 |
IL198618A0 (en) | 2010-02-17 |
WO2008058679A2 (en) | 2008-05-22 |
US20100098629A1 (en) | 2010-04-22 |
EP2099815A2 (en) | 2009-09-16 |
GB0622826D0 (en) | 2006-12-27 |
ES2389271T3 (es) | 2012-10-24 |
IL198618A (en) | 2013-07-31 |
AU2007321460A1 (en) | 2008-05-22 |
CA2669162A1 (en) | 2008-05-22 |
AU2007321460B2 (en) | 2012-05-03 |
US8227502B2 (en) | 2012-07-24 |
NZ576781A (en) | 2012-02-24 |
WO2008058679A3 (en) | 2008-07-10 |
KR20090091166A (ko) | 2009-08-26 |
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Legal Events
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FG | Grant or registration | ||
GB | Transfer or rights |