ECSP055967A - N-ARILHETEROCICLOS REPLACED, PROCEDURES FOR THEIR PREPARATION, AND ITS EMPLOYMENT AS MEDICATIONS - Google Patents
N-ARILHETEROCICLOS REPLACED, PROCEDURES FOR THEIR PREPARATION, AND ITS EMPLOYMENT AS MEDICATIONSInfo
- Publication number
- ECSP055967A ECSP055967A EC2005005967A ECSP055967A ECSP055967A EC SP055967 A ECSP055967 A EC SP055967A EC 2005005967 A EC2005005967 A EC 2005005967A EC SP055967 A ECSP055967 A EC SP055967A EC SP055967 A ECSP055967 A EC SP055967A
- Authority
- EC
- Ecuador
- Prior art keywords
- preparation
- procedures
- arilheterociclos
- medications
- employment
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 3
- 239000003814 drug Substances 0.000 title abstract 2
- 229940079593 drug Drugs 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 239000002830 appetite depressant Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member 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 ring carbon atoms
- C07D207/24—Oxygen or sulfur atoms
- C07D207/26—2-Pyrrolidones
-
- 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
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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
- A61P25/20—Hypnotics; Sedatives
-
- 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
- A61P25/22—Anxiolytics
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- 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
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D205/04—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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 ring carbon atoms
- C07D207/14—Nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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 ring carbon atoms
- C07D207/16—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members 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 ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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 ring carbon atoms
- C07D211/56—Nitrogen atoms
- C07D211/58—Nitrogen atoms attached in position 4
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- 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
- C07D405/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Diabetes (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Psychiatry (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Endocrinology (AREA)
- Urology & Nephrology (AREA)
- Pain & Pain Management (AREA)
- Child & Adolescent Psychology (AREA)
- Addiction (AREA)
- Emergency Medicine (AREA)
- Anesthesiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Hydrogenated Pyridines (AREA)
- Pyrrole Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
N-Arilheterociclos sustituidos, procedimientos para su preparación, y su empleo como medicamentos La invención se refiere a N-arilheterociclos sustituidos, y a sus sales fisiológicamente tolerables y derivados fisiológicamente funcionales.Se describen compuestos de fórmula I,en la cual los radicales tienen los significados que se indican, sus N-óxidos y sus sales fisiológicamente tolerables, y procedimientos para su preparación. Los compuestos son útiles, por ejemplo, como anorexígenos.Substituted N-Arylheterocycles, methods for their preparation, and their use as medicaments The invention relates to substituted N-arylheterocycles, and their physiologically tolerable salts and physiologically functional derivatives. Compounds of formula I are described, in which the radicals have the meanings which are indicated, their N-oxides and their physiologically tolerable salts, and procedures for their preparation. The compounds are useful, for example, as anorexigens.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10306250A DE10306250A1 (en) | 2003-02-14 | 2003-02-14 | Substituted N-aryl heterocycles, processes for their preparation and their use as pharmaceuticals |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ECSP055967A true ECSP055967A (en) | 2006-01-16 |
Family
ID=32841665
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EC2005005967A ECSP055967A (en) | 2003-02-14 | 2005-08-11 | N-ARILHETEROCICLOS REPLACED, PROCEDURES FOR THEIR PREPARATION, AND ITS EMPLOYMENT AS MEDICATIONS |
Country Status (29)
| Country | Link |
|---|---|
| EP (1) | EP1597228A2 (en) |
| JP (1) | JP2006517563A (en) |
| KR (1) | KR20050101215A (en) |
| CN (1) | CN100506792C (en) |
| AR (1) | AR044496A1 (en) |
| AU (1) | AU2004212145B2 (en) |
| BR (1) | BRPI0407504A (en) |
| CA (1) | CA2516118A1 (en) |
| CO (1) | CO5690548A2 (en) |
| DE (1) | DE10306250A1 (en) |
| EC (1) | ECSP055967A (en) |
| HR (1) | HRP20050710A2 (en) |
| MA (1) | MA27735A1 (en) |
| MX (1) | MXPA05008449A (en) |
| MY (1) | MY139102A (en) |
| NO (1) | NO20054220L (en) |
| NZ (1) | NZ541823A (en) |
| OA (1) | OA13027A (en) |
| PA (1) | PA8595901A1 (en) |
| PE (1) | PE20040952A1 (en) |
| PL (1) | PL378065A1 (en) |
| RS (1) | RS20050666A (en) |
| RU (1) | RU2005128551A (en) |
| TN (1) | TNSN05194A1 (en) |
| TW (1) | TW200510297A (en) |
| UA (1) | UA86760C2 (en) |
| UY (1) | UY28186A1 (en) |
| WO (1) | WO2004072025A2 (en) |
| ZA (1) | ZA200506369B (en) |
Families Citing this family (118)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7351719B2 (en) | 2002-10-31 | 2008-04-01 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Amide compounds having MCH-antagonistic activity and medicaments comprising these compounds |
| CA2526285A1 (en) | 2003-05-15 | 2004-12-23 | Arqule, Inc. | Inhibitors of p38 and methods of using the same |
| DE602004017316D1 (en) * | 2003-07-24 | 2008-12-04 | Euro Celtique Sa | HETEROARYL TETRAHYDROPYRIDYL COMPOUNDS RELATING TO THE TREATMENT THE PREVENTION OF PAIN EQUIPMENTS |
| EP1867644B1 (en) * | 2003-07-24 | 2009-05-20 | Euro-Celtique S.A. | Heteroaryl-tetrahydropiperidyl compounds useful for treating or preventing pain |
| WO2005016910A1 (en) | 2003-08-18 | 2005-02-24 | Sankio Chemical Co., Ltd. | Pyridyltetrahydropyridines, pyridylpiperidines, and process for the production of both |
| US7592373B2 (en) | 2003-12-23 | 2009-09-22 | Boehringer Ingelheim International Gmbh | Amide compounds with MCH antagonistic activity and medicaments comprising these compounds |
| DE10360745A1 (en) * | 2003-12-23 | 2005-07-28 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | New amide compounds having MCH antagonist activity and medicaments containing these compounds |
| US7319108B2 (en) | 2004-01-25 | 2008-01-15 | Sanofi-Aventis Deutschland Gmbh | Aryl-substituted heterocycles, process for their preparation and their use as medicaments |
| DE102004003812A1 (en) * | 2004-01-25 | 2005-08-11 | Aventis Pharma Deutschland Gmbh | Aryl-substituted heterocycles, methods of their preparation and their use as pharmaceuticals |
| WO2006010082A1 (en) * | 2004-07-08 | 2006-01-26 | Arqule, Inc. | 1,4-disubstituted naphtalenes as inhibitors of p38 map kinase |
| WO2006022442A1 (en) * | 2004-08-24 | 2006-03-02 | Santen Pharmaceutical Co., Ltd. | Novel heterocyclic amide derivatives having dihydroorotate dehydrogenase inhibiting activity |
| GB0420722D0 (en) | 2004-09-17 | 2004-10-20 | Addex Pharmaceuticals Sa | Novel allosteric modulators |
| CN101084211A (en) * | 2004-09-20 | 2007-12-05 | 泽农医药公司 | Heterocyclic derivatives and their use as therapeutic agents |
| WO2006038680A1 (en) * | 2004-10-01 | 2006-04-13 | Banyu Pharmaceutical Co.,Ltd | 2-arylcarboxamide-nitrogeneous heterocycle compound |
| CN101094846A (en) | 2004-10-18 | 2007-12-26 | 伊莱利利公司 | 1-(Hetero)aryl-3-amino-pyrrolidine derivatives useful as MGLUR3 receptor antagonists |
| EP2258704A1 (en) | 2004-10-19 | 2010-12-08 | ArQule, Inc. | Synthesis of imidazooxazole and imidazothiazole inhibitors of p38 map kinase |
| DE102004051277A1 (en) * | 2004-10-21 | 2006-04-27 | Merck Patent Gmbh | Heterocyclic carbonyl compounds |
| JPWO2006054793A1 (en) * | 2004-11-19 | 2008-06-05 | 財団法人新産業創造研究機構 | Benzofuran compound and pharmaceutical composition containing the same |
| NZ590148A (en) | 2004-12-30 | 2012-04-27 | Janssen Pharmaceutica Nv | Piperazinyl and piperidinyl ureas as modulators of fatty acid amide hydrolase |
| EP1846388A4 (en) * | 2005-01-25 | 2011-12-07 | Synta Pharmaceuticals Corp | Thiophene compounds for inflammation and immune-related uses |
| ATE429428T1 (en) | 2005-09-30 | 2009-05-15 | Hoffmann La Roche | INDANDERIVATES AS ANTAGONISTS OF THE MCH RECEPTOR |
| CN101379060B (en) * | 2006-02-10 | 2012-05-23 | 转化技术制药公司 | Benzoxazole Derivatives, Compositions and Methods of Use as Aurora Kinase Inhibitors |
| WO2007093365A2 (en) * | 2006-02-15 | 2007-08-23 | Sanofi-Aventis | Novel amino alcohol-substituted arylthienopyrimidinones, process for their preparation and their use as medicaments |
| BRPI0707869A2 (en) * | 2006-02-15 | 2011-05-10 | Sanofi Aventis | azacyclyl substituted arylthienopyrimidinones, process for their preparation and their use as medicines |
| AR059898A1 (en) | 2006-03-15 | 2008-05-07 | Janssen Pharmaceutica Nv | DERIVATIVES OF 3-CIANO-PIRIDONA 1,4-DISUSTITUTED AND ITS USE AS ALLOSTERIC MODULATORS OF MGLUR2 RECEIVERS |
| CA2649288C (en) | 2006-04-19 | 2015-11-24 | Novartis Ag | 6-o-substituted benzoxazole and benzothiazole compounds and methods of inhibiting csf-1r signaling |
| JP5182088B2 (en) | 2006-04-19 | 2013-04-10 | アステラス製薬株式会社 | Azole carboxamide derivatives |
| UA93548C2 (en) | 2006-05-05 | 2011-02-25 | Айерем Елелсі | Compounds and compositions as hedgehog pathway modulators |
| CN103435595A (en) | 2006-05-08 | 2013-12-11 | 阿里亚德医药股份有限公司 | Acetylenic heteroaryl compounds |
| US8278307B2 (en) | 2006-05-08 | 2012-10-02 | Ariad Pharmaceuticals, Inc. | Monocyclic Heteroaryl compounds |
| EP2061767B1 (en) | 2006-08-08 | 2014-12-17 | Sanofi | Arylaminoaryl-alkyl-substituted imidazolidine-2,4-diones, processes for preparing them, medicaments comprising these compounds, and their use |
| MX2009002019A (en) | 2006-08-24 | 2009-03-09 | Novartis Ag | 2- (pyrazin-2-yl) -thiazole and 2- (1h-pyraz0l-3-yl) -thiazole derivatives as well as related compounds as stearoyl-coa desaturase (scd) inhibitors for the treatment of metabolic, cardiovascular and other disorders. |
| WO2008031772A1 (en) * | 2006-09-11 | 2008-03-20 | Glaxo Group Limited | Azabicyclic compounds as inhibitors of monoamines reuptake |
| US20080076770A1 (en) * | 2006-09-25 | 2008-03-27 | Arete Therapeutics, Inc. | Soluble epoxide hydrolase inhibitors |
| AR063311A1 (en) | 2006-10-18 | 2009-01-21 | Novartis Ag | ORGANIC COMPOUNDS |
| AU2008205252B2 (en) * | 2007-01-09 | 2013-02-21 | Amgen Inc. | Bis-aryl amide derivatives useful for the treatment of cancer |
| TW200845978A (en) | 2007-03-07 | 2008-12-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-tetrahydropyran-phenyl)-pyridin-2-one derivatives |
| TW200900065A (en) | 2007-03-07 | 2009-01-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-pyridinyloxy-phenyl)-pyridin-2-one derivatives |
| GB0706793D0 (en) * | 2007-04-05 | 2007-05-16 | Evotec Ag | Compounds |
| ES2536406T3 (en) * | 2007-06-08 | 2015-05-25 | Janssen Pharmaceutica, N.V. | Piperidine / Piperazine Derivatives |
| EP2152271B1 (en) | 2007-06-08 | 2015-10-21 | Janssen Pharmaceutica, N.V. | Piperidine/piperazine derivatives |
| JO2972B1 (en) | 2007-06-08 | 2016-03-15 | جانسين فارماسوتيكا ان. في | Piperidine/Piperazine derivatives |
| JP5464709B2 (en) | 2007-06-08 | 2014-04-09 | 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 | Piperidine / piperazine derivatives |
| TWI452044B (en) | 2007-06-15 | 2014-09-11 | Mitsubishi Tanabe Pharma Corp | Morpholine derivative |
| TW200918521A (en) * | 2007-08-31 | 2009-05-01 | Astrazeneca Ab | Heterocyclic amides and methods of use thereof |
| SI2203439T1 (en) | 2007-09-14 | 2011-05-31 | Ortho Mcneil Janssen Pharm | 1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2h, 1'h-y1, 4' bipyridinyl-2'-ones |
| PL2200985T3 (en) | 2007-09-14 | 2011-12-30 | Ortho Mcneil Janssen Pharmaceuticals Inc | 1,3-disubstituted 4-(aryl-x-phenyl)-1h-pyridin-2-ones |
| CN101801930B (en) | 2007-09-14 | 2013-01-30 | 奥梅-杨森制药有限公司 | 1,3-disubstituted-4-phenyl-1 h-pyridin-2-ones |
| SI2215058T1 (en) * | 2007-10-17 | 2012-03-30 | Sanofi Sa | Substituted n-phenyl-bipyrrolidine ureas and therapeutic use thereof |
| EP2205558B1 (en) * | 2007-10-17 | 2012-07-25 | Sanofi | Substituted n-phenyl-pyrrolidinylmethylpyrrolidine amides and therapeutic use thereof as histamine h3 receptor modulators |
| SI2212282T1 (en) * | 2007-10-17 | 2012-01-31 | Sanofi Sa | Substituted n-phenyl-bipyrrolidine carboxamides and therapeutic use thereof |
| ES2372332T3 (en) * | 2007-10-17 | 2012-01-18 | Sanofi | N-PHENYL-BIPIRROLIDINE SUBSTITUTED CARBOXAMIDS AND THERAPEUTIC USE. |
| EP2206707B1 (en) | 2007-10-24 | 2014-07-23 | Astellas Pharma Inc. | Azolecarboxamide compound or salt thereof |
| CN101861316B (en) | 2007-11-14 | 2013-08-21 | 奥梅-杨森制药有限公司 | Imidazo[1,2-a]pyridine derivatives and their use as positive allosteric modulators of the MGLUR2 receptor |
| EP2070925A1 (en) | 2007-12-10 | 2009-06-17 | Bayer Schering Pharma Aktiengesellschaft | New 2-substituted tiazol-4-carboxylic acid derivatives, their manufacture and use as medicine |
| EP2070924A1 (en) | 2007-12-10 | 2009-06-17 | Bayer Schering Pharma Aktiengesellschaft | New 2 hetarylthiazol-4-carboxylic acid derivatives, their manufacture and use as medicine |
| EP2070916A1 (en) | 2007-12-10 | 2009-06-17 | Bayer Schering Pharma Aktiengesellschaft | 2-Arylthiazol-4-carboxylic acid derivatives, their manufacture and use as medicine |
| RU2364597C1 (en) * | 2007-12-14 | 2009-08-20 | Андрей Александрович Иващенко | HETEROCYCLIC INHIBITORS OF Hh-SYGNAL CASCADE, BASED ON THEM MEDICINAL COMPOSITIONS AND METHOD OF TREATING DISEASES INDUCED BY ABBARANT ACTIVITY OF Hh-SIGNAL SYSTEM |
| PE20100083A1 (en) * | 2008-06-05 | 2010-02-17 | Janssen Pharmaceutica Nv | DRUG COMBINATIONS INCLUDING A DGAT INHIBITOR AND A PPAR AGONIST |
| UY31968A (en) | 2008-07-09 | 2010-01-29 | Sanofi Aventis | NEW HETEROCYCLIC DERIVATIVES, THEIR PROCESSES FOR THEIR PREPARATION, AND THEIR THERAPEUTIC USES |
| EP2344470B1 (en) | 2008-09-02 | 2013-11-06 | Janssen Pharmaceuticals, Inc. | 3-azabicyclo[3.1.0]hexyl derivatives as modulators of metabotropic glutamate receptors |
| CA2737699A1 (en) * | 2008-09-16 | 2010-03-25 | Merck Sharp & Dohme Corp. | Phthalimide derivative metabotropic glutamate r4 ligands |
| JP2012006837A (en) * | 2008-09-30 | 2012-01-12 | Mochida Pharmaceut Co Ltd | 2-indoleacrylamide analogue |
| WO2010043396A1 (en) | 2008-10-16 | 2010-04-22 | Ortho-Mcneil-Janssen Pharmaceuticals, Inc. | Indole and benzomorpholine derivatives as modulators of metabotropic glutamate receptors |
| CA2743449C (en) | 2008-11-12 | 2016-10-18 | Ariad Pharmaceuticals, Inc. | Pyrazinopyrazines and derivatives as kinase inhibitors |
| JP5690277B2 (en) | 2008-11-28 | 2015-03-25 | ジャンセン ファーマシューティカルズ, インコーポレイテッド. | Indole and benzoxazine derivatives as modulators of metabotropic glutamate receptors |
| AR074466A1 (en) * | 2008-12-05 | 2011-01-19 | Sanofi Aventis | PIPERIDINE ESPIRO PIRROLIDINONA AND PIPERIDINONA REPLACED AND ITS THERAPEUTIC USE IN DISEASES MEDIATED BY THE MODULATION OF H3 RECEPTORS. |
| WO2010068601A1 (en) | 2008-12-08 | 2010-06-17 | Sanofi-Aventis | A crystalline heteroaromatic fluoroglycoside hydrate, processes for making, methods of use and pharmaceutical compositions thereof |
| UA103918C2 (en) | 2009-03-02 | 2013-12-10 | Айерем Элелси | N-(hetero)aryl, 2-(hetero)aryl-substituted acetamides for use as wnt signaling modulators |
| JP5642661B2 (en) * | 2009-03-05 | 2014-12-17 | 塩野義製薬株式会社 | Piperidine and pyrrolidine derivatives having NPYY5 receptor antagonistic activity |
| JP5685181B2 (en) * | 2009-03-05 | 2015-03-18 | 塩野義製薬株式会社 | Cyclohexane derivative having NPYY5 receptor antagonistic action |
| BRPI1010831A2 (en) | 2009-05-12 | 2016-04-05 | Addex Pharmaceuticals Sa | 1,2,4-triazolo [4,3-a] pyridine derivatives and their as positive allosteric modulators of mglur2 receptors |
| CN102439008B (en) | 2009-05-12 | 2015-04-29 | 杨森制药有限公司 | 1,2,4-Triazolo[4,3-A]pyridine derivatives and their use for the treatment or prevention of neurological and psychiatric disorders |
| MY153913A (en) | 2009-05-12 | 2015-04-15 | Janssen Pharmaceuticals Inc | 7-aryl-1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors |
| KR20120060207A (en) | 2009-08-26 | 2012-06-11 | 사노피 | Novel crystalline heteroaromatic fluoroglycoside hydrates, pharmaceuticals comprising these compounds and their use |
| US20120225097A1 (en) | 2009-11-12 | 2012-09-06 | Hawryluk Natalie A | Piperazinecarboxamide derivative useful as a modulator of fatty acid amide hydrolase (faah) |
| US9452980B2 (en) * | 2009-12-22 | 2016-09-27 | Hoffmann-La Roche Inc. | Substituted benzamides |
| UA108233C2 (en) | 2010-05-03 | 2015-04-10 | Fatty acid amide hydrolysis activity modulators | |
| EP2569280B1 (en) * | 2010-05-11 | 2015-02-25 | Sanofi | Substituted phenyl cycloalkyl pyrrolidine (piperidine) spirolactams and amides, preparation and therapeutic use thereof |
| EP2569294B1 (en) * | 2010-05-11 | 2015-03-11 | Sanofi | Substituted n-heteroaryl bipyrrolidine carboxamides, preparation and therapeutic use thereof |
| WO2011143148A1 (en) * | 2010-05-11 | 2011-11-17 | Sanofi | Substituted n-heteroaryl spirolactam bipyrrolidines, preparation and therapeutic use thereof |
| UY33469A (en) | 2010-06-29 | 2012-01-31 | Irm Llc Y Novartis Ag | COMPOSITIONS AND METHODS TO MODULATE THE WNT SIGNALING ROAD |
| US9271967B2 (en) | 2010-11-08 | 2016-03-01 | Janssen Pharmaceuticals, Inc. | 1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mGluR2 receptors |
| ES2536433T3 (en) | 2010-11-08 | 2015-05-25 | Janssen Pharmaceuticals, Inc. | 1,2,4-Triazolo [4,3-a] pyridine derivatives and their use as positive allosteric modulators of mGluR2 receptors |
| AU2011328203B2 (en) | 2010-11-08 | 2015-03-19 | Janssen Pharmaceuticals, Inc. | 1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mGluR2 receptors |
| WO2012120051A1 (en) | 2011-03-08 | 2012-09-13 | Sanofi | Benzyl-oxathiazine derivates substituted with adamantane or noradamantane, medicaments containing said compounds and use thereof |
| EP2683704B1 (en) | 2011-03-08 | 2014-12-17 | Sanofi | Branched oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
| EP2683699B1 (en) | 2011-03-08 | 2015-06-24 | Sanofi | Di- and tri-substituted oxathiazine derivates, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
| EP2683702B1 (en) | 2011-03-08 | 2014-12-24 | Sanofi | New substituted phenyl oxathiazine derivatives, method for their manufacture, medicines containing these compounds and their application |
| EP2766349B1 (en) | 2011-03-08 | 2016-06-01 | Sanofi | Oxathiazine derivatives substituted with carbocycles or heterocycles, method for producing same, drugs containing said compounds, and use thereof |
| WO2012120058A1 (en) | 2011-03-08 | 2012-09-13 | Sanofi | Oxathiazine derivatives which are substituted with benzyl or heteromethylene groups, method for producing them, their use as medicine and drug containing said derivatives and the use thereof |
| WO2012120056A1 (en) | 2011-03-08 | 2012-09-13 | Sanofi | Tetrasubstituted oxathiazine derivatives, method for producing them, their use as medicine and drug containing said derivatives and the use thereof |
| US8828994B2 (en) | 2011-03-08 | 2014-09-09 | Sanofi | Di- and tri-substituted oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
| US8895547B2 (en) | 2011-03-08 | 2014-11-25 | Sanofi | Substituted phenyl-oxathiazine derivatives, method for producing them, drugs containing said compounds and the use thereof |
| US9051265B2 (en) | 2011-06-06 | 2015-06-09 | The Scripps Research Institute | N-benzylindole modulators of PPARG |
| US8957093B2 (en) | 2011-06-06 | 2015-02-17 | The Scripps Research Institute | N-biphenylmethylindole modulators of PPARG |
| US9309227B2 (en) | 2011-11-22 | 2016-04-12 | The Scripps Research Institute | N-biphenylmethylbenzimidazole modulators of PPARG |
| WO2013085957A1 (en) | 2011-12-06 | 2013-06-13 | Janssen Pharmaceutica Nv | Substituted piperidinyl-pyridazinyl derivatives useful as scd 1 inhibitors |
| WO2013085954A1 (en) | 2011-12-06 | 2013-06-13 | Janssen Pharmaceutica Nv | Substituted piperidinyl-carboxamide derivatives useful as scd 1 inhibitors |
| CN104684906B (en) * | 2012-05-11 | 2017-06-09 | 艾伯维公司 | Nampt inhibitor |
| EP2914253B1 (en) * | 2012-11-05 | 2018-01-03 | NantBioScience, Inc. | Cyclic sulfonamide containing derivatives as inhibitors of hedgehog signaling pathway |
| AR094929A1 (en) | 2013-02-28 | 2015-09-09 | Bristol Myers Squibb Co | DERIVATIVES OF PHENYLPIRAZOL AS POWERFUL INHIBITORS OF ROCK1 AND ROCK2 |
| CN105102448B (en) | 2013-02-28 | 2018-03-06 | 百时美施贵宝公司 | Phenylpyrazole derivatives as ROCK1 and ROCK2 inhibitor |
| JO3368B1 (en) | 2013-06-04 | 2019-03-13 | Janssen Pharmaceutica Nv | 6, 7- dihydropyrazolu [5,1-a] pyrazine-4 (5 hands) -on compounds and their use as negative excretory regulators of Miglore 2 receptors. |
| JO3367B1 (en) | 2013-09-06 | 2019-03-13 | Janssen Pharmaceutica Nv | 1,2,4-TRIAZOLO[4,3-a]PYRIDINE COMPOUNDS AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS |
| ME03518B (en) | 2014-01-21 | 2020-04-20 | Janssen Pharmaceutica Nv | COMBINATIONS INCLUDING POSITIVE ALOSTERIC MODULATORS OR ORTHOSTERIC AGONISTS OF METABOTROPIC GLUTAMATERGIC RECEPTOR SUBTYPE 2 AND THEIR APPLICATIONS |
| MX386697B (en) | 2014-01-21 | 2025-03-19 | Janssen Pharmaceutica Nv | Combinations comprising positive allosteric modulators or orthosteric agonists of metabotropic glutamatergic receptor subtype 2 and their use |
| WO2015161108A1 (en) | 2014-04-16 | 2015-10-22 | The Scripps Research Institute | Pparg modulators for treatment of osteoporosis |
| US20170152226A1 (en) * | 2014-07-16 | 2017-06-01 | Novogen Ltd. | Functionalised and substituted indoles as anti-cancer agents |
| JP6633618B2 (en) * | 2014-08-21 | 2020-01-22 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | Tideback benzamide derivatives as potent ROCK inhibitors |
| JP2017526706A (en) * | 2014-09-10 | 2017-09-14 | エピザイム,インコーポレイティド | Isoxazole carboxamide compounds |
| HK1257756A1 (en) * | 2015-08-28 | 2019-10-25 | Glenmark Pharmaceuticals S.A. | Novel carbocyclic compounds as ror gamma modulators |
| CN108713019B (en) | 2016-03-17 | 2021-06-15 | 豪夫迈·罗氏有限公司 | 5-Ethyl-4-methyl-pyrazole-3-carboxamide derivatives having activity as agonists of TAAR |
| CN108815167B (en) * | 2017-05-24 | 2021-04-13 | 四川晶华生物科技有限公司 | Application of compound in preparing medicine for treating tumor |
| TW202136238A (en) * | 2020-01-06 | 2021-10-01 | 大陸商廣東東陽光藥業有限公司 | ROR[gamma]T inhibitor, preparation method therefor and use thereof |
| WO2022150962A1 (en) * | 2021-01-12 | 2022-07-21 | Westlake Pharmaceutical (Hangzhou) Co., Ltd. | Protease inhibitors, preparation, and uses thereof |
| CN115160269A (en) * | 2021-04-02 | 2022-10-11 | 北京大学 | Arylcarboxamide derivatives as positive allosteric modulators of NMDAR |
| MX2024008868A (en) | 2022-01-18 | 2024-09-23 | Maze Therapeutics Inc | Apol1 inhibitors and methods of use. |
Family Cites Families (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2663336B1 (en) | 1990-06-18 | 1992-09-04 | Adir | NOVEL PEPTIDE DERIVATIVES, THEIR PREPARATION PROCESS AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME. |
| JP3933198B2 (en) * | 1994-10-26 | 2007-06-20 | ファルマシア・アンド・アップジョン・カンパニー | Phenyloxazolidinone antibacterial agent |
| EP0876379A1 (en) | 1996-01-17 | 1998-11-11 | Novo Nordisk A/S | Fused 1,2,4-thiadiazine and fused 1,4-thiazine derivatives, their preparation and use |
| IL128332A0 (en) | 1996-08-30 | 2000-01-31 | Novo Nordisk As | GLP-1 derivatives |
| ES2199366T3 (en) | 1996-12-31 | 2004-02-16 | Dr. Reddy's Laboratories Ltd. | HETEROCICLICAL COMPOUNDS, PROCEDURE FOR THE PREPARATION AND PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM AND THEIR USE IN THE TREATMENT OF DIABETES AND RELATED ILLNESSES. |
| DE19726167B4 (en) | 1997-06-20 | 2008-01-24 | Sanofi-Aventis Deutschland Gmbh | Insulin, process for its preparation and pharmaceutical preparation containing it |
| RU2215004C2 (en) | 1997-07-16 | 2003-10-27 | Ново Нордиск А/С | Condensed derivative of 1,2,4-thiadiazine, pharmaceutical composition and method for preparing medicine |
| CO4970713A1 (en) | 1997-09-19 | 2000-11-07 | Sanofi Synthelabo | DERIVATIVES OF CARBOXAMIDOTIAZOLES, THEIR PREPARATION, PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM |
| EP1028948B1 (en) * | 1997-11-07 | 2003-01-29 | Schering Corporation | Phenyl-alkyl-imidazoles as h3 receptor antagonists |
| US6221897B1 (en) | 1998-06-10 | 2001-04-24 | Aventis Pharma Deutschland Gmbh | Benzothiepine 1,1-dioxide derivatives, a process for their preparation, pharmaceuticals comprising these compounds, and their use |
| DE19845405C2 (en) | 1998-10-02 | 2000-07-13 | Aventis Pharma Gmbh | Aryl-substituted propanolamine derivatives and their use |
| US6492400B1 (en) | 1998-12-18 | 2002-12-10 | Bristol-Myers Squibb Pharma Company | N-ureidoalkyl-piperidines as modulators of chemokine receptor activity |
| GB9900416D0 (en) | 1999-01-08 | 1999-02-24 | Alizyme Therapeutics Ltd | Inhibitors |
| MXPA01008142A (en) * | 1999-02-10 | 2003-07-21 | Welfide Corp | Amide compounds and medicinal use thereof. |
| CZ20013608A3 (en) * | 1999-04-09 | 2002-05-15 | Astrazeneca Ab | Adamantane derivatives |
| WO2000063208A1 (en) | 1999-04-16 | 2000-10-26 | Novo Nordisk A/S | Substituted imidazoles, their preparation and use |
| WO2000066585A1 (en) | 1999-04-30 | 2000-11-09 | Neurogen Corporation | 9H-PYRIMIDO[4,5-b]INDOLE DERIVATIVES: CRF1 SPECIFIC LIGANDS |
| GB9911863D0 (en) | 1999-05-21 | 1999-07-21 | Knoll Ag | Therapeutic agents |
| SE9901875D0 (en) * | 1999-05-25 | 1999-05-25 | Astra Pharma Prod | Novel compounds |
| US6399640B1 (en) | 1999-06-18 | 2002-06-04 | Merck & Co., Inc. | Arylthiazolidinedione and aryloxazolidinedione derivatives |
| EP1204654B1 (en) | 1999-07-29 | 2003-07-23 | Eli Lilly And Company | Benzofurylpiperazines: 5-ht2c serotonin receptor agonists |
| KR20020033778A (en) | 1999-09-01 | 2002-05-07 | 로버트 흐라이탁, 미쉘 베스트 | Sulfonyl carboxamide derivatives, method for their production and their use as medicaments |
| ATE369337T1 (en) | 2000-04-28 | 2007-08-15 | Asahi Kasei Pharma Corp | NEW BIZYCLIC COMPOUNDS |
| ATE310728T1 (en) | 2000-05-11 | 2005-12-15 | Bristol Myers Squibb Co | TETRAHYDROISOCHINOLINE ANALOGUE AS GROWTH HORMONE SECRETAGOGEN |
| JP2003534377A (en) | 2000-05-30 | 2003-11-18 | メルク エンド カムパニー インコーポレーテッド | Melanocortin receptor agonist |
| HUP0302918A2 (en) * | 2000-07-17 | 2003-12-29 | Ranbaxy Laboratories Limited | Antimicrobial oxazolidinone derivatives, and pharmaceutical compositions containing the same and process for preparation of compounds |
| US6525202B2 (en) * | 2000-07-17 | 2003-02-25 | Wyeth | Cyclic amine phenyl beta-3 adrenergic receptor agonists |
| BR0112856A (en) * | 2000-07-31 | 2003-07-01 | Smithkline Beecham Plc | Method for treating the disorder, compound or a salt or solvate thereof, process for preparing the disorder, pharmaceutical composition, method of treatment and / or prophylaxis of one or more of the disorders, use of a compound, and method for treatment of diabetes, major depression, manic depression, anxiety, schizophrenia, and sleep disorders in human and non-human mammals |
| JO2654B1 (en) * | 2000-09-04 | 2012-06-17 | شركة جانسين فارماسوتيكا ان. في | Polyarylcarboxamides useful as lipid lowering agents |
| JO2409B1 (en) * | 2000-11-21 | 2007-06-17 | شركة جانسين فارماسوتيكا ان. في | Biphenylcarboxamides useful as lipid lowering agents |
| JP2002338537A (en) * | 2001-05-16 | 2002-11-27 | Mitsubishi Pharma Corp | Amide compounds and their pharmaceutical uses |
| WO2002098871A1 (en) * | 2001-06-01 | 2002-12-12 | Tanabe Seiyaku Co., Ltd. | Phenylcarboxamides and process for preparation thereof |
| WO2002098839A1 (en) * | 2001-06-01 | 2002-12-12 | Tanabe Seiyaku Co., Ltd. | Biphenylcarboxamides and process for preparation thereof |
| WO2002099388A2 (en) * | 2001-06-07 | 2002-12-12 | Merck & Co., Inc. | Benzodiazepine bradykinin antagonists |
| DE10142734A1 (en) | 2001-08-31 | 2003-03-27 | Aventis Pharma Gmbh | New (((oxazolylalkyl)-cycloalkyl)-alkyl)-benzoic acid derivatives, are peroxisome proliferator activated receptor agonists or antagonists used e.g. for treating lipid metabolism disorders, type II diabetes, syndrome X and obesity |
| US7662826B2 (en) * | 2002-04-23 | 2010-02-16 | Shionogi & Co., Ltd. | Pyrazolo [1,5-a] pyrimidine derivative and nad (p) h oxidase inhibitor containing the same |
| JP2004175739A (en) * | 2002-11-28 | 2004-06-24 | Tanabe Seiyaku Co Ltd | Pharmaceutical composition |
-
2003
- 2003-02-14 DE DE10306250A patent/DE10306250A1/en not_active Withdrawn
-
2004
- 2004-02-13 OA OA1200500227A patent/OA13027A/en unknown
- 2004-02-13 WO PCT/EP2004/001342 patent/WO2004072025A2/en not_active Ceased
- 2004-02-13 UY UY28186A patent/UY28186A1/en unknown
- 2004-02-13 TW TW093103412A patent/TW200510297A/en unknown
- 2004-02-13 KR KR1020057014989A patent/KR20050101215A/en not_active Ceased
- 2004-02-13 JP JP2006501827A patent/JP2006517563A/en active Pending
- 2004-02-13 PA PA20048595901A patent/PA8595901A1/en unknown
- 2004-02-13 PE PE2004000158A patent/PE20040952A1/en not_active Application Discontinuation
- 2004-02-13 BR BRPI0407504-8A patent/BRPI0407504A/en not_active IP Right Cessation
- 2004-02-13 UA UAA200508733A patent/UA86760C2/en unknown
- 2004-02-13 MX MXPA05008449A patent/MXPA05008449A/en active IP Right Grant
- 2004-02-13 NZ NZ541823A patent/NZ541823A/en unknown
- 2004-02-13 PL PL378065A patent/PL378065A1/en not_active Application Discontinuation
- 2004-02-13 AU AU2004212145A patent/AU2004212145B2/en not_active Ceased
- 2004-02-13 MY MYPI20040479A patent/MY139102A/en unknown
- 2004-02-13 CN CNB2004800098606A patent/CN100506792C/en not_active Expired - Fee Related
- 2004-02-13 CA CA002516118A patent/CA2516118A1/en not_active Abandoned
- 2004-02-13 HR HR20050710A patent/HRP20050710A2/en not_active Application Discontinuation
- 2004-02-13 RS YUP-2005/0666A patent/RS20050666A/en unknown
- 2004-02-13 EP EP04710808A patent/EP1597228A2/en not_active Withdrawn
- 2004-02-13 RU RU2005128551/04A patent/RU2005128551A/en not_active Application Discontinuation
- 2004-02-16 AR ARP040100469A patent/AR044496A1/en unknown
-
2005
- 2005-08-10 ZA ZA200506369A patent/ZA200506369B/en unknown
- 2005-08-11 CO CO05079788A patent/CO5690548A2/en not_active Application Discontinuation
- 2005-08-11 EC EC2005005967A patent/ECSP055967A/en unknown
- 2005-08-11 MA MA28430A patent/MA27735A1/en unknown
- 2005-08-12 TN TNP2005000194A patent/TNSN05194A1/en unknown
- 2005-09-12 NO NO20054220A patent/NO20054220L/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| TW200510297A (en) | 2005-03-16 |
| PE20040952A1 (en) | 2005-02-08 |
| NZ541823A (en) | 2009-01-31 |
| WO2004072025A3 (en) | 2004-12-23 |
| DE10306250A1 (en) | 2004-09-09 |
| CN100506792C (en) | 2009-07-01 |
| RS20050666A (en) | 2007-12-31 |
| EP1597228A2 (en) | 2005-11-23 |
| ZA200506369B (en) | 2006-07-26 |
| AU2004212145B2 (en) | 2010-06-17 |
| MA27735A1 (en) | 2006-02-01 |
| MY139102A (en) | 2009-08-28 |
| BRPI0407504A (en) | 2006-02-14 |
| PA8595901A1 (en) | 2004-09-16 |
| CO5690548A2 (en) | 2006-10-31 |
| HRP20050710A2 (en) | 2006-07-31 |
| PL378065A1 (en) | 2006-02-20 |
| OA13027A (en) | 2006-11-10 |
| KR20050101215A (en) | 2005-10-20 |
| CA2516118A1 (en) | 2004-08-26 |
| RU2005128551A (en) | 2006-02-10 |
| AR044496A1 (en) | 2005-09-14 |
| AU2004212145A1 (en) | 2004-08-26 |
| NO20054220L (en) | 2005-10-28 |
| CN1774418A (en) | 2006-05-17 |
| NO20054220D0 (en) | 2005-09-12 |
| TNSN05194A1 (en) | 2007-06-11 |
| MXPA05008449A (en) | 2006-05-25 |
| JP2006517563A (en) | 2006-07-27 |
| WO2004072025A2 (en) | 2004-08-26 |
| UA86760C2 (en) | 2009-05-25 |
| UY28186A1 (en) | 2004-09-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ECSP055967A (en) | N-ARILHETEROCICLOS REPLACED, PROCEDURES FOR THEIR PREPARATION, AND ITS EMPLOYMENT AS MEDICATIONS | |
| SV2004001690A (en) | NEW DERIVATIVES OF HETEROCICLIC FLUOROGLYCOSIDS, MEDICINES CONTAINING THESE COMPOUNDS, AND THE USE OF THE SAME | |
| UY27761A1 (en) | DERIVATIVES OF ACIL-4-CARBOXIFENILUREA, PROCEDURES FOR PREPARATION AND USE. | |
| UY28123A1 (en) | NEW DERIVATIVES OF AROMATIC FLUOROGLYCHIDS, MEDICINES CONTAINING THESE COMPOUNDS AND THEIR USES. | |
| UY28955A1 (en) | NEW FLUOROGLYCOSIDE DERIVATIVES OF PIRAZOLES, MEDICINES CONTAINING THESE COMPOUNDS, AND THE USE OF THEMSELVES | |
| ECSP066734A (en) | ACID DERIVATIVES 7-PHENYLAMINE-4-QUINOLONA-3-CARBOXYL, METHODS FOR PRODUCTION AND USE AS MEDICATIONS | |
| PA8577001A1 (en) | HETEROCICLICALLY SUBSTITUTED BENZOILUREAS, PROCEDURE FOR PREPARATION AND USE AS PHARMACOS | |
| PY0219683A (en) | AMINO-ALKYL SUBSTITUTED AROMATIC BICYCLIC COMPOUNDS, PROCESS FOR THEIR PREPARATION AND THEIR USE AS MEDICINES | |
| UY29781A1 (en) | DIAZASPIRO SUBSTITUTE COMPOUNDS, PHARMACEUTICALLY ACCEPTABLE SALTS, PHARMACEUTICAL COMPOSITIONS CONTAINING THE COMPOUNDS OR SALTS, PREPARATION METHODS AND USES | |
| UY30498A1 (en) | NEW CLASS OF BENZIMIDAZOLILO COMPOUNDS, ITS SALTS, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM AND APPLICATIONS | |
| UY28572A1 (en) | NEW COMPOUNDS | |
| PA8657501A1 (en) | PIPERIDA DERIVATIVES AND THEIR USE AS ANTI-INFLAMMATORY AGENTS | |
| NI200900076A (en) | NEW DERIVATIVES OF 1,4-BENZOTHYPINE-1,1-DIOXIDE REPLACED WITH BENZYL RADICALS, A METHOD FOR THEIR PREPARATION, PHARMACEUTICAL PRODUCTS THAT INCLUDE THESE COMPOUNDS AND THEIR USE. | |
| UY31481A1 (en) | NEW PIRIMIDINE DERIVATIVES, PREPARATION PROCESSES, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM AND APPLICATIONS | |
| UY27891A1 (en) | NEW DERIVATIVES OF THIOPHEN GLYCOSIDE, PROCEDURES FOR THE PREPARATION OF THE SAME, MEDICINES CONTAINING THESE COMPOUNDS, AND THE USE OF THEM. | |
| UY27851A1 (en) | DIFENILAZETIDINONAS REPLACED IN RING, PROCEDURE FOR PREPARATION, MEDICATIONS UNDERSTANDING THESE COMPOUNDS AND THEIR USE. | |
| CY1114669T1 (en) | Substituted Sulfonamide Derivatives | |
| UY28443A1 (en) | SUBSTITUTED DERIVATIVES OF THE TIAZOL-BENZOISOTIAZOL DIOXIDE, PROCEDURE FOR PREPARATION AND USE. | |
| AR071120A1 (en) | DERIVATIVES OF DIOSMETINE, ITS PREPARATION PROCEDURE, THE PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM AND THEIR USE IN THE TREATMENT OF CHRONIC VENOUS DISEASES. | |
| CR10497A (en) | USEFUL PIPERAZINYL DERIVATIVES IN THE TREATMENT OF DISEASES MEDIATED BY THE GPR38 RECEIVER | |
| UY29258A1 (en) | HYDROXIBYPHYL CARBOXYLIC ACIDS AND DERIVATIVES, PROCEDURES TO PREPARE THEM AND USE | |
| UY28356A1 (en) | DERIVATIVES OF BENZIMIDAZOL, COMPOSITIONS THAT CONTAIN THEM, PREPARATIONS OF THE SAME AND ITS USES | |
| UY28357A1 (en) | DERIVATIVES OF BENZIMIDAZOL, COMPOSITIONS THAT CONTAIN THEM, PREPARATION OF THE SAME AND ITS USES | |
| CR11584A (en) | OXINDOL DERIVATIVES SUBSTITUTED AND USE OF THE SAME FOR THE TREATMENT OF VASOPRESINE DEPENDENT DISEASES | |
| UY30424A1 (en) | DERIVATIVES OF QUINOLINA, ITS PREPARATION, ITS USE AND MEDICINES THAT UNDERSTAND THE SAME. |