BRPI0514319A - composto ou sal farmaceuticamente aceitável do mesmo, composição farmacêutica, métodos para reduzir a condutáncia de cálcio de um receptor de capsaicina celular, e para inibir a ligação de ligando de vanilóide a um receptor de capsaicina, método para tratar uma condição respondente a modulação do receptor de capsaicina, dor, coceira, tosse ou soluço e incontinência urinária ou bexiga superativa em um paciente, métodos para promover perda de peso em um paciente obeso, para identificar um agente que liga ao receptor de capsaicina, e para determinar a presença ou ausência de receptor de capsaicina em uma amostra, preparação farmacêutica acondicionada, e, uso do composto ou sal - Google Patents
composto ou sal farmaceuticamente aceitável do mesmo, composição farmacêutica, métodos para reduzir a condutáncia de cálcio de um receptor de capsaicina celular, e para inibir a ligação de ligando de vanilóide a um receptor de capsaicina, método para tratar uma condição respondente a modulação do receptor de capsaicina, dor, coceira, tosse ou soluço e incontinência urinária ou bexiga superativa em um paciente, métodos para promover perda de peso em um paciente obeso, para identificar um agente que liga ao receptor de capsaicina, e para determinar a presença ou ausência de receptor de capsaicina em uma amostra, preparação farmacêutica acondicionada, e, uso do composto ou salInfo
- Publication number
- BRPI0514319A BRPI0514319A BRPI0514319-5A BRPI0514319A BRPI0514319A BR PI0514319 A BRPI0514319 A BR PI0514319A BR PI0514319 A BRPI0514319 A BR PI0514319A BR PI0514319 A BRPI0514319 A BR PI0514319A
- Authority
- BR
- Brazil
- Prior art keywords
- receptor
- capsaicin
- methods
- capsaicin receptor
- compound
- Prior art date
Links
Classifications
-
- 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
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/14—Antitussive agents
-
- 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
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- 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
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
-
- 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
- C07D403/14—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 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
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- 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
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Urology & Nephrology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Diabetes (AREA)
- Obesity (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Hematology (AREA)
- Child & Adolescent Psychology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
COMPOSTO OU SAL FARMACEUTICAMENTE ACEITáVEL DO MESMO COMPOSIçãO FARMACêUTICA MéTODOS PARA REDUZIR A CONDUTáNCIA DE CáLCIO DE UM RECEPTOR DE CAPSAICINA CELULAR, E PARA INIBIR A LIGAçãO DE LIGANDO DE VANILóIDE A UM RECEPTOR DE CAPSAICINA, MéTODO PARA TRATAR UMA CONDIçãO RESPONDENTE A MODULAçãO DO RECEPTOR DE CAPSAICINA, DOR, COCEIRA, TOSSE OU SOLUçO E INCONTINêNCIA URINáRIA OU BEXIGA SUPERATIVA EM UM PACIENTE, MéTODOS PARA PROMOVER PERDA DE PESO EM UM PACIENTE OBESO, PARA IDENTIFICAR UM AGENTE QUE LIGA AO RECEPTOR DE CAPSAICINA, E PARA DETERMINAR A PRESENçA OU AUSêNCIA DE RECEPTOR DE CAPSAICINA EM UMA AMOSTRA, PREPARAçãO FARMACêUTICA ACONDICIONADA, E, USO DO COMPOSTO OU SAL Análogos de biaril piperazinil-piridina substituídos são providos de fórmula (I): em que as variáveis são como aqui descritas. Estes compostos são ligandos que podem ser usados para modular a atividade de receptor específica in vivo ou in vitro, e são particularmente utilizáveis no tratamento de condições associadas com a ativação de receptor patológico em humanos, animais de estimação domesticados e animais de criação. As composições farmacêuticas e métodos para usar estes compostos para tratar estes distúrbios são providos, assim como os métodos para usar estes ligandos para os estudos de localização de receptor.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US60172104P | 2004-08-13 | 2004-08-13 | |
US64179605P | 2005-01-05 | 2005-01-05 | |
PCT/US2005/028969 WO2006026135A2 (en) | 2004-08-13 | 2005-08-13 | Substituted biaryl piperazinyl-pyridine analogues |
Publications (1)
Publication Number | Publication Date |
---|---|
BRPI0514319A true BRPI0514319A (pt) | 2008-06-10 |
Family
ID=36000525
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BRPI0514319-5A BRPI0514319A (pt) | 2004-08-13 | 2005-08-13 | composto ou sal farmaceuticamente aceitável do mesmo, composição farmacêutica, métodos para reduzir a condutáncia de cálcio de um receptor de capsaicina celular, e para inibir a ligação de ligando de vanilóide a um receptor de capsaicina, método para tratar uma condição respondente a modulação do receptor de capsaicina, dor, coceira, tosse ou soluço e incontinência urinária ou bexiga superativa em um paciente, métodos para promover perda de peso em um paciente obeso, para identificar um agente que liga ao receptor de capsaicina, e para determinar a presença ou ausência de receptor de capsaicina em uma amostra, preparação farmacêutica acondicionada, e, uso do composto ou sal |
Country Status (24)
Country | Link |
---|---|
US (2) | US7662830B2 (pt) |
EP (1) | EP1786800B1 (pt) |
JP (1) | JP4955554B2 (pt) |
KR (1) | KR20070046924A (pt) |
CN (1) | CN101014587B (pt) |
AR (1) | AR050194A1 (pt) |
BR (1) | BRPI0514319A (pt) |
CA (1) | CA2577301C (pt) |
CR (1) | CR8992A (pt) |
EC (1) | ECSP077318A (pt) |
HN (1) | HN2007006799A (pt) |
IL (1) | IL181040A0 (pt) |
MA (1) | MA28857B1 (pt) |
MX (1) | MX2007001696A (pt) |
MY (1) | MY145822A (pt) |
NI (1) | NI200700040A (pt) |
NO (1) | NO20071243L (pt) |
NZ (1) | NZ553388A (pt) |
PE (1) | PE20060620A1 (pt) |
RU (1) | RU2413726C2 (pt) |
SG (1) | SG157399A1 (pt) |
TW (1) | TW200605889A (pt) |
WO (1) | WO2006026135A2 (pt) |
ZA (1) | ZA200701530B (pt) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003018563A1 (en) | 2001-08-31 | 2003-03-06 | Northwestern University | Anti-inflammatory and protein kinase inhibitor composition and method of use |
WO2005007648A2 (en) * | 2003-07-16 | 2005-01-27 | Neurogen Corporation | Biaryl piperazinyl-pyridine analogues |
MY145822A (en) * | 2004-08-13 | 2012-04-30 | Neurogen Corp | Substituted biaryl piperazinyl-pyridine analogues |
WO2006050389A2 (en) | 2004-11-02 | 2006-05-11 | Northwestern University | Pyridazine compounds, compositions and methods |
CA2589102C (en) | 2004-11-02 | 2013-08-13 | Northwestern University | Pyridazine compounds and methods for using the compounds to treat inflammatory diseases |
JP2008523152A (ja) * | 2004-12-13 | 2008-07-03 | ニューロジェン・コーポレーション | ピペラジニル−ピリジン類縁体 |
US20080124384A1 (en) * | 2005-01-19 | 2008-05-29 | Blum Charles A | Heteroaryl Substituted Piperazinyl-Pyridine Analogues |
AU2007243280A1 (en) | 2006-04-28 | 2007-11-08 | Northwestern University | Formulations containing pyridazine compounds for treating neuroinflammatory diseases |
EP2015750A2 (en) | 2006-04-28 | 2009-01-21 | Northwestern University | Compositions and treatments using pyridazine compounds and cholinesterase inhibitors |
US20080153845A1 (en) * | 2006-10-27 | 2008-06-26 | Redpoint Bio Corporation | Trpv1 antagonists and uses thereof |
ME02123B (me) * | 2007-04-27 | 2014-08-29 | Purdue Pharma Lp | Antagonisti trpv1 i njihova upotreba |
US8343966B2 (en) * | 2008-01-11 | 2013-01-01 | Novartis Ag | Organic compounds |
CA2829558A1 (en) * | 2011-03-09 | 2012-09-13 | Celgene Avilomics Research, Inc. | Pi3 kinase inhibitors and uses thereof |
ES2390326B1 (es) * | 2011-04-05 | 2013-08-14 | Universidad Miguel Hernández De Elche | Antagonistas de trpv1 y sus usos. |
EP2771337B1 (en) | 2011-09-27 | 2017-08-02 | Novartis AG | 3-(pyrimidin-4-yl)-oxazolidin-2-ones as inhibitors of mutant idh |
JP6129199B2 (ja) * | 2011-12-02 | 2017-05-17 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | ピペリジン誘導体、その医薬組成物及び使用 |
UY34632A (es) | 2012-02-24 | 2013-05-31 | Novartis Ag | Compuestos de oxazolidin- 2- ona y usos de los mismos |
US9296733B2 (en) | 2012-11-12 | 2016-03-29 | Novartis Ag | Oxazolidin-2-one-pyrimidine derivative and use thereof for the treatment of conditions, diseases and disorders dependent upon PI3 kinases |
JP6387360B2 (ja) | 2013-03-14 | 2018-09-05 | ノバルティス アーゲー | 変異idhの阻害薬としての3−ピリミジン−4−イル−オキサゾリジン−2−オン |
JP6397912B2 (ja) | 2013-07-30 | 2018-09-26 | ヤンセン・サイエンシズ・アイルランド・ユーシー | Rsv抗ウイルス化合物としての置換ピリジンピペラジニルアナログ |
CN115060832B (zh) * | 2022-08-18 | 2022-11-29 | 上海奥科达生物医药科技有限公司 | 奥卡西平口服混悬液中奥卡西平及防腐剂含量检测方法 |
Family Cites Families (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4921148B1 (pt) * | 1970-12-28 | 1974-05-30 | ||
US3775326A (en) | 1972-04-17 | 1973-11-27 | Addressograph Multigraph | Pressure fixable electroscopic printing powder |
FR2262512A1 (en) | 1974-03-01 | 1975-09-26 | Synthelabo | 2,4,6-Tri-substd. -1,3,5-triazines - with analgesic and psychotropic activity |
DE2643753A1 (de) * | 1976-09-29 | 1978-04-06 | Thomae Gmbh Dr K | Neue 1h-pyrazolo eckige klammer auf 3,4-b eckige klammer zu pyridine |
FI70411C (fi) * | 1980-12-29 | 1986-09-19 | Pfizer | Foerfarande foer framstaellning av nya antihypertensiva 4-amino-6,7-dimetoxi-2-piperazinokinazolin derivat |
DE3609596A1 (de) * | 1986-03-21 | 1987-10-01 | Hoechst Ag | 2-azolylmethyl-2-aryl-1,3-dioxolane und deren salze, verfahren zu ihrer herstellung, sie enthaltende mittel und ihre verwendung |
GB9012311D0 (en) | 1990-06-01 | 1990-07-18 | Wellcome Found | Pharmacologically active cns compounds |
AU8405991A (en) * | 1990-08-31 | 1992-03-30 | Nippon Shinyaku Co. Ltd. | Pyrimidine derivative and medicine |
BR9508539A (pt) | 1994-08-08 | 1997-10-28 | Nippon Shinyaku Co Ltd | Derivado de triazina e medicamento |
US5962453A (en) * | 1995-08-08 | 1999-10-05 | Nippon Shinyaku Co. Ltd. | Triazine derivative and medicine |
TW520362B (en) | 1996-12-05 | 2003-02-11 | Amgen Inc | Substituted pyrimidine compounds and pharmaceutical composition comprising same |
EP1087963B1 (en) * | 1998-06-19 | 2004-08-25 | Chiron Corporation | Inhibitors of glycogen synthase kinase 3 |
DE19836697A1 (de) | 1998-08-13 | 2000-02-17 | Hoechst Marion Roussel De Gmbh | Substituierte 4-Amino-2-aryl-pyrimidine, ihre Herstellung, ihre Verwendung und sie enthaltende pharmazeutische Präparate |
CZ20013465A3 (cs) * | 1999-04-01 | 2002-10-16 | Pfizer Products Inc. | Aminopyrimidiny jako inhibitory sorbitoldehydrogenasy |
AU2001262150A1 (en) | 2000-03-23 | 2001-10-03 | Mitsubishi Pharma Corporation | 2-(nitrogen-heterocyclic)pyrimidone derivatives |
EP1136483A1 (en) | 2000-03-23 | 2001-09-26 | Sanofi-Synthelabo | 2-[Piperazinyl]pyrimidone derivatives |
JP2004502681A (ja) * | 2000-06-29 | 2004-01-29 | アボット・ラボラトリーズ | アリールフェニル複素環スルフィド誘導体および細胞接着を阻止する抗炎症性および免疫抑制性物質としてのその使用 |
AU8066701A (en) | 2000-07-20 | 2002-02-05 | Neurogen Corp | Capsaicin receptor ligands |
US6710058B2 (en) * | 2000-11-06 | 2004-03-23 | Bristol-Myers Squibb Pharma Company | Monocyclic or bicyclic carbocycles and heterocycles as factor Xa inhibitors |
EP1247809A3 (en) * | 2001-03-30 | 2003-12-17 | Pfizer Products Inc. | Triazine compounds useful as sorbitol dehydrogenase inhibitors |
ES2332505T3 (es) * | 2001-06-01 | 2010-02-08 | F. Hoffmann-La Roche Ag | Derivados de pirimidina, triazina y pirazina como receptores de glutamato. |
WO2004000820A2 (en) | 2002-06-21 | 2003-12-31 | Cellular Genomics, Inc. | Certain aromatic monocycles as kinase modulators |
US7423148B2 (en) * | 2002-11-21 | 2008-09-09 | Chiron Corporation | Small molecule PI 3-kinase inhibitors and methods of their use |
EP1651636A1 (en) * | 2003-07-10 | 2006-05-03 | Neurogen Corporation | Substituted heterocyclic diarylamine analogues |
WO2005007648A2 (en) * | 2003-07-16 | 2005-01-27 | Neurogen Corporation | Biaryl piperazinyl-pyridine analogues |
US20070161637A1 (en) * | 2003-07-22 | 2007-07-12 | Neurogen Corporation | Substituted pyridin-2-ylamine analogues |
MY145822A (en) * | 2004-08-13 | 2012-04-30 | Neurogen Corp | Substituted biaryl piperazinyl-pyridine analogues |
JP2008523152A (ja) | 2004-12-13 | 2008-07-03 | ニューロジェン・コーポレーション | ピペラジニル−ピリジン類縁体 |
US20080124384A1 (en) | 2005-01-19 | 2008-05-29 | Blum Charles A | Heteroaryl Substituted Piperazinyl-Pyridine Analogues |
US8258143B2 (en) * | 2006-06-28 | 2012-09-04 | Duquesne University Of The Holy Ghost | Methods of using substituted pyrrolo[2,3-d]pyrimidines for targeting tumor cells and treating cancer |
-
2005
- 2005-06-22 MY MYPI20052848A patent/MY145822A/en unknown
- 2005-07-01 TW TW094122269A patent/TW200605889A/zh unknown
- 2005-08-02 AR ARP050103213A patent/AR050194A1/es unknown
- 2005-08-11 PE PE2005000929A patent/PE20060620A1/es not_active Application Discontinuation
- 2005-08-13 JP JP2007525874A patent/JP4955554B2/ja not_active Expired - Fee Related
- 2005-08-13 US US11/204,202 patent/US7662830B2/en active Active
- 2005-08-13 NZ NZ553388A patent/NZ553388A/en unknown
- 2005-08-13 RU RU2007106042/04A patent/RU2413726C2/ru not_active IP Right Cessation
- 2005-08-13 EP EP05810146.0A patent/EP1786800B1/en active Active
- 2005-08-13 MX MX2007001696A patent/MX2007001696A/es not_active Application Discontinuation
- 2005-08-13 WO PCT/US2005/028969 patent/WO2006026135A2/en active Application Filing
- 2005-08-13 SG SG200907610-0A patent/SG157399A1/en unknown
- 2005-08-13 CA CA2577301A patent/CA2577301C/en not_active Expired - Fee Related
- 2005-08-13 ZA ZA200701530A patent/ZA200701530B/xx unknown
- 2005-08-13 KR KR1020077005831A patent/KR20070046924A/ko not_active Application Discontinuation
- 2005-08-13 BR BRPI0514319-5A patent/BRPI0514319A/pt not_active IP Right Cessation
- 2005-08-13 CN CN2005800275501A patent/CN101014587B/zh not_active Expired - Fee Related
-
2007
- 2007-01-29 IL IL181040A patent/IL181040A0/en unknown
- 2007-02-09 NI NI200700040A patent/NI200700040A/es unknown
- 2007-02-23 HN HN2007006799A patent/HN2007006799A/es unknown
- 2007-03-07 NO NO20071243A patent/NO20071243L/no not_active Application Discontinuation
- 2007-03-13 MA MA29749A patent/MA28857B1/fr unknown
- 2007-03-13 CR CR8992A patent/CR8992A/es not_active Application Discontinuation
- 2007-03-13 EC EC2007007318A patent/ECSP077318A/es unknown
-
2010
- 2010-02-15 US US12/705,964 patent/US8334382B2/en active Active
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
BRPI0514319A (pt) | composto ou sal farmaceuticamente aceitável do mesmo, composição farmacêutica, métodos para reduzir a condutáncia de cálcio de um receptor de capsaicina celular, e para inibir a ligação de ligando de vanilóide a um receptor de capsaicina, método para tratar uma condição respondente a modulação do receptor de capsaicina, dor, coceira, tosse ou soluço e incontinência urinária ou bexiga superativa em um paciente, métodos para promover perda de peso em um paciente obeso, para identificar um agente que liga ao receptor de capsaicina, e para determinar a presença ou ausência de receptor de capsaicina em uma amostra, preparação farmacêutica acondicionada, e, uso do composto ou sal | |
BR0317168A (pt) | Composto ou uma forma farmaceuticamente aceitável do mesmo, composição farmacêutica, métodos de reduzir condutância de cálcio de um receptor de capsaicina celular, e de inibir ligação de ligante vanilóide a um receptor de capsaicina, métodos de tratar uma condição responsiva à modulação de receptor de capsaicina, dor, coceira, tosse ou soluços, incontinência urinária, de promover perda de peso em paciente, e de determinar a presença ou ausência de receptor de capsaicina em uma amostra, preparação farmacêutica embalada, e, uso de um composto | |
BR0306982A (pt) | Composto ou um sal deste farmaceuticamente aceitável, composição farmacêutica, métodos para reduzir a condutância de cálcio de um receptor da capsaicina celular, para inibir a ligação de ligando vanilóide a um receptor da capsaicina in vitro e em um paciente, para tratar uma condição responsiva à modulação do receptor da capsaicina em um paciente, para tratar a dor em um paciente, para tratar coceira em um paciente, para tratar tosse ou soluço em um paciente, promover a perda de peso em um paciente obeso, e para determinar a presença ou ausência de receptor da capsaicina em uma amostra, preparação farmacêutica embalada, e, uso de um composto | |
MXPA03010612A (es) | Ligandos receptores de la hormona concentradora de melanina: analogos de 1-bencil-4-aril piperazina substiruidos. | |
WO2006078992A3 (en) | Heteroaryl substituted piperazinyl-pyridine analogues | |
TW200716594A (en) | Substituted heteroaryl CB1 antagonists | |
EA200970931A1 (ru) | Аналоги гетероариламидов | |
MY150731A (en) | Heteroaryl amide derivatives | |
WO2007140383A3 (en) | Spirocyclic sulfonamides and related compounds | |
PH12014501677A1 (en) | 5-membered heterocyclic amides and related compounds | |
WO2006076646A3 (en) | Heteroaryl substituted quinolin-4-ylamine analogues | |
WO2004056774A3 (en) | Substituted biphenyl-4-carboxylic acid arylamide analogues as capsaicin receptor modulators | |
WO2007101007A3 (en) | Aryl sulfonyl heterocycles | |
TW200510373A (en) | Substituted quinolin-4-ylamine analogues | |
WO2006081388A3 (en) | Substituted pyridazinyl-and pyrimidinyl-quinolin-4-ylamine analogues | |
WO2005110982A3 (en) | Substituted 1-benzyl-4-substituted piperazine analogues | |
TW200609219A (en) | Aryl-substituted piperazine derivatives | |
WO2008024433A3 (en) | Haloalkyl-substituted pyrimidinone derivatives | |
WO2008033739A3 (en) | Benzimidazole carboxamide derivatives | |
WO2006052542A3 (en) | Arylalkyl ureas as cb1 antagonists | |
WO2008066664A3 (en) | Cis-cyclohexyl substituted pyrimidinone derivatives | |
TW200621251A (en) | Substituted biaryl quinolin-4-ylamine analogues | |
WO2005084401A3 (en) | Aryl substituted purine analogues | |
WO2005084368A3 (en) | Heteroalkyl-substituted biphenyl-4-carboxylic acid arylamide analogues | |
WO2006071538A3 (en) | Substituted biaryl analogues |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
B08F | Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette] |
Free format text: REFERENTE A 7A ANUIDADE. |
|
B08K | Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette] |
Free format text: NAO APRESENTADA A GUIA DE CUMPRIMENTO DE EXIGENCIA. REFERENTE A 7A ANUIDADE. |