BRPI0517232A - composto ou um sal farmaceuticamente aceitável do mesmo, composição farmacêutica, ativador da glicocinase, e, agentes terapêuticos e/ou profiláticos para diabetes e para obesidade - Google Patents
composto ou um sal farmaceuticamente aceitável do mesmo, composição farmacêutica, ativador da glicocinase, e, agentes terapêuticos e/ou profiláticos para diabetes e para obesidadeInfo
- Publication number
- BRPI0517232A BRPI0517232A BRPI0517232-2A BRPI0517232A BRPI0517232A BR PI0517232 A BRPI0517232 A BR PI0517232A BR PI0517232 A BRPI0517232 A BR PI0517232A BR PI0517232 A BRPI0517232 A BR PI0517232A
- Authority
- BR
- Brazil
- Prior art keywords
- obesity
- diabetes
- pharmaceutically acceptable
- therapeutic
- hydrogen
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/22—Hormones
- A61K38/31—Somatostatins
-
- 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
- A61K31/13—Amines
- A61K31/155—Amidines (), e.g. guanidine (H2N—C(=NH)—NH2), isourea (N=C(OH)—NH2), isothiourea (—N=C(SH)—NH2)
-
- 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
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- 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
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- 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
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/22—Hormones
- A61K38/28—Insulins
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
- A61P3/08—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
-
- 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
- C07D401/14—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
- 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
- C07D413/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
Abstract
COMPOSTO OU UM SAL FARMACEUTICAMENTE ACEITáVEL DO MESMO, COMPOSIçãO FARMACêUTICA, ATIVADOR DA GLICOCINASE, E, AGENTES TERAPêUTICOS E/OU PROFILáTICOS PARA DIABETES E PARA OBESIDADE. Compostos representados pela fórmula geral (I), ou seus sais farmaceuticamente aceitáveis, que têm atividade ativadora da glicocinase e são úteis como agentes terapêuticos para diabetes e obesidade: em que R¬ 1¬ e R¬ 2¬ são cada um hidrogênio ou similar; R¬ 3¬ é hidrogênio, halogênio ou similar; R¬ 4¬ é hidrogênio, alquila inferior ou similar; Q é um carbono, nitrogênio ou átomo de enxofre (com a condição de que o átomo de enxofre possa ser mono ou di-substituído por oxo); R¬ 5¬ e R¬ 6¬ são cada um hidrogênio, alquila inferior, ou similar; X, X, X e X¬ 4¬ são, cada um independentemente, carbono ou nitrogênio; Z é oxigênio, enxofre ou nitrogênio; Ar é arila ou heteroarila; A é um grupo heterocíclico aromático nitrogenoso de 5 ou 6 membros; m é um inteiro de 1 a 6; n é um inteiro de 0 a 3; p é um inteiro de 0 a 2 (com a condição de que pelo menos dois de X a X¬ 4¬ sejam cada um carbono); e q é 0 ou 1.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004319339 | 2004-11-02 | ||
JP2005178628 | 2005-06-17 | ||
PCT/JP2005/020483 WO2006049304A1 (ja) | 2004-11-02 | 2005-11-01 | アリールオキシ置換ベンズイミダゾール誘導体 |
Publications (1)
Publication Number | Publication Date |
---|---|
BRPI0517232A true BRPI0517232A (pt) | 2008-10-07 |
Family
ID=36319300
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BRPI0517232-2A BRPI0517232A (pt) | 2004-11-02 | 2005-11-01 | composto ou um sal farmaceuticamente aceitável do mesmo, composição farmacêutica, ativador da glicocinase, e, agentes terapêuticos e/ou profiláticos para diabetes e para obesidade |
Country Status (17)
Country | Link |
---|---|
US (1) | US7932394B2 (pt) |
EP (1) | EP1810969B1 (pt) |
JP (1) | JP5036316B2 (pt) |
KR (1) | KR20070083939A (pt) |
CN (1) | CN101094847B (pt) |
AU (1) | AU2005301608B2 (pt) |
BR (1) | BRPI0517232A (pt) |
CA (1) | CA2586056C (pt) |
CR (1) | CR9078A (pt) |
EC (1) | ECSP077422A (pt) |
IL (1) | IL182679A0 (pt) |
MA (1) | MA29043B1 (pt) |
MX (1) | MX2007005289A (pt) |
NO (1) | NO20072806L (pt) |
NZ (1) | NZ554440A (pt) |
RU (1) | RU2398773C2 (pt) |
WO (1) | WO2006049304A1 (pt) |
Families Citing this family (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20060105872A (ko) * | 2003-12-29 | 2006-10-11 | 반유 세이야꾸 가부시끼가이샤 | 신규한 2-헤테로아릴 치환된 벤즈이미다졸 유도체 |
AU2006267338B2 (en) * | 2005-07-13 | 2012-08-16 | Msd K.K. | Heterocycle-substituted benzimidazole derivative |
US20080293775A1 (en) * | 2005-12-15 | 2008-11-27 | Astrazeneca Ab | Substituted Diphenylethers, -Amines, -Sulfides and -Methanes for the Treatment of Respiratory Disease |
PE20080251A1 (es) | 2006-05-04 | 2008-04-25 | Boehringer Ingelheim Int | Usos de inhibidores de dpp iv |
ATE523507T1 (de) | 2007-01-04 | 2011-09-15 | Prosidion Ltd | Piperidin-gpcr-agonisten |
US8242140B2 (en) | 2007-08-03 | 2012-08-14 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
EP2221301B1 (en) | 2007-11-12 | 2014-06-04 | Msd K.K. | Heteroaryloxy quinazoline derivative |
US8476257B2 (en) | 2007-12-19 | 2013-07-02 | Boehringer Ingelheim International Gmbh | Viral polymerase inhibitors |
CN101896483B (zh) | 2007-12-20 | 2013-11-20 | 株式会社Lg生命科学 | 葡糖激酶激活剂和包含其作为活性成分的药物组合物 |
US8592428B2 (en) | 2008-08-15 | 2013-11-26 | Msd K. K. | Acetyl pyrrolidinyl indole derivative |
CA2734981A1 (en) * | 2008-08-29 | 2010-03-04 | Banyu Pharmaceutical Co., Ltd. | Oxotetrahydrofuran-2-yl-benzimidazole derivative |
CN101607923B (zh) * | 2009-07-21 | 2012-12-19 | 焦宁 | 芳基腈类化合物或其衍生物及其合成方法和应用 |
SG10201509157QA (en) * | 2010-11-09 | 2015-12-30 | Fujian Haixi Pharmaceuticals Inc | Compound for increasing kinase active and application thereof |
US20120258891A1 (en) | 2011-04-07 | 2012-10-11 | Nimblegen Systems Gmbh | Diarylsulfide backbone containing photolabile protecting groups |
WO2015161016A1 (en) * | 2014-04-17 | 2015-10-22 | Merck Sharp & Dohme Corp. | Bicyclic cgrp receptor antagonists |
AR106728A1 (es) * | 2015-11-17 | 2018-02-14 | Viamet Pharmaceuticals Inc | 4-((6-(2-(2,4difluorofenil)-1,1-difluoro-2-hidroxi-3-(1h-1,2,4-triazol-1-il)propil)piridin-3-il)oxi)benzonitrilo y proceso para su preparación |
AR106729A1 (es) * | 2015-11-17 | 2018-02-14 | Viamet Pharmaceuticals Inc | 4-((6-(2-(2,4-difluorofenil)-1,1-difluoro-2-oxoetil)piridin-3-il)oxi)benzonitrilo y proceso para su preparación |
AR106731A1 (es) * | 2015-11-17 | 2018-02-14 | Viamet Pharmaceuticals Inc | 4-((6-(2-(2,4-difluorofenil)-1,1-difluoro-2-hidroxi-3-(1h-1,2,4-triazol-1-il)propil)piridin-3-il)oxi)benzonitrilo y proceso para su preparación |
CA3049728A1 (en) * | 2017-01-10 | 2018-07-19 | Eth Zurich | Inhibitors of g-protein-coupled receptor kinase 2 and their use |
EP4367112A1 (en) | 2021-07-09 | 2024-05-15 | Plexium, Inc. | Aryl compounds and pharmaceutical compositions that modulate ikzf2 |
WO2024033677A1 (en) * | 2022-08-09 | 2024-02-15 | Faculdade De Farmácia Da Universidade De Lisboa | One-pot method for the synthesis of 3-acetamido-furfural from n-acetylglucosamine |
JP7356203B1 (ja) | 2023-08-03 | 2023-10-04 | Towa Corporation 株式会社 | WD and tetratricopeptide repeats 1遺伝子発現亢進用医薬組成物及び食品組成物 |
Family Cites Families (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3536809A (en) | 1969-02-17 | 1970-10-27 | Alza Corp | Medication method |
US3598123A (en) | 1969-04-01 | 1971-08-10 | Alza Corp | Bandage for administering drugs |
US3630200A (en) | 1969-06-09 | 1971-12-28 | Alza Corp | Ocular insert |
US3845770A (en) | 1972-06-05 | 1974-11-05 | Alza Corp | Osmatic dispensing device for releasing beneficial agent |
US3916899A (en) | 1973-04-25 | 1975-11-04 | Alza Corp | Osmotic dispensing device with maximum and minimum sizes for the passageway |
US4008719A (en) | 1976-02-02 | 1977-02-22 | Alza Corporation | Osmotic system having laminar arrangement for programming delivery of active agent |
DK337086A (da) * | 1985-08-12 | 1987-02-13 | Hoffmann La Roche | Benzimidazolderivater |
IL102183A (en) | 1991-06-27 | 1999-11-30 | Takeda Chemical Industries Ltd | The heterocyclic compounds are converted into biphenyl groups, their production and the pharmaceutical compositions containing them |
US5349045A (en) | 1993-01-26 | 1994-09-20 | United States Surgical Corporation | Polymer derived from cyclic amide and medical devices manufactured therefrom |
PE92198A1 (es) | 1996-08-01 | 1999-01-09 | Banyu Pharma Co Ltd | Derivados de 1,4-piperidina disustituida que contienen fluor |
US20020032330A1 (en) | 1996-12-24 | 2002-03-14 | Yutaka Nomura | Propionic acid derivatives |
JPH10306076A (ja) | 1997-03-06 | 1998-11-17 | Nippon Chemiphar Co Ltd | プロピオン酸誘導体 |
US6162804A (en) * | 1997-09-26 | 2000-12-19 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
EP1415987B1 (en) | 2000-10-20 | 2007-02-28 | Eisai R&D Management Co., Ltd. | Nitrogenous aromatic ring compounds as anti cancer agents |
US6433188B1 (en) | 2000-12-06 | 2002-08-13 | Wendy Lea Corbett | Fused heteroaromatic glucokinase activators |
PT1341774E (pt) * | 2000-12-06 | 2006-05-31 | Hoffmann La Roche | Activadores heteroaromaticos, fundidos de glicocinase |
WO2003011836A1 (en) | 2001-08-01 | 2003-02-13 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
AU2003254795A1 (en) | 2002-08-02 | 2004-02-23 | Sankyo Company, Limited | Resorcinol derivative |
JP2004123711A (ja) | 2002-08-02 | 2004-04-22 | Sankyo Co Ltd | レゾルシノール誘導体 |
JP2004067629A (ja) | 2002-08-09 | 2004-03-04 | Yamanouchi Pharmaceut Co Ltd | ミトコンドリア機能活性化剤及び新規なベンゾイミダゾール誘導体 |
NZ540791A (en) | 2003-02-13 | 2009-09-25 | Banyu Pharma Co Ltd | Novel 2-pyridinecarboxamide derivatives |
KR20060105872A (ko) | 2003-12-29 | 2006-10-11 | 반유 세이야꾸 가부시끼가이샤 | 신규한 2-헤테로아릴 치환된 벤즈이미다졸 유도체 |
-
2005
- 2005-11-01 KR KR1020077010065A patent/KR20070083939A/ko not_active Application Discontinuation
- 2005-11-01 NZ NZ554440A patent/NZ554440A/en not_active IP Right Cessation
- 2005-11-01 JP JP2006542472A patent/JP5036316B2/ja not_active Expired - Fee Related
- 2005-11-01 WO PCT/JP2005/020483 patent/WO2006049304A1/ja active Application Filing
- 2005-11-01 CA CA2586056A patent/CA2586056C/en not_active Expired - Fee Related
- 2005-11-01 MX MX2007005289A patent/MX2007005289A/es active IP Right Grant
- 2005-11-01 AU AU2005301608A patent/AU2005301608B2/en not_active Ceased
- 2005-11-01 BR BRPI0517232-2A patent/BRPI0517232A/pt not_active IP Right Cessation
- 2005-11-01 US US11/666,555 patent/US7932394B2/en active Active
- 2005-11-01 CN CN2005800456884A patent/CN101094847B/zh not_active Expired - Fee Related
- 2005-11-01 RU RU2007120519/04A patent/RU2398773C2/ru not_active IP Right Cessation
- 2005-11-01 EP EP05803447.1A patent/EP1810969B1/en active Active
-
2007
- 2007-04-19 IL IL182679A patent/IL182679A0/en unknown
- 2007-04-20 CR CR9078A patent/CR9078A/es not_active Application Discontinuation
- 2007-04-27 EC EC2007007422A patent/ECSP077422A/es unknown
- 2007-05-28 MA MA29946A patent/MA29043B1/fr unknown
- 2007-06-01 NO NO20072806A patent/NO20072806L/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
IL182679A0 (en) | 2007-09-20 |
MX2007005289A (es) | 2007-07-19 |
CN101094847A (zh) | 2007-12-26 |
RU2007120519A (ru) | 2008-12-10 |
NO20072806L (no) | 2007-07-27 |
EP1810969A1 (en) | 2007-07-25 |
US7932394B2 (en) | 2011-04-26 |
CR9078A (es) | 2007-10-01 |
WO2006049304A1 (ja) | 2006-05-11 |
EP1810969A4 (en) | 2011-05-25 |
RU2398773C2 (ru) | 2010-09-10 |
AU2005301608A1 (en) | 2006-05-11 |
US20080125429A1 (en) | 2008-05-29 |
EP1810969B1 (en) | 2013-08-07 |
JP5036316B2 (ja) | 2012-09-26 |
MA29043B1 (fr) | 2007-11-01 |
KR20070083939A (ko) | 2007-08-24 |
CA2586056C (en) | 2012-03-13 |
NZ554440A (en) | 2010-01-29 |
CN101094847B (zh) | 2011-06-15 |
AU2005301608B2 (en) | 2012-09-13 |
ECSP077422A (es) | 2007-05-30 |
CA2586056A1 (en) | 2006-05-11 |
JPWO2006049304A1 (ja) | 2008-05-29 |
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