BR0315681A - Composto e seus sais e hidratos farmaceuticamente aceitáveis, composição farmacêutica, métodos para o tratamento de doenças mediadas pela prostaglandina d2, para o tratamento de congestão nasal, para o tratamento de asma alérgica, e para o tratamento de rinite alérgica, composto ou um seu sal ou solvato farmaceuticamente aceitável, sal ou hidrato do composto, e, uso de um composto ou de um seu sal ou solvato farmaceuticamente aceitável - Google Patents
Composto e seus sais e hidratos farmaceuticamente aceitáveis, composição farmacêutica, métodos para o tratamento de doenças mediadas pela prostaglandina d2, para o tratamento de congestão nasal, para o tratamento de asma alérgica, e para o tratamento de rinite alérgica, composto ou um seu sal ou solvato farmaceuticamente aceitável, sal ou hidrato do composto, e, uso de um composto ou de um seu sal ou solvato farmaceuticamente aceitávelInfo
- Publication number
- BR0315681A BR0315681A BR0315681-8A BR0315681A BR0315681A BR 0315681 A BR0315681 A BR 0315681A BR 0315681 A BR0315681 A BR 0315681A BR 0315681 A BR0315681 A BR 0315681A
- Authority
- BR
- Brazil
- Prior art keywords
- compound
- pharmaceutically acceptable
- salt
- treating
- solvate
- Prior art date
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
- C07D471/14—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4375—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
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- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P11/02—Nasal agents, e.g. decongestants
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
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- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Physical Education & Sports Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Rheumatology (AREA)
- Pulmonology (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pain & Pain Management (AREA)
- Ophthalmology & Optometry (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pregnancy & Childbirth (AREA)
- Diabetes (AREA)
- Gynecology & Obstetrics (AREA)
- Biomedical Technology (AREA)
- Anesthesiology (AREA)
- Vascular Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Transplantation (AREA)
- Hematology (AREA)
- Urology & Nephrology (AREA)
- Otolaryngology (AREA)
- Oncology (AREA)
Abstract
"COMPOSTO E SEUS SAIS E HIDRATOS FARMACEUTICAMENTE ACEITáVEIS, COMPOSIçãO FARMACêUTICA, MéTODOS PARA O TRATAMENTO DE DOENçAS MEDIADAS PELA PROSTAGLANDINA D2, PARA O TRATAMENTO DE CONGESTãO NASAL, PARA O TRATAMENTO DE ASMA ALéRGICA E PARA O TRATAMENTO DE RINITE ALéRGICA COMPOSTO OU UM SEU SAL OU SOLVATO FARMACEUTICAMENTE ACEITáVEL, SAL OU HIDRATO DO COMPOSTO, E, USO DE UM COMPOSTO OU DE UM SEU SAL OU SOLVATO FARMACEUTICAMENTE ACEITáVEL". Os derivados de piridopirrolizina e de piridoindolizina são antagonistas do receptor da prostaglandina úteis para o tratamento de doenças mediadas pela prostaglandina, tais como as rinites alérgicas, a congestão nasal e a asma.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US42244302P | 2002-10-30 | 2002-10-30 | |
US48262603P | 2003-06-26 | 2003-06-26 | |
PCT/CA2003/001658 WO2004039807A1 (en) | 2002-10-30 | 2003-10-28 | Pyridopyrrolizine and pyridoindolizine derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
BR0315681A true BR0315681A (pt) | 2005-09-06 |
Family
ID=32233493
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BR0315681-8A BR0315681A (pt) | 2002-10-30 | 2003-10-28 | Composto e seus sais e hidratos farmaceuticamente aceitáveis, composição farmacêutica, métodos para o tratamento de doenças mediadas pela prostaglandina d2, para o tratamento de congestão nasal, para o tratamento de asma alérgica, e para o tratamento de rinite alérgica, composto ou um seu sal ou solvato farmaceuticamente aceitável, sal ou hidrato do composto, e, uso de um composto ou de um seu sal ou solvato farmaceuticamente aceitável |
Country Status (15)
Country | Link |
---|---|
US (1) | US7618979B2 (pt) |
EP (1) | EP1558614B1 (pt) |
JP (1) | JP4332151B2 (pt) |
KR (1) | KR20050084890A (pt) |
AT (1) | ATE479686T1 (pt) |
AU (1) | AU2003275868B2 (pt) |
BR (1) | BR0315681A (pt) |
CA (1) | CA2503767C (pt) |
DE (1) | DE60334015D1 (pt) |
MX (1) | MXPA05004715A (pt) |
NO (1) | NO20052591L (pt) |
NZ (1) | NZ539406A (pt) |
PL (1) | PL376440A1 (pt) |
RU (1) | RU2342386C2 (pt) |
WO (1) | WO2004039807A1 (pt) |
Families Citing this family (44)
Publication number | Priority date | Publication date | Assignee | Title |
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BRPI0410445B1 (pt) * | 2003-05-21 | 2017-11-28 | Prosidion Limited | Pyrrolopyridine-2-carboxylic acid amide inhibitor compound of glycogen phosphorylase, pharmaceutical composition comprising the same, process for its production and intermediate compounds |
US7405210B2 (en) | 2003-05-21 | 2008-07-29 | Osi Pharmaceuticals, Inc. | Pyrrolopyridine-2-carboxylic acid amide inhibitors of glycogen phosphorylase |
DK1725553T3 (da) | 2004-03-11 | 2008-08-18 | Actelion Pharmaceuticals Ltd | Tetrahydropyridoindolderivater |
GB0412914D0 (en) * | 2004-06-10 | 2004-07-14 | Oxagen Ltd | Compounds |
AU2005318372A1 (en) | 2004-12-23 | 2006-06-29 | Glaxo Group Limited | Pyridine compounds for the treatment of prostaglandin mediated diseases |
BRPI0519280A2 (pt) | 2004-12-27 | 2009-01-06 | Actelion Pharmaceuticals Ltd | composto, composiÇço farmacÊutica e uso de um composto |
GB0500604D0 (en) * | 2005-01-13 | 2005-02-16 | Astrazeneca Ab | Novel process |
EP1916245B1 (en) | 2005-07-22 | 2011-10-26 | Shionogi & Co., Ltd. | Indole derivative having pgd2 receptor antagonist activity |
WO2007010965A1 (ja) * | 2005-07-22 | 2007-01-25 | Shionogi & Co., Ltd. | Pgd2受容体アンタゴニスト活性を有するアザインドール酸誘導体 |
JP5147401B2 (ja) | 2005-09-06 | 2013-02-20 | 塩野義製薬株式会社 | Pgd2受容体アンタゴニスト活性を有するインドールカルボン酸誘導体 |
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EP2197438B1 (en) * | 2007-10-10 | 2015-07-15 | Cspc Zhongqi Pharmaceutical Technology (Shijiazhuang) Co., Ltd. | Heterocyclic compounds as crth2 receptor antagonists |
EP2245002A4 (en) * | 2008-02-01 | 2011-08-17 | Amira Pharmaceuticals Inc | AMINOALKYLBIPHENYL ANTAGONISTS N, N 'DISUBSTITUTED FROM D2 RECEPTORS OF PROSTAGLANDIN |
CA2713139C (en) * | 2008-02-01 | 2013-04-23 | Amira Pharmaceuticals, Inc. | N,n-disubstituted aminoalkylbiphenyl antagonists of prostaglandin d2 receptors |
WO2009102893A2 (en) * | 2008-02-14 | 2009-08-20 | Amira Pharmaceuticals, Inc. | CYCLIC DIARYL ETHER COMPOUNDS AS ANTAGONISTS OF PROSTAGLANDIN D2 receptors |
JP2011513242A (ja) * | 2008-02-25 | 2011-04-28 | アミラ ファーマシューティカルズ,インク. | プロスタグランジンd2受容体アンタゴニスト |
JP2011518130A (ja) * | 2008-04-02 | 2011-06-23 | アミラ ファーマシューティカルズ,インク. | プロスタグランジンd2受容体のアミノアルキルフェニルアンタゴニスト |
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EP2149554A1 (de) | 2008-07-30 | 2010-02-03 | Bayer Schering Pharma Aktiengesellschaft | Indolylamide als Modulatoren des EP2-Rezeptors |
EP2149552A1 (de) | 2008-07-30 | 2010-02-03 | Bayer Schering Pharma AG | 5,6 substituierte Benzamid-Derivate als Modulatoren des EP2-Rezeptors |
EP2149551A1 (de) | 2008-07-30 | 2010-02-03 | Bayer Schering Pharma AG | N-(Indol-3-ylalkyl)-(hetero)arylamidderivate als Modulatoren des EP2-Rezeptors |
JP2012502928A (ja) * | 2008-09-22 | 2012-02-02 | メルク カナダ インコーポレイテッド | Crth2受容体アンタゴニストとしてのアザインドール誘導体 |
WO2010031183A1 (en) * | 2008-09-22 | 2010-03-25 | Merck Frosst Canada Ltd. | Indole derivatives as crth2 receptor antagonists |
GB2463788B (en) * | 2008-09-29 | 2010-12-15 | Amira Pharmaceuticals Inc | Heteroaryl antagonists of prostaglandin D2 receptors |
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GB2465062B (en) * | 2008-11-06 | 2011-04-13 | Amira Pharmaceuticals Inc | Cycloalkane(B)azaindole antagonists of prostaglandin D2 receptors |
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US20100173313A1 (en) * | 2009-01-08 | 2010-07-08 | Amira Pharmaceuticals, Inc. | Biomarkers of inflammation |
CA2768492A1 (en) | 2009-07-31 | 2011-02-03 | Panmira Pharmaceuticals, Llc | Ophthalmic pharmaceutical compositions of dp2 receptor antagonists |
CN102596902A (zh) * | 2009-08-05 | 2012-07-18 | 潘米拉制药公司 | Dp2拮抗剂及其用途 |
DE102009049662A1 (de) | 2009-10-13 | 2011-04-14 | Bayer Schering Pharma Aktiengesellschaft | 2,5-Disubstituierte 2H-Indazole als EP2-Rezeptor-Antagonisten |
MX2012007927A (es) | 2010-01-06 | 2012-08-15 | Panmira Pharmaceuticals Llc | Antagonistas de dp2 y usos del mismo. |
SI2558447T1 (sl) | 2010-03-22 | 2015-01-30 | Actelion Pharmaceuticals Ltd. | Derivati 3-(heteroaril-amino)-1,2,3,4-tetrahidro-9h-karbazola in njihova uporaba kot modulatorji prostaglandinskega receptorja d2 |
JP2014510156A (ja) * | 2011-04-07 | 2014-04-24 | ネクスメッド ホールディングス,インコーポレイテッド | レイノー病を治療する方法および組成物 |
BR112013026283A8 (pt) | 2011-04-14 | 2018-01-30 | Actelion Pharmaceuticals Ltd | derivados de ácido 7-(heteroaril-amino)-6,7,8,9-tetrahidropirido[1,2-a]indol acético e seu uso como moduladores do receptor d2 de prostaglandina |
EP2757883B1 (en) | 2011-09-22 | 2021-01-13 | Merck Sharp & Dohme Corp. | Triazolopyridyl compounds as aldosterone synthase inhibitors |
US9351973B2 (en) | 2011-09-22 | 2016-05-31 | Merck Sharp & Dohme Corp. | Pyrazolopyridyl compounds as aldosterone synthase inhibitors |
EP2757882B1 (en) | 2011-09-22 | 2020-11-04 | Merck Sharp & Dohme Corp. | Imidazopyridyl compounds as aldosterone synthase inhibitors |
JP6496246B2 (ja) | 2012-10-05 | 2019-04-03 | メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. | アルドステロンシンターゼインヒビター関連用途としてのインドリン化合物 |
AR099767A1 (es) | 2014-03-17 | 2016-08-17 | Actelion Pharmaceuticals Ltd | Derivados del ácido acético azaindol y su uso como moduladores del receptor de prostaglandina d2 |
CN106103437A (zh) | 2014-03-18 | 2016-11-09 | 埃科特莱茵药品有限公司 | 氮杂吲哚乙酸衍生物及其作为前列腺素d2受体调节剂的用途 |
US10351560B2 (en) | 2015-09-15 | 2019-07-16 | Idorsia Pharmaceuticals Ltd | Crystalline forms |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
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CA1241660A (en) * | 1984-06-25 | 1988-09-06 | Yvan Guindon | Indole-2-alkanoic acids |
US4808608A (en) | 1986-01-23 | 1989-02-28 | Merck & Co., Inc. | Tetrahydrocarbazole 1-alkanoic acids, pharmaceutical compositions and use |
TW197442B (pt) | 1990-02-08 | 1993-01-01 | Pfizer | |
US5128364A (en) * | 1991-03-28 | 1992-07-07 | Merck Frosst Canada, Inc. | Pyrrolo[1,2-a]indole hydroxylamine derivatives as inhibitors of leukotriene biosynthesis |
CA2225250C (en) | 1995-06-21 | 2005-03-22 | Shionogi & Co., Ltd. | Bicyclic amino derivatives and pgd2 antagonist containing the same |
CZ297324B6 (cs) | 1996-12-13 | 2006-11-15 | Shionogi & Co., Ltd. | Benzothiofenkarboxamidové deriváty a antagonisty PGD2, které je obsahují |
JP3857525B2 (ja) | 1998-06-03 | 2006-12-13 | 塩野義製薬株式会社 | Pgd2拮抗剤を含有する痒みの治療剤 |
DE60215000T2 (de) | 2001-05-23 | 2007-08-09 | Merck Frosst Canada & Co, Kirkland | Dihydropyrroloil[1,2-a]indol- und Tetrahydropyridol[1,2-a]indol-Derivate als Prostaglandin-D2-Rezeptor-Antagonisten |
-
2003
- 2003-10-28 JP JP2005501791A patent/JP4332151B2/ja not_active Expired - Fee Related
- 2003-10-28 KR KR1020057007434A patent/KR20050084890A/ko not_active Application Discontinuation
- 2003-10-28 NZ NZ539406A patent/NZ539406A/en unknown
- 2003-10-28 WO PCT/CA2003/001658 patent/WO2004039807A1/en active Application Filing
- 2003-10-28 CA CA002503767A patent/CA2503767C/en not_active Expired - Fee Related
- 2003-10-28 PL PL03376440A patent/PL376440A1/xx not_active Application Discontinuation
- 2003-10-28 AT AT03809672T patent/ATE479686T1/de not_active IP Right Cessation
- 2003-10-28 BR BR0315681-8A patent/BR0315681A/pt not_active IP Right Cessation
- 2003-10-28 MX MXPA05004715A patent/MXPA05004715A/es unknown
- 2003-10-28 US US10/532,633 patent/US7618979B2/en not_active Expired - Fee Related
- 2003-10-28 DE DE60334015T patent/DE60334015D1/de not_active Expired - Lifetime
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- 2003-10-28 RU RU2005116254/04A patent/RU2342386C2/ru active
- 2003-10-28 EP EP03809672A patent/EP1558614B1/en not_active Expired - Lifetime
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2005
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RU2342386C2 (ru) | 2008-12-27 |
CA2503767C (en) | 2009-09-22 |
NO20052591D0 (no) | 2005-05-27 |
ATE479686T1 (de) | 2010-09-15 |
AU2003275868B2 (en) | 2009-07-09 |
US7618979B2 (en) | 2009-11-17 |
AU2003275868A1 (en) | 2004-05-25 |
CA2503767A1 (en) | 2004-05-13 |
EP1558614B1 (en) | 2010-09-01 |
PL376440A1 (en) | 2005-12-27 |
NZ539406A (en) | 2007-05-31 |
US20050272756A1 (en) | 2005-12-08 |
RU2005116254A (ru) | 2006-01-20 |
NO20052591L (no) | 2005-07-29 |
MXPA05004715A (es) | 2005-08-03 |
WO2004039807A1 (en) | 2004-05-13 |
JP4332151B2 (ja) | 2009-09-16 |
JP2006506457A (ja) | 2006-02-23 |
DE60334015D1 (de) | 2010-10-14 |
EP1558614A1 (en) | 2005-08-03 |
KR20050084890A (ko) | 2005-08-29 |
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