ATE423122T1 - Kondensierte heterocyclen als inhibitoren von glutamatracemase (muri) - Google Patents
Kondensierte heterocyclen als inhibitoren von glutamatracemase (muri)Info
- Publication number
- ATE423122T1 ATE423122T1 AT04743692T AT04743692T ATE423122T1 AT E423122 T1 ATE423122 T1 AT E423122T1 AT 04743692 T AT04743692 T AT 04743692T AT 04743692 T AT04743692 T AT 04743692T AT E423122 T1 ATE423122 T1 AT E423122T1
- Authority
- AT
- Austria
- Prior art keywords
- glutamatracemase
- muri
- inhibitors
- condensed heterocycles
- heterocycles
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
- C07D487/14—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- 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
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US49561503P | 2003-08-15 | 2003-08-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
ATE423122T1 true ATE423122T1 (de) | 2009-03-15 |
Family
ID=34193331
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT04743692T ATE423122T1 (de) | 2003-08-15 | 2004-08-12 | Kondensierte heterocyclen als inhibitoren von glutamatracemase (muri) |
Country Status (6)
Country | Link |
---|---|
US (1) | US7371757B2 (de) |
EP (1) | EP1664052B1 (de) |
JP (1) | JP2007502307A (de) |
AT (1) | ATE423122T1 (de) |
DE (1) | DE602004019548D1 (de) |
WO (1) | WO2005016929A1 (de) |
Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7371757B2 (en) | 2003-08-15 | 2008-05-13 | Astrazeneca Ab | Fused heterocycles as inhibitors of glutamate racemase(MURI) |
WO2009134666A1 (en) | 2008-04-29 | 2009-11-05 | Boehringer Ingelheim International Gmbh | Indazole compounds as ccr1 receptor antagonists |
WO2009137338A1 (en) * | 2008-05-06 | 2009-11-12 | Boehringer Ingelheim International Gmbh | Pyrazole compounds as ccr1 antagonists |
JP5507567B2 (ja) | 2008-09-26 | 2014-05-28 | 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 | Ccr1受容体拮抗薬としてのアザインダゾール化合物 |
US9040528B2 (en) | 2008-10-14 | 2015-05-26 | Astrazeneca Ab | Chemical compounds 542 |
ES2565611T3 (es) * | 2008-10-14 | 2016-04-05 | Entasis Therapeutics Limited | Compuestos heteroaromáticos espirocíclicos y condensados para el tratamiento de infecciones bacterianas |
KR20120087923A (ko) | 2009-10-21 | 2012-08-07 | 베링거 인겔하임 인터내셔날 게엠베하 | Ccr1 수용체 길항제로서의 인다졸 및 피라졸로피리딘 화합물 |
US8927550B2 (en) | 2009-10-27 | 2015-01-06 | Boehringer Ingelheim International Gmbh | Heterocyclic compounds as CCR1 receptor antagonists |
BR112012013582A2 (pt) * | 2009-12-08 | 2016-07-05 | Boehringer Ingelheim Int | processo para síntese de intermediários úteis para a produção de compostos de indazol e azaindazol substituídos |
US8871786B2 (en) | 2010-04-30 | 2014-10-28 | Boehringer Ingelheim International Gmbh | Azaindazole amide compounds as CCR1 receptor antagonists |
JP5684406B2 (ja) | 2010-12-23 | 2015-03-11 | 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 | Ccr1受容体アンタゴニストとしてのピラゾロピペリジン化合物 |
PE20150229A1 (es) | 2012-05-31 | 2015-03-02 | Phenex Pharmaceuticals Ag | Tiazoles sustituidos por carboxamida o sulfonamida y derivados relacionados como moduladores para el receptor nuclear huerfano rory |
JO3215B1 (ar) | 2012-08-09 | 2018-03-08 | Phenex Pharmaceuticals Ag | حلقات غير متجانسة بها 5 ذرات تحتوي على النيتروجين بها استبدال بكربوكساميد أو سلفوناميد كمعدلات لمستقبل نووي غير محمي RORy |
US8889671B2 (en) | 2013-01-23 | 2014-11-18 | Astrazeneca Ab | Compounds and methods for treating bacterial infections |
WO2014160405A1 (en) * | 2013-03-13 | 2014-10-02 | University Of Iowa Research Foundation | Compounds, compositions comprising same, and methods related thereto |
MX365261B (es) | 2014-05-29 | 2019-05-27 | Entasis Therapeutics Ltd | Compuestos heteroaromaticos espirociclicos, fusionados para el tratamiento de infecciones bacterianas. |
TN2017000483A1 (en) | 2015-05-20 | 2019-04-12 | Amgen Inc | Triazole agonists of the apj receptor. |
US10118910B2 (en) | 2015-12-09 | 2018-11-06 | The Board Of Trustees Of The University Of Illinois | Benzothiophene-based selective estrogen receptor downregulators |
WO2017192485A1 (en) | 2016-05-03 | 2017-11-09 | Amgen Inc. | Heterocyclic triazole compounds as agonists of the apj receptor |
WO2018081168A2 (en) | 2016-10-24 | 2018-05-03 | The Board Of Trustees Of The University Of Illinois | Benzothiophene-based selective mixed estrogen receptor downregulators |
MA46824A (fr) | 2016-11-16 | 2019-09-25 | Amgen Inc | Composés de triazole substitués par alkyle en tant qu'agonistes du récepteur apj |
US11020395B2 (en) | 2016-11-16 | 2021-06-01 | Amgen Inc. | Cycloalkyl substituted triazole compounds as agonists of the APJ receptor |
US10689367B2 (en) | 2016-11-16 | 2020-06-23 | Amgen Inc. | Triazole pyridyl compounds as agonists of the APJ receptor |
WO2018097945A1 (en) | 2016-11-16 | 2018-05-31 | Amgen Inc. | Heteroaryl-substituted triazoles as apj receptor agonists |
EP3541792B1 (de) | 2016-11-16 | 2020-12-23 | Amgen Inc. | Triazol-furan-verbindungen als agonisten des apj-rezeptors |
WO2018093579A1 (en) | 2016-11-16 | 2018-05-24 | Amgen Inc. | Triazole phenyl compounds as agonists of the apj receptor |
CN110177554B (zh) | 2017-01-06 | 2023-06-02 | G1治疗公司 | 用于治疗癌症的组合疗法 |
CN110461853A (zh) | 2017-02-10 | 2019-11-15 | G1治疗公司 | 苯并噻吩雌激素受体调节剂 |
MA50509A (fr) | 2017-11-03 | 2021-06-02 | Amgen Inc | Agonistes de triazole fusionnés du récepteur apj |
WO2019213006A1 (en) | 2018-05-01 | 2019-11-07 | Amgen Inc. | Substituted pyrimidinones as agonists of the apj receptor |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SE0102315D0 (sv) | 2001-06-28 | 2001-06-28 | Astrazeneca Ab | Compounds |
US7371757B2 (en) | 2003-08-15 | 2008-05-13 | Astrazeneca Ab | Fused heterocycles as inhibitors of glutamate racemase(MURI) |
-
2004
- 2004-08-12 US US10/567,797 patent/US7371757B2/en not_active Expired - Fee Related
- 2004-08-12 WO PCT/GB2004/003464 patent/WO2005016929A1/en active Search and Examination
- 2004-08-12 AT AT04743692T patent/ATE423122T1/de not_active IP Right Cessation
- 2004-08-12 DE DE602004019548T patent/DE602004019548D1/de not_active Expired - Fee Related
- 2004-08-12 EP EP04743692A patent/EP1664052B1/de not_active Not-in-force
- 2004-08-12 JP JP2006523672A patent/JP2007502307A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
US7371757B2 (en) | 2008-05-13 |
US20060252781A1 (en) | 2006-11-09 |
EP1664052A1 (de) | 2006-06-07 |
EP1664052B1 (de) | 2009-02-18 |
JP2007502307A (ja) | 2007-02-08 |
WO2005016929A1 (en) | 2005-02-24 |
DE602004019548D1 (de) | 2009-04-02 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
ATE423122T1 (de) | Kondensierte heterocyclen als inhibitoren von glutamatracemase (muri) | |
CY1107747T1 (el) | Υποκατεστημενα τετρακυκλικα παραγωγα πυρρολοκινολονης χρησιμα ως αναστολεις της φωσφοδιεστερασης | |
DK1853602T3 (da) | Kemiske forbindelser | |
CY1108275T1 (el) | Χημικες ενωσεις | |
ATE433447T1 (de) | Pyrimiidinverbindungen | |
BRPI0510177B8 (pt) | composto, composição farmacêutica e uso do mesmo | |
BG66084B1 (bg) | Циклопентаноиндоли, състави,съдържащи такива съединения и използването им | |
EA200401436A1 (ru) | Ингибиторы протеазы вич для лечения инфекции вич и фармацевтическая композиция | |
NO20063275L (no) | Anvendelse av substituerte 2-aminotetraliner for forebyggende behandling av Parkinsons sykdom | |
ATE368031T1 (de) | Neue gamma secretase inhibitoren | |
EA200500312A1 (ru) | Новые спироконденсированные хиназолиноны и их применение в качестве ингибиторов фосфодиэстераз | |
EA200601007A1 (ru) | 7-фенилалкилзамещённые 2-хинолиноны и 2-хиноксалиноны в качестве ингибиторов поли(адф-рибоза)полимеразы | |
ATE466860T1 (de) | Cgrp-rezeptorantagonisten | |
CY1109906T1 (el) | Παραγωγα c3-kyano εποθιλονης | |
ATE553077T1 (de) | Peptidaseinhibitoren | |
PL378107A1 (pl) | 1,2,4-triazyny hamujące HIV | |
ATE538651T1 (de) | Spiropiperidininhibitoren von beta-secretase zur behandlung von alzheimer-krankheit | |
ATE307810T1 (de) | Imidazol-2-carbonsäureamid derivate als raf- kinase-inhibitoren | |
EP1689713A4 (de) | Benzylether und benzylaminoverbindungen als inhibitoren von beta-secretase zur behandlung von alzheimer-krankheit | |
DE602004008959D1 (de) | Benzoäbüä1,4üdioxepinderivate | |
PL376324A1 (en) | Piperazinyl and diazapanyl benzamides and benzthioamides | |
MX2009006473A (es) | Inhibidores de receptor vainilloide de bencimidazol. | |
DE60310767D1 (de) | PYRAZOL-3,4-d-PYRIMIDINDERIVATE UND IHRE VERWENDUNG BEI DER BEHANDLUNG VON H.PYLORI-INFEKTIONEN | |
DE60220385D1 (de) | Benzimidazole zur behandlung sexueller fehlfunktionen | |
DE602004029355D1 (de) | Sulfopyrrolderivate |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
RER | Ceased as to paragraph 5 lit. 3 law introducing patent treaties |