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 |
---|---|---|---|---|
EP1664052B1 (de) | 2003-08-15 | 2009-02-18 | AstraZeneca AB | Kondensierte heterocyclen als inhibitoren von glutamatracemase (muri) |
EP2285783B1 (de) | 2008-04-29 | 2014-05-21 | Boehringer Ingelheim International GmbH | Indazolverbindungen als ccr1-rezeptorantagonisten |
JP5411927B2 (ja) * | 2008-05-06 | 2014-02-12 | 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アンタゴニストとしてのピラゾール化合物 |
PE20110854A1 (es) | 2008-09-26 | 2011-12-23 | Boehringer Ingelheim Int | DERIVADOS DE 1-FENIL-1H-PIRAZOLO[3,4-c]PIRIDINA-4-CARBONILAMINA COMO ANTAGONISTAS DE LOS RECEPTORES CCR1 |
US9040528B2 (en) | 2008-10-14 | 2015-05-26 | Astrazeneca Ab | Chemical compounds 542 |
AU2009305203B2 (en) * | 2008-10-14 | 2013-03-07 | Entasis Therapeutics Limited | Fused, spirocyclic heteroaromatic compounds for the treatment of bacterial infections |
SI2491028T1 (sl) | 2009-10-21 | 2014-03-31 | Boehringer Ingelheim International Gmbh | Indazolne in pirazolopiridinske spojine kot antagonisti receptorja CCR1 |
JP5542214B2 (ja) | 2009-10-27 | 2014-07-09 | 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複素環化合物 |
IN2012DN05081A (de) * | 2009-12-08 | 2015-10-09 | Boehringer Ingelheim Int | |
US8871786B2 (en) | 2010-04-30 | 2014-10-28 | Boehringer Ingelheim International Gmbh | Azaindazole amide compounds as CCR1 receptor antagonists |
WO2012087782A1 (en) | 2010-12-23 | 2012-06-28 | Boehringer Ingelheim International Gmbh | Pyrazolopiperidine compounds as ccr1 receptor antagonists |
EP2855440A1 (de) | 2012-05-31 | 2015-04-08 | Phenex Pharmaceuticals AG | Carboxamid- oder sulfonamidsubstituierte thiazole und zugehörige derivate als modulatoren für orphan-nuklearrezeptor ror? |
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 |
EP3148546A1 (de) | 2014-05-29 | 2017-04-05 | Entasis Therapeutics Limited | Kondensierte spirocyclische heteroaromatische verbindungen zur behandlung von bakteriellen infektionen |
HUE050317T2 (hu) | 2015-05-20 | 2020-11-30 | Amgen Inc | APJ receptor triazol agonistái |
DK3386500T3 (da) | 2015-12-09 | 2022-12-12 | Univ Illinois | Benzothiophen-baserede selektive østrogenreceptor ned-regulatorer |
EP3452466B1 (de) | 2016-05-03 | 2020-08-12 | Amgen Inc. | Heterocyclische triazolverbindungen als agonisten des apj-rezeptors |
WO2018081168A2 (en) | 2016-10-24 | 2018-05-03 | The Board Of Trustees Of The University Of Illinois | Benzothiophene-based selective mixed estrogen receptor downregulators |
MA46827A (fr) | 2016-11-16 | 2019-09-25 | Amgen Inc | Composés de triazole à substitution cycloalkyle en tant qu'agonistes du récepteur apj |
WO2018093576A1 (en) | 2016-11-16 | 2018-05-24 | Amgen Inc. | Alkyl substituted triazole compounds as agonists of the apj receptor |
WO2018097944A1 (en) | 2016-11-16 | 2018-05-31 | Amgen Inc. | Triazole furan compounds as agonists of the apj receptor |
WO2018093579A1 (en) | 2016-11-16 | 2018-05-24 | Amgen Inc. | Triazole phenyl compounds as agonists of the apj receptor |
EP3541805B1 (de) | 2016-11-16 | 2020-10-14 | Amgen Inc. | Heteroaryl-substituierte triazole als apj-rezeptoragonisten |
US10689367B2 (en) | 2016-11-16 | 2020-06-23 | Amgen Inc. | Triazole pyridyl 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 |
KR20190117582A (ko) | 2017-02-10 | 2019-10-16 | 쥐원 쎄라퓨틱스, 인크. | 벤조티오펜 에스트로겐 수용체 조정제 |
US11149040B2 (en) | 2017-11-03 | 2021-10-19 | Amgen Inc. | Fused triazole agonists of the APJ receptor |
US11807624B2 (en) | 2018-05-01 | 2023-11-07 | 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 |
EP1664052B1 (de) | 2003-08-15 | 2009-02-18 | AstraZeneca AB | Kondensierte heterocyclen als inhibitoren von glutamatracemase (muri) |
-
2004
- 2004-08-12 EP EP04743692A patent/EP1664052B1/de not_active Not-in-force
- 2004-08-12 DE DE602004019548T patent/DE602004019548D1/de not_active Expired - Fee Related
- 2004-08-12 US US10/567,797 patent/US7371757B2/en not_active Expired - Fee Related
- 2004-08-12 AT AT04743692T patent/ATE423122T1/de not_active IP Right Cessation
- 2004-08-12 JP JP2006523672A patent/JP2007502307A/ja active Pending
- 2004-08-12 WO PCT/GB2004/003464 patent/WO2005016929A1/en active Search and Examination
Also Published As
Publication number | Publication date |
---|---|
US7371757B2 (en) | 2008-05-13 |
EP1664052B1 (de) | 2009-02-18 |
JP2007502307A (ja) | 2007-02-08 |
WO2005016929A1 (en) | 2005-02-24 |
DE602004019548D1 (de) | 2009-04-02 |
EP1664052A1 (de) | 2006-06-07 |
US20060252781A1 (en) | 2006-11-09 |
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 | |
DK1853588T3 (da) | Kemiske forbindelser | |
CY1110900T1 (el) | Χημικες ενωσεις | |
ATE443043T1 (de) | Phenylcarboxamide als beta-sekretase-hemmer zur behandlung von alzheimer | |
BRPI0510177B8 (pt) | composto, composição farmacêutica e uso do mesmo | |
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 | |
EA200500453A1 (ru) | Имидазопиридины и способы их получения и применения | |
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 | |
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 | |
DE60310767D1 (de) | PYRAZOL-3,4-d-PYRIMIDINDERIVATE UND IHRE VERWENDUNG BEI DER BEHANDLUNG VON H.PYLORI-INFEKTIONEN | |
NO20070980L (no) | Selekterte kondenserte heterocykler og anvendelser derav | |
DE60220385D1 (de) | Benzimidazole zur behandlung sexueller fehlfunktionen | |
DE602004029355D1 (de) | Sulfopyrrolderivate | |
DK1511472T3 (da) | Anvendelige forbindelser til behandling af Anthrax og hæmning af letalfaktor |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
RER | Ceased as to paragraph 5 lit. 3 law introducing patent treaties |