ATE504582T1 - Substituierte benzopyrane als selektive östrogenrezeptor-beta-agonisten - Google Patents
Substituierte benzopyrane als selektive östrogenrezeptor-beta-agonistenInfo
- Publication number
- ATE504582T1 ATE504582T1 AT05807448T AT05807448T ATE504582T1 AT E504582 T1 ATE504582 T1 AT E504582T1 AT 05807448 T AT05807448 T AT 05807448T AT 05807448 T AT05807448 T AT 05807448T AT E504582 T1 ATE504582 T1 AT E504582T1
- Authority
- AT
- Austria
- Prior art keywords
- sub
- sup
- alkyl
- estrogen receptor
- selective estrogen
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/94—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems condensed with rings other than six-membered or with ring systems containing such rings
-
- 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
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P39/00—General protective or antinoxious agents
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Toxicology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyrane Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US61962704P | 2004-10-18 | 2004-10-18 | |
PCT/US2005/035472 WO2006044176A1 (en) | 2004-10-18 | 2005-10-05 | Substituted benzopyrans as selective estrogen receptor-beta agonists |
Publications (1)
Publication Number | Publication Date |
---|---|
ATE504582T1 true ATE504582T1 (de) | 2011-04-15 |
Family
ID=36010977
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT05807448T ATE504582T1 (de) | 2004-10-18 | 2005-10-05 | Substituierte benzopyrane als selektive östrogenrezeptor-beta-agonisten |
Country Status (8)
Country | Link |
---|---|
US (1) | US7354951B2 (de) |
EP (1) | EP1805160B1 (de) |
JP (1) | JP2008516949A (de) |
AT (1) | ATE504582T1 (de) |
CA (1) | CA2578300A1 (de) |
DE (1) | DE602005027378D1 (de) |
ES (1) | ES2361031T3 (de) |
WO (1) | WO2006044176A1 (de) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2518819A1 (en) | 2003-04-21 | 2004-11-04 | Eli Lilly And Company | Substituted benzopyrans as selective estrogen receptor-beta agonists |
EP1853578A1 (de) | 2005-02-15 | 2007-11-14 | Eli Lilly And Company | Substituierte tetraline als selektive östrogenrezeptor-beta-agonisten |
US9623021B2 (en) | 2007-01-22 | 2017-04-18 | Gtx, Inc. | Nuclear receptor binding agents |
CN101641013B (zh) | 2007-01-22 | 2014-07-30 | Gtx公司 | 核受体结合剂 |
US9604931B2 (en) | 2007-01-22 | 2017-03-28 | Gtx, Inc. | Nuclear receptor binding agents |
US10154988B2 (en) | 2012-11-14 | 2018-12-18 | The Johns Hopkins University | Methods and compositions for treating schizophrenia |
EP3827820A1 (de) | 2013-03-15 | 2021-06-02 | The Johns Hopkins University | Brivaracetam zur verbesserung der kognitiven funktion |
AU2014228512A1 (en) | 2013-03-15 | 2015-10-01 | Agenebio, Inc. | Methods and compositions for improving cognitive function |
JP2016539954A (ja) | 2013-12-05 | 2016-12-22 | カロ ファーマ エービーKaro Pharma Ab | 中皮腫の処置で使用するためのエストロゲン受容体ベータアゴニスト |
CN112843005B (zh) | 2015-05-22 | 2023-02-21 | 艾吉因生物股份有限公司 | 左乙拉西坦的延时释放药物组合物 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE529419T1 (de) | 2000-03-01 | 2011-11-15 | Organon Nv | Chromanderivate als estrogene verbindungen |
ES2286322T3 (es) * | 2001-11-19 | 2007-12-01 | Eli Lilly And Company | Benzopirianos como agosnistas selectivos de receptores de estrogenos beta. |
US6630508B1 (en) | 2002-02-11 | 2003-10-07 | Eli Lilly And Company | Substituted benzopyrans as selective estrogen receptor β agonists |
CA2518819A1 (en) | 2003-04-21 | 2004-11-04 | Eli Lilly And Company | Substituted benzopyrans as selective estrogen receptor-beta agonists |
WO2004094401A1 (en) | 2003-04-21 | 2004-11-04 | Eli Lilly And Company | Substituted benzopyrans as selective estrogen receptor-beta agonists |
-
2005
- 2005-10-05 WO PCT/US2005/035472 patent/WO2006044176A1/en active Application Filing
- 2005-10-05 US US11/574,034 patent/US7354951B2/en not_active Expired - Fee Related
- 2005-10-05 ES ES05807448T patent/ES2361031T3/es active Active
- 2005-10-05 DE DE602005027378T patent/DE602005027378D1/de active Active
- 2005-10-05 EP EP05807448A patent/EP1805160B1/de not_active Not-in-force
- 2005-10-05 JP JP2007536726A patent/JP2008516949A/ja not_active Ceased
- 2005-10-05 CA CA002578300A patent/CA2578300A1/en not_active Abandoned
- 2005-10-05 AT AT05807448T patent/ATE504582T1/de not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
DE602005027378D1 (de) | 2011-05-19 |
EP1805160A1 (de) | 2007-07-11 |
JP2008516949A (ja) | 2008-05-22 |
WO2006044176A1 (en) | 2006-04-27 |
EP1805160B1 (de) | 2011-04-06 |
ES2361031T3 (es) | 2011-06-13 |
US20080064742A1 (en) | 2008-03-13 |
US7354951B2 (en) | 2008-04-08 |
CA2578300A1 (en) | 2006-04-27 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
ATE504582T1 (de) | Substituierte benzopyrane als selektive östrogenrezeptor-beta-agonisten | |
MY136959A (en) | Quinoline intermediates of receptor tyrosine kinase inhibitors and the synthesis thereof | |
Zhang et al. | Potent nonsteroidal progesterone receptor agonists: synthesis and SAR study of 6-aryl benzoxazines | |
BRPI0309534B8 (pt) | derivados de triazol como antagonistas do receptor de taquicinina, seu uso, e composição farmacêutica | |
TW200540174A (en) | Indole derivative having piperidine ring | |
BG106038A (en) | Aminopyridines as sorbitol dehydrogenase inhibitors | |
ATE415462T1 (de) | Flüssigkristallines medium | |
ATE399546T1 (de) | Cycloalkyl-lactam-derivate als inhibitoren von 11-beta-hydroxysteroiddehydrogenase 1 | |
AU2001231710A1 (en) | Pyridine derivatives inhibiting angiogenesis and/or vegf receptor tyrosine kinase | |
GT200800226A (es) | Derivados de acido benzoazepin-oxi-acetico como agonistas de receptores activados por proliferador de peroxisoma delta usados para incrementar la lipoproteina de alta densidad-colesterol, reducir la lipoproteina de baja densidad-colesterol y reducir | |
DE60113032D1 (de) | Glucocorticoid Rezeptor Modulatoren | |
Wood et al. | Challenges in the development of an M4 PAM in vivo tool compound: the discovery of VU0467154 and unexpected DMPK profiles of close analogs | |
ATE327974T1 (de) | Modulatoren des glucocorticoid-rezeptors | |
Zarghi et al. | Design, synthesis, and biological evaluation of 1, 3-diarylprop-2-en-1-ones: A novel class of cyclooxygenase-2 inhibitors | |
MXPA05004507A (es) | 4-amino-1-(piridilmetil)piperidina sustituida como antagonista del receptor muscarinico. | |
Sharma et al. | Microwave-assisted One-pot Efficient Synthesis of Functionalized 2-Oxo-2-phenylethylidenes-linked 2-Oxobenzo [1, 4] oxazines and 2-Oxoquino [1, 4] oxalines: Synthetic Applications, Antioxidant Activity, SAR and Cytotoxic Studies. | |
BR0109838A (pt) | Metabólitos de agonista/antagonista de estrogênio | |
Liu et al. | Design, synthesis and bioevaluation of 2, 7-diaryl-pyrazolo [1, 5-a] pyrimidines as tubulin polymerization inhibitors | |
Loksha et al. | Synthesis and biological screening of some novel 6‐substituted 2‐alkylpyridazin‐3 (2H)‐ones as anti‐inflammatory and analgesic agents | |
Soussi et al. | Palladium‐Catalyzed Coupling of 3‐Halo‐Substituted Coumarins, Chromenes, and Quinolones with Various Nitrogen‐Containing Nucleophiles | |
SI1626974T1 (sl) | Substituirani benzopirani kot selektivni agonistiestrogenskega receptorja beta | |
Takahashi et al. | Discovery and SAR study of novel dihydroquinoline containing glucocorticoid receptor ligands | |
Cube et al. | 3-(2-Ethoxy-4-{4-[3-hydroxy-2-methyl-4-(3-methylbutanoyl) phenoxy] butoxy} phenyl) propanoic acid: a brain penetrant allosteric potentiator at the metabotropic glutamate receptor 2 (mGluR2) | |
ATE276995T1 (de) | Halogenierte triphenylethylene derivate als selektive östrogenrezeptormodulatoren | |
Roth et al. | Design, synthesis and evaluation of MCH receptor 1 antagonists—Part II: Optimization of pyridazines toward reduced phospholipidosis and hERG inhibition |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
RER | Ceased as to paragraph 5 lit. 3 law introducing patent treaties |