ATE504582T1 - Substituierte benzopyrane als selektive östrogenrezeptor-beta-agonisten - Google Patents

Substituierte benzopyrane als selektive östrogenrezeptor-beta-agonisten

Info

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
Application number
AT05807448T
Other languages
English (en)
Inventor
Bryan Norman
Timothy Richardson
Original Assignee
Lilly Co Eli
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Lilly Co Eli filed Critical Lilly Co Eli
Application granted granted Critical
Publication of ATE504582T1 publication Critical patent/ATE504582T1/de

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic 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
    • C07D311/94Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/08Drugs for disorders of the urinary system of the prostate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P39/00General 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)
AT05807448T 2004-10-18 2005-10-05 Substituierte benzopyrane als selektive östrogenrezeptor-beta-agonisten ATE504582T1 (de)

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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

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