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

    • 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)
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
EP1626974B1 (de) * 2003-04-21 2008-08-27 Eli Lilly And Company Substituierte benzopyrane als selektive antagonisten am östrogenrezeptor-beta
US8093302B2 (en) 2005-02-15 2012-01-10 Eli Lilly And Company Substituted tetralins as selective estrogen receptor-β agonists
US9623021B2 (en) 2007-01-22 2017-04-18 Gtx, Inc. Nuclear receptor binding agents
US9604931B2 (en) 2007-01-22 2017-03-28 Gtx, Inc. Nuclear receptor binding agents
KR101638035B1 (ko) 2007-01-22 2016-07-11 지티엑스, 인코포레이티드 핵 수용체에 결합하는 물질
US10154988B2 (en) 2012-11-14 2018-12-18 The Johns Hopkins University Methods and compositions for treating schizophrenia
CA2904767C (en) 2013-03-15 2022-06-21 Agenebio, Inc. Methods and compositions for improving cognitive function
US10806717B2 (en) 2013-03-15 2020-10-20 The Johns Hopkins University Methods and compositions for improving cognitive function
CN105960236A (zh) 2013-12-05 2016-09-21 卡罗医药股份公司 用于治疗间皮瘤的雌激素受体β激动剂
EA034167B8 (ru) 2015-05-22 2021-04-27 Эйджинбайо, Инк. Фармацевтические композиции леветирацетама пролонгированного высвобождения

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7214706B2 (en) 2000-03-01 2007-05-08 Akzo Nobel N.V. Chroman derivatives as estrogenic compounds
DE60220179T2 (de) 2001-11-19 2008-02-07 Eli Lilly And Co., Indianapolis Substituierte benzopyrane als selektive agonisten am östrogenrezeptor-beta
US6630508B1 (en) * 2002-02-11 2003-10-07 Eli Lilly And Company Substituted benzopyrans as selective estrogen receptor β agonists
US7279499B2 (en) * 2003-04-21 2007-10-09 Eli Lilly And Company Substituted benzopyrans as selective estrogen receptor-beta agonists
EP1626974B1 (de) * 2003-04-21 2008-08-27 Eli Lilly And Company Substituierte benzopyrane als selektive antagonisten am östrogenrezeptor-beta

Also Published As

Publication number Publication date
US7354951B2 (en) 2008-04-08
EP1805160B1 (de) 2011-04-06
JP2008516949A (ja) 2008-05-22
CA2578300A1 (en) 2006-04-27
US20080064742A1 (en) 2008-03-13
DE602005027378D1 (de) 2011-05-19
EP1805160A1 (de) 2007-07-11
WO2006044176A1 (en) 2006-04-27
ES2361031T3 (es) 2011-06-13

Similar Documents

Publication Publication Date Title
DE602005027378D1 (de) Substituierte benzopyrane als selektive östrogenrezeptor-beta-agonisten
Zhang et al. Potent nonsteroidal progesterone receptor agonists: synthesis and SAR study of 6-aryl benzoxazines
MY136959A (en) Quinoline intermediates of receptor tyrosine kinase inhibitors and the synthesis thereof
BRPI0309534B8 (pt) derivados de triazol como antagonistas do receptor de taquicinina, seu uso, e composição farmacêutica
Jain et al. Identification and Structure− Activity Relationships of Chromene-Derived Selective Estrogen Receptor Modulators for Treatment of Postmenopausal Symptoms
AU637500B2 (en) Bicyclic heterocyclic compounds
ATE295365T1 (de) Pyridinderivative als angiogenese- und/oder vegf- rezeptor-tyrosinkinase-inhibitoren
BG106038A (en) Aminopyridines as sorbitol dehydrogenase inhibitors
NO20061797L (no) Trombinreseptorantagonister
Zarghi et al. Design, synthesis, and biological evaluation of 1, 3-diarylprop-2-en-1-ones: A novel class of cyclooxygenase-2 inhibitors
CY1110443T1 (el) Υποκατεστημενα βενζοπυρανια ως εκλεκτικοι αγωνιστες υποδοχεα-βητα οιστρογονων
Row et al. Design, synthesis and evaluation of furanocoumarin monomers as inhibitors of CYP3A4
Ostrowska et al. Synthesis of a new series of aryl/heteroarylpiperazinyl derivatives of 8-acetyl-7-hydroxy-4-methylcoumarin with low nanomolar 5-HT1A affinities
Lamie et al. Synthesis and biological evaluation of tetrazole derivatives as TNF-α, IL-6 and COX-2 inhibitors with antimicrobial activity: Computational analysis, molecular modeling study and region-specific cyclization using 2D NMR tools
ATE399546T1 (de) Cycloalkyl-lactam-derivate als inhibitoren von 11-beta-hydroxysteroiddehydrogenase 1
Lanter et al. The discovery of a potent orally efficacious indole androgen receptor antagonist through in vivo screening
DE60105785D1 (de) Halogenierte triphenylethylene derivate als selektive östrogenrezeptormodulatoren
CN1602307A (zh) 作为雌激素制剂的取代的6H-二苯并[c,h]色烯
ECSP045113A (es) Benzopiranos sustituidos como agonistas selectivos del receptor estrogenico beta
Liao et al. Discovery of thiadiazoleamide derivatives as potent, selective, and orally available antagonists disrupting androgen receptor homodimer
Bromidge et al. 8-[2-(4-Aryl-1-piperazinyl) ethyl]-2H-1, 4-benzoxazin-3 (4H)-ones: Dual-acting 5-HT1 receptor antagonists and serotonin reuptake inhibitors—Part II
Zarghi et al. Design and synthesis of new 2-aryl, 3-benzyl-(1, 3-oxazolidine or 1, 3-thiazolidine)-4-ones as selective cyclooxygenase (COX-2) inhibitors
DK1381608T3 (da) Cyclohexylphenylvasopressinagonister
Li et al. Regioselective [3+ 2] cycloaddition of diazo reagents and internal alkynes: Accessing regiosomers of highly substituted trifluoromethylpyrazoles
DE60117517D1 (de) Indolderivate als mcp-1 rezeptor antagonisten

Legal Events

Date Code Title Description
RER Ceased as to paragraph 5 lit. 3 law introducing patent treaties