NO20051942L - Substituerte 4-cindazol-3-yl)fenoler som ostrogenreseptor-(ER) ligander og deres anvendelse ved behandling av inflammatoriske sykdommer - Google Patents

Substituerte 4-cindazol-3-yl)fenoler som ostrogenreseptor-(ER) ligander og deres anvendelse ved behandling av inflammatoriske sykdommer

Info

Publication number
NO20051942L
NO20051942L NO20051942A NO20051942A NO20051942L NO 20051942 L NO20051942 L NO 20051942L NO 20051942 A NO20051942 A NO 20051942A NO 20051942 A NO20051942 A NO 20051942A NO 20051942 L NO20051942 L NO 20051942L
Authority
NO
Norway
Prior art keywords
treatment
cindazol
phenols
ligands
substituted
Prior art date
Application number
NO20051942A
Other languages
English (en)
Norwegian (no)
Other versions
NO20051942D0 (no
Inventor
Robert John Steffan
Mark Anthony Ashwell
Edward Martin Matelan
William Ronad Solvibile
Original Assignee
Wyeth Corp
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 Wyeth Corp filed Critical Wyeth Corp
Publication of NO20051942D0 publication Critical patent/NO20051942D0/no
Publication of NO20051942L publication Critical patent/NO20051942L/no

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/54Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
    • C07D231/56Benzopyrazoles; Hydrogenated benzopyrazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles
    • A61K31/4161,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
    • AHUMAN NECESSITIES
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    • C07D409/04Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Immunology (AREA)
  • Rheumatology (AREA)
  • Cardiology (AREA)
  • Endocrinology (AREA)
  • Obesity (AREA)
  • Dermatology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Urology & Nephrology (AREA)
  • Pulmonology (AREA)
  • Reproductive Health (AREA)
  • Ophthalmology & Optometry (AREA)
  • Psychiatry (AREA)
  • Hospice & Palliative Care (AREA)
  • Oncology (AREA)
  • Pain & Pain Management (AREA)
  • Biochemistry (AREA)
  • Communicable Diseases (AREA)
  • Child & Adolescent Psychology (AREA)
NO20051942A 2002-09-25 2005-04-20 Substituerte 4-cindazol-3-yl)fenoler som ostrogenreseptor-(ER) ligander og deres anvendelse ved behandling av inflammatoriske sykdommer NO20051942L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US41393102P 2002-09-25 2002-09-25
PCT/US2003/030252 WO2004031159A1 (en) 2002-09-25 2003-09-24 Substituted 4-(indazol-3-yl)phenols as estrogen receptor (er) ligands and their use in the treatment of inflammatory diseases

Publications (2)

Publication Number Publication Date
NO20051942D0 NO20051942D0 (no) 2005-04-20
NO20051942L true NO20051942L (no) 2005-06-14

Family

ID=32069719

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20051942A NO20051942L (no) 2002-09-25 2005-04-20 Substituerte 4-cindazol-3-yl)fenoler som ostrogenreseptor-(ER) ligander og deres anvendelse ved behandling av inflammatoriske sykdommer

Country Status (21)

Country Link
US (2) US7241791B2 (de)
EP (1) EP1542976B1 (de)
JP (1) JP4459813B2 (de)
KR (1) KR20050053702A (de)
CN (2) CN1321984C (de)
AR (1) AR041378A1 (de)
AT (1) ATE422202T1 (de)
AU (1) AU2003276940A1 (de)
BR (1) BR0314475A (de)
CA (1) CA2499736A1 (de)
CR (1) CR7769A (de)
DE (1) DE60326077D1 (de)
DK (1) DK1542976T3 (de)
EC (1) ECSP055704A (de)
ES (1) ES2319519T3 (de)
MX (1) MXPA05003275A (de)
NO (1) NO20051942L (de)
RU (1) RU2005109387A (de)
TW (1) TW200409759A (de)
WO (1) WO2004031159A1 (de)
ZA (1) ZA200502462B (de)

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EP1704856A4 (de) * 2003-12-26 2009-08-19 Kyowa Hakko Kirin Co Ltd Proteininhibitor der hsp90-familie
US7592363B2 (en) * 2004-08-03 2009-09-22 Wyeth Indazoles
DE102004039280A1 (de) * 2004-08-13 2006-02-23 Merck Patent Gmbh 1,5-Diphenyl-pyrazole
WO2006028875A1 (en) 2004-09-02 2006-03-16 Wyeth Phenanthridine carbonyl phenols as cytokine modulators
EP1647549A1 (de) 2004-10-14 2006-04-19 Laboratoire Theramex Indazole, Benzisoxazole und Benzisothiazole mit oestrogenen Eigenschaften
US7601847B2 (en) * 2004-10-26 2009-10-13 Wyeth Preparation and purification of 4-(indazol-3-yl)phenols
TW200621237A (en) * 2004-11-01 2006-07-01 Wyeth Corp [(1-h-indazol-3-yl)methyl]phenols and (hydroxyphenyl)(1h-indazol-3-yl)methanones
CN100516049C (zh) * 2004-11-16 2009-07-22 永信药品工业股份有限公司 抗血管生成药n2-(取代的芳基甲基)-3-(取代的苯基)吲唑的合成
MX2007008495A (es) 2005-01-19 2007-09-14 Wyeth Corp Estructura receptora de estrogenos.
AU2007296555B2 (en) 2006-09-12 2012-07-12 Gilead Sciences, Inc. Process and intermediates for preparing integrase inhibitors
EP2184987A4 (de) * 2007-07-31 2011-09-28 Burnham Inst Medical Research Bidentatverbindungen als kinasehemmer
AR068403A1 (es) 2007-09-11 2009-11-18 Gilead Sciences Inc Proceso e intermediarios para la preparacion de inhibidores de integrasa
EP2298767A4 (de) 2008-07-17 2011-10-19 Asahi Kasei Pharma Corp Nitrogenierte bicyclische und heterocyclische verbindung
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AU2013296289B2 (en) 2012-08-03 2017-10-05 Gilead Sciences, Inc. Process and intermediates for preparing integrase inhibitors
JP2014133739A (ja) * 2012-12-12 2014-07-24 Dainippon Sumitomo Pharma Co Ltd インダゾール誘導体またはピロロピリジン誘導体からなる医薬
KR20240122922A (ko) 2013-03-27 2024-08-13 세다르스-신나이 메디칼 센터 Tl1a 기능 및 관련된 신호전달 경로의 저해에 의한 섬유증 및 염증의 완화 및 반전
EP4105236A1 (de) 2013-07-19 2022-12-21 Cedars-Sinai Medical Center Anti-tl1a (tnfsf15) antikörper zur behandlung von entzündlichen darmerkrankungen
KR102412146B1 (ko) 2015-02-11 2022-06-22 주식회사 아이엔테라퓨틱스 소디움 채널 차단제
CN109462996A (zh) 2016-03-17 2019-03-12 西达-赛奈医疗中心 通过rnaset2诊断炎性肠病的方法
CN106511350A (zh) * 2016-09-26 2017-03-22 张德芳 6‑羟基‑7‑芳甲酰基喹啉酮类化合物在治疗溃疡性结肠炎中的应用
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CA2499736A1 (en) 2004-04-15
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