NO20055565D0 - Anvendelse av derivater av 2,4-dihydro-[1,2,4]triazol-3-thion som inhibitorer av enzymet myeloperoksidase (MPO) - Google Patents

Anvendelse av derivater av 2,4-dihydro-[1,2,4]triazol-3-thion som inhibitorer av enzymet myeloperoksidase (MPO)

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Publication number
NO20055565D0
NO20055565D0 NO20055565A NO20055565A NO20055565D0 NO 20055565 D0 NO20055565 D0 NO 20055565D0 NO 20055565 A NO20055565 A NO 20055565A NO 20055565 A NO20055565 A NO 20055565A NO 20055565 D0 NO20055565 D0 NO 20055565D0
Authority
NO
Norway
Prior art keywords
mpo
thione
triazol
dihydro
inhibitors
Prior art date
Application number
NO20055565A
Other languages
English (en)
Other versions
NO20055565L (no
Inventor
Anna-Karin Tiden
Mats Svensson
Dominika Turek
Original Assignee
Astrazeneca Ab
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Filing date
Publication date
Application filed by Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of NO20055565D0 publication Critical patent/NO20055565D0/no
Publication of NO20055565L publication Critical patent/NO20055565L/no

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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • A61K31/41961,2,4-Triazoles
    • AHUMAN NECESSITIES
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    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
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    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16Anti-Parkinson drugs
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    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • C07D249/101,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D417/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond

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  • Physical Education & Sports Medicine (AREA)
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  • Plural Heterocyclic Compounds (AREA)
NO20055565A 2003-04-25 2005-11-24 Anvendelse av derivater av 2,4-dihydro-[1,2,4]triazol-3-thion som inhibitorer av enzymet myeloperoksidase (MPO) NO20055565L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE0301232A SE0301232D0 (sv) 2003-04-25 2003-04-25 Novel use
PCT/SE2004/000618 WO2004096781A1 (en) 2003-04-25 2004-04-22 Use of derivatives of 2, 4-dihydro-[1,2,4]triazole-3-thione as inhibitors o fteh enzyme myeloperoxidase (mpo)

Publications (2)

Publication Number Publication Date
NO20055565D0 true NO20055565D0 (no) 2005-11-24
NO20055565L NO20055565L (no) 2006-01-25

Family

ID=20291142

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20055565A NO20055565L (no) 2003-04-25 2005-11-24 Anvendelse av derivater av 2,4-dihydro-[1,2,4]triazol-3-thion som inhibitorer av enzymet myeloperoksidase (MPO)

Country Status (13)

Country Link
US (1) US20070093483A1 (no)
EP (1) EP1620410A1 (no)
JP (1) JP2006524686A (no)
KR (1) KR20060006064A (no)
CN (1) CN1780822A (no)
AU (1) AU2004234320A1 (no)
BR (1) BRPI0409498A (no)
CA (1) CA2523020A1 (no)
MX (1) MXPA05011207A (no)
NO (1) NO20055565L (no)
SE (1) SE0301232D0 (no)
WO (1) WO2004096781A1 (no)
ZA (1) ZA200508623B (no)

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AR039385A1 (es) 2002-04-19 2005-02-16 Astrazeneca Ab Derivados de tioxantina como inhibidores de la mieloperoxidasa
SE0302756D0 (sv) * 2003-10-17 2003-10-17 Astrazeneca Ab Novel Compounds
SE0402591D0 (sv) * 2004-10-25 2004-10-25 Astrazeneca Ab Novel use
KR101374553B1 (ko) 2004-11-18 2014-03-17 신타 파마슈티칼스 코프. Hsp90 활성을 조절하는 트리아졸 화합물
MY140748A (en) 2004-12-06 2010-01-15 Astrazeneca Ab Novel pyrrolo [3,2-d] pyrimidin-4-one derivatives and their use in therapy
TW200804383A (en) 2006-06-05 2008-01-16 Astrazeneca Ab New compounds
PE20110371A1 (es) 2006-08-15 2011-06-24 Novartis Ag COMPUESTOS HETEROCICLICOS QUE MODULAN LA ACTIVIDAD DE LA ESTEROIL-CoA-DESATURASA
EP1921073A1 (en) 2006-11-10 2008-05-14 Laboratorios del Dr. Esteve S.A. 1,2,4-Triazole derivatives as sigma receptor inhibitors
US20090053176A1 (en) * 2007-08-23 2009-02-26 Astrazeneca Ab New Combination 937
CN101945848A (zh) 2007-12-20 2011-01-12 英维沃医药有限公司 四取代的苯
NZ592603A (en) * 2008-10-21 2013-02-22 Metabolex Inc Aryl gpr120 receptor agonists and uses thereof
CN101723909B (zh) * 2008-10-29 2011-12-28 天津药物研究院 三唑酮类化合物、其制备方法和用途
WO2011133581A1 (en) 2010-04-19 2011-10-27 General Atomics Methods and compositions for assaying enzymatic activity of myeloperoxidase in blood samples
EP2560640A1 (en) 2010-04-19 2013-02-27 Synta Pharmaceuticals Corp. Cancer therapy using a combination of a hsp90 inhibitory compounds and a egfr inhibitor
EP2773345A1 (en) 2011-11-02 2014-09-10 Synta Pharmaceuticals Corp. Cancer therapy using a combination of hsp90 inhibitors with topoisomerase i inhibitors
EP2776025A1 (en) 2011-11-02 2014-09-17 Synta Pharmaceuticals Corp. Combination therapy of hsp90 inhibitors with platinum-containing agents
PE20161219A1 (es) * 2011-11-11 2016-11-17 Pfizer 2-tiopirimidinonas
AU2012339679A1 (en) 2011-11-14 2014-06-12 Synta Pharmaceuticals Corp. Combination therapy of Hsp90 inhibitors with BRAF inhibitors
FR2988000A1 (fr) * 2012-03-16 2013-09-20 Thomas Wandji Composition pharmaceutique active dans la therapie des affections virales humaines et animales
KR102639231B1 (ko) 2017-10-30 2024-02-22 뉴로포레 테라피스, 인코포레이티드 치환된 페닐 설폰일 페닐 트리아졸 싸이온 및 이의 용도
KR20200083843A (ko) 2018-12-31 2020-07-09 공주대학교 산학협력단 4-(2-플루오로페닐)-3-(3-메톡시벤질)-1h-1,2,4-트리아졸-5(4h)-온 및 이의 퇴행성 뇌질환 및 대사성 질환 치료제로서의 용도
CN110313401A (zh) * 2019-07-12 2019-10-11 华南农业大学 一种促进企剑白墨墨兰组织培养过程中芽分化的方法
JP2023524241A (ja) * 2020-05-06 2023-06-09 バイオヘイブン・セラピューティクス・リミテッド ベルジペルスタットの調製のためのプロセス
US11926602B1 (en) * 2023-08-23 2024-03-12 King Faisal University 4-amino-5-(4-fluoro-3-phenoxyphenyl)-4H-1,2,4-triazole-3-thiol derivatives as antifungal agents

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Publication number Publication date
JP2006524686A (ja) 2006-11-02
SE0301232D0 (sv) 2003-04-25
MXPA05011207A (es) 2005-12-14
CN1780822A (zh) 2006-05-31
CA2523020A1 (en) 2004-11-11
AU2004234320A1 (en) 2004-11-11
BRPI0409498A (pt) 2006-05-02
US20070093483A1 (en) 2007-04-26
KR20060006064A (ko) 2006-01-18
EP1620410A1 (en) 2006-02-01
WO2004096781A1 (en) 2004-11-11
NO20055565L (no) 2006-01-25
ZA200508623B (en) 2007-07-25

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