RU2170730C2 - Хинолиновые карбоксамиды и фармацевтическая композиция на их основе - Google Patents

Хинолиновые карбоксамиды и фармацевтическая композиция на их основе Download PDF

Info

Publication number
RU2170730C2
RU2170730C2 RU98123074/04A RU98123074A RU2170730C2 RU 2170730 C2 RU2170730 C2 RU 2170730C2 RU 98123074/04 A RU98123074/04 A RU 98123074/04A RU 98123074 A RU98123074 A RU 98123074A RU 2170730 C2 RU2170730 C2 RU 2170730C2
Authority
RU
Russia
Prior art keywords
carboxamide
methoxyquinolin
dichloropyridin
compound
optionally substituted
Prior art date
Application number
RU98123074/04A
Other languages
English (en)
Russian (ru)
Other versions
RU98123074A (ru
Inventor
Хэйзел Джоан ДАЙК (GB)
Хэйзел Джоан ДАЙК
Джон Гари МОНТАНА (GB)
Джон Гари Монтана
Кристофер ЛОУ (GB)
Кристофер Лоу
Ханнах Джэйн КЕНДАЛЛ (GB)
Ханнах Джэйн Кендалл
Верити Маргарет САБИН (GB)
Верити Маргарет Сабин
Original Assignee
Дарвин Дискавери Лимитед
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
Priority claimed from GBGB9610506.9A external-priority patent/GB9610506D0/en
Priority claimed from GBGB9623234.3A external-priority patent/GB9623234D0/en
Priority claimed from GBGB9626883.4A external-priority patent/GB9626883D0/en
Priority claimed from GBGB9708072.5A external-priority patent/GB9708072D0/en
Application filed by Дарвин Дискавери Лимитед filed Critical Дарвин Дискавери Лимитед
Publication of RU98123074A publication Critical patent/RU98123074A/ru
Application granted granted Critical
Publication of RU2170730C2 publication Critical patent/RU2170730C2/ru

Links

Classifications

    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • 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
    • C07D401/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D215/48Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • 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
    • C07D401/14Heterocyclic 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 three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic 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
    • C07D417/02Heterocyclic 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
    • C07D417/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Neurology (AREA)
  • Oncology (AREA)
  • Biomedical Technology (AREA)
  • Communicable Diseases (AREA)
  • Neurosurgery (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pulmonology (AREA)
  • Virology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Quinoline Compounds (AREA)
RU98123074/04A 1996-05-20 1997-05-20 Хинолиновые карбоксамиды и фармацевтическая композиция на их основе RU2170730C2 (ru)

Applications Claiming Priority (8)

Application Number Priority Date Filing Date Title
GB9610506.9 1996-05-20
GBGB9610506.9A GB9610506D0 (en) 1996-05-20 1996-05-20 Novel compounds
GBGB9623234.3A GB9623234D0 (en) 1996-11-07 1996-11-07 Novel compounds
GB9623234.3 1996-11-07
GBGB9626883.4A GB9626883D0 (en) 1996-12-24 1996-12-24 Compounds
GB9626883.4 1996-12-24
GBGB9708072.5A GB9708072D0 (en) 1997-04-22 1997-04-22 Compounds
GB9708072.5 1997-04-22

Publications (2)

Publication Number Publication Date
RU98123074A RU98123074A (ru) 2000-10-10
RU2170730C2 true RU2170730C2 (ru) 2001-07-20

Family

ID=27451451

Family Applications (1)

Application Number Title Priority Date Filing Date
RU98123074/04A RU2170730C2 (ru) 1996-05-20 1997-05-20 Хинолиновые карбоксамиды и фармацевтическая композиция на их основе

Country Status (19)

Country Link
US (1) US5804588A (enExample)
EP (1) EP0952832B1 (enExample)
JP (1) JP2000510865A (enExample)
KR (1) KR20000065219A (enExample)
CN (1) CN1148189C (enExample)
AT (1) ATE406163T1 (enExample)
AU (1) AU722472B2 (enExample)
BR (1) BR9709015A (enExample)
CA (1) CA2252531A1 (enExample)
CZ (1) CZ296163B6 (enExample)
DE (1) DE69738949D1 (enExample)
IL (1) IL126557A (enExample)
NO (1) NO312099B1 (enExample)
NZ (1) NZ332341A (enExample)
PL (1) PL329922A1 (enExample)
RU (1) RU2170730C2 (enExample)
SK (1) SK283162B6 (enExample)
TR (1) TR199802385T2 (enExample)
WO (1) WO1997044036A1 (enExample)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2332405C2 (ru) * 2003-02-28 2008-08-27 Новартис Аг Способ получения соли 5-[(r)-2-(5, 6-диэтилиндан-2-иламино)-1-гидроксиэтил]-8-гидрокси-(1н)-хинолин-2-она, полезной в качестве адренорецепторного агониста
RU2339621C2 (ru) * 2003-04-02 2008-11-27 Новартис Аг Способ получения 5-(альфа-галогенацетил)-8-(замещенный окси)-(1н)-хинолин-2-онов
RU2348618C2 (ru) * 2002-07-16 2009-03-10 Прана Биотехнолоджи Лимитэд Производные 8-гидроксихинолина
RU2383534C2 (ru) * 2004-06-22 2010-03-10 Новартис Аг Энантиоселективный способ получения производных хинолина
RU2391338C2 (ru) * 2004-10-19 2010-06-10 Ф.Хоффманн-Ля Рош Аг Производные хинолина
RU2411043C2 (ru) * 2004-04-01 2011-02-10 Юниверсите Де Льеж Фармацевтические композиции пиримидин-2,4,6-трионов
RU2495029C2 (ru) * 2007-02-09 2013-10-10 Альмираль, С.А. ГЕМИНАПАДИЗИЛАТ 5-(2-{[6-(2,2-ДИФТОР-2-ФЕНИЛЭТОКСИ)ГЕКСИЛ]АМИНО}-1-ГИДРОКСИЭТИЛ)-8-ГИДРОКСИХИНОЛИН-2(1H)-ОНА КАК АГОНИСТ β2 АДРЕНЕРГИЧЕСКОГО РЕЦЕПТОРА
RU2624906C2 (ru) * 2015-12-22 2017-07-10 федеральное государственное бюджетное учреждение "Федеральный научно-исследовательский центр эпидемиологии и микробиологии имени почетного академика Н.Ф. Гамалеи" Министерства здравоохранения Российской Федерации Производные 2-хинальдинкарбоновой кислоты и их противогриппозная активность

Families Citing this family (79)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11514361A (ja) * 1995-10-16 1999-12-07 藤沢薬品工業株式会社 H+−ATPaseとしての複素環式化合物
GB9712761D0 (en) * 1997-06-17 1997-08-20 Chiroscience Ltd Quinolines and their therapeutic use
US6262070B1 (en) 1998-11-04 2001-07-17 Darwin Discovery Ltd. Heterocyclic compounds and their therapeutic use
GB9824160D0 (en) * 1998-11-04 1998-12-30 Darwin Discovery Ltd Heterocyclic compounds and their therapeutic use
CA2715683A1 (en) * 1999-08-21 2001-03-01 Nycomed Gmbh Synergistic combination
AU1053501A (en) * 1999-11-02 2001-05-14 Ajinomoto Co., Inc. Polyazanaphthalene compound and medicinal use thereof
JP4603646B2 (ja) * 1999-11-15 2010-12-22 富士フイルムファインケミカルズ株式会社 新規なジピリジル誘導体
US7217722B2 (en) * 2000-02-01 2007-05-15 Kirin Beer Kabushiki Kaisha Nitrogen-containing compounds having kinase inhibitory activity and drugs containing the same
GB0003256D0 (en) * 2000-02-11 2000-04-05 Darwin Discovery Ltd Heterocyclic compounds and their therapeutic use
US6521618B2 (en) 2000-03-28 2003-02-18 Wyeth 3-cyanoquinolines, 3-cyano-1,6-naphthyridines, and 3-cyano-1,7-naphthyridines as protein kinase inhibitors
DE10035928A1 (de) * 2000-07-21 2002-03-07 Asta Medica Ag Neue Heteroaryl-Derivate und deren Verwendung als Arzneimittel
EP1310488A4 (en) * 2000-08-09 2005-08-10 Mitsubishi Pharma Corp CONCENTRATED BICYCLIC AMID COMPOUNDS AND THEIR MEDICAL USE
US6953774B2 (en) 2000-08-11 2005-10-11 Applied Research Systems Ars Holding N.V. Methods of inducing ovulation
JP2002300373A (ja) * 2001-03-30 2002-10-11 Minolta Co Ltd 画像処理方法、画像処理装置、記録媒体及びプログラム
CN1537018A (zh) 2001-05-23 2004-10-13 田边制药株式会社 一种用于软骨疾病再生治疗的组合物
EP1389468A4 (en) * 2001-05-23 2007-01-10 Tanabe Seiyaku Co COMPOSITIONS FOR PROMOTING BONE FRACTURE HEALING
WO2003008409A1 (en) 2001-07-16 2003-01-30 Astrazeneca Ab Quinoline derivatives and their use as tyrosine kinase inhibitors
CN100506817C (zh) * 2001-08-15 2009-07-01 纳幕尔杜邦公司 用于防治无脊椎害虫的邻-杂环取代的芳基酰胺类化合物
US7507707B2 (en) 2001-12-14 2009-03-24 Laboratoires Serono Sa Methods of inducing ovulation using a non-polypeptide camp level modulator
MY140561A (en) 2002-02-20 2009-12-31 Nycomed Gmbh Dosage form containing pde 4 inhibitor as active ingredient
SE0200920D0 (sv) * 2002-03-25 2002-03-25 Astrazeneca Ab Novel compounds
ES2195785B1 (es) * 2002-05-16 2005-03-16 Almirall Prodesfarma, S.A. Nuevos derivados de piridazin-3(2h)-ona.
ES2211344B1 (es) * 2002-12-26 2005-10-01 Almirall Prodesfarma, S.A. Nuevos derivados de piridazin-3(2h)-ona.
US7153824B2 (en) 2003-04-01 2006-12-26 Applied Research Systems Ars Holding N.V. Inhibitors of phosphodiesterases in infertility
MXPA05012705A (es) * 2003-05-29 2006-02-08 Astrazeneca Ab Una composicion farmaceutica que comprende un antagonista del receptor p2x7 y un factor alfa de necrosis tumoral.
WO2004105797A1 (en) * 2003-05-29 2004-12-09 Astrazeneca Ab A pharmaceutical composition comprising a p2x7 antagonist and sulfasalazine
US20070281931A1 (en) * 2003-05-29 2007-12-06 Nigel Boughton-Smith Pharmaceutical Composition Containing a P2x7 Receptor Antagonist and Methotrexate
GB0312609D0 (en) * 2003-06-02 2003-07-09 Astrazeneca Ab Novel compounds
SE0302139D0 (sv) * 2003-07-28 2003-07-28 Astrazeneca Ab Novel compounds
SE0302192D0 (sv) * 2003-08-08 2003-08-08 Astrazeneca Ab Novel compounds
ATE366728T1 (de) * 2003-09-15 2007-08-15 Schering Corp Synthese von für die herstellung von pde-iv- inhibitoren geeigneten chinolin-5-carboxamiden
SE0302488D0 (sv) * 2003-09-18 2003-09-18 Astrazeneca Ab New combination
AU2004298486A1 (en) 2003-12-12 2005-06-30 Wyeth Quinolines useful in treating cardiovascular disease
US7569536B2 (en) * 2003-12-26 2009-08-04 Masatoshi Hagiwara Method for controlling SR protein phosphorylation, and antiviral agents whose active ingredients comprise agents that control SR protein activity
AP2006003685A0 (en) * 2004-02-04 2006-08-31 Pfizer Prod Inc Substituted quinoline compounds
CA2565599C (en) * 2004-05-18 2012-07-31 Schering Corporation Substituted 2-quinolyl-oxazoles useful as pde4 inhibitors
ES2251866B1 (es) * 2004-06-18 2007-06-16 Laboratorios Almirall S.A. Nuevos derivados de piridazin-3(2h)-ona.
ES2251867B1 (es) * 2004-06-21 2007-06-16 Laboratorios Almirall S.A. Nuevos derivados de piridazin-3(2h)-ona.
LT2502911T (lt) 2004-06-24 2017-09-11 Vertex Pharmaceuticals Incorporated Atp surišančios kasetės transporterių moduliatoriai
US8354427B2 (en) * 2004-06-24 2013-01-15 Vertex Pharmaceutical Incorporated Modulators of ATP-binding cassette transporters
SA05260265A (ar) * 2004-08-30 2005-12-03 استرازينيكا ايه بي مركبات جديدة
BRPI0515979A (pt) * 2004-10-12 2008-08-12 Actelion Pharmaceuticals Ltd composto, processo para a preparação do mesmo, composições, uso de um ou mais compostos, e, método de tratamento de um paciente sofrendo de um distúrbio
SE0402925D0 (sv) * 2004-11-30 2004-11-30 Astrazeneca Ab Novel Compounds
WO2007022946A1 (de) 2005-08-21 2007-03-01 Abbott Gmbh & Co. Kg Heterocyclische verbindungen und ihre verwendung als bindungspartner für 5-ht5-rezeptoren
EP2275095A3 (en) 2005-08-26 2011-08-17 Braincells, Inc. Neurogenesis by muscarinic receptor modulation
EP2258358A3 (en) 2005-08-26 2011-09-07 Braincells, Inc. Neurogenesis with acetylcholinesterase inhibitor
EP1940389A2 (en) 2005-10-21 2008-07-09 Braincells, Inc. Modulation of neurogenesis by pde inhibition
AU2006308889A1 (en) 2005-10-31 2007-05-10 Braincells, Inc. GABA receptor mediated modulation of neurogenesis
CA2634113A1 (en) * 2005-12-24 2007-07-05 Vertex Pharmaceuticals Incorporated Quinolin- 4 - one derivatives as modulators of abc transporters
WO2007079139A2 (en) 2005-12-28 2007-07-12 Vertex Pharmaceuticals, Inc. Solid forms of n-[2,4-bis(1,1-dimethylethyl)-5-hydroxyphenyl]-1,4-dihydro-4-oxoquinoline-3-carboxamide
KR100821649B1 (ko) 2006-01-24 2008-04-11 서울시립대학교 산학협력단 클리오퀴놀을 유효성분으로 포함하는 HIF-1α 활성제
US20100216734A1 (en) 2006-03-08 2010-08-26 Braincells, Inc. Modulation of neurogenesis by nootropic agents
EP2382975A3 (en) 2006-05-09 2012-02-29 Braincells, Inc. Neurogenesis by modulating angiotensin
CA2657902A1 (en) * 2006-07-11 2008-01-17 Schering Corporation Xinafoate salt of a substituted 5-oxazol-2-yl-quinoline compound
CA2661850A1 (en) 2006-09-01 2008-03-06 Kyorin Pharmaceutical Co., Ltd. Pyrazolopyridine carboxamide derivative and phosphodiesterase (pde) inhibitor containing the same
US20100184806A1 (en) 2006-09-19 2010-07-22 Braincells, Inc. Modulation of neurogenesis by ppar agents
CL2007003874A1 (es) * 2007-01-03 2008-05-16 Boehringer Ingelheim Int Compuestos derivados de benzamida; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar enfermedades cardiovasculares, hipertension, aterosclerosis, reestenosis, ictus, insuficiencia cardiaca, lesion isquemica, hipertensio
ES2320954B1 (es) * 2007-03-02 2010-03-16 Laboratorio Almirall S.A. Nuevo procedimiento de preparacion de 3-metil-4-fenilisoxazolo (3,4-d)iridazin-7(6h)-ona.
CA2680761A1 (en) * 2007-03-22 2008-09-25 Astrazeneca Ab Quinoline derivatives for the treatment of inflammatory diseases
US9321730B2 (en) * 2007-08-21 2016-04-26 The Hong Kong Polytechnic University Method of making and administering quinoline derivatives as anti-cancer agents
PE20091036A1 (es) 2007-11-30 2009-08-15 Astrazeneca Ab Derivado de quinolina como antagonista del receptor p2x7
US20100074949A1 (en) 2008-08-13 2010-03-25 William Rowe Pharmaceutical composition and administration thereof
US12458635B2 (en) 2008-08-13 2025-11-04 Vertex Pharmaceuticals Incorporated Pharmaceutical composition and administrations thereof
WO2010099217A1 (en) 2009-02-25 2010-09-02 Braincells, Inc. Modulation of neurogenesis using d-cycloserine combinations
SI2408750T1 (sl) 2009-03-20 2015-11-30 Vertex Pharmaceuticals Incorporated Postopek za izdelavo modulatorjev cistično-fibroznega transmembranskega regulatorja prevodnosti
JP2011042643A (ja) * 2009-07-24 2011-03-03 Bayer Cropscience Ag 殺虫性カルボキサミド類
CA2796826A1 (en) 2010-05-10 2011-11-17 Gilead Sciences, Inc. Bifunctional quinoline derivatives
UY33373A (es) 2010-05-10 2011-12-30 Gilead Sciences Inc ?Compuestos de pirazolopiridina bifuncionales, su uso en terapia y composiciones que los comprenden?.
WO2013074059A2 (en) * 2010-11-05 2013-05-23 Regents Of The University Of Minnesota Cytosine deaminase modulators for enhancement of dna transfection
US8802700B2 (en) 2010-12-10 2014-08-12 Vertex Pharmaceuticals Incorporated Modulators of ATP-Binding Cassette transporters
WO2012083866A1 (en) 2010-12-22 2012-06-28 The Hong Kong Polytechnic University Quinoline derivatives as anti-cancer agents
WO2013106547A1 (en) 2012-01-10 2013-07-18 President And Fellows Of Harvard College Beta-cell replication promoting compounds and methods of their use
EP2819670A1 (en) 2012-02-27 2015-01-07 Vertex Pharmaceuticals Incorporated Pharmaceutical composition and administration thereof
CN103254291B (zh) * 2013-05-30 2014-06-25 常州亚当生物技术有限公司 肿瘤坏死因子-α多肽抑制剂及其应用
CN103285373A (zh) * 2013-05-30 2013-09-11 苏州普罗达生物科技有限公司 肿瘤坏死因子-α多肽抑制剂制备及其应用
SG10202103278TA (en) * 2013-10-14 2021-04-29 Eisai R&D Man Co Ltd Selectively substituted quinoline compounds
KR20170063954A (ko) 2014-10-07 2017-06-08 버텍스 파마슈티칼스 인코포레이티드 낭성 섬유증 막횡단 전도도 조절자의 조정제의 공-결정
WO2019053015A1 (en) 2017-09-13 2019-03-21 Syngenta Participations Ag MICROBIOCIDE DERIVATIVES OF QUINOLINE (THIO) CARBOXAMIDE
CN107812006A (zh) * 2017-11-13 2018-03-20 全椒先奇医药科技有限公司 一种治疗急性肾衰药物组合物及其应用

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SU1477247A3 (ru) * 1985-05-07 1989-04-30 Алкалоида Ведьесети Дьяр (Инопредприятие) Способ получени триазолилхинолиновых производных или их солей присоединени кислот
WO1994022852A1 (en) * 1993-03-31 1994-10-13 Syntex (U.S.A.) Inc. Quinolines as type iv phosphodiesterase inhibitors

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2517229A1 (de) * 1975-04-18 1976-10-28 Boehringer Mannheim Gmbh Phenylalkylcarbonsaeure-derivate und verfahren zu ihrer herstellung
US4186201A (en) * 1977-02-07 1980-01-29 Riker Laboratories, Inc. Methods of using 8(tetrazol-5-ylcarbamoyl)isoquinoline compounds
US4147694A (en) * 1977-02-07 1979-04-03 Riker Laboratories, Inc. 8-(1H-Tetrazol-5-yl-carbamoyl)quinoline compounds
ES2104862T3 (es) * 1991-02-07 1997-10-16 Roussel Uclaf Derivados biciclicos nitrogenados, su procedimiento de preparacion, sus productos intermedios obtenidos, su aplicacion como medicamentos y composiciones farmaceuticas que los contienen.
SE9302490D0 (sv) * 1993-07-26 1993-07-26 Kabi Pharmacia Ab New use of old drugs

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SU1477247A3 (ru) * 1985-05-07 1989-04-30 Алкалоида Ведьесети Дьяр (Инопредприятие) Способ получени триазолилхинолиновых производных или их солей присоединени кислот
WO1994022852A1 (en) * 1993-03-31 1994-10-13 Syntex (U.S.A.) Inc. Quinolines as type iv phosphodiesterase inhibitors

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2348618C2 (ru) * 2002-07-16 2009-03-10 Прана Биотехнолоджи Лимитэд Производные 8-гидроксихинолина
US7619091B2 (en) 2002-07-16 2009-11-17 Prana Biotechnology Limited 8-hydroxy quinoline derivatives
US8975278B2 (en) 2002-07-16 2015-03-10 Prana Biotechnology Limited 8-hydroxy quinoline derivatives
US9169211B2 (en) 2002-07-16 2015-10-27 Prana Biotechnology Limited 8-hydroxy quinoline derivatives
US9302993B2 (en) 2002-07-16 2016-04-05 Prana Biotechnology Limited 8-hydroxy quinoline derivatives
RU2332405C2 (ru) * 2003-02-28 2008-08-27 Новартис Аг Способ получения соли 5-[(r)-2-(5, 6-диэтилиндан-2-иламино)-1-гидроксиэтил]-8-гидрокси-(1н)-хинолин-2-она, полезной в качестве адренорецепторного агониста
RU2339621C2 (ru) * 2003-04-02 2008-11-27 Новартис Аг Способ получения 5-(альфа-галогенацетил)-8-(замещенный окси)-(1н)-хинолин-2-онов
RU2411043C2 (ru) * 2004-04-01 2011-02-10 Юниверсите Де Льеж Фармацевтические композиции пиримидин-2,4,6-трионов
RU2383534C2 (ru) * 2004-06-22 2010-03-10 Новартис Аг Энантиоселективный способ получения производных хинолина
RU2391338C2 (ru) * 2004-10-19 2010-06-10 Ф.Хоффманн-Ля Рош Аг Производные хинолина
RU2495029C2 (ru) * 2007-02-09 2013-10-10 Альмираль, С.А. ГЕМИНАПАДИЗИЛАТ 5-(2-{[6-(2,2-ДИФТОР-2-ФЕНИЛЭТОКСИ)ГЕКСИЛ]АМИНО}-1-ГИДРОКСИЭТИЛ)-8-ГИДРОКСИХИНОЛИН-2(1H)-ОНА КАК АГОНИСТ β2 АДРЕНЕРГИЧЕСКОГО РЕЦЕПТОРА
RU2624906C2 (ru) * 2015-12-22 2017-07-10 федеральное государственное бюджетное учреждение "Федеральный научно-исследовательский центр эпидемиологии и микробиологии имени почетного академика Н.Ф. Гамалеи" Министерства здравоохранения Российской Федерации Производные 2-хинальдинкарбоновой кислоты и их противогриппозная активность

Also Published As

Publication number Publication date
CN1219131A (zh) 1999-06-09
NO312099B1 (no) 2002-03-18
NO985376D0 (no) 1998-11-19
CN1148189C (zh) 2004-05-05
JP2000510865A (ja) 2000-08-22
CZ365198A3 (cs) 1999-03-17
NZ332341A (en) 2000-05-26
EP0952832A1 (en) 1999-11-03
ATE406163T1 (de) 2008-09-15
CZ296163B6 (cs) 2006-01-11
IL126557A0 (en) 1999-08-17
SK283162B6 (sk) 2003-03-04
WO1997044036A1 (en) 1997-11-27
EP0952832B1 (en) 2008-08-27
PL329922A1 (en) 1999-04-26
IL126557A (en) 2002-09-12
US5804588A (en) 1998-09-08
DE69738949D1 (de) 2008-10-09
CA2252531A1 (en) 1997-11-27
AU2905897A (en) 1997-12-09
NO985376L (no) 1998-11-19
BR9709015A (pt) 1999-08-03
TR199802385T2 (xx) 1999-04-21
KR20000065219A (ko) 2000-11-06
SK160598A3 (en) 1999-12-10
AU722472B2 (en) 2000-08-03

Similar Documents

Publication Publication Date Title
RU2170730C2 (ru) Хинолиновые карбоксамиды и фармацевтическая композиция на их основе
US6069151A (en) Quinolines and their therapeutic use
US5925636A (en) Benzofuran carboxamides and their therapeutic use
TW530048B (en) New hydroxyindoles, their use as inhibitors of phosphodiesterase 4 and processes for their preparation
EP0946541B1 (en) Quinolines and their therapeutic use
US6353010B1 (en) Bicyclic aryl carboxamides and their therapeutic use
JP2005537247A (ja) 置換されたキノリンccr5受容体アンタゴニスト
BR112014021148B1 (pt) Pirazol-1-il benzeno sulfonamidas como antagonistas de ccr9, sua composição e método de modular função ccr (9) em uma célula
TWI386402B (zh) N-(雜芳基)-1-雜芳基烷基-1h-吲哚-2-甲醯胺衍生物,其製備方法及其治療用途
ES2231439T3 (es) Derivados benzooxazol como inhibidores de tnf y de pde iv.
EA018984B1 (ru) Производные пиразолона как ингибиторы pde4
ES2204171T3 (es) Derivados de furopiridina y su utilizacion terapeutica.
US5792774A (en) Quinolones and their therapeutic use
JP2002528541A (ja) Tnfおよびpde−iv阻害活性を有する複素環式化合物のn−オキシド
US7482457B2 (en) Substituted quinoline-4-carboxylic hydrazides as NK-2/NK-3 receptor ligands
MXPA98009740A (en) Quinoline carboxamides as fnt inhibitors and as fde inhibitors
JPS603397B2 (ja) イソインドリン誘導体
TW201910325A (zh) 吲哚衍生物及其用途

Legal Events

Date Code Title Description
MM4A The patent is invalid due to non-payment of fees

Effective date: 20050521