AP3272A - Multiheteroaryl compounds as inhibitors of H-PGDS and their use for treating prosaglandin D2 mediated diseases - Google Patents

Multiheteroaryl compounds as inhibitors of H-PGDS and their use for treating prosaglandin D2 mediated diseases

Info

Publication number
AP3272A
AP3272A AP2011005682A AP2011005682A AP3272A AP 3272 A AP3272 A AP 3272A AP 2011005682 A AP2011005682 A AP 2011005682A AP 2011005682 A AP2011005682 A AP 2011005682A AP 3272 A AP3272 A AP 3272A
Authority
AP
ARIPO
Prior art keywords
prosaglandin
pgds
inhibitors
treating
mediated diseases
Prior art date
Application number
AP2011005682A
Other languages
English (en)
Other versions
AP2011005682A0 (en
Inventor
Pil Heui Lee
Gregory W Endres
James Bernard Kramer
Original Assignee
Cayman Chem Co
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 Cayman Chem Co filed Critical Cayman Chem Co
Publication of AP2011005682A0 publication Critical patent/AP2011005682A0/xx
Application granted granted Critical
Publication of AP3272A publication Critical patent/AP3272A/xx

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/04—Heterocyclic 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/14—Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/02—Nasal agents, e.g. decongestants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/06—Antiasthmatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/08—Bronchodilators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/04—Centrally acting analgesics, e.g. opioids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A61P27/14—Decongestants or antiallergics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/04—Immunostimulants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/08—Antiallergic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/14—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic 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
    • C07D417/02—Heterocyclic 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
    • C07D417/04—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic 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
    • C07D417/14—Heterocyclic 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 three or more hetero rings

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Pulmonology (AREA)
  • Immunology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Rheumatology (AREA)
  • Dermatology (AREA)
  • Pain & Pain Management (AREA)
  • Neurosurgery (AREA)
  • Ophthalmology & Optometry (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Neurology (AREA)
  • Otolaryngology (AREA)
  • Biomedical Technology (AREA)
  • Nutrition Science (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Cardiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
AP2011005682A 2008-09-22 2009-09-22 Multiheteroaryl compounds as inhibitors of H-PGDS and their use for treating prosaglandin D2 mediated diseases AP3272A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US9894208P 2008-09-22 2008-09-22
PCT/US2009/057813 WO2010033977A2 (fr) 2008-09-22 2009-09-22 Composes multiheteroaryles servant d'inhibiteurs de la h-pgds, ainsi que leur utilisation dans le traitement des maladies induites par la prostaglandine d2

Publications (2)

Publication Number Publication Date
AP2011005682A0 AP2011005682A0 (en) 2011-04-30
AP3272A true AP3272A (en) 2015-05-31

Family

ID=42038293

Family Applications (1)

Application Number Title Priority Date Filing Date
AP2011005682A AP3272A (en) 2008-09-22 2009-09-22 Multiheteroaryl compounds as inhibitors of H-PGDS and their use for treating prosaglandin D2 mediated diseases

Country Status (21)

Country Link
US (3) US8536185B2 (fr)
EP (1) EP2350059B1 (fr)
JP (1) JP2014001228A (fr)
KR (2) KR20130105914A (fr)
AP (1) AP3272A (fr)
AU (1) AU2009292931B2 (fr)
BR (1) BRPI0919004A2 (fr)
CA (1) CA2736955C (fr)
CL (2) CL2011000604A1 (fr)
CO (1) CO6362005A2 (fr)
CR (1) CR20110196A (fr)
EC (1) ECSP11010995A (fr)
IL (3) IL211629A0 (fr)
MX (1) MX2011003011A (fr)
MY (1) MY154000A (fr)
NI (1) NI201100056A (fr)
NZ (1) NZ592297A (fr)
PE (1) PE20110843A1 (fr)
PH (1) PH12013502370A1 (fr)
SG (1) SG2014014013A (fr)
WO (1) WO2010033977A2 (fr)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PE20110843A1 (es) 2008-09-22 2011-12-08 Cayman Chem Co Derivados de 5-(1h-imidazol-5-il)-2-fenilpirimidina, como inhibidores de prostaglandina d sintasa hematopoyetica
AU2010239253A1 (en) * 2009-04-23 2011-11-24 Merck Sharp & Dohme Corp. 2-alkyl piperidine mGluR5 receptor modulators
JP5933554B2 (ja) * 2010-09-01 2016-06-15 アムビト ビオスシエンセス コルポラチオン 光学活性のあるピラゾリルアミノキナゾリン及びその医薬組成物及び使用方法
US9199975B2 (en) 2011-09-30 2015-12-01 Asana Biosciences, Llc Biaryl imidazole derivatives for regulating CYP17
US8809372B2 (en) 2011-09-30 2014-08-19 Asana Biosciences, Llc Pyridine derivatives
WO2014066568A1 (fr) 2012-10-24 2014-05-01 Winthrop-University Hospital Biomarqueur non invasif permettant d'identifier des sujets risquant un accouchement avant terme
JP6401261B2 (ja) * 2013-07-10 2018-10-10 バンブ・デザイン・アンド・リサーチ・インスティテュート・フォー・グラス・インダストリー 電気絶縁モジュール支持体を備えたソーラーモジュールおよびこれの製造方法
BR112016015285A8 (pt) * 2014-02-11 2020-06-09 Merck Patent Gmbh pirimidina imidazol aminas como moduladores da atividade de quinase, seus usos e seu processo de preparação, composição farmacêutica, e kit
RU2018126105A (ru) 2015-12-17 2020-01-17 Астекс Терапьютикс Лимитед Хинолин-3-карбоксамиды в качестве ингибиторов h-pgds
JOP20190072A1 (ar) 2016-10-13 2019-04-07 Glaxosmithkline Ip Dev Ltd مشتقات 1، 3 سيكلوبوتان ثنائي الاستبدال أو آزيتيدين كمثبطات للإنزيم المخلق للبروستاجلاندين d المكون للدم
BR112019026452A2 (pt) 2017-06-13 2020-07-14 Glaxosmithkline Intellectual Property Development Limited compostos químicos como inibidores de h-pgds
KR20200109293A (ko) 2017-09-13 2020-09-22 프로제너티, 인크. 자간전증 바이오마커 및 관련된 시스템 및 방법
WO2019116256A1 (fr) 2017-12-13 2019-06-20 Glaxosmithkline Intellectual Property Development Limited Pyridines fusionnées agissant en tant qu'inhibiteurs de h-pgds
EP3877384A1 (fr) 2018-11-08 2021-09-15 GlaxoSmithKline Intellectual Property Development Ltd Composés chimiques
EP4070113A4 (fr) 2019-12-04 2023-12-20 Biora Therapeutics, Inc. Évaluation de la prééclampsie à l'aide de dosages du facteur de croissance placentaire libre et dissocié
EP3916015A1 (fr) 2020-05-28 2021-12-01 Geneuro SA Anticorps de la protéine d'enveloppe anti-herv-w destiné à utiliser dans le traitement de maladies psychotiques
JPWO2021256569A1 (fr) 2020-06-19 2021-12-23
JPWO2023113023A1 (fr) 2021-12-17 2023-06-22
CN115403526A (zh) * 2022-09-21 2022-11-29 韶远科技（上海)有限公司 一种5-乙酰基嘧啶的制备方法

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001052845A1 (fr) * 2000-01-18 2001-07-26 Vertex Pharmaceuticals Incorpoated Inhibiteurs de la gyrase et leurs applications
WO2005075468A2 (fr) * 2004-02-06 2005-08-18 Cyclacel Limited Composes
WO2007040440A1 (fr) * 2005-10-03 2007-04-12 Astrazeneca Ab Nouveaux derives de pyrimidine et leur utilisation en therapie et pour la production d'un medicament pour la prevention et/ou le traitement de la maladie d'alzheimer

Family Cites Families (51)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4435396A (en) 1982-05-10 1984-03-06 Pfizer Inc. Antiulcer 2-guanidino-4-(2-substituted-amino-4-imidazolyl)thiazoles and process therefor
IL83467A0 (en) 1986-08-15 1988-01-31 Fujisawa Pharmaceutical Co Imidazole derivatives,processes for their preparation and pharmaceutical compositions containing the same
DD294255A5 (de) 1990-05-14 1991-09-26 Adw Forschungsstelle Fuer Chemische Toxikologie,De Verfahren zur herstellung tetrazolylsubstituierter pyrimidinderivate
US5196537A (en) 1991-03-21 1993-03-23 G. D. Searle & Co. 5-apylheteroarylalkyl-1,3,5-trisubstituted-1,2,4-triazole compounds for treatment of circulatory disorders
JPH04368375A (ja) * 1991-06-17 1992-12-21 Otsuka Pharmaceut Factory Inc イソオキサゾール誘導体
US5668148A (en) 1995-04-20 1997-09-16 Merck & Co., Inc. Alpha1a adrenergic receptor antagonists
JP3003922B2 (ja) * 1995-11-09 2000-01-31 住友ベークライト株式会社 ４層プリント配線板
AU711927B2 (en) 1996-02-27 1999-10-21 Sankyo Company Limited Isoxazole derivatives
JP2000507590A (ja) 1996-04-03 2000-06-20 メルク エンド カンパニー インコーポレーテッド ファルネシル―タンパク質トランスフェラーゼ阻害剤
AU8460798A (en) * 1997-08-01 1999-02-22 Nissan Chemical Industries Ltd. Tetrazole compounds and pest control agent
WO2001052846A1 (fr) 2000-01-18 2001-07-26 Vertex Pharmaceuticals Incorporated Inhibiteurs de la gyrase et utilisations de ces derniers
CA2409819C (fr) * 2000-05-19 2009-09-15 Yamanouchi Pharmaceutical Co., Ltd. Derives de triazole
US20030216385A1 (en) 2000-05-19 2003-11-20 Takahiko Tobe Triazole derivatives
AU2002331227B2 (en) * 2001-08-13 2008-01-24 Janssen Pharmaceutica N.V. 2,4,5-trisubstituted thiazolyl derivatives and their antiinflammatory activity
CA2461360A1 (fr) 2001-09-26 2003-04-03 Bayer Pharmaceuticals Corporation Thiazoles 3-pyridyle ou 4-isoquinolinyle utilises comme inhibiteurs de lyase c17,20
JP4071477B2 (ja) 2001-11-12 2008-04-02 財団法人大阪バイオサイエンス研究所 プロスタグランジンｄ合成酵素の３次元立体構造及びその使用
US20060235035A1 (en) 2002-04-09 2006-10-19 7Tm Pharma A/S Novel methoxybenzamibe compounds for use in mch receptor related disorders
US7361665B2 (en) 2002-07-09 2008-04-22 Vertex Pharmaceuticals Incorporated Inhibitors of c-Jun N-terminal kinases (JNK) and other protein kinases
WO2004035563A1 (fr) 2002-10-17 2004-04-29 Syngenta Participations Ag Derives de 3-heterocyclylpyridine utilises comme herbicides
AU2003276201A1 (en) 2002-11-11 2004-06-03 Bayer Healthcare Ag Phenyl or heteroaryl amino alkane derivatives as ip receptor antagonist
WO2004060367A1 (fr) 2002-12-30 2004-07-22 Fujisawa Pharmaceutical Co., Ltd. Derives d'imidazole et de triazole utiles en tant qu'inhibiteurs de cox-1 selectifs
WO2004069394A2 (fr) 2003-02-03 2004-08-19 The Trustees Of Columbia University In The City Of New York Procede synthetique d'arylation directe d'arenes heterocycliques
WO2004089415A2 (fr) 2003-04-11 2004-10-21 Novo Nordisk A/S Therapie combinatoire utilisant un inhibiteur de 11$g(b)-hydroxysteroide deshydrogenase de type 1 et agoniste du recepteur de glucocorticoides pour minimiser les effets secondaires associes a la therapie a base d'agoniste du recepteur de glucocorticoides
CA2531061A1 (fr) 2003-07-02 2005-01-13 Vertex Pharmaceuticals Incorporated Pyrimidines utilisees comme modulateurs des canaux ioniques sensibles au voltage
CA2533870A1 (fr) 2003-07-30 2005-02-10 Shudong Wang Derives de pyridinylamino-pyrimidine utiles comme inhibiteurs de la proteine kinase
EP1673355A1 (fr) 2003-09-22 2006-06-28 Pfizer Limited Derives de triazoles substitues en tant qu'antagonistes de l'oxytocine
JP4550394B2 (ja) 2003-10-14 2010-09-22 財団法人大阪バイオサイエンス研究所 筋変性疾患の治療用医薬組成物およびそのスクリーニング方法
WO2005047281A1 (fr) 2003-11-13 2005-05-26 Syngenta Participations Ag Nouveaux herbicides
CA2547198A1 (fr) 2003-12-17 2005-06-30 Merck & Co., Inc. Carboxylates propanoiques 3,4-disusbstitues utilises en tant qu'agonistes du recepteur s1p (edg)
US7745630B2 (en) 2003-12-22 2010-06-29 Justin Stephen Bryans Triazolyl piperidine arginine vasopressin receptor modulators
NZ547965A (en) 2003-12-24 2009-12-24 Prosidion Ltd 1,2,4-Oxadiazole derivatives as GPCR receptor agonists
PT1745040E (pt) * 2004-02-23 2010-03-08 Glaxo Group Ltd Derivados do azabiciclo3.1.0-hexano úteis como moduladores dos receptores d3 da dopamina
JP2007527890A (ja) 2004-03-08 2007-10-04 グラクソ　グループ　リミテッド ドーパミンｄ３受容体のモジュレーター（抗精神病剤）としてのテトラヒドロベンゾアゼピン誘導体
WO2005094805A1 (fr) 2004-04-01 2005-10-13 Institute Of Medicinal Molecular Design. Inc. Dérivé imine et dérivé amide
GB0507602D0 (en) * 2005-04-14 2005-05-18 Glaxo Group Ltd Compounds
TW200720255A (en) 2005-07-13 2007-06-01 Taiho Pharmaceutical Co Ltd Benzoimidazole compound capable of inhibiting prostaglandin d synthetase
PE20110118A1 (es) 2005-10-04 2011-03-08 Aventis Pharma Inc Compuestos de pirimidina amida como inhibidores de pgds
EP1983980A4 (fr) 2006-01-25 2010-05-05 Synta Pharmaceuticals Corp Composes thiazole et thiadiazole destines a des utilisations associees a une inflammation et au système immunitaire
GB0606774D0 (en) 2006-04-03 2006-05-10 Novartis Ag Organic compounds
WO2007125061A1 (fr) 2006-04-27 2007-11-08 Glaxo Group Limited Composés spiro utiles en tant que modulateurs de récepteurs de la dopamine d3
JP2009535388A (ja) 2006-05-03 2009-10-01 アストラゼネカ アクチボラグ ピラゾール誘導体、及びそのｐｉ３ｋ阻害薬としての使用
US7659270B2 (en) * 2006-08-11 2010-02-09 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
AR061841A1 (es) 2006-09-07 2008-09-24 Actelion Pharmaceuticals Ltd Derivados de tiofen-oxadiazoles, agonistas del receptor s1p1/edg1, composiciones farmaceuticas que los contienen y usos como agentes inmunomoduladores.
WO2008075172A2 (fr) * 2006-12-19 2008-06-26 Pfizer Products Inc. Dérivés de nicotinamide
EP2132196A1 (fr) 2007-02-26 2009-12-16 Pfizer Products Inc. Composés hétérocycliques utiles dans le traitement de maladies et de conditions
WO2008121670A1 (fr) 2007-03-30 2008-10-09 Sanofi-Aventis Composés d'hydrazide de pyrimidine en tant qu'inhibiteurs de pgds
JP5313229B2 (ja) 2007-04-19 2013-10-09 グラクソ グループ リミテッド スフィンゴシン１−リン酸（ｓ１ｐ）アゴニストとして用いるためのオキサジアゾール置換インダゾール誘導体
TW200934771A (en) * 2007-10-19 2009-08-16 Astrazeneca Ab New compounds
US8080544B2 (en) 2008-02-05 2011-12-20 Merck Sharp & Dohme Corp. Prodrugs of CGRP receptor antagonists
AU2009253046A1 (en) 2008-05-30 2009-12-03 Foster Wheeler Energia Oy Method of and system for generating power by oxyfuel combustion
PE20110843A1 (es) 2008-09-22 2011-12-08 Cayman Chem Co Derivados de 5-(1h-imidazol-5-il)-2-fenilpirimidina, como inhibidores de prostaglandina d sintasa hematopoyetica

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001052845A1 (fr) * 2000-01-18 2001-07-26 Vertex Pharmaceuticals Incorpoated Inhibiteurs de la gyrase et leurs applications
WO2005075468A2 (fr) * 2004-02-06 2005-08-18 Cyclacel Limited Composes
WO2007040440A1 (fr) * 2005-10-03 2007-04-12 Astrazeneca Ab Nouveaux derives de pyrimidine et leur utilisation en therapie et pour la production d'un medicament pour la prevention et/ou le traitement de la maladie d'alzheimer

Also Published As

Publication number Publication date
AU2009292931B2 (en) 2014-09-11
KR20130105914A (ko) 2013-09-26
IL211629A0 (en) 2011-05-31
CA2736955C (fr) 2016-02-16
MX2011003011A (es) 2011-09-01
JP5653356B2 (ja) 2015-01-14
BRPI0919004A2 (pt) 2019-09-24
MY154000A (en) 2015-04-30
CA2736955A1 (fr) 2010-03-25
US8536185B2 (en) 2013-09-17
AP2011005682A0 (en) 2011-04-30
NI201100056A (es) 2011-09-08
WO2010033977A2 (fr) 2010-03-25
IL240048A0 (en) 2015-08-31
JP2012503021A (ja) 2012-02-02
KR20110059778A (ko) 2011-06-03
US20150099748A1 (en) 2015-04-09
WO2010033977A3 (fr) 2010-07-01
CR20110196A (es) 2011-09-05
CL2012003104A1 (es) 2013-03-08
US9126973B2 (en) 2015-09-08
US20130079375A1 (en) 2013-03-28
PE20110843A1 (es) 2011-12-08
NZ592297A (en) 2012-11-30
PH12013502370A1 (en) 2014-08-27
CO6362005A2 (es) 2012-01-20
EP2350059B1 (fr) 2016-03-23
AU2009292931A1 (en) 2010-03-25
SG2014014013A (en) 2014-07-30
US20100075990A1 (en) 2010-03-25
IL228105A0 (en) 2013-09-30
EP2350059A2 (fr) 2011-08-03
CL2011000604A1 (es) 2011-06-24
ECSP11010995A (es) 2011-06-30
KR101406433B1 (ko) 2014-06-13
EP2350059A4 (fr) 2012-05-02
JP2014001228A (ja) 2014-01-09
IL240048A (en) 2016-05-31

Similar Documents

Publication Publication Date Title
AP3272A (en) Multiheteroaryl compounds as inhibitors of H-PGDS and their use for treating prosaglandin D2 mediated diseases
HK1154575A1 (zh) 用於治療增生性疾病的不對稱吡咯並苯並二氮雜卓二聚物
IL213068A0 (en) Pyridyloxyindoles inhibitors of vegf-r2 and use thereof for treatment of disease
EP2429292A4 (fr) Composés et compositions comprenant des inhibiteurs des cdk et méthodes de traitement du cancer
IL207752A0 (en) Methods of treating inflammation
EP2211881A4 (fr) Compositions et procédés de prévention et de traitement de maladies touchant des mammifères
HK1217763A1 (zh) 用於治療疾病的方法
HK1146894A1 (en) Compositions and methods for treating diseases of the nail
EP2331564A4 (fr) Procédés de traitement de l'inflammation
ZA201006988B (en) Method and compositions for treatment of cancer
EP2497482A4 (fr) Fig. 2:composition destinée à prévenir et à traiter des maladies induites par le virus de la grippe
HK1165791A1 (en) Triazolopyridines as phosphodiesterase inhibitors for treatment of dermal diseases
EP2254411A4 (fr) Inhibiteurs du complément en tant qu'agents thérapeutiques pour le traitement du cancer
EP2242501A4 (fr) Inhibiteurs thérapeutiques de la fonction de pai-i, et leurs procédés d'utilisation
EP2291284A4 (fr) Compositions pour traiter des matériaux et procédés de traitement associés
EP2411020A4 (fr) Compositions et procédés pour le traitement de l'hémorragie
EP2462435A4 (fr) Identification et utilisation de composés dans le traitement de la douleur persistante
GB0805119D0 (en) Treatment of myelination diseases
ZA201006046B (en) Methods of treating inflammation
HUP0900567A2 (en) Composition for heat treatment of wood and process for treatment of it