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PE20060301A1 - DERIVADOS PIRROLOPIRIDINAS COMO ANTAGONISTAS DE CRTh2 - Google Patents

DERIVADOS PIRROLOPIRIDINAS COMO ANTAGONISTAS DE CRTh2

Info

Publication number
PE20060301A1
PE20060301A1 PE2005000686A PE2005000686A PE20060301A1 PE 20060301 A1 PE20060301 A1 PE 20060301A1 PE 2005000686 A PE2005000686 A PE 2005000686A PE 2005000686 A PE2005000686 A PE 2005000686A PE 20060301 A1 PE20060301 A1 PE 20060301A1
Authority
PE
Peru
Prior art keywords
alkyl
methyl
pyridin
benzyl
halogen
Prior art date
Application number
PE2005000686A
Other languages
English (en)
Inventor
Kamlesh Jagdis Bala
Catherine Leblanc
Katharine Louise Turner
Brian Cox
Lyndon Nigel Brown
Simon James Watson
David Andrew Sandham
Original Assignee
Novartis Ag
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 GB0413619A external-priority patent/GB0413619D0/en
Priority claimed from GB0507693A external-priority patent/GB0507693D0/en
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of PE20060301A1 publication Critical patent/PE20060301A1/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • 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
    • A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • 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
    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
    • 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
    • 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
    • A61P11/08—Bronchodilators
    • 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
    • A61P11/14—Antitussive agents
    • 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
    • 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
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Pulmonology (AREA)
  • Immunology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Biomedical Technology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)

Abstract

SE REFIERE A UN COMPUESTO DE LA FORMULA I, DONDE Q ES UN ENLACE, ALQUILENO C1-C10 SUSTITUIDO O NO POR HALOGENO; R1 Y R2 SON CADA UNO H, HALOGENO, ALQUILO C1-C8, ENTRE OTROS; R3 ES H, ALQUILO C1-C8, CARBOCICLO C3-C15, HALOALQUILO C1-C8, ENTRE OTROS; R4 Y R5 SON CADA UNO HALOGENO, ALQUILO C1-C8, HALOALQUILO C1-C8, ENTRE OTROS; R6 ES H, ALQUILO C1-C8; W ES CARBOCICLICO AROMATICO DE C6-C15, HETEROCICLICO DE 4-10 MIEMBROS CON AL MENOS UN HETEROATOMO SELECCIONADO DE N, O, S; X ES -SO2-, -CH2-, -CON- (ALQUILO C1-C8), ENTRE OTROS; m Y n SON CADA UNO 0-3; p ES 1. SON COMPUESTOS PREFERIDOS: ACIDO (1-BENCIL-2-METIL-1H-PIRROLO-[2,3-b]-PIRIDIN-3-IL)-ACETICO; [1-(3,4-DICLORO-BENCIL)-2-METIL-1H-PIRROLO-[2,3-b]-PIRIDIN-3-IL)-ACETICO; ACIDO [2-METIL-1-(2-METIL-BENCIL)-1H-PIRROLO-[2,3-b]-PIRIDIN-3-IL]-ACETICO. SE REFIERE TAMBIEN A UN PROCESO DE PREPARACION. DICHOS COMPUESTOS SON ANTAGONISTAS DE LA CRTh2 RECEPTORA QUIMIOATRAYENTE ACOPLADA CON PROTEINA-G SIENDO UTILES EN EL TRATAMIENTO DE CONDICIONES ALERGICAS, INFLAMATORIAS TALES COMO ASMA, PSORIASIS, CONJUNTIVITIS, ANEMIA APLASICA, ENTRE OTROS
PE2005000686A 2004-06-17 2005-06-15 DERIVADOS PIRROLOPIRIDINAS COMO ANTAGONISTAS DE CRTh2 PE20060301A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB0413619A GB0413619D0 (en) 2004-06-17 2004-06-17 Organic compounds
GB0507693A GB0507693D0 (en) 2005-04-15 2005-04-15 Organic compounds

Publications (1)

Publication Number Publication Date
PE20060301A1 true PE20060301A1 (es) 2006-05-18

Family

ID=35510318

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2005000686A PE20060301A1 (es) 2004-06-17 2005-06-15 DERIVADOS PIRROLOPIRIDINAS COMO ANTAGONISTAS DE CRTh2

Country Status (28)

Country Link
US (5) US7666878B2 (es)
EP (1) EP1761529B3 (es)
JP (1) JP4886680B2 (es)
KR (1) KR101183330B1 (es)
AR (1) AR049443A1 (es)
AT (1) ATE378338T1 (es)
AU (1) AU2005254681B2 (es)
BR (1) BRPI0512060B8 (es)
CA (1) CA2569125C (es)
CY (1) CY1107851T1 (es)
DE (1) DE602005003365T3 (es)
DK (1) DK1761529T3 (es)
EC (1) ECSP067077A (es)
ES (1) ES2294717T7 (es)
HR (1) HRP20080022T4 (es)
IL (1) IL179604A (es)
MA (1) MA28666B1 (es)
MX (1) MXPA06014694A (es)
MY (1) MY144903A (es)
NO (1) NO338319B1 (es)
NZ (1) NZ551439A (es)
PE (1) PE20060301A1 (es)
PL (1) PL1761529T6 (es)
PT (1) PT1761529E (es)
RS (1) RS50552B (es)
RU (1) RU2379309C2 (es)
TW (1) TWI352702B (es)
WO (1) WO2005123731A2 (es)

Families Citing this family (56)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7435837B2 (en) 2003-10-24 2008-10-14 Wyeth Dihydrobenzofuranyl alkanamine derivatives and methods for using same
MY144903A (en) 2004-06-17 2011-11-30 Novartis Ag Pyrrolopyridine derivatives and their use as crth2 antagonists
GB0525144D0 (en) * 2005-12-09 2006-01-18 Novartis Ag Organic compounds
GB0525143D0 (en) 2005-12-09 2006-01-18 Novartis Ag Organic compounds
GB0525337D0 (en) * 2005-12-13 2006-01-18 Novartis Ag Organic compounds
SI1986633T1 (sl) 2006-02-10 2015-03-31 Summit Corporation Plc Zdravljenje Duchennove mišične distrofije
GB0611695D0 (en) * 2006-06-13 2006-07-26 Novartis Ag Organic compounds
ATE530523T1 (de) 2006-08-07 2011-11-15 Actelion Pharmaceuticals Ltd (3-amino-1,2,3,4-tetrahydro-9h-carbazol-9-yl)- essigsäurederivate
CN101678107A (zh) * 2007-08-03 2010-03-24 萨米特公开有限公司 用于治疗杜兴型肌营养不良的药物组合物
GB0715937D0 (en) * 2007-08-15 2007-09-26 Vastox Plc Method of treatment og duchenne muscular dystrophy
WO2009102462A1 (en) * 2008-02-15 2009-08-20 Abbott Laboratories Thienopyrroles and pyrrolothiazoles as new therapeutic agents
HRP20170019T1 (hr) 2008-08-15 2017-03-10 Nivalis Therapeutics, Inc. Novi pirol-inhibitori od reduktaze s-nitrozoglutationa kao terapeutska sredstva
DK2318007T3 (da) 2008-08-15 2013-03-25 N30 Pharmaceuticals Inc Nye pyrrol-inhibitorer af s-nitrosoglutathion-reduktase som terapeutiske midler
EP2315590B1 (en) * 2008-08-15 2012-09-26 N30 Pharmaceuticals, LLC Pyrrole inhibitors of s-nitrosoglutathione reductase
MA34094B1 (fr) 2010-03-22 2013-03-05 Actelion Pharmaceuticals Ltd Dérivés de 3-(hétéroarylamino)-1,2,3,4-tétrahydro-9h-carbazole et leur utilisation comme modulateurs du récepteur de la prostaglandine d2
EP2457900A1 (en) 2010-11-25 2012-05-30 Almirall, S.A. New pyrazole derivatives having CRTh2 antagonistic behaviour
US9290453B2 (en) 2010-12-23 2016-03-22 Merck Sharp & Dohme Corp. Quinolines and aza-quinolines as CRTH2 receptor modulators
CN103702985B (zh) * 2010-12-23 2016-02-17 默沙东公司 作为crth2受体调节剂的喹喔啉和氮杂喹喔啉
AU2012241442B2 (en) 2011-04-14 2017-01-12 Idorsia Pharmaceuticals Ltd 7-(heteroaryl-amino)-6,7,8,9-tetrahydropyrido(1,2-a)indol acetic acid derivatives and their use as prostaglandin D2 receptor modulators
EP2545964A1 (en) 2011-07-13 2013-01-16 Phenex Pharmaceuticals AG Novel FXR (NR1H4) binding and activity modulating compounds
BR112014009108A2 (pt) 2011-10-25 2017-04-18 Shionogi & Co derivado heterocíclico tendo atividade antagonista de receptor de pgd2
SG11201402796SA (en) 2011-12-16 2014-06-27 Atopix Therapeutics Ltd Combination of crth2 antagonist and a proton pump inhibitor for the treatment of eosinophilic esophagitis
PL3119779T3 (pl) 2014-03-17 2019-01-31 Idorsia Pharmaceuticals Ltd Pochodne kwasu azaindolooctowego i ich zastosowanie jako modulatorów receptora prostaglandyny d2
TW201620909A (zh) 2014-03-18 2016-06-16 艾克泰聯製藥有限公司 氮雜吲哚乙酸衍生物及彼等作為前列腺素ｄ２受體調節劑之用途
US10689383B2 (en) 2014-08-04 2020-06-23 Nuevolution A/S Optionally fused heterocyclyl-substituted derivatives of pyrimidine useful for the treatment of inflammatory, metabolic, oncologic and autoimmune diseases
WO2016128565A1 (en) 2015-02-13 2016-08-18 Institut National De La Sante Et De La Recherche Medicale (Inserm) Ptgdr-1 and/or ptgdr-2 antagonists for preventing and/or treating systemic lupus erythematosus
AU2016297005A1 (en) 2015-07-23 2018-01-18 Merck Sharp & Dohme Corp. Genetic markers associated with response to CRTH2 receptor antagonists
UA123156C2 (uk) 2015-09-15 2021-02-24 Ідорсія Фармасьютікалз Лтд КРИСТАЛІЧНА ФОРМА (S)-2-(8-((5-ХЛОРПІРИМІДИН-2-ІЛ)(МЕТИЛ)АМІНО)-2-ФТОР-6,7,8,9-ТЕТРАГІДРО-5H-ПІРИДО[3,2-b]ІНДОЛ-5-ІЛ)ОЦТОВОЇ КИСЛОТИ, ЇЇ ЗАСТОСУВАННЯ ТА ФАРМАЦЕВТИЧНА КОМПОЗИЦІЯ, ЩО ЇЇ МІСТИТЬ
EP3353145B1 (en) 2015-09-23 2022-09-28 XWPharma Ltd. Prodrugs of gamma-hydroxybutyric acid, compositions and uses thereof
RU2744976C1 (ru) * 2015-09-29 2021-03-17 Новартис Аг Способ получения 1-(4-метансульфонил-2-трифторметилбензил)-2-метил-1н-пирроло[2,3-b]пиридин-3-ил-уксусной кислоты
WO2017210261A1 (en) * 2016-05-31 2017-12-07 Concert Pharmaceuticals, Inc. Deuterated fevipiprant
CA2968836A1 (en) 2016-06-13 2017-12-13 Gilead Sciences, Inc. Fxr (nr1h4) modulating compounds
JP6678779B2 (ja) 2016-06-13 2020-04-08 ギリアード サイエンシーズ， インコーポレイテッド Ｆｘｒ（ｎｒ１ｈ４）調節化合物
CN106188040B (zh) * 2016-06-28 2018-03-23 浙江宏鑫染化材料有限公司 一种Fevipiprant及其中间体的制备方法
US11524958B2 (en) 2016-07-21 2022-12-13 Chia Tai Tianqing Pharmaceutical Group Co., Ltd. Tricyclic compound as CRTH2 inhibitor
KR20220119520A (ko) 2017-03-28 2022-08-29 길리애드 사이언시즈, 인코포레이티드 간 질환을 치료하기 위한 치료 조합물
JP6991239B2 (ja) 2017-03-30 2022-01-12 エックスダブリューファルマ リミテッド 二環式ヘテロアリール誘導体ならびにその調製および使用
JOP20190223A1 (ar) * 2017-04-01 2019-09-26 Novartis Ag عملية لتحضير حمض 1-(4- ميثان سلفونيل -2- تراي فلورو ميثيل - بنزيل)-2- ميثيل -1h- بيرولو [2، 3-b] بيريدين -3- يل- أسيتيك
IL305317B1 (en) 2017-06-30 2025-07-01 Univ California Compositions and methods for modulating hair growth
WO2019011337A1 (zh) * 2017-07-14 2019-01-17 苏州科睿思制药有限公司 Qaw-039的晶型及其制备方法和用途
WO2019130166A1 (en) * 2017-12-26 2019-07-04 Mankind Pharma Ltd. Preparation of 2-[2-methyl-1-[[4-methylsulfonyl-2-(trifluoro methyl)phenyl]methyl] pyrrolo[2,3-b]pyridin-3-yl]acetic acid
EP3741754A4 (en) 2018-01-19 2021-06-09 Chia Tai Tianqing Pharmaceutical Group Co., Ltd. INDOLE DERIVATIVE CRYSTALLINE FORM AND PROCESS OF PREPARATION AND USE
CN110467612B (zh) * 2018-05-09 2020-09-25 新发药业有限公司 一种前列腺素d2受体抑制剂化合物的简便制备方法
JP6996029B2 (ja) 2018-09-30 2022-01-17 エックスダブリューファルマ リミテッド ニューロンヒスタミン受容体－３アンタゴニストとしての化合物およびその使用
CR20210385A (es) 2019-01-15 2021-09-14 Gilead Sciences Inc Compuestos moduladores de fxr (nr1h4)
KR102725082B1 (ko) 2019-02-19 2024-11-04 길리애드 사이언시즈, 인코포레이티드 Fxr 효능제의 고체 형태
GB201905721D0 (en) 2019-04-24 2019-06-05 Univ Dundee Compounds
CA3162919A1 (en) 2019-12-20 2021-06-24 XWPharma Ltd. Methods of synthesizing 4-valyloxybutyric acid
JP2021098692A (ja) 2019-12-20 2021-07-01 ヌエヴォリューション・アクティーゼルスカブＮｕｅｖｏｌｕｔｉｏｎ Ａ／Ｓ 核内受容体に対して活性の化合物
JP7713953B2 (ja) 2020-03-31 2025-07-28 ヌエヴォリューション・アクティーゼルスカブ 核内受容体に対して活性な化合物
WO2021198956A1 (en) 2020-03-31 2021-10-07 Nuevolution A/S Compounds active towards nuclear receptors
WO2021257886A1 (en) 2020-06-18 2021-12-23 XWPharma Ltd. Controlled release granulations of water-soluble active pharmaceutical ingredients
CN115803017A (zh) 2020-06-18 2023-03-14 凯瑞康宁生物工程有限公司 水溶性活性药物成分的药物造粒物
CN116261451A (zh) 2020-07-24 2023-06-13 凯瑞康宁生物工程有限公司 γ-羟基丁酸衍生物的药物组合物和药物动力学
CN119970650A (zh) 2020-10-05 2025-05-13 凯瑞康宁生物工程有限公司 γ-羟基丁酸衍生物的修饰释放组合物
CN117098533A (zh) 2021-03-19 2023-11-21 凯瑞康宁公司 γ-羟基丁酸衍生物的组合释放型制剂的药物动力学

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3320268A (en) * 1964-08-14 1967-05-16 Merck & Co Inc 1-aroyl or heteroaroyl-7-azaindole-3-carboxylates and derivatives
US5212195A (en) * 1992-05-13 1993-05-18 Syntex (U.S.A.) Inc. Substituted indole antagonists derivatives which are angiotensin II
GB9319297D0 (en) 1993-09-17 1993-11-03 Wellcome Found Indole derivatives
US6075037A (en) 1994-06-09 2000-06-13 Smithkline Beecham Corporation Endothelin receptor antagonists
DE69510940T2 (de) * 1994-06-16 1999-11-11 Pfizer Inc., New York Pyrazolo und pyrrolopyridine
TWI262920B (en) 2000-10-27 2006-10-01 Elbion Ag New 7-azaindoles, their use as inhibitors of phosphodiesterase 4, and a method for synthesizing them
EP1424325A4 (en) 2001-09-07 2005-12-21 Ono Pharmaceutical Co INDOLE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND MEDICAMENTS CONTAINING THEM AS AN ACTIVE AGENT
SE0200356D0 (sv) * 2002-02-05 2002-02-05 Astrazeneca Ab Novel use
SE0200411D0 (sv) 2002-02-05 2002-02-05 Astrazeneca Ab Novel use
US7534897B2 (en) * 2002-05-16 2009-05-19 Shionogi & Co., Ltd. Indole arylsulfonaimide compounds exhibiting PGD 2 receptor antagonism
SE0201635D0 (sv) * 2002-05-30 2002-05-30 Astrazeneca Ab Novel compounds
SE0202241D0 (sv) * 2002-07-17 2002-07-17 Astrazeneca Ab Novel Compounds
WO2005040112A1 (en) * 2003-10-14 2005-05-06 Oxagen Limited Compounds with pgd2 antagonist activity
GB0412914D0 (en) * 2004-06-10 2004-07-14 Oxagen Ltd Compounds
MY144903A (en) 2004-06-17 2011-11-30 Novartis Ag Pyrrolopyridine derivatives and their use as crth2 antagonists
GB0525144D0 (en) * 2005-12-09 2006-01-18 Novartis Ag Organic compounds
GB0525143D0 (en) * 2005-12-09 2006-01-18 Novartis Ag Organic compounds
GB0525337D0 (en) * 2005-12-13 2006-01-18 Novartis Ag Organic compounds

Also Published As

Publication number Publication date
CY1107851T1 (el) 2013-06-19
HRP20080022T3 (en) 2008-02-29
DE602005003365T2 (de) 2008-09-11
TWI352702B (en) 2011-11-21
IL179604A0 (en) 2007-05-15
PL1761529T3 (pl) 2008-04-30
ECSP067077A (es) 2007-01-26
US20140309254A1 (en) 2014-10-16
US9169251B2 (en) 2015-10-27
US20100204225A1 (en) 2010-08-12
KR20070032694A (ko) 2007-03-22
CA2569125A1 (en) 2005-12-29
MA28666B1 (fr) 2007-06-01
PL1761529T6 (pl) 2011-11-30
NO338319B1 (no) 2016-08-08
DE602005003365D1 (de) 2011-01-05
US20080114022A1 (en) 2008-05-15
AU2005254681A1 (en) 2005-12-29
MXPA06014694A (es) 2007-02-12
EP1761529B1 (en) 2007-11-14
NZ551439A (en) 2009-09-25
HRP20080022T4 (hr) 2011-10-31
TW200617009A (en) 2006-06-01
EP1761529A2 (en) 2007-03-14
WO2005123731A3 (en) 2006-05-04
JP4886680B2 (ja) 2012-02-29
PT1761529E (pt) 2008-02-11
HK1103730A1 (en) 2007-12-28
ATE378338T1 (de) 2007-11-15
CA2569125C (en) 2013-01-08
WO2005123731A2 (en) 2005-12-29
US20100210610A1 (en) 2010-08-19
DE602005003365T3 (de) 2012-08-30
BRPI0512060B1 (pt) 2018-08-07
JP2008502638A (ja) 2008-01-31
RS50552B (sr) 2010-05-07
EP1761529B3 (en) 2011-06-15
BRPI0512060B8 (pt) 2021-05-25
NO20070323L (no) 2007-03-12
US7666878B2 (en) 2010-02-23
US8791256B2 (en) 2014-07-29
US8455645B2 (en) 2013-06-04
US20130267518A1 (en) 2013-10-10
ES2294717T3 (es) 2008-04-01
KR101183330B1 (ko) 2012-09-17
AU2005254681B2 (en) 2009-01-29
IL179604A (en) 2014-04-30
ES2294717T7 (es) 2012-06-14
AR049443A1 (es) 2006-08-02
DK1761529T3 (da) 2008-03-25
RU2379309C2 (ru) 2010-01-20
BRPI0512060A (pt) 2008-02-06
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MY144903A (en) 2011-11-30
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