NO20084291L - 2,6-substituert-4-monosubstituert aminopyridin som prostaglandin D2 reseptor-antagonister - Google Patents

2,6-substituert-4-monosubstituert aminopyridin som prostaglandin D2 reseptor-antagonister

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Publication number
NO20084291L
NO20084291L NO20084291A NO20084291A NO20084291L NO 20084291 L NO20084291 L NO 20084291L NO 20084291 A NO20084291 A NO 20084291A NO 20084291 A NO20084291 A NO 20084291A NO 20084291 L NO20084291 L NO 20084291L
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Norway
Prior art keywords
pharmaceutically acceptable
accompanied
urticaria
itching
solvate
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NO20084291A
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English (en)
Inventor
Timothy Alan Gillespy
Keith John Harris
David Stefany
Joacy C Aguiar
Charles J Gardner
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Sanofi Aventis
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Publication of NO20084291L publication Critical patent/NO20084291L/no

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic 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
    • C07D403/04Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • 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
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs 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
    • 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
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/02Nasal agents, e.g. decongestants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/08Bronchodilators
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • AHUMAN NECESSITIES
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    • A61P17/00Drugs for dermatological disorders
    • A61P17/04Antipruritics
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    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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    • A61P25/20Hypnotics; Sedatives
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    • A61P27/02Ophthalmic agents
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • A61P27/14Decongestants or antiallergics
    • 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]
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • C07DHETEROCYCLIC COMPOUNDS
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    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
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    • C07DHETEROCYCLIC COMPOUNDS
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    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • 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)
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  • Life Sciences & Earth Sciences (AREA)
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  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
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  • Engineering & Computer Science (AREA)
  • Pulmonology (AREA)
  • Diabetes (AREA)
  • Obesity (AREA)
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  • Ophthalmology & Optometry (AREA)
  • Hematology (AREA)
  • Dermatology (AREA)
  • Rheumatology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Emergency Medicine (AREA)
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  • Child & Adolescent Psychology (AREA)
  • Cardiology (AREA)
  • Pain & Pain Management (AREA)
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  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Urology & Nephrology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Otolaryngology (AREA)

Abstract

Foreliggende oppfinnelse angår en forbindelse med formel (I) hvori Rog Rer som definert heri, eller et farmasøytisk akseptabelt salt, hydrat eller solvat derav, et farmasøytisk akseptabelt prodmg derav eller et farmasøytisk akseptabelt salt, hydrat eller solvat av prodmget, en farmasøytisk sammensetning som innbefatter en farmasøytisk effektiv mengde av en eller flere forbindelser ifølge oppfinnelsen blandet med en farmasøytisk akseptabel bærer, en fremgangsmåte for behandling av en pasient som lider av en PGD2 forstyrrelse som inkluderer, men er ikke begrenset til, allergisk sykdom (slik som allergisk rinitt, allergisk konjunktivitt, topisk dermatitt, bronkial astma og matallergi), systemisk mastocytose, forstyrrelser ledsaget av systemisk mastcelleaktivering, anafylaksisjokk, bronkokonstriksjon, bronkitt, urtikari, eksem, sykdommer ledsaget av kløe (slik som atopisk dermatitt og urtikari), sykdommer (slike som katarakt, retinal løsning, inflammasjon, infeksjon og søvnforstyrrelser) som genereres sekundært som et resultat av atferd ledsaget av kløen, (slik som skraping og banking), inflammasjon, kronisk obstruktiv lungesykdom, iskemisk reperfunksjonsskade, cerebrovaskulær ulykke, kronisk reumatoid artritt, pleurisy, ulcerativ kolitt og lignende ved administrering til nevnte pasient en farmasøytisk effektiv mengde av en forbindelse ifølge oppfinnelsen.
NO20084291A 2006-04-12 2008-10-14 2,6-substituert-4-monosubstituert aminopyridin som prostaglandin D2 reseptor-antagonister NO20084291L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US74467606P 2006-04-12 2006-04-12
PCT/US2007/066481 WO2007121280A1 (en) 2006-04-12 2007-04-12 2,6-substituted-4-monosubstituted amino-pyrimidine as prostaglandin d2 receptor antagonists

Publications (1)

Publication Number Publication Date
NO20084291L true NO20084291L (no) 2008-11-11

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NO20084291A NO20084291L (no) 2006-04-12 2008-10-14 2,6-substituert-4-monosubstituert aminopyridin som prostaglandin D2 reseptor-antagonister

Country Status (26)

Country Link
US (1) US20090036469A1 (no)
EP (1) EP2010503A1 (no)
JP (1) JP2009533473A (no)
KR (1) KR20080108287A (no)
CN (1) CN101421252B (no)
AR (1) AR060403A1 (no)
AU (1) AU2007238052B2 (no)
BR (1) BRPI0710710A2 (no)
CA (1) CA2649083C (no)
CR (1) CR10249A (no)
DO (1) DOP2007000068A (no)
EC (1) ECSP088813A (no)
HK (1) HK1131975A1 (no)
HN (1) HN2008001530A (no)
MA (1) MA30409B1 (no)
MX (1) MX2008011369A (no)
NO (1) NO20084291L (no)
NZ (1) NZ571793A (no)
PE (1) PE20080186A1 (no)
RU (1) RU2431631C2 (no)
TN (1) TNSN08339A1 (no)
TW (1) TW200815395A (no)
UA (1) UA95950C2 (no)
UY (1) UY30283A1 (no)
WO (1) WO2007121280A1 (no)
ZA (1) ZA200807380B (no)

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JP5039594B2 (ja) * 2008-02-08 2012-10-03 株式会社日立ハイテクノロジーズ レビュー装置,検査領域設定支援システム、および、欠陥の画像得方法
AR074776A1 (es) * 2008-12-18 2011-02-09 Sanofi Aventis Metodo para tratar la degeneracion macular; modulando el sistema inmunitario del paciente
RU2012143897A (ru) * 2010-03-16 2014-04-27 Авентис Фармасьютикалз Инк. Замещенные пиримидины как антагонисты рецепторов простагландина d2
JP2013522307A (ja) * 2010-03-16 2013-06-13 アベンティス・ファーマスーティカルズ・インコーポレイテツド プロスタグランジンd2受容体アンタゴニストとしての置換ピリミジン
WO2012004722A1 (en) 2010-07-05 2012-01-12 Actelion Pharmaceuticals Ltd 1-phenyl-substituted heterocyclyl derivatives and their use as prostaglandin d2 receptor modulators
EP2621276B1 (en) * 2010-09-30 2017-12-27 Merck Sharp & Dohme Corp. 2-alkoxy pyrimidine pde10 inhibitors
RU2014129613A (ru) 2011-12-21 2016-02-10 Актелион Фармасьютиклз Лтд Гетероциклильные производные и их применение в качестве модуляторов рецептора простагландина d2
CN104428305A (zh) 2012-07-05 2015-03-18 埃科特莱茵药品有限公司 1-苯基-取代的杂环衍生物及其作为前列腺素d2受体调节剂的用途
EP3382391A1 (en) 2012-10-24 2018-10-03 NYU Winthrop Hospital Non-invasive biomarker to identify subjects at risk of preterm delivery
EP3067349B1 (en) * 2013-11-08 2018-02-28 Kissei Pharmaceutical Co., Ltd. Carboxymethyl piperidine derivative
WO2016020288A1 (en) 2014-08-04 2016-02-11 Nuevolution A/S Optionally fused heterocyclyl-substituted derivatives of pyrimidine useful for the treatment of inflammatory, metabolic, oncologic and autoimmune diseases
CR20180323A (es) 2015-11-20 2018-08-06 Idorsia Pharmaceuticals Ltd Derivados de indol n-sustituídos como moduladores de los receptores de pge2
TW201900178A (zh) 2017-05-18 2019-01-01 瑞士商愛杜西亞製藥有限公司 作為pge2受體調節劑之嘧啶衍生物
CN110621671A (zh) 2017-05-18 2019-12-27 爱杜西亚药品有限公司 作为pge2受体调节剂的苯并呋喃及苯并噻吩衍生物
ES2896476T3 (es) 2017-05-18 2022-02-24 Idorsia Pharmaceuticals Ltd Derivados de pirimidina
HUE056080T2 (hu) 2017-05-18 2022-01-28 Idorsia Pharmaceuticals Ltd Fenilszármazékok mint PGE2 receptor modulátorok
KR20200109293A (ko) 2017-09-13 2020-09-22 프로제너티, 인크. 자간전증 바이오마커 및 관련된 시스템 및 방법
EP4029380A4 (en) * 2019-09-13 2023-09-13 Meiji Co., Ltd SOLID FOOD, AND SOLID MILK
EP4070113A4 (en) 2019-12-04 2023-12-20 Biora Therapeutics, Inc. ASSESSMENT OF PREECAMPSIA USING FREE AND DISSOCIATE PLACENTAL GROWTH FACTOR ASSAYS
EP4076657A1 (en) 2019-12-20 2022-10-26 Nuevolution A/S Compounds active towards nuclear receptors
CA3174176A1 (en) 2020-03-31 2021-10-07 Sanne Schroder Glad Compounds active towards nuclear receptors
MX2022012260A (es) 2020-03-31 2022-11-30 Nuevolution As Compuestos activos frente a receptores nucleares.

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DE3644799A1 (de) * 1986-06-04 1987-12-10 Hoechst Ag Neue pyrimidin-derivate, deren herstellung und verwendung
SE0200411D0 (sv) * 2002-02-05 2002-02-05 Astrazeneca Ab Novel use
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GT200600457A (es) * 2005-10-13 2007-04-27 Aventis Pharma Inc Sal de fosfato dihidrogeno como antagonistas del receptor de prostaglandina d2

Also Published As

Publication number Publication date
EP2010503A1 (en) 2009-01-07
DOP2007000068A (es) 2007-10-31
CN101421252A (zh) 2009-04-29
HK1131975A1 (en) 2010-02-12
AU2007238052B2 (en) 2011-12-22
TW200815395A (en) 2008-04-01
ZA200807380B (en) 2009-05-27
ECSP088813A (es) 2008-11-27
NZ571793A (en) 2011-08-26
UA95950C2 (en) 2011-09-26
HN2008001530A (es) 2012-01-17
RU2431631C2 (ru) 2011-10-20
US20090036469A1 (en) 2009-02-05
WO2007121280A1 (en) 2007-10-25
MA30409B1 (fr) 2009-05-04
KR20080108287A (ko) 2008-12-12
CR10249A (es) 2008-11-26
BRPI0710710A2 (pt) 2011-08-16
JP2009533473A (ja) 2009-09-17
CN101421252B (zh) 2011-10-12
AR060403A1 (es) 2008-06-11
AU2007238052A1 (en) 2007-10-25
MX2008011369A (es) 2008-09-18
RU2008144578A (ru) 2010-05-20
CA2649083C (en) 2011-06-28
TNSN08339A1 (en) 2009-12-29
CA2649083A1 (en) 2007-10-25
PE20080186A1 (es) 2008-04-15
UY30283A1 (es) 2007-11-30

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