MA30991B1 - Utilisation de dérivés du benzamide comme agonistes des récepteurs ep4 - Google Patents

Utilisation de dérivés du benzamide comme agonistes des récepteurs ep4

Info

Publication number
MA30991B1
MA30991B1 MA31990A MA31990A MA30991B1 MA 30991 B1 MA30991 B1 MA 30991B1 MA 31990 A MA31990 A MA 31990A MA 31990 A MA31990 A MA 31990A MA 30991 B1 MA30991 B1 MA 30991B1
Authority
MA
Morocco
Prior art keywords
agonists
receptors
benzamide derivatives
compounds
benzamide
Prior art date
Application number
MA31990A
Other languages
English (en)
Inventor
Alessandra Gaiba
Mark Patrick Healy
Christopher Norbert Johnson
Susan Roomans
Steven James Stanway
Martin Edward Swarbrick
Original Assignee
Glaxo Group Ltd
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 GB0625098A external-priority patent/GB0625098D0/en
Priority claimed from GB0715145A external-priority patent/GB0715145D0/en
Application filed by Glaxo Group Ltd filed Critical Glaxo Group Ltd
Publication of MA30991B1 publication Critical patent/MA30991B1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
    • C07C235/42—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton
    • C07C235/44—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring
    • C07C235/56—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a six-membered aromatic ring
    • 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
    • A61K31/16—Amides, e.g. hydroxamic acids
    • A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • A61K31/167—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
    • 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
    • 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
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/06—Antimigraine agents
    • 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
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (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)
  • Pain & Pain Management (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Rheumatology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Immunology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Hydrogenated Pyridines (AREA)

Abstract

CETTE INVENTION CONCERNE UN COMPOSÉ DE FORMULE (I) OU SON DÉRIVÉ PHARMACEUTIQUEMENT ACCEPTABLE, OÙ R1, R2, R3, R4, R5, M, N ET X SONT TELS QUE DÉFINIS DANS LE MÉMOIRE. L'INVENTION DÉCRIT ÉGALEMENT UN PROCÉDÉ PERMETTANT DE PRÉPARER DE TELS COMPOSÉS, UNE COMPOSITION PHARMACEUTIQUE COMPRENANT CES COMPOSÉS, AINSI QUE L'UTILISATION PHARMACOLOGIQUE DE CES COMPOSÉS.
MA31990A 2006-12-15 2009-06-15 Utilisation de dérivés du benzamide comme agonistes des récepteurs ep4 MA30991B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB0625098A GB0625098D0 (en) 2006-12-15 2006-12-15 Novel compounds
GB0715145A GB0715145D0 (en) 2007-08-03 2007-08-03 Novel compounds

Publications (1)

Publication Number Publication Date
MA30991B1 true MA30991B1 (fr) 2009-12-01

Family

ID=39149241

Family Applications (1)

Application Number Title Priority Date Filing Date
MA31990A MA30991B1 (fr) 2006-12-15 2009-06-15 Utilisation de dérivés du benzamide comme agonistes des récepteurs ep4

Country Status (21)

Country Link
US (3) US20080167377A1 (fr)
EP (1) EP2101751A1 (fr)
JP (1) JP5069752B2 (fr)
KR (1) KR20090089868A (fr)
AR (1) AR064361A1 (fr)
AU (1) AU2007331471C1 (fr)
BR (1) BRPI0720254A2 (fr)
CA (1) CA2672631A1 (fr)
CL (1) CL2007003640A1 (fr)
CR (1) CR10849A (fr)
DO (1) DOP2009000124A (fr)
EA (1) EA015931B1 (fr)
IL (1) IL198931A0 (fr)
MA (1) MA30991B1 (fr)
MX (1) MX2009006474A (fr)
NO (1) NO20092314L (fr)
NZ (1) NZ577109A (fr)
PE (1) PE20081579A1 (fr)
SG (1) SG177203A1 (fr)
TW (1) TW200848014A (fr)
WO (1) WO2008071736A1 (fr)

Families Citing this family (25)

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EP2172447A4 (fr) * 2007-07-03 2011-08-24 Astellas Pharma Inc Composé amide
GB0721611D0 (en) 2007-11-02 2007-12-12 Glaxo Group Ltd Novel compounds
WO2009085177A1 (fr) * 2007-12-19 2009-07-09 Amgen Inc. Dérivés de l'acide phénylacétique utiles comme modulateurs de l'inflammation
AU2009247262B2 (en) * 2008-05-14 2013-01-31 Astellas Pharma Inc. Amide compound
GB0810313D0 (en) * 2008-06-05 2008-07-09 Glaxo Group Ltd Novel compounds
GB0810617D0 (en) * 2008-06-10 2008-07-16 Glaxo Group Ltd Novel pharmaceutical
GB0810615D0 (en) * 2008-06-10 2008-07-16 Glaxo Group Ltd Novel pharmaceutical
ES2512727T3 (es) * 2009-09-29 2014-10-24 Glaxo Group Limited Nuevos compuestos
CN104292154A (zh) * 2009-09-29 2015-01-21 葛兰素集团有限公司 新化合物
CN102655859A (zh) 2009-10-14 2012-09-05 格穆斯药业股份有限公司 病毒感染的组合疗法治疗
AR082428A1 (es) * 2010-07-30 2012-12-05 Allergan Inc Uso de un compuesto agonista de ep4 para preparar una composicion farmaceutica util para tratar una imperfeccion de la piel y metodos para reparar la piel relacionados
US8894992B2 (en) 2010-08-19 2014-11-25 Allergan, Inc. Compositions and soft tissue replacement methods
US8926963B2 (en) 2010-08-19 2015-01-06 Allergan, Inc. Compositions and soft tissue replacement methods
US8900571B2 (en) 2010-08-19 2014-12-02 Allergan, Inc. Compositions and soft tissue replacement methods
HUE031408T2 (en) 2010-09-21 2017-07-28 Eisai R&D Man Co Ltd Pharmaceutical preparation
US20120142684A1 (en) * 2010-12-02 2012-06-07 Allergan, Inc. Compounds and methods for skin repair
EP2814527A1 (fr) * 2012-02-16 2014-12-24 Allergan, Inc. Compositions et procédés perfectionnés de remplacement de tissu mou
EP2765128A1 (fr) 2013-02-07 2014-08-13 Almirall, S.A. Benzamides substitués présentant une activité vis-à-vis de récepteurs EP4
CN105979959B (zh) 2013-08-09 2021-11-30 阿德利克斯公司 用于抑制磷酸盐转运的化合物和方法
ES2919346T3 (es) * 2014-03-06 2022-07-26 Elanco Animal Health Incorporated Forma cristalina x2 de grapiprant
US10407376B2 (en) 2015-01-16 2019-09-10 Nederlandse Organisatie Voor Toegepast-Natuurwetenschappelijk Onderzoek Tno Method to prepare phenolics from biomass
EP3184505A1 (fr) 2015-12-22 2017-06-28 Nederlandse Organisatie voor toegepast- natuurwetenschappelijk onderzoek TNO Procédé de préparation de composés phénoliques à l'aide d'un catalyseur
US20220202774A1 (en) * 2019-04-09 2022-06-30 Neurobit Science Co., Ltd. Pharmaceutical composition for prevention or treatment of spinal cord injury or spinal stenosis
WO2020237096A1 (fr) 2019-05-21 2020-11-26 Ardelyx, Inc. Combinaison pour baisser le phosphate sérique chez un patient
CN111454150B (zh) * 2019-12-25 2023-03-28 南京工业大学 一种(s)-2-芳基丙酸酯类化合物的合成方法

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JPH10265454A (ja) 1997-01-27 1998-10-06 Ono Pharmaceut Co Ltd ３，７−ジチアプロスタン酸誘導体、それらの製造方法およびそれらを有効成分として含有する薬剤
AUPO713297A0 (en) 1997-06-02 1997-06-26 Fujisawa Pharmaceutical Co., Ltd. Oxazole compound
US6043275A (en) 1998-04-16 2000-03-28 Ono Pharmaceutical Co., Ltd. 3,7-dithiaprostanoic acid derivative
TWI249520B (en) 1998-07-15 2006-02-21 Ono Pharmaceutical Co 5-Thia-omega-substituted phenyl prostaglandin E derivatives, method for producing the same and medicines containing the same as the active ingredient
WO2000015608A1 (fr) 1998-09-14 2000-03-23 Ono Pharmaceutical Co., Ltd. Derives e de phenyl-prostaglandine a substitution-φ et medicaments les contenant comme ingredient actif
AUPP608898A0 (en) 1998-09-23 1998-10-15 Fujisawa Pharmaceutical Co., Ltd. New use of prostaglandin E2 antagonists
US6437146B1 (en) 1998-09-25 2002-08-20 Fujisawa Pharmaceutical Co., Ltd. Oxazole compounds as prostaglandin e2 agonists or antagonists
WO2000021532A1 (fr) 1998-10-15 2000-04-20 Merck & Co., Inc. Inhibition de la resorption osseuse
GB0031315D0 (en) 2000-12-21 2001-02-07 Glaxo Group Ltd Indole derivatives
GB0031295D0 (en) 2000-12-21 2001-01-31 Glaxo Group Ltd Naphthalene derivatives
GB0031302D0 (en) 2000-12-21 2001-01-31 Glaxo Group Ltd Napthalene derivatives
GB0103269D0 (en) 2001-02-09 2001-03-28 Glaxo Group Ltd Napthalene derivatives
SE0102300D0 (sv) * 2001-06-26 2001-06-26 Astrazeneca Ab Compounds
SE0102764D0 (sv) * 2001-08-17 2001-08-17 Astrazeneca Ab Compounds
JP2005531516A (ja) 2002-03-18 2005-10-20 ファイザー・プロダクツ・インク 選択的ｅｐ４受容体アゴニストによる治療方法
NZ535748A (en) 2002-04-12 2007-06-29 Pfizer Use of EP4 receptor ligands in the treatment of IL-6 involved diseases
WO2003103604A2 (fr) 2002-06-01 2003-12-18 Applied Research Systems Ars Holding N.V Gamma lactames utilises en tant qu'agonistes de la prostaglandine et leur utilisation
AU2003275838A1 (en) 2002-10-25 2004-05-13 Beunard, Jean-Luc Pyrrolidin-2-on derivatives as ep4 receptor agonists
US7053085B2 (en) 2003-03-26 2006-05-30 Merck & Co. Inc. EP4 receptor agonist, compositions and methods thereof
RU2311409C2 (ru) * 2003-01-10 2007-11-27 Ф.Хоффманн-Ля Рош Аг Производные 2-пиперидона в качестве агонистов простагландина
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WO2005021508A1 (fr) 2003-09-03 2005-03-10 Pfizer Inc. Composes de phenyle ou de pyridyle amide utiles comme antagonistes de la prostaglandine e2
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US7326732B2 (en) * 2004-02-12 2008-02-05 Pharmagene Laboratories Limited EP2 receptor agonists
CA2565813C (fr) 2004-05-04 2010-10-26 Pfizer Inc. Composes methylaryl- ou heteroarylamides substitues
AP2006003769A0 (en) * 2004-05-04 2006-10-31 Pfizer Ortho substituted aryl or heteroaryl amide compounds
WO2005116010A1 (fr) 2004-05-26 2005-12-08 Merck Frosst Canada Ltd. Agoniste du recepteur ep4, compositions et methodes associees ep4 receptor agonist, compositions and methods thereof
JP5289046B2 (ja) * 2005-05-19 2013-09-11 メルク カナダ インコーポレイテッド Ｅｐ４アンタゴニストとしてのキノリン誘導体

Also Published As

Publication number Publication date
EA200970585A1 (ru) 2009-10-30
KR20090089868A (ko) 2009-08-24
EA015931B1 (ru) 2011-12-30
AU2007331471B2 (en) 2013-01-10
TW200848014A (en) 2008-12-16
IL198931A0 (en) 2010-02-17
JP5069752B2 (ja) 2012-11-07
AR064361A1 (es) 2009-04-01
US20100022650A1 (en) 2010-01-28
DOP2009000124A (es) 2010-03-31
CR10849A (es) 2009-08-12
CL2007003640A1 (es) 2008-07-11
BRPI0720254A2 (pt) 2014-01-07
EP2101751A1 (fr) 2009-09-23
NZ577109A (en) 2011-12-22
JP2010513242A (ja) 2010-04-30
US8314147B2 (en) 2012-11-20
AU2007331471C1 (en) 2013-07-25
MX2009006474A (es) 2009-06-26
US20130261185A1 (en) 2013-10-03
NO20092314L (no) 2009-08-31
US20080167377A1 (en) 2008-07-10
AU2007331471A1 (en) 2008-06-19
CA2672631A1 (fr) 2008-06-19
WO2008071736A1 (fr) 2008-06-19
PE20081579A1 (es) 2009-01-01
SG177203A1 (en) 2012-01-30

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