MA28111A1 - Derives des - Google Patents

Derives des

Info

Publication number
MA28111A1
MA28111A1 MA28965A MA28965A MA28111A1 MA 28111 A1 MA28111 A1 MA 28111A1 MA 28965 A MA28965 A MA 28965A MA 28965 A MA28965 A MA 28965A MA 28111 A1 MA28111 A1 MA 28111A1
Authority
MA
Morocco
Prior art keywords
mch
anxiety
obesity
diabetes
depression
Prior art date
Application number
MA28965A
Other languages
English (en)
Inventor
Kevin K Barvian
Anthony L Handlon
Donald L Hertzog
Clifton E Hyman
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
Application filed by Glaxo Group Ltd filed Critical Glaxo Group Ltd
Publication of MA28111A1 publication Critical patent/MA28111A1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04—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
    • A61K31/495—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
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • 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
    • A61P25/22—Anxiolytics
    • 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
    • A61P25/24—Antidepressants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/04—Anorexiants; Antiobesity agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • 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)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Diabetes (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Biomedical Technology (AREA)
  • Pain & Pain Management (AREA)
  • Psychiatry (AREA)
  • Child & Adolescent Psychology (AREA)
  • Endocrinology (AREA)
  • Emergency Medicine (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

Dérivés de 3-(4-aminophényl)-thiénopyrimid-4-one servant d'antagonistes de MCH R1 pour le traitement de l'obésité, du diabète, de la dépression et de l'anxiété La présente invention concerne des arylamines nouvelles qui sont des antagonistes du récepteur 1 de l'hormone concentrant la mélanine (MCH R1), des compositions pharmaceutiques les contenant, des procédés pour leur préparation, et leur utilisation dans des médicaments pour le traitement de l'obésité, du diabète, de la dépression et/ou de l'anxiété. Les composés de la présente invention répondent à la formule:
MA28965A 2003-10-23 2006-04-25 Derives des MA28111A1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US51380003P 2003-10-23 2003-10-23

Publications (1)

Publication Number Publication Date
MA28111A1 true MA28111A1 (fr) 2006-08-01

Family

ID=34549304

Family Applications (1)

Application Number Title Priority Date Filing Date
MA28965A MA28111A1 (fr) 2003-10-23 2006-04-25 Derives des

Country Status (15)

Country Link
US (1) US20070078125A1 (fr)
EP (1) EP1678184A1 (fr)
JP (1) JP2007509158A (fr)
KR (1) KR20060100412A (fr)
CN (1) CN1871242A (fr)
AU (1) AU2004285913A1 (fr)
BR (1) BRPI0415667A (fr)
CA (1) CA2543122A1 (fr)
CO (1) CO5690599A2 (fr)
IL (1) IL174693A0 (fr)
MA (1) MA28111A1 (fr)
MX (1) MXPA06003997A (fr)
NO (1) NO20061909L (fr)
WO (1) WO2005042541A1 (fr)
ZA (1) ZA200603181B (fr)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080221107A1 (en) * 2005-07-15 2008-09-11 Astrazeneca Ab Therapeutic Agents
AU2006298852A1 (en) 2005-09-30 2007-04-12 F. Hoffmann-La Roche Ag Indane derivatives as MCH receptor antagonists
US8618115B2 (en) * 2005-10-26 2013-12-31 Bristol-Myers Squibb Company Substituted thieno[3,2-d]pyrimidinones as MCHR1 antagonists and methods for using them
US7745447B2 (en) 2005-10-26 2010-06-29 Bristol-Myers Squibb Company Substituted thieno[3,2-D]pyrimidines as non-basic melanin concentrating hormone receptor-1 antagonists
JP5193878B2 (ja) 2005-12-21 2013-05-08 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ Ｍｃｈ−１が媒介する疾患における使用のための新規な置換ピラジノン誘導体
US7553836B2 (en) 2006-02-06 2009-06-30 Bristol-Myers Squibb Company Melanin concentrating hormone receptor-1 antagonists
TW200801022A (en) 2006-02-15 2008-01-01 Sanofi Aventis Novel amino alcohol-substituted arylthienopyrimidinones, process for their preparation and their use as medicaments
ATE495157T1 (de) 2006-02-15 2011-01-15 Sanofi Aventis Neue aminoalkohol-substituierte aryldihydroisochinolinone, herstellungsverfahren und ihre verwendung als medikamente
JP5175228B2 (ja) 2006-02-15 2013-04-03 サノフイ 新規なアザシクリル置換アリールジヒドロイソキノリノン、それらの製造方法及び薬剤としてそれらの使用
JP2009526792A (ja) * 2006-02-15 2009-07-23 サノフィ−アベンティス 新規なアザシクリル置換アリールチエノピリミジノン、それらの製造方法及び薬剤としてのそれらの使用
CN101454328A (zh) * 2006-06-08 2009-06-10 伊莱利利公司 新的mch受体拮抗剂
JP2010501553A (ja) 2006-08-18 2010-01-21 アストラゼネカ アクチボラグ Ｍｃｈｒ１アンタゴニストとしてのチエノピリミジン−４−オン誘導体およびチエノピリダジン−７−オン誘導体
BRPI0806537A2 (pt) 2007-01-10 2014-04-22 Albany Molecular Res Inc Indazóis substituídos por 5-piridinona
WO2008134480A1 (fr) * 2007-04-25 2008-11-06 Bristol-Myers Squibb Company Antagonistes du récepteur 1 de l'hormone de mélano-concentration non basiques
ATE544759T1 (de) 2007-07-21 2012-02-15 Albany Molecular Res Inc 5-pyridinon-substituierte indazole und pharmazeutische zusammensetzungen davon
PE20091928A1 (es) 2008-05-29 2009-12-31 Bristol Myers Squibb Co Tienopirimidinas hidroxisustituidas como antagonistas de receptor-1 de hormona concentradora de melanina no basicos
US8278316B2 (en) 2009-03-09 2012-10-02 Bristol-Myers Squibb Company Aza pyridone analogs useful as melanin concentrating hormone receptor-1 antagonists
HUP1100241A3 (en) 2011-05-06 2013-12-30 Richter Gedeon Nyrt Oxetane substituted pyrimidones
KR20130013199A (ko) * 2011-07-27 2013-02-06 한미약품 주식회사 신규 피리미딘 유도체 및 이를 활성성분으로 포함하는 약학 조성물
WO2013032535A1 (fr) 2011-08-26 2013-03-07 O'neil Michael P Système et procédé de détatouage
AU2021206286A1 (en) * 2020-01-10 2024-08-08 Consynance Therapeutics, Inc. Therapeutic combinations of drugs and methods of using them
HUP2200222A1 (hu) 2022-06-17 2023-12-28 Richter Gedeon Nyrt MCHR1 antagonisták a Prader-Willi szindróma kezelésére

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0124627D0 (en) * 2001-10-15 2001-12-05 Smithkline Beecham Plc Novel compounds

Also Published As

Publication number Publication date
EP1678184A1 (fr) 2006-07-12
ZA200603181B (en) 2008-01-30
AU2004285913A1 (en) 2005-05-12
JP2007509158A (ja) 2007-04-12
IL174693A0 (en) 2006-08-20
KR20060100412A (ko) 2006-09-20
CN1871242A (zh) 2006-11-29
US20070078125A1 (en) 2007-04-05
CO5690599A2 (es) 2006-10-31
BRPI0415667A (pt) 2006-12-19
WO2005042541A1 (fr) 2005-05-12
MXPA06003997A (es) 2006-07-05
NO20061909L (no) 2006-05-03
CA2543122A1 (fr) 2005-05-12

Similar Documents

Publication Publication Date Title
MA28111A1 (fr) Derives des
MA30539B1 (fr) Derives de piperazinyle utiles dans le traitement de maladies induites par le recepteur gpr38.
ATE422887T1 (de) Kondensierte heterozyklische verbindungen
MA29693B1 (fr) Derives de xanthine en tant qu'agonistes hm74a selectifs
ATE423769T1 (de) Fluor- und sulfonylaminohaltige, 3,6- disubstituierte azabicyclo 3.1.0 hexanderivate als muscarinrezeptorantagonisten
SE9902987D0 (sv) Novel compounds
TNSN08137A1 (fr) Derives de carboxamides servant d'antagonistes des recepteurs muscariniques
PL1716152T3 (pl) Skondensowane związki heterocykliczne i ich zastosowanie jako antagonistów receptora metabotropowego do leczenia zaburzeń żołądkowo-jelitowych
MA26722A1 (fr) Nouveaux composes et medicaments les contenant
MA30778B1 (fr) Derives de sulfonamides servant d'agonistes adrenergique et d'antagonistes muscariniques
MA30999B1 (fr) Composés.
MA30289B1 (fr) Dérivés d'amines
MA27448A1 (fr) Derives de pyridine modulateurs du recepteur cb2
TW200510429A (en) Heterocyclic MCHR1 antagonists
TR199901710T2 (xx) IL-8 resept�r antagonistleri.
DE60237528D1 (de) Neue aminoazetidin-, aminopyrrolidin- und aminopiperidinderivative
MA30696B1 (fr) Derives de l'acide (3-amino-1,2,3,4-tetrahydro-9h-carbazol-9-yl)-acetique
TNSN04194A1 (fr) Derives de tropane servant de modulateurs de ccr5
EP2042490A3 (fr) Dérivés du benzoimidazole comme antagonistes du recepteur Vanilloid
TR200402529T4 (tr) Yeni Fenalliloksi fenil türevleri.
DE60226906D1 (de) 3,6-disubstituierte azabicyclo ä3.1.0ühexanderivate, die sich als muscarinrezeptorantagonisten eignen
ATE276246T1 (de) Chemische verbindungen
EP2202222A3 (fr) Dérivés d'indène, leur préparation et leur utilisation en tant que médicaments
TR199901761T2 (xx) IL-8 resept�r antagonistleri.
TR200103638T2 (tr) IL-8 Reseptör antagonistleri