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WO2004030637A3 - Treatment of obesity and other disorders associated with excessive food intake - Google Patents

Treatment of obesity and other disorders associated with excessive food intake Download PDF

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Publication number
WO2004030637A3
WO2004030637A3 PCT/US2003/009717 US0309717W WO2004030637A3 WO 2004030637 A3 WO2004030637 A3 WO 2004030637A3 US 0309717 W US0309717 W US 0309717W WO 2004030637 A3 WO2004030637 A3 WO 2004030637A3
Authority
WO
WIPO (PCT)
Prior art keywords
obesity
food intake
disorders associated
treatment
excessive food
Prior art date
Legal status (The legal status 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 status listed.)
Ceased
Application number
PCT/US2003/009717
Other languages
French (fr)
Other versions
WO2004030637A2 (en
Inventor
Margaret J Bradbury
Nicholas D P Cosford
Mark A Varney
Jeffery J Anderson
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Merck and Co Inc
Original Assignee
Merck and Co Inc
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 PCT/US2002/031294 external-priority patent/WO2003029210A2/en
Priority claimed from PCT/US2002/041720 external-priority patent/WO2003051315A2/en
Priority claimed from PCT/US2002/040147 external-priority patent/WO2003051833A2/en
Priority claimed from PCT/US2002/040237 external-priority patent/WO2003053922A2/en
Priority claimed from PCT/US2002/040486 external-priority patent/WO2003059904A1/en
Application filed by Merck and Co Inc filed Critical Merck and Co Inc
Priority to AU2003218462A priority Critical patent/AU2003218462A1/en
Publication of WO2004030637A2 publication Critical patent/WO2004030637A2/en
Publication of WO2004030637A3 publication Critical patent/WO2004030637A3/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/4353Heterocyclic 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
    • A61K31/437Heterocyclic 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
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/04Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/14Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • 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
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic 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
    • C07D413/04Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic 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
    • C07D417/02Heterocyclic 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
    • C07D417/04Heterocyclic 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

Modulators of metabotropic glutamate receptor-5 (mGluR5) are useful in treating disorders associated with excessive food intake, including obesity and obesity-related disorders. In particular, mGluR5 antagonists of structural formulae IA-IF are useful in treating these conditions, either as single agents or in combination with other compounds useful for treating obesity.
PCT/US2003/009717 2002-10-01 2003-03-31 Treatment of obesity and other disorders associated with excessive food intake Ceased WO2004030637A2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU2003218462A AU2003218462A1 (en) 2002-10-01 2003-03-31 Treatment of obesity and other disorders associated with excessive food intake

Applications Claiming Priority (10)

Application Number Priority Date Filing Date Title
PCT/US2002/031294 WO2003029210A2 (en) 2001-10-04 2002-10-01 Heteroaryl substituted tetrazole modulators of metabotropic glutamate receptor-5
USPCT/US02/31294 2002-10-01
USPCT/US02/40147 2002-12-13
PCT/US2002/041720 WO2003051315A2 (en) 2001-12-18 2002-12-13 Heteroaryl substituted triazole modulators of metabotropic glutamate receptor-5
PCT/US2002/040147 WO2003051833A2 (en) 2001-12-18 2002-12-13 Heteroaryl substituted pyrazole modulators of metabotropic glutamate receptor-5
USPCT/US02/41720 2002-12-13
USPCT/US02/40237 2002-12-16
PCT/US2002/040237 WO2003053922A2 (en) 2001-12-19 2002-12-16 Heteroaryl substituted imidazole modulators of metabotropic glutamate receptor-5
PCT/US2002/040486 WO2003059904A1 (en) 2001-12-21 2002-12-17 Heteroaryl substituted pyrrole modulators of metabotropic glutamate receptor-5
USPCT/US02/40486 2002-12-17

Publications (2)

Publication Number Publication Date
WO2004030637A2 WO2004030637A2 (en) 2004-04-15
WO2004030637A3 true WO2004030637A3 (en) 2004-09-23

Family

ID=32074735

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2003/009717 Ceased WO2004030637A2 (en) 2002-10-01 2003-03-31 Treatment of obesity and other disorders associated with excessive food intake

Country Status (2)

Country Link
AU (1) AU2003218462A1 (en)
WO (1) WO2004030637A2 (en)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006071730A1 (en) * 2004-12-27 2006-07-06 Astrazeneca Ab Pyrazolone compounds as metabotropic glutamate receptor agonists for the treatment of neurological and psychiatric disorders
EP2513087A1 (en) * 2009-12-18 2012-10-24 NeuroSearch A/S Tetrazole derivatives as nicotinic acetylcholine receptor moudlators
ME03564B (en) 2013-03-13 2020-07-20 Forma Therapeutics Inc 2-hydroxy-1-{4-[(4-phenylphenyl)carbonyl]piperazin-1-yl}ethan-1-one derivatives and related compounds as fatty acid synthase (fasn) inhibitors for the treatment of cancer
US8652527B1 (en) 2013-03-13 2014-02-18 Upsher-Smith Laboratories, Inc Extended-release topiramate capsules
US9101545B2 (en) 2013-03-15 2015-08-11 Upsher-Smith Laboratories, Inc. Extended-release topiramate capsules
CN112020500A (en) 2017-12-22 2020-12-01 拉文纳制药公司 Aminopyridine derivatives as phosphatidylinositol phosphokinase inhibitors
TWI767148B (en) 2018-10-10 2022-06-11 美商弗瑪治療公司 Inhibiting fatty acid synthase (fasn)
CN113382633A (en) 2018-10-29 2021-09-10 福马治疗股份有限公司 Solid forms of (4- (2-fluoro-4- (1-methyl-1H-benzo [ d ] imidazol-5-yl) benzoyl) piperazin-1-yl) (1-hydroxycyclopropyl) methanone
TW202112767A (en) 2019-06-17 2021-04-01 美商佩特拉製藥公司 Aminopyridine derivatives as phosphatidylinositol phosphate kinase inhibitors
MX2023009059A (en) 2021-02-02 2023-09-15 Liminal Biosciences Ltd GPR84 ANTAGONISTS AND USES OF THESE.
PL247051B1 (en) * 2022-11-29 2025-05-05 Univ Medyczny W Lublinie N-substituted derivatives of 1-(1-phenyl-3-aryl)-1H-pyrazol-4-yl) methanamine, method of their preparation and use
WO2025212908A1 (en) * 2024-04-04 2025-10-09 Nimbus Clio, Inc. Cbl-b modulators and uses thereof

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
DATABASE CAPLUS [online] 3 January 2001 (2001-01-03), REIMANN E. ET AL: "Intramolecular alkylation of aromatic compounds. Part XXXIV. Synthesis of (pyridinylmethyl)indoles as potential precursors of ergolines", XP002981277, Database accession no. (ACC178709) *
KOST ET AL: "Reactions of Hydrazine Derivatives", OBSHCH. KHIM., vol. 33, no. 11, 1963, pages 3603 - 3613, XP002981296 *
PHAMAZIE, vol. 55, no. 12, 2000, pages 907 - 912, XP002903667 *

Also Published As

Publication number Publication date
AU2003218462A8 (en) 2004-04-23
AU2003218462A1 (en) 2004-04-23
WO2004030637A2 (en) 2004-04-15

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