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NO20082214L - 1,1-Diokso-tiomorfolinyl-indolyl-metanonderivater for anvendelse som H3-modulatorer - Google Patents

1,1-Diokso-tiomorfolinyl-indolyl-metanonderivater for anvendelse som H3-modulatorer

Info

Publication number
NO20082214L
NO20082214L NO20082214A NO20082214A NO20082214L NO 20082214 L NO20082214 L NO 20082214L NO 20082214 A NO20082214 A NO 20082214A NO 20082214 A NO20082214 A NO 20082214A NO 20082214 L NO20082214 L NO 20082214L
Authority
NO
Norway
Prior art keywords
thiomorpholinyl
dioxo
indolyl
modulators
methanone derivatives
Prior art date
Application number
NO20082214A
Other languages
English (en)
Inventor
Sven Taylor
Olivier Roche
Jean-Marc Plancher
Hans Richter
Matthias Heinrich Nettekoven
Rosa Maria Rodriguez Sarmiento
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of NO20082214L publication Critical patent/NO20082214L/no

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    • 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
    • C07D401/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links
    • 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
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404Indoles, e.g. pindolol
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P11/00Drugs for disorders of the respiratory system
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    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
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    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
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    • C07ORGANIC CHEMISTRY
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    • 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
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    • 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
    • C07D403/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Diabetes (AREA)
  • Pain & Pain Management (AREA)
  • Pulmonology (AREA)
  • Hematology (AREA)
  • Psychiatry (AREA)
  • Obesity (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Anesthesiology (AREA)
  • Psychology (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Rheumatology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Addiction (AREA)
  • Immunology (AREA)
  • Hospice & Palliative Care (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Foreliggende oppfinnelse angår forbindelser med formel I hvor R1, R2 og G er som definert i beskrivelsen og kravene, samt farmasøytisk akseptable salter derav. Forbindelsene er anvendelige for behandling og/eller forebygging av sykdommer som er relaterte til modulering av H3-reseptorer.
NO20082214A 2005-11-30 2008-05-14 1,1-Diokso-tiomorfolinyl-indolyl-metanonderivater for anvendelse som H3-modulatorer NO20082214L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP05111479 2005-11-30
PCT/EP2006/068649 WO2007062997A1 (en) 2005-11-30 2006-11-20 1,1-dioxo-thiomorpholinyl indolyl methanone derivatives for use as h3 modulators

Publications (1)

Publication Number Publication Date
NO20082214L true NO20082214L (no) 2008-07-31

Family

ID=37715997

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20082214A NO20082214L (no) 2005-11-30 2008-05-14 1,1-Diokso-tiomorfolinyl-indolyl-metanonderivater for anvendelse som H3-modulatorer

Country Status (17)

Country Link
US (1) US7538101B2 (no)
EP (1) EP1968967B1 (no)
JP (1) JP4879996B2 (no)
KR (1) KR101047204B1 (no)
CN (1) CN101316838B (no)
AR (1) AR057197A1 (no)
AT (1) ATE507222T1 (no)
AU (1) AU2006319232B2 (no)
BR (1) BRPI0619266A2 (no)
CA (1) CA2630307A1 (no)
DE (1) DE602006021626D1 (no)
ES (1) ES2362929T3 (no)
NO (1) NO20082214L (no)
RU (1) RU2412182C2 (no)
TW (1) TWI327144B (no)
WO (1) WO2007062997A1 (no)
ZA (1) ZA200804349B (no)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2630314A1 (en) * 2005-11-30 2007-06-07 F. Hoffmann-La Roche Ag 1,5-substituted indol-2-yl amide derivatives
JP2009517434A (ja) * 2005-11-30 2009-04-30 エフ.ホフマン−ラ ロシュ アーゲー 5−置換インドール−2−カルボキサミド誘導体
US8012955B2 (en) * 2006-12-28 2011-09-06 Rigel Pharmaceuticals, Inc. N-substituted-heterocycloalkyloxybenzamide compounds and methods of use
EP2183237A1 (en) 2007-07-25 2010-05-12 F. Hoffmann-Roche AG Benzofuran- and benzo[b]thiophene-2-carboxylic acid amide derivatives and use thereof as histamine 3 receptor modulators
MX2010005298A (es) 2007-11-16 2010-06-30 Rigel Pharmaceuticals Inc Compuestos de carboxamida, sulfonamida y amina para trastornos metabolicos.
EP2231666B1 (en) 2007-12-12 2015-07-29 Rigel Pharmaceuticals, Inc. Carboxamide, sulfonamide and amine compounds for metabolic disorders
KR101662333B1 (ko) 2008-04-23 2016-10-04 리겔 파마슈티칼스, 인크. 대사성 장애의 치료를 위한 카르복스아미드 화합물
US8785435B2 (en) * 2011-10-20 2014-07-22 Hoffmann-La Roche Inc. Solid forms
EA025136B1 (ru) * 2012-08-23 2016-11-30 Сувен Лайф Сайенсиз Лимитед Соединения акриламида в качестве лигандов h-рецептора гистамина

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CA1247547A (en) 1983-06-22 1988-12-28 Paul Hadvary Leucine derivatives
US5246960A (en) 1984-12-21 1993-09-21 Hoffmann-La Roche Inc. Oxetanones
CA1328881C (en) 1984-12-21 1994-04-26 Pierre Barbier Process for the manufacture of oxetanones
CA1270837A (en) 1984-12-21 1990-06-26 Hoffmann-La Roche Limited Oxetanones
CA2035972C (en) 1990-02-23 2006-07-11 Martin Karpf Process for the preparation of oxetanones
US5338755A (en) * 1990-07-31 1994-08-16 Elf Sanofi N-sulfonylindoline derivatives, their preparation and the pharmaceutical compositions in which they are present
US5274143A (en) 1991-07-23 1993-12-28 Hoffmann-La Roche Inc. Process for the preparation of (R)-3-hexyl-5,6-dihydro-4-hydroxy-6-undecyl-2H-pyran-2-one and (R)-5,6-dihydro-6-undecyl-2H-pyran-2,4(3H)-dione
US6004996A (en) 1997-02-05 1999-12-21 Hoffman-La Roche Inc. Tetrahydrolipstatin containing compositions
CA2316172C (en) * 1997-12-24 2010-02-02 Aventis Pharma Deutschland Gmbh Indole derivatives as inhibitors of factor xa
US6267952B1 (en) 1998-01-09 2001-07-31 Geltex Pharmaceuticals, Inc. Lipase inhibiting polymers
EP0978512A1 (en) * 1998-07-29 2000-02-09 Societe Civile Bioprojet Non-imidazole aryloxy (or arylthio) alkylamines as histamine H3-receptor antagonists and their therapeutic applications
TR200100471T2 (tr) 1998-08-14 2001-07-23 F.Hoffmann-La Roche Ag Lipaz inhibitörleri içeren farmasötik bileşimler
DK1105123T3 (da) 1998-08-14 2004-08-09 Hoffmann La Roche Farmaceutiske præparater indeholdende lipase-inhibitorer og chitosan
CZ301366B6 (cs) 1999-03-29 2010-02-03 F. Hoffmann-La Roche Ag 2-Fenyl-3-cykloalkylpropionamidová sloucenina, zpusob její prípravy a farmaceutický prostredek s jejím obsahem
AU2002336273A1 (en) * 2001-03-09 2002-09-24 Ortho-Mcneil Pharmaceutical, Inc. Heterocyclic compounds and their use as histamine h4 ligands.
GB0224084D0 (en) * 2002-10-16 2002-11-27 Glaxo Group Ltd Novel compounds
US20060052597A1 (en) * 2002-10-22 2006-03-09 Best Desmond J Aryloxyalkylamine derivatives as h3 receptor ligands
WO2005123716A1 (en) * 2004-06-21 2005-12-29 F. Hoffmann-La Roche Ag Indole derivatives as histamine receptor antagonists
CA2630314A1 (en) * 2005-11-30 2007-06-07 F. Hoffmann-La Roche Ag 1,5-substituted indol-2-yl amide derivatives

Also Published As

Publication number Publication date
ZA200804349B (en) 2009-04-29
JP4879996B2 (ja) 2012-02-22
KR20080076979A (ko) 2008-08-20
JP2009517431A (ja) 2009-04-30
US7538101B2 (en) 2009-05-26
WO2007062997A1 (en) 2007-06-07
RU2008126389A (ru) 2010-01-10
US20070123526A1 (en) 2007-05-31
BRPI0619266A2 (pt) 2011-09-27
CN101316838B (zh) 2013-01-30
ATE507222T1 (de) 2011-05-15
KR101047204B1 (ko) 2011-07-06
AR057197A1 (es) 2007-11-21
TWI327144B (en) 2010-07-11
TW200804339A (en) 2008-01-16
DE602006021626D1 (de) 2011-06-09
EP1968967A1 (en) 2008-09-17
ES2362929T3 (es) 2011-07-15
EP1968967B1 (en) 2011-04-27
CN101316838A (zh) 2008-12-03
CA2630307A1 (en) 2007-06-07
RU2412182C2 (ru) 2011-02-20
AU2006319232B2 (en) 2012-09-13
AU2006319232A1 (en) 2007-06-07

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