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AU1734401A - Carboxyamido derivatives - Google Patents

Carboxyamido derivatives

Info

Publication number
AU1734401A
AU1734401A AU17344/01A AU1734401A AU1734401A AU 1734401 A AU1734401 A AU 1734401A AU 17344/01 A AU17344/01 A AU 17344/01A AU 1734401 A AU1734401 A AU 1734401A AU 1734401 A AU1734401 A AU 1734401A
Authority
AU
Australia
Prior art keywords
carboxyamido
derivatives
carboxyamido derivatives
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.)
Abandoned
Application number
AU17344/01A
Inventor
Ryoichi Ando
Keiichi Aritomo
Kenichi Saito
Aya Shoda
Fumiaki Uehara
Kazutoshi Watanabe
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.)
Mitsubishi Pharma Corp
Original Assignee
Mitsubishi Tokyo Pharmaceuticals 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
Application filed by Mitsubishi Tokyo Pharmaceuticals Inc filed Critical Mitsubishi Tokyo Pharmaceuticals Inc
Publication of AU1734401A publication Critical patent/AU1734401A/en
Abandoned legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/04—Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
    • C07D235/26—Oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/12—Heterocyclic 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (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)
AU17344/01A 1999-12-09 2000-12-08 Carboxyamido derivatives Abandoned AU1734401A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP35041399 1999-12-09
JP11/350413 1999-12-09
PCT/JP2000/008690 WO2001042224A1 (en) 1999-12-09 2000-12-08 Carboxyamido derivatives

Publications (1)

Publication Number Publication Date
AU1734401A true AU1734401A (en) 2001-06-18

Family

ID=18410336

Family Applications (1)

Application Number Title Priority Date Filing Date
AU17344/01A Abandoned AU1734401A (en) 1999-12-09 2000-12-08 Carboxyamido derivatives

Country Status (2)

Country Link
AU (1) AU1734401A (en)
WO (1) WO2001042224A1 (en)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2002216314A1 (en) * 2000-10-12 2002-04-22 Scott A Henderson Heterocyclic angiogenesis inhibitors
DK1674456T3 (en) 2001-09-21 2008-10-27 Sanofi Aventis New 1,4-benzothiazepine-1,1-dioxide derivatives with improved properties, process for their preparation, drugs containing these compounds and their use
EP1295885A1 (en) * 2001-09-21 2003-03-26 Sanofi-Synthelabo Substituted 2-pyridinyl-6,7,8,9-tetrahydropyrimido(1,2-a)pyrimidin-4-one and 7-pyridinyl-2,3-dihydroimidazo(1,2-a)pyrimidin-5(1H)one derivatives
EA012784B1 (en) * 2004-06-25 2009-12-30 Янссен Фармацевтика Н.В. Quaternary salt ccr2 antagonists
SI1809622T1 (en) * 2004-09-22 2010-11-30 Janssen Pharmaceutica Nv Inhibitors of the interaction between mdm2 and p53
CA2620333A1 (en) 2005-08-26 2007-03-01 Braincells, Inc. Neurogenesis by muscarinic receptor modulation
EP2258357A3 (en) 2005-08-26 2011-04-06 Braincells, Inc. Neurogenesis with acetylcholinesterase inhibitor
EP2377530A3 (en) 2005-10-21 2012-06-20 Braincells, Inc. Modulation of neurogenesis by PDE inhibition
EP1942879A1 (en) 2005-10-31 2008-07-16 Braincells, Inc. Gaba receptor mediated modulation of neurogenesis
US20100216734A1 (en) 2006-03-08 2010-08-26 Braincells, Inc. Modulation of neurogenesis by nootropic agents
MX2008011791A (en) 2006-03-15 2008-09-25 Wyeth Corp N-substituted-azacyclylamines as histamine-3 antagonists.
EP2382975A3 (en) 2006-05-09 2012-02-29 Braincells, Inc. Neurogenesis by modulating angiotensin
WO2007136668A2 (en) * 2006-05-19 2007-11-29 Wyeth N-benzoyl-and n-benzylpyrrolidin-3-ylamines as histamine-3 antagonists
US20100184806A1 (en) 2006-09-19 2010-07-22 Braincells, Inc. Modulation of neurogenesis by ppar agents
PE20081152A1 (en) 2006-10-06 2008-08-10 Wyeth Corp N-SUBSTITUTED AZACYCLYLAMINES AS HISTAMINE-3 ANTAGONISTS
EP2170875A1 (en) 2007-07-16 2010-04-07 Wyeth LLC Aminoalkylazole derivatives as histamine-3 antagonists
ES2534899T3 (en) 2007-08-06 2015-04-30 Janssen Pharmaceutica, N.V. Substituted phenylenediamines as inhibitors of the interaction between MDM2 and p53
JO2704B1 (en) 2007-09-21 2013-03-03 جانسين فارماسوتيكا ان في Inhibitors of the interaction between mdm2 and p53
WO2010089327A2 (en) 2009-02-04 2010-08-12 Janssen Pharmaceutica Nv Indole derivatives as anticancer agents
US20100216805A1 (en) 2009-02-25 2010-08-26 Braincells, Inc. Modulation of neurogenesis using d-cycloserine combinations

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57149277A (en) * 1981-03-10 1982-09-14 Taiho Yakuhin Kogyo Kk Heterocyclic compound
IT1250629B (en) * 1991-07-04 1995-04-21 Boehringer Ingelheim Italia USE OF BENZIMIDAZOLIN-2-OXO-1-CARBOXYLIC ACID DERIVATIVES.
GB9726695D0 (en) * 1997-12-17 1998-02-18 Smithkline Beecham Plc Novel compounds

Also Published As

Publication number Publication date
WO2001042224A1 (en) 2001-06-14

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Legal Events

Date Code Title Description
MK6 Application lapsed section 142(2)(f)/reg. 8.3(3) - pct applic. not entering national phase