NO20050088L - Cationically substituted diphenylazofidinones, processes for their preparation, medicaments containing said compounds, and use thereof - Google Patents

Cationically substituted diphenylazofidinones, processes for their preparation, medicaments containing said compounds, and use thereof

Info

Publication number
NO20050088L
NO20050088L NO20050088A NO20050088A NO20050088L NO 20050088 L NO20050088 L NO 20050088L NO 20050088 A NO20050088 A NO 20050088A NO 20050088 A NO20050088 A NO 20050088A NO 20050088 L NO20050088 L NO 20050088L
Authority
NO
Norway
Prior art keywords
compounds
diphenylazofidinones
processes
preparation
medicaments containing
Prior art date
Application number
NO20050088A
Other languages
Norwegian (no)
Inventor
Heiner Glombik
Hubert Heuer
Werner Kramer
Wendelin Frick
Hans-Ludwig Schaefer
Andreas Lindenschmidt
Gerhard Jaehne
Stefanie Flohr
Original Assignee
Sanofi Aventis Deutschland
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 Sanofi Aventis Deutschland filed Critical Sanofi Aventis Deutschland
Publication of NO20050088L publication Critical patent/NO20050088L/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/08—Bridged systems
    • 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
    • A61P3/06—Antihyperlipidemics
    • 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
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
    • C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
    • C07D205/06—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D205/08—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with one oxygen atom directly attached in position 2, e.g. beta-lactams
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems

Abstract

The invention relates to compounds of formula (I), in which R1, R2, R3, R4, R5 and R6 are defined as cited, in addition to their physiologically compatible salts. The compounds are suitable for use e.g. as hypolipidaemics.
NO20050088A 2002-06-19 2005-01-06 Cationically substituted diphenylazofidinones, processes for their preparation, medicaments containing said compounds, and use thereof NO20050088L (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10227507A DE10227507A1 (en) 2002-06-19 2002-06-19 Cationically substituted diphenylazetidinones, processes for their preparation, medicaments containing these compounds and their use
PCT/EP2003/005814 WO2004000803A1 (en) 2002-06-19 2003-06-04 Cationically substituted diphenyl azetidinones, method for their production, medicaments containing said compounds and use thereof

Publications (1)

Publication Number Publication Date
NO20050088L true NO20050088L (en) 2005-01-06

Family

ID=29719282

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20050088A NO20050088L (en) 2002-06-19 2005-01-06 Cationically substituted diphenylazofidinones, processes for their preparation, medicaments containing said compounds, and use thereof

Country Status (26)

Country Link
EP (1) EP1517890B1 (en)
JP (1) JP2005533071A (en)
KR (1) KR20050010061A (en)
CN (1) CN1662494A (en)
AT (1) ATE401304T1 (en)
AU (1) AU2003238209B2 (en)
BR (1) BR0311984A (en)
CA (1) CA2490108A1 (en)
DE (2) DE10227507A1 (en)
DK (1) DK1517890T3 (en)
ES (1) ES2310662T3 (en)
HR (1) HRP20041202A2 (en)
IL (1) IL165790A (en)
MA (1) MA27251A1 (en)
MX (1) MXPA04012308A (en)
NO (1) NO20050088L (en)
PA (1) PA8575601A1 (en)
PL (1) PL372660A1 (en)
PT (1) PT1517890E (en)
RS (1) RS108604A (en)
RU (1) RU2315753C2 (en)
SV (1) SV2004001555A (en)
TW (1) TW200406380A (en)
UY (1) UY27852A1 (en)
WO (1) WO2004000803A1 (en)
ZA (1) ZA200409379B (en)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0215579D0 (en) 2002-07-05 2002-08-14 Astrazeneca Ab Chemical compounds
US7871998B2 (en) 2003-12-23 2011-01-18 Astrazeneca Ab Diphenylazetidinone derivatives possessing cholesterol absorption inhibitory activity
NZ555320A (en) 2004-12-03 2010-11-26 Schering Corp Substituted piperazines as CB1 antagonists
MX2007012253A (en) * 2005-04-04 2007-12-07 Univ Pontificia Catolica Chile The use of ezetimibe in the prevention and treatment of cholesterol gallstones.
ATE450526T1 (en) 2005-06-20 2009-12-15 Schering Corp PIPERIDINE DERIVATIVES SUITABLE AS ANTAGONISTS OF HISTAMINE H3
SA06270191B1 (en) 2005-06-22 2010-03-29 استرازينيكا ايه بي Novel 2-Azetidinone Derivatives as Cholesterol Absorption Inhibitors for the Treatment of Hyperlipidaemic Conditions
TW200811098A (en) 2006-04-27 2008-03-01 Astrazeneca Ab Chemical compounds
CA2666193A1 (en) 2006-08-08 2008-02-14 Sanofi-Aventis Arylaminoaryl-alkyl-substituted imidazolidine-2,4-diones, process for preparing them, medicaments comprising these compounds, and their use
DE102007002260A1 (en) 2007-01-16 2008-07-31 Sanofi-Aventis Use of substituted pyranonic acid derivatives for the preparation of medicaments for the treatment of the metabolic syndrome
EP2025674A1 (en) 2007-08-15 2009-02-18 sanofi-aventis Substituted tetra hydro naphthalines, method for their manufacture and their use as drugs
DE102007054497B3 (en) 2007-11-13 2009-07-23 Sanofi-Aventis Deutschland Gmbh New crystalline hydrate form of dodecanedioic acid 4-((2S,3R)-3-((S)-3-(4-fluoro-phenyl)-3-hydroxy-propyl)-2-(4-methoxy-phenyl)-4-oxo-azetidin-1-yl)-benzylamide ((2S,3R,4R,5R)-pentahydroxy-hexyl)-amide useful e.g. to treat hyperlipidemia
EP2310372B1 (en) 2008-07-09 2012-05-23 Sanofi Heterocyclic compounds, processes for their preparation, medicaments comprising these compounds, and the use thereof
WO2010068601A1 (en) 2008-12-08 2010-06-17 Sanofi-Aventis A crystalline heteroaromatic fluoroglycoside hydrate, processes for making, methods of use and pharmaceutical compositions thereof
US9212175B2 (en) 2009-03-06 2015-12-15 Lipideon Biotechnology Ag Pharmaceutical hypocholesterolemic compositions
CN101993403B (en) 2009-08-11 2012-07-11 浙江海正药业股份有限公司 Azetidinone compound and medical applications thereof
DK2470552T3 (en) 2009-08-26 2014-02-17 Sanofi Sa NOVEL, CRYSTALLINE, heteroaromatic FLUORGLYCOSIDHYDRATER, MEDICINES COVERING THESE COMPOUNDS AND THEIR USE
US8933024B2 (en) 2010-06-18 2015-01-13 Sanofi Azolopyridin-3-one derivatives as inhibitors of lipases and phospholipases
WO2012120055A1 (en) 2011-03-08 2012-09-13 Sanofi Di- and tri-substituted oxathiazine derivates, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof
US8828994B2 (en) 2011-03-08 2014-09-09 Sanofi Di- and tri-substituted oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof
EP2683700B1 (en) 2011-03-08 2015-02-18 Sanofi Tetra-substituted oxathiazine derivatives, method for their preparation, their usage as medicament and medicament containing same and its use
US8901114B2 (en) 2011-03-08 2014-12-02 Sanofi Oxathiazine derivatives substituted with carbocycles or heterocycles, method for producing same, drugs containing said compounds, and use thereof
WO2012120053A1 (en) 2011-03-08 2012-09-13 Sanofi Branched oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof
EP2567959B1 (en) 2011-09-12 2014-04-16 Sanofi 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10042447A1 (en) * 2000-08-29 2002-03-28 Aventis Pharma Gmbh Vertebrate intestinal protein that absorbs cholesterol and use of this protein to identify inhibitors of intestinal cholesterol transport
DE50110906D1 (en) * 2000-12-21 2006-10-12 Sanofi Aventis Deutschland DIPHENYLAZETIDINONE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF, THE MEDICAMENT CONTAINING THESE COMPOUNDS AND THEIR USE
JP4605990B2 (en) * 2000-12-21 2011-01-05 サノフィ−アベンティス・ドイチュラント・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング Novel 1,2-diphenylazetidinone, process for its preparation, medicament containing the compound, and use thereof for treating lipid metabolism disorders
IL156552A0 (en) * 2000-12-21 2004-01-04 Aventis Pharma Gmbh Diphenyl azetidinone derivatives, method for the production thereof, medicaments containing these compounds, and their use

Also Published As

Publication number Publication date
ES2310662T3 (en) 2009-01-16
HRP20041202A2 (en) 2005-06-30
DE50310161D1 (en) 2008-08-28
WO2004000803A1 (en) 2003-12-31
AU2003238209A1 (en) 2004-01-06
RS108604A (en) 2007-02-05
JP2005533071A (en) 2005-11-04
ATE401304T1 (en) 2008-08-15
CA2490108A1 (en) 2003-12-31
DK1517890T3 (en) 2008-11-10
AU2003238209B2 (en) 2009-01-22
RU2315753C2 (en) 2008-01-27
EP1517890B1 (en) 2008-07-16
IL165790A (en) 2010-04-15
IL165790A0 (en) 2006-01-15
EP1517890A1 (en) 2005-03-30
RU2005101088A (en) 2005-06-27
UY27852A1 (en) 2003-12-31
BR0311984A (en) 2005-04-26
MA27251A1 (en) 2005-03-01
CN1662494A (en) 2005-08-31
TW200406380A (en) 2004-05-01
DE10227507A1 (en) 2004-01-08
ZA200409379B (en) 2006-05-31
PL372660A1 (en) 2005-07-25
SV2004001555A (en) 2004-03-19
KR20050010061A (en) 2005-01-26
MXPA04012308A (en) 2005-02-25
PA8575601A1 (en) 2004-02-07
PT1517890E (en) 2008-10-14

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