SK7522003A3 - Biphenylcarboxamides useful as lipid lowering agents - Google Patents

Biphenylcarboxamides useful as lipid lowering agents Download PDF

Info

Publication number
SK7522003A3
SK7522003A3 SK752-2003A SK7522003A SK7522003A3 SK 7522003 A3 SK7522003 A3 SK 7522003A3 SK 7522003 A SK7522003 A SK 7522003A SK 7522003 A3 SK7522003 A3 SK 7522003A3
Authority
SK
Slovakia
Prior art keywords
formula
alkyl
hydrogen
amino
halo
Prior art date
Application number
SK752-2003A
Other languages
English (en)
Slovak (sk)
Inventor
Lieven Meerpoel
Leo Jacobus Jozef Backx
Original Assignee
Janssen Pharmaceutica Nv
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 Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Publication of SK7522003A3 publication Critical patent/SK7522003A3/sk

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
    • C07C237/20—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton containing six-membered aromatic rings
    • 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
    • A61P3/06—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
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00—Carboxylic acid amides
    • C07C233/64—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C233/77—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups
    • C07C233/80—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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 to ring carbon atoms
    • C07D207/14—Nitrogen atoms not forming part of a nitro radical
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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 to ring carbon atoms
    • C07D211/56—Nitrogen atoms
    • C07D211/58—Nitrogen atoms attached in position 4
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00—Systems containing only non-condensed rings
    • C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
    • C07C2601/08—Systems containing only non-condensed rings with a five-membered ring the ring being saturated
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00—Systems containing only non-condensed rings
    • C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/14—The ring being saturated

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Diabetes (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Child & Adolescent Psychology (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Hydrogenated Pyridines (AREA)
  • Pyrrole Compounds (AREA)
SK752-2003A 2000-11-21 2001-11-15 Biphenylcarboxamides useful as lipid lowering agents SK7522003A3 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP00204150 2000-11-21
PCT/EP2001/013316 WO2002042271A2 (fr) 2000-11-21 2001-11-15 Biphenylcarboxamides utiles comme hypolipidemiants

Publications (1)

Publication Number Publication Date
SK7522003A3 true SK7522003A3 (en) 2004-04-06

Family

ID=8172315

Family Applications (1)

Application Number Title Priority Date Filing Date
SK752-2003A SK7522003A3 (en) 2000-11-21 2001-11-15 Biphenylcarboxamides useful as lipid lowering agents

Country Status (32)

Country Link
US (5) US7135586B2 (fr)
EP (1) EP1339685B1 (fr)
JP (1) JP4190283B2 (fr)
KR (1) KR20030051718A (fr)
CN (1) CN1289481C (fr)
AR (1) AR035072A1 (fr)
AT (1) ATE344243T1 (fr)
AU (2) AU2002219115B2 (fr)
BG (1) BG107805A (fr)
CA (1) CA2427660C (fr)
CZ (1) CZ20031638A3 (fr)
DE (1) DE60124296T2 (fr)
DK (1) DK1339685T3 (fr)
EA (1) EA006101B1 (fr)
EE (1) EE200300234A (fr)
ES (1) ES2275759T3 (fr)
GC (1) GC0000312A (fr)
HK (1) HK1073310A1 (fr)
HU (1) HUP0400926A3 (fr)
IL (2) IL155945A0 (fr)
JO (1) JO2409B1 (fr)
MX (1) MXPA03004465A (fr)
MY (1) MY134167A (fr)
NO (1) NO20032272D0 (fr)
NZ (1) NZ526495A (fr)
PA (1) PA8532001A1 (fr)
PL (1) PL205290B1 (fr)
PT (1) PT1339685E (fr)
SI (1) SI1339685T1 (fr)
SK (1) SK7522003A3 (fr)
WO (1) WO2002042271A2 (fr)
ZA (1) ZA200303910B (fr)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JO2654B1 (en) 2000-09-04 2012-06-17 شركة جانسين فارماسوتيكا ان. في Multiple aryl caroxa amides are useful as lipid - lowering agents
JO2409B1 (en) 2000-11-21 2007-06-17 شركة جانسين فارماسوتيكا ان. في Second-phenyl carboxy amides are useful as lipid-lowering agents
WO2002098839A1 (fr) * 2001-06-01 2002-12-12 Tanabe Seiyaku Co., Ltd. Biphenylcarboxamides et procede de preparation de ceux-ci
ZA200502496B (en) 2002-02-28 2005-10-12 Japan Tobacco Inc Ester compound and medicinal use thereof.
DE60321548D1 (de) 2002-03-13 2008-07-24 Janssen Pharmaceutica Nv Carbonylamino- derivativate als neue inhibitoren von histone deacetylase
ATE521592T1 (de) 2002-03-13 2011-09-15 Janssen Pharmaceutica Nv Histone-deacetylase-inhibitoren
UA79300C2 (en) * 2002-08-12 2007-06-11 Janssen Pharmaceutica Nv N-aryl piperidine substituted biphenylcarboxamides as inhibitors of apolipoprotein b secretion
WO2004056775A1 (fr) * 2002-12-20 2004-07-08 Pfizer Products Inc. Inhibiteurs de proteine de transfert de triglyceride microsomale
US7223788B2 (en) 2003-02-14 2007-05-29 Sanofi-Aventis Deutschland Gmbh Substituted N-aryl heterocycles, process for their preparation and their use as medicaments
DE10306250A1 (de) 2003-02-14 2004-09-09 Aventis Pharma Deutschland Gmbh Substituierte N-Arylheterozyklen, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
EP1669345A4 (fr) 2003-08-29 2008-02-20 Japan Tobacco Inc Derive d'ester et utilisation medicale de celui-ci
FR2871463B1 (fr) * 2004-06-11 2006-09-22 Merck Sante Soc Par Actions Si Derives a structure aroyl-o-piperidine, leurs procedes de preparation, les compositions pharmaceutiques qui les contiennent et leurs applications en therapeutique
JP4948403B2 (ja) 2004-07-28 2012-06-06 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 ヒストン・デアセチラーゼの新インヒビターとしての置換インドリルアルキルアミノ誘導体
US8101774B2 (en) 2004-10-18 2012-01-24 Japan Tobacco Inc. Ester derivatives and medicinal use thereof
WO2007053436A1 (fr) 2005-10-31 2007-05-10 Janssen Pharmaceutica N.V. Piperazines et piperidines substituees en tant que modulateurs du recepteur du neuropeptide y2
US9101160B2 (en) 2005-11-23 2015-08-11 The Coca-Cola Company Condiments with high-potency sweetener
JP5247470B2 (ja) 2006-01-19 2013-07-24 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 ヒストンデアセチラーゼのインヒビターとしてのピリジン及びピリミジン誘導体
US8017168B2 (en) 2006-11-02 2011-09-13 The Coca-Cola Company High-potency sweetener composition with rubisco protein, rubiscolin, rubiscolin derivatives, ace inhibitory peptides, and combinations thereof, and compositions sweetened therewith
WO2009006185A1 (fr) * 2007-07-03 2009-01-08 Janssen Pharmaceutica, N.V. Dérivés pipérazinylés utiles comme modulateurs du récepteur de neuropeptide y2
US10491357B2 (en) * 2010-07-12 2019-11-26 Entropic Communications Llc Method and apparatus for using dynamic subchannels in a communications network

Family Cites Families (81)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3910930A (en) 1973-01-04 1975-10-07 Janssen Pharmaceutica Nv 1-{55 1-{8 2-(1,4-Benzodioxan-2-yl)-2-hydroxyethyl{9 -4-piperidyl{56 -2-benzimidazolinones
US3929801A (en) 1973-11-20 1975-12-30 Janssen Pharmaceutica Nv 2-Benzimidazolinones
US3929601A (en) * 1974-03-26 1975-12-30 Us Energy Synthesis of pentafluorides
DE2852203C3 (de) * 1978-12-02 1982-03-11 Ibm Deutschland Gmbh, 7000 Stuttgart Lichtleiteinrichtung für eine mit Auflicht betriebene Abbildungsvorrichtung
US4231576A (en) * 1979-02-21 1980-11-04 Perkins Sonnie J Golf club head alignment apparatus
US4329348A (en) 1979-02-26 1982-05-11 Ciba-Geigy Corporation N-Oxacyclic-alkylpiperidines as psychostimulants
US4231938A (en) 1979-06-15 1980-11-04 Merck & Co., Inc. Hypocholesteremic fermentation products and process of preparation
US4444764A (en) * 1979-08-06 1984-04-24 The Dow Chemical Company Phosphorus esters of alkylcycloalkyl-5-pyrimidinols and control of corn rootworm and western spotted cucumber beetle with them
US4444784A (en) 1980-08-05 1984-04-24 Merck & Co., Inc. Antihypercholesterolemic compounds
DK149080C (da) 1980-06-06 1986-07-28 Sankyo Co Fremgangsmaade til fremstilling af derivater af ml-236b-carboxylsyre
DE3124366A1 (de) 1981-06-20 1982-12-30 Hoechst Ag, 6000 Frankfurt N-oxacyclyl-alkylpiperidin-derivate, verfahren zu ihrer herstellung, sie enthaltende pharmazeutische praeparate und deren verwendung
US4739073A (en) 1983-11-04 1988-04-19 Sandoz Pharmaceuticals Corp. Intermediates in the synthesis of indole analogs of mevalonolactone and derivatives thereof
DE3410498A1 (de) * 1984-03-22 1985-10-03 Hoechst Ag, 6230 Frankfurt N-bicycloheptyl- und n-bicycloheptenyl-imidazole, verfahren zu ihrer herstellung, ihre verwendung sowie pharmazeutische praeparate
US4647576A (en) 1984-09-24 1987-03-03 Warner-Lambert Company Trans-6-[2-(substitutedpyrrol-1-yl)alkyl]-pyran-2-one inhibitors of cholesterol synthesis
US4847271A (en) 1986-01-27 1989-07-11 Merck & Co., Inc. Antihypercholesterolemic β-lactones
US5041432A (en) 1987-01-30 1991-08-20 E. I. Du Pont De Nemours And Company Steroid derivatives useful as hypocholesterolemics
GB8716059D0 (en) * 1987-07-08 1987-08-12 Anderson Strathclyde Plc Mining machine
DE3901814A1 (de) 1988-07-28 1990-02-01 Bayer Ag Substituierte aminomethylzetraline sowie ihre heterocyclischen analoga
US5064858A (en) * 1988-08-17 1991-11-12 Spectrum Pharmaceutical Corporation Protected complex of procaine for the treatment of symptoms from narcotics addiction, tinnitus and Alzheimer's disease
US5232833A (en) * 1988-09-14 1993-08-03 Stressgen Biotechnologies Corporation Accumulation of heat shock proteins for evaluating biological damage due to chronic exposure of an organism to sublethal levels of pollutants
US5064856A (en) 1989-07-31 1991-11-12 Merck & Co., Inc. Novel hmg-coa synthase inhibitors
US5120729A (en) 1990-06-20 1992-06-09 Merck & Co., Inc. Beta-lactams as antihypercholesterolemics
US5177080A (en) 1990-12-14 1993-01-05 Bayer Aktiengesellschaft Substituted pyridyl-dihydroxy-heptenoic acid and its salts
DE4040203A1 (de) 1990-12-15 1992-06-17 Roehm Gmbh Eingetruebte kunststoffelemente
WO1992018113A1 (fr) * 1991-04-18 1992-10-29 The United States Of America, Represented By The Secretary, Department Of Health And Human Services Identification d'une nouvelle espece d'ehrlichia a partir d'un patient souffrant d'ehrlichiose
DE4140540A1 (de) 1991-12-09 1993-06-17 Bayer Ag Neue azaheterocyclylmethyl-chromane
WO1993011782A1 (fr) 1991-12-19 1993-06-24 Southwest Foundation For Biomedical Research Polypeptide inhibant la proteine de transfert aux esters de cholesteryl, anticorps contre le polypeptide synthetique et traitements prophylactiques et therapeutiques anti-atherosclerose
SI9300097B (en) 1992-02-27 2001-12-31 Janssen Pharmaceutica Nv (benzodioxan, benzofuran or benzopyran) alkylamino) alkyl substituted guanidines
CA2091102C (fr) 1992-03-06 2009-05-26 John R. Ii Wetterau Proteine de transfert de triglycerides microsomaux
US5595872A (en) * 1992-03-06 1997-01-21 Bristol-Myers Squibb Company Nucleic acids encoding microsomal trigyceride transfer protein
EP0567026B1 (fr) 1992-04-20 2003-03-26 Takeda Chemical Industries, Ltd. Dérivés de 4,1-benzoxazepine comme inhibiteurs de la synthétase du squalène et leur application dans le traitement d'hypercholesteremie et comme fongicides
US5279454A (en) 1992-04-24 1994-01-18 Eastman Kodak Company Straight through lateral constraint
US5327875A (en) * 1993-02-19 1994-07-12 Hall S Franklin Vapor enhanced carburetion system
DE4319038A1 (de) 1993-06-08 1994-12-15 Bayer Ag Verwendung von teilweise bekannten substituierten Chromanen als Arzneimittel, neue Wirkstoffe und Verfahren zu ihrer Herstellung
US5780248A (en) * 1993-07-15 1998-07-14 Ortho Diagnostic Systems, Inc. Foil sealed cassette for agglutination reactions and liner therefor
FI93396C (fi) 1993-08-17 1995-03-27 Petetronic Tmi P Kinnunen Optinen menetelmä nesteen pinnankorkeuden mittaamiseksi
RO116900B1 (ro) 1993-08-19 2001-07-30 Janssen Pharmaceutica N.V. Derivaţi de dihidrobenzopiran, procedeu pentru prepararea acestora, intermediar pentru realizarea procedeului, compoziţie farmaceutică şi metodă de tratament
US5739135A (en) 1993-09-03 1998-04-14 Bristol-Myers Squibb Company Inhibitors of microsomal triglyceride transfer protein and method
AU678503B2 (en) 1993-09-24 1997-05-29 Takeda Chemical Industries Ltd. Condensed heterocyclic compounds and their use as squalene synthetase inhibitors
US5492916A (en) 1993-12-23 1996-02-20 Merck & Co., Inc. Di- and tri-substituted piperidines, pyrrolidines and hexahydro-1H-azepines promote release of growth hormone
CZ286403B6 (en) * 1993-12-07 2000-04-12 S & R Maschb Gmbh Apparatus for baking pies
JPH086412A (ja) * 1994-06-20 1996-01-12 Canon Inc 加熱装置および画像形成装置
EP0784612A1 (fr) 1994-10-04 1997-07-23 Fujisawa Pharmaceutical Co., Ltd. Derives d'uree et leur utilisation comme inhibiteurs de l'acat
US5510379A (en) 1994-12-19 1996-04-23 Warner-Lambert Company Sulfonate ACAT inhibitors
US5536859A (en) 1995-02-27 1996-07-16 Amoco Corporation Alpha-olefin catalyst and process
GB9504066D0 (en) 1995-03-01 1995-04-19 Pharmacia Spa Phosphate derivatives of ureas and thioureas
US5541199A (en) 1995-06-02 1996-07-30 American Home Products Corporation Chroman-2-ylmethylamino derivatives
EP0832069B1 (fr) 1995-06-07 2003-03-05 Pfizer Inc. DERIVES DE BIPHENYL-2-ACIDE CARBOXYLIQUE-TETRAHYDRO-ISOQUINOLEINE-6-YL AMIDES, PREPARATION DE CES AMIDES ET UTILISATION EN TANT QU'INHIBITEURS DE LA PROTEINE DE TRANSFERT DE TRIGLYCERIDE MICROSOMAL ET/OU DE LA SECRETION D'APOLIPOPROTEINES B (Apo B)
MX9709914A (es) 1995-06-07 1998-03-31 Pfizer Derivados de acido bifenil-2-carboxilico-tetrahidro-isoquinolin-6-ilo, su preparacion y el uso de los mismos.
US5696196A (en) * 1995-09-15 1997-12-09 Egyptian Lacquer Mfg. Co. EMI/RFI-shielding coating
US5827875A (en) 1996-05-10 1998-10-27 Bristol-Myers Squibb Company Inhibitors of microsomal triglyceride transfer protein and method
US6542607B1 (en) 1996-09-03 2003-04-01 Siemens Aktiengesellschaft Device and method for the cryptographic processing of a digital data stream presenting any number of data
FR2756027B1 (fr) 1996-11-15 1999-01-15 Dimos Crochet de securite
WO1998023593A1 (fr) 1996-11-27 1998-06-04 Pfizer Inc. AMIDES INHIBANT LA SECRETION D'Apo B ET/OU LA PROTEINE MTP
DE19649751C2 (de) 1996-11-30 1999-12-30 Cts Fahrzeug Dachsysteme Gmbh Dachaufbau für Fahrzeuge, insbesondere Personenkraftwagen
US5876070A (en) 1996-12-11 1999-03-02 Kennecott Holdings Corporation Pipe flange connection for pressure retaining, abrasive/corrosive service
GB9626045D0 (en) 1996-12-14 1997-01-29 Rover Group A vehicle roll stabilising system
US5760246A (en) 1996-12-17 1998-06-02 Biller; Scott A. Conformationally restricted aromatic inhibitors of microsomal triglyceride transfer protein and method
WO1998027979A1 (fr) 1996-12-20 1998-07-02 Bristol-Myers Squibb Company Inhibiteurs heterocycliques de la proteine de transfert des triglycerides microsomiques et methode associee
US5966677A (en) 1997-02-28 1999-10-12 Fiekowsky; Peter J. High accuracy particle dimension measurement system
GB9705206D0 (en) 1997-03-13 1997-04-30 Automotive Prod Italia Drum brakes
US5968950A (en) 1997-06-23 1999-10-19 Pfizer Inc Apo B-secretion/MTP inhibitor hydrochloride salt
US5988950A (en) * 1997-11-18 1999-11-23 Atlantic Richfield Company Method and system for preventing upward migration of contaminants in soil
US6133277A (en) 1997-12-05 2000-10-17 Janssen Pharmaceutica N.V. (Benzodioxan, benzofuran or benzopyran) derivatives having fundic relaxation properties
GB9725782D0 (en) 1997-12-05 1998-02-04 Pfizer Ltd Therapeutic agents
US5989950A (en) * 1998-01-26 1999-11-23 Texas Instruments - Acer Incorporated Reduced mask CMOS salicided process
US6173351B1 (en) 1998-06-15 2001-01-09 Sun Microsystems, Inc. Multi-processor system bridge
US6133217A (en) 1998-08-28 2000-10-17 Huntsman Petrochemical Corporation Solubilization of low 2-phenyl alkylbenzene sulfonates
US5985577A (en) * 1998-10-14 1999-11-16 The Trustees Of Columbia University In The City Of New York Protein conjugates containing multimers of green fluorescent protein
GB9826412D0 (en) * 1998-12-03 1999-01-27 Glaxo Group Ltd Chemical compounds
WO2000032532A1 (fr) 1998-12-03 2000-06-08 Lucio Alvaro Procede de traitement thermique de materiaux inorganiques et organiques dans une serie de petites cuves et appareil pour le mettre en oeuvre
SI1187829T1 (en) 1999-06-02 2004-04-30 Janssen Pharmaceutica N.V. Aminoalkyl substituted (benzodioxan, benzofuran or benzopyran) derivatives
ATE279409T1 (de) 1999-06-02 2004-10-15 Janssen Pharmaceutica Nv Pyrrolidinyl, piperidinyl oder homopiperidinyl substituierte (benzodioxan, benzofuran oder benzopyran) derivate
AU2001262185A1 (en) 2000-04-10 2001-10-23 Novartis Ag Substituted (hetero)aryl carboxamide derivatives as microsomal triglyceride transfer protein (mtp) and apolipoprotein b (apo b) secretion
GB0013346D0 (en) * 2000-06-01 2000-07-26 Glaxo Group Ltd Therapeutic benzamide derivatives
JO2352B1 (en) 2000-06-22 2006-12-12 جانسين فارماسيوتيكا ان. في Compounds for the treatment of non-adaptation of the bottom of the uterus
JO2654B1 (en) 2000-09-04 2012-06-17 شركة جانسين فارماسوتيكا ان. في Multiple aryl caroxa amides are useful as lipid - lowering agents
JO2409B1 (en) 2000-11-21 2007-06-17 شركة جانسين فارماسوتيكا ان. في Second-phenyl carboxy amides are useful as lipid-lowering agents
JO2390B1 (en) 2001-04-06 2007-06-17 شركة جانسين فارماسوتيكا ان. في Diphenylcarboxamides act as lipid-lowering agents
US7101891B2 (en) 2001-04-09 2006-09-05 Eli Lilly And Company Compounds and pharmaceutical compositions for inhibiting MRP1
GB0423422D0 (en) * 2004-10-21 2004-11-24 Bard Inc C R Medical device for fluid flow, and method of forming such device

Also Published As

Publication number Publication date
SI1339685T1 (sl) 2007-04-30
US20080275087A1 (en) 2008-11-06
JO2409B1 (en) 2007-06-17
US20080009522A1 (en) 2008-01-10
BG107805A (bg) 2004-01-30
JP4190283B2 (ja) 2008-12-03
US7135586B2 (en) 2006-11-14
WO2002042271A3 (fr) 2002-11-21
US7304167B2 (en) 2007-12-04
US20060128973A1 (en) 2006-06-15
NO20032272L (no) 2003-05-20
US20060128972A1 (en) 2006-06-15
CZ20031638A3 (cs) 2004-02-18
NZ526495A (en) 2004-06-25
PL205290B1 (pl) 2010-03-31
CN1289481C (zh) 2006-12-13
ATE344243T1 (de) 2006-11-15
US7538124B2 (en) 2009-05-26
CA2427660C (fr) 2010-01-19
EA200300597A1 (ru) 2003-10-30
IL155945A (en) 2009-06-15
PA8532001A1 (es) 2002-10-28
MXPA03004465A (es) 2003-08-19
CA2427660A1 (fr) 2002-05-30
MY134167A (en) 2007-11-30
DK1339685T3 (da) 2007-03-12
ZA200303910B (en) 2004-09-01
AR035072A1 (es) 2004-04-14
EP1339685B1 (fr) 2006-11-02
US7244848B2 (en) 2007-07-17
PT1339685E (pt) 2007-02-28
HUP0400926A2 (hu) 2004-07-28
DE60124296D1 (de) 2006-12-14
ES2275759T3 (es) 2007-06-16
US7405307B2 (en) 2008-07-29
JP2004521870A (ja) 2004-07-22
EP1339685A2 (fr) 2003-09-03
GC0000312A (en) 2006-11-01
PL361633A1 (en) 2004-10-04
DE60124296T2 (de) 2007-05-31
KR20030051718A (ko) 2003-06-25
AU2002219115B2 (en) 2007-01-04
CN1568312A (zh) 2005-01-19
IL155945A0 (en) 2003-12-23
EA006101B1 (ru) 2005-08-25
EE200300234A (et) 2003-08-15
HK1073310A1 (en) 2005-09-30
US20040102490A1 (en) 2004-05-27
HUP0400926A3 (en) 2008-03-28
NO20032272D0 (no) 2003-05-20
WO2002042271A2 (fr) 2002-05-30
AU1911502A (en) 2002-06-03

Similar Documents

Publication Publication Date Title
SK7522003A3 (en) Biphenylcarboxamides useful as lipid lowering agents
BG107581A (bg) Полиарилкарбоксамиди и използването им като средства, понижаващи липидите
AU2003250215B2 (en) N-aryl piperidine substituted biphenylcarboxamides as inhibitors of apolipoprotein B secretion
AU2002219115A1 (en) Biphenylcarboxamides useful as lipid lowering agents
EP1379515B1 (fr) Biphenylcarboxamides hypolipidemiants
AU2002253171A1 (en) Lipid lowering biphenylcarboxamides
KR101387459B1 (ko) Ｍｔｐ를 저해하는 테트라하이드로-나프탈렌-1-카복실산 유도체
MXPA06006507A (en) N-aryl piperidine substituted biphenylcarboxamides as inhibitors of apolipoprote in b