UA79300C2 - N-aryl piperidine substituted biphenylcarboxamides as inhibitors of apolipoprotein b secretion - Google Patents

N-aryl piperidine substituted biphenylcarboxamides as inhibitors of apolipoprotein b secretion Download PDF

Info

Publication number
UA79300C2
UA79300C2 UAA200501990A UA2005001990A UA79300C2 UA 79300 C2 UA79300 C2 UA 79300C2 UA A200501990 A UAA200501990 A UA A200501990A UA 2005001990 A UA2005001990 A UA 2005001990A UA 79300 C2 UA79300 C2 UA 79300C2
Authority
UA
Ukraine
Prior art keywords
compounds
acid
formula
osm
compound
Prior art date
Application number
UAA200501990A
Other languages
English (en)
Ukrainian (uk)
Inventor
Lieven Meerpoel
Leo Jacobus Jozef Backx
Peter Walter Maria Roevens
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 UA79300C2 publication Critical patent/UA79300C2/uk

Links

Classifications

    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/06Antihyperlipidemics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic 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
    • C07D211/08Heterocyclic 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 hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
    • C07D211/18Heterocyclic 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 hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D211/34Heterocyclic 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 hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic 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
    • C07D211/36Heterocyclic 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
    • C07D211/60Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D211/62Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals attached in position 4

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Diabetes (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Child & Adolescent Psychology (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Plural Heterocyclic Compounds (AREA)
UAA200501990A 2002-08-12 2003-05-08 N-aryl piperidine substituted biphenylcarboxamides as inhibitors of apolipoprotein b secretion UA79300C2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP02078309 2002-08-12
PCT/EP2003/008694 WO2004017969A1 (en) 2002-08-12 2003-08-05 N-aryl piperidine substituted biphenylcarboxamides as inhibitors of apolipoprotein b secretion

Publications (1)

Publication Number Publication Date
UA79300C2 true UA79300C2 (en) 2007-06-11

Family

ID=31896911

Family Applications (1)

Application Number Title Priority Date Filing Date
UAA200501990A UA79300C2 (en) 2002-08-12 2003-05-08 N-aryl piperidine substituted biphenylcarboxamides as inhibitors of apolipoprotein b secretion

Country Status (31)

Country Link
US (2) US20060040989A1 (de)
EP (1) EP1536796B1 (de)
JP (1) JP4559856B2 (de)
KR (1) KR101052204B1 (de)
CN (3) CN100366252C (de)
AR (1) AR040968A1 (de)
AT (1) ATE385796T1 (de)
AU (1) AU2003250215B2 (de)
BR (1) BR0313377A (de)
CA (1) CA2494208C (de)
CY (1) CY1107945T1 (de)
DE (1) DE60319097T2 (de)
DK (1) DK1536796T3 (de)
EA (1) EA008061B1 (de)
EG (1) EG25699A (de)
ES (1) ES2301873T3 (de)
HR (1) HRP20050103B1 (de)
IL (1) IL166795A (de)
IS (1) IS2726B (de)
MX (1) MXPA05001712A (de)
MY (1) MY136632A (de)
NO (1) NO329308B1 (de)
NZ (1) NZ538680A (de)
PA (1) PA8579901A1 (de)
PL (1) PL212405B1 (de)
PT (1) PT1536796E (de)
SI (1) SI1536796T1 (de)
TW (1) TWI342775B (de)
UA (1) UA79300C2 (de)
WO (1) WO2004017969A1 (de)
ZA (1) ZA200501225B (de)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
UA83510C2 (en) * 2003-12-09 2008-07-25 Янссен Фармацевтика Н.В. N-aryl piperidine substituted biphenylcarboxamides as inhibitors of apolipoprotein b
FR2883000B1 (fr) * 2005-03-14 2007-06-01 Merck Sante Soc Par Actions Si Derives de trifluoromethylbenzamide et leurs utilisations en therapeutique
US7754717B2 (en) 2005-08-15 2010-07-13 Amgen Inc. Bis-aryl amide compounds and methods of use
WO2007053436A1 (en) 2005-10-31 2007-05-10 Janssen Pharmaceutica N.V. Substituted piperazines and piperidines as modulators of the neuropeptide y2 receptor
CA2648132C (en) 2006-04-03 2019-05-28 Santaris Pharma A/S Pharmaceutical composition comprising anti-mirna antisense oligonucleotides
EP2666859B1 (de) * 2006-04-03 2019-01-02 Roche Innovation Center Copenhagen A/S Pharmazeutische zusammensetzungen mit anti-mirna-antisense-oligonukleotiden
WO2008100423A1 (en) * 2007-02-09 2008-08-21 Sirtris Pharmaceuticals, Inc. Gut microsomal triglyceride transport protein inhibitors
CA2681406A1 (en) * 2007-03-22 2008-09-25 Santaris Pharma A/S Rna antagonist compounds for the inhibition of apo-b100 expression
WO2008113832A2 (en) * 2007-03-22 2008-09-25 Santaris Pharma A/S SHORT RNA ANTAGONIST COMPOUNDS FOR THE MODULATION OF TARGET mRNA
WO2009027527A2 (en) * 2007-08-30 2009-03-05 Santaris Pharma A/S Rna antagonist compounds for the modulation of fabp4/ap2
ES2360929T3 (es) * 2007-09-20 2011-06-10 Amgen Inc. Derivados del ácido 1-(4-(4-bencilbenzamido)-bencil)azetidin-3-carboxílico y compuestos relacionados como moduladores del receptor s1p para el tratamiento de trastornos inmunitarios.
EP2623599B1 (de) * 2007-10-04 2019-01-02 Roche Innovation Center Copenhagen A/S Mikromir-Moleküle
EP2268811A1 (de) * 2008-03-07 2011-01-05 Santaris Pharma A/S Pharmazeutische zusammensetzungen zur behandlung von krankheiten in verbindung mit microrna
ES2541442T3 (es) 2008-08-01 2015-07-20 Roche Innovation Center Copenhagen A/S Modulación mediada por microARN de factores estimulantes de colonias
ES2599979T3 (es) * 2009-04-24 2017-02-06 Roche Innovation Center Copenhagen A/S Composiciones farmacéuticas para el tratamiento de pacientes de VHC que no responden al interferón
US8563528B2 (en) 2009-07-21 2013-10-22 Santaris Pharma A/S Antisense oligomers targeting PCSK9
ES2770667T3 (es) 2013-06-27 2020-07-02 Roche Innovation Ct Copenhagen As Oligómeros antisentido y conjugados que se dirigen a PCSK9
US9790237B2 (en) 2014-06-16 2017-10-17 Johnson Matthey Public Limited Company Processes for making alkylated arylpiperazine and alkylated arylpiperidine compounds including novel intermediates

Family Cites Families (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4231938A (en) * 1979-06-15 1980-11-04 Merck & Co., Inc. Hypocholesteremic fermentation products and process of preparation
US4444784A (en) * 1980-08-05 1984-04-24 Merck & Co., Inc. Antihypercholesterolemic compounds
MX7065E (es) * 1980-06-06 1987-04-10 Sankyo Co Un procedimiento microbiologico para preparar derivados de ml-236b
US4739073A (en) * 1983-11-04 1988-04-19 Sandoz Pharmaceuticals Corp. Intermediates in the synthesis of indole analogs of mevalonolactone and derivatives thereof
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
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
EP0618803A4 (de) * 1991-12-19 1995-03-22 Southwest Found Biomed Res Polypeptide als inhibitoren gegen cholesterylester-transferase, antikörper gegen die synthetischen polypeptide und prophylaktische und therapeutische behandlungsweisen der atherosklerose.
DE69332792T2 (de) 1992-04-20 2004-01-15 Takeda Chemical Industries Ltd 4,1-Benzoxazepinderivate als Squalen-Synthetase Inhibitoren und ihre Verwendung zur Behandlung von Hypercholesterämie und als Fungizide
AU678503B2 (en) 1993-09-24 1997-05-29 Takeda Chemical Industries Ltd. Condensed heterocyclic compounds and their use as squalene synthetase inhibitors
EP0784612A1 (de) 1994-10-04 1997-07-23 Fujisawa Pharmaceutical Co., Ltd. Harnstoffderivate und ihre verwendung als acat-inhibitoren
US5510379A (en) * 1994-12-19 1996-04-23 Warner-Lambert Company Sulfonate ACAT inhibitors
GB9504066D0 (en) 1995-03-01 1995-04-19 Pharmacia Spa Phosphate derivatives of ureas and thioureas
US6147214A (en) * 1997-04-18 2000-11-14 Pfizer Inc Process and intermediates for the preparation of 4'-trifluoromethyl-biphenyl-2-carboxylic acid (1,2,3,4-tetrahydro-isoquinolin-6-yl)-amide
GB9826412D0 (en) * 1998-12-03 1999-01-27 Glaxo Group Ltd Chemical compounds
GB0013383D0 (en) * 2000-06-01 2000-07-26 Glaxo Group Ltd Therapeutic benzamide derivatives
GB0013378D0 (en) * 2000-06-01 2000-07-26 Glaxo Group Ltd Use of therapeutic benzamide derivatives
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
US6884750B2 (en) * 2001-06-27 2005-04-26 Rs Tech Corp. Chiral salen catalyst and methods for the preparation of chiral compounds from racemic epoxides by using new catalyst
GB0129015D0 (en) * 2001-12-04 2002-01-23 Glaxo Group Ltd Compounds

Also Published As

Publication number Publication date
CY1107945T1 (el) 2013-09-04
IS7622A (is) 2004-12-29
SI1536796T1 (sl) 2008-08-31
CN1674900A (zh) 2005-09-28
US20060040989A1 (en) 2006-02-23
NZ538680A (en) 2006-01-27
PL373379A1 (en) 2005-08-22
MXPA05001712A (es) 2005-04-19
DK1536796T3 (da) 2008-06-09
IL166795A0 (en) 2006-01-15
KR20050026483A (ko) 2005-03-15
PL212405B1 (pl) 2012-09-28
IS2726B (is) 2011-03-15
ATE385796T1 (de) 2008-03-15
PA8579901A1 (es) 2005-03-03
HRP20050103B1 (hr) 2013-09-30
CN100366252C (zh) 2008-02-06
US8258304B2 (en) 2012-09-04
WO2004017969A1 (en) 2004-03-04
EA008061B1 (ru) 2007-02-27
MY136632A (en) 2008-11-28
AU2003250215B2 (en) 2009-01-22
ES2301873T3 (es) 2008-07-01
DE60319097D1 (de) 2008-03-27
DE60319097T2 (de) 2009-06-04
NO329308B1 (no) 2010-09-27
TWI342775B (en) 2011-06-01
AR040968A1 (es) 2005-04-27
CA2494208C (en) 2011-05-10
HK1083451A1 (en) 2006-07-07
EP1536796B1 (de) 2008-02-13
HRP20050103A2 (en) 2006-09-30
EA200500348A1 (ru) 2005-08-25
JP4559856B2 (ja) 2010-10-13
ZA200501225B (en) 2006-07-26
CN101165053A (zh) 2008-04-23
IL166795A (en) 2010-11-30
NO20050563L (no) 2005-01-31
CN101165052B (zh) 2012-04-18
TW200412954A (en) 2004-08-01
BR0313377A (pt) 2005-07-12
KR101052204B1 (ko) 2011-07-29
CN101165052A (zh) 2008-04-23
EP1536796A1 (de) 2005-06-08
JP2006500371A (ja) 2006-01-05
PT1536796E (pt) 2008-05-13
CA2494208A1 (en) 2004-03-04
EG25699A (en) 2012-05-22
US20090156623A1 (en) 2009-06-18
AU2003250215A1 (en) 2004-03-11

Similar Documents

Publication Publication Date Title
UA79300C2 (en) N-aryl piperidine substituted biphenylcarboxamides as inhibitors of apolipoprotein b secretion
JP7204676B2 (ja) 疾患の予防および治療用の化合物およびその使用
EA005855B1 (ru) Полиарилкарбоксамиды, применимые в качестве агентов, снижающих содержание липидов
RS56332B1 (sr) Antagonisti c5ar
CN1312140C (zh) 降低脂质的联苯基甲酰胺
CA2427660C (en) Biphenylcarboxamides useful as lipid lowering agents
AU2002253171A1 (en) Lipid lowering biphenylcarboxamides
WO2021233133A1 (zh) 用作ret激酶抑制剂的化合物及其应用
JP4790626B2 (ja) N−アリールピペリジン置換ビフェニルカルボキサアミド
JP7016352B2 (ja) ベンゾイミダゾール直接ampk活性化剤
JP2024504720A (ja) 官能化長鎖炭化水素モノカルボン酸及びジカルボン酸ならびにそれらの誘導体、ならびに疾患の予防または治療のためのそれらの使用
JP5525261B2 (ja) Mtp阻害性テトラヒドロ−ナフタレン−1−カルボン酸誘導体
CN114751874A (zh) 作为TRPV4-KCa2.3促耦联剂的1-苄基-4-乙基哌嗪衍生物及其应用
HK1100559B (en) N-aryl piperidine substituted biphenylcarboxamides as inhibitors of apolipoprotein b
HK1083451B (en) N-aryl piperidine substituted biphenylcarboxamides as inhibitors of apolipoprotein b secretion