ZA200501225B - 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

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Publication number
ZA200501225B
ZA200501225B ZA200501225A ZA200501225A ZA200501225B ZA 200501225 B ZA200501225 B ZA 200501225B ZA 200501225 A ZA200501225 A ZA 200501225A ZA 200501225 A ZA200501225 A ZA 200501225A ZA 200501225 B ZA200501225 B ZA 200501225B
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ZA
South Africa
Prior art keywords
compound
formula
carbon
compounds
4alkyl
Prior art date
Application number
ZA200501225A
Other languages
English (en)
Inventor
Lieven Meerpoel
Peter W M Roevens
Leo J J 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 ZA200501225B publication Critical patent/ZA200501225B/en

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    • 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
ZA200501225A 2002-08-12 2005-02-10 N-aryl piperidine substituted biphenylcarboxamides as inhibitors of apolipoprotein B secretion ZA200501225B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP02078309 2002-08-12

Publications (1)

Publication Number Publication Date
ZA200501225B true ZA200501225B (en) 2006-07-26

Family

ID=31896911

Family Applications (1)

Application Number Title Priority Date Filing Date
ZA200501225A ZA200501225B (en) 2002-08-12 2005-02-10 N-aryl piperidine substituted biphenylcarboxamides as inhibitors of apolipoprotein B secretion

Country Status (32)

Country Link
US (2) US20060040989A1 (hr)
EP (1) EP1536796B1 (hr)
JP (1) JP4559856B2 (hr)
KR (1) KR101052204B1 (hr)
CN (3) CN101165053A (hr)
AR (1) AR040968A1 (hr)
AT (1) ATE385796T1 (hr)
AU (1) AU2003250215B2 (hr)
BR (1) BR0313377A (hr)
CA (1) CA2494208C (hr)
CY (1) CY1107945T1 (hr)
DE (1) DE60319097T2 (hr)
DK (1) DK1536796T3 (hr)
EA (1) EA008061B1 (hr)
EG (1) EG25699A (hr)
ES (1) ES2301873T3 (hr)
HK (1) HK1083451A1 (hr)
HR (1) HRP20050103B1 (hr)
IL (1) IL166795A (hr)
IS (1) IS2726B (hr)
MX (1) MXPA05001712A (hr)
MY (1) MY136632A (hr)
NO (1) NO329308B1 (hr)
NZ (1) NZ538680A (hr)
PA (1) PA8579901A1 (hr)
PL (1) PL212405B1 (hr)
PT (1) PT1536796E (hr)
SI (1) SI1536796T1 (hr)
TW (1) TWI342775B (hr)
UA (1) UA79300C2 (hr)
WO (1) WO2004017969A1 (hr)
ZA (1) ZA200501225B (hr)

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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
EP3431602A1 (en) * 2006-04-03 2019-01-23 Roche Innovation Center Copenhagen A/S Pharmaceutical composition comprising anti-mirna antisense oligonucleotides
JP5814505B2 (ja) 2006-04-03 2015-11-17 ロシュ・イノベーション・センター・コペンハーゲン・アクティーゼルスカブRoche Innovation Center Copenhagen A/S antimiRNAアンチセンスオリゴヌクレオチドを含む医薬組成物
WO2008100423A1 (en) * 2007-02-09 2008-08-21 Sirtris Pharmaceuticals, Inc. Gut microsomal triglyceride transport protein inhibitors
DK2149605T3 (da) * 2007-03-22 2013-09-30 Santaris Pharma As Korte RNA antagonist forbindelser til modulering af det ønskede mRNA
AU2008228243B2 (en) * 2007-03-22 2014-05-15 Santaris Pharma A/S RNA antagonist compounds for the inhibition of Apo-B100 expression
US20110054011A1 (en) * 2007-08-30 2011-03-03 Mccullagh Keith RNA Antagonist Compounds for the Modulation of FABP4/AP2
MX2010002885A (es) * 2007-09-20 2010-04-01 Amgen Inc Derivados de acido 1-(4-(bencilbenzamido)-bencil)-azetidin-3-carbo xilico y compuestos relacionados como moduladores de receptores de s1p para el tratamiento de trastornos inmunitarios.
AU2008306327B2 (en) * 2007-10-04 2014-05-15 Roche Innovation Center Copenhagen A/S Micromirs
US8404659B2 (en) * 2008-03-07 2013-03-26 Santaris Pharma A/S Pharmaceutical compositions for treatment of MicroRNA related diseases
ES2541442T3 (es) 2008-08-01 2015-07-20 Roche Innovation Center Copenhagen A/S Modulación mediada por microARN de factores estimulantes de colonias
WO2010122538A1 (en) * 2009-04-24 2010-10-28 Santaris Pharma A/S Pharmaceutical compositions for treatment of hcv patients that are non-responders to interferon
US8563528B2 (en) 2009-07-21 2013-10-22 Santaris Pharma A/S Antisense oligomers targeting PCSK9
CN112263682A (zh) 2013-06-27 2021-01-26 罗氏创新中心哥本哈根有限公司 靶向pcsk9的反义寡聚体和缀合物
SI3154967T1 (sl) 2014-06-16 2020-11-30 Johnson Matthey Public Limited Company, Postopki za pripravo alkiliranih arilpiperazinskih in alkiliranih arilpiperidinskih spojin, ki vključujejo nove intermediate

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US4444784A (en) * 1980-08-05 1984-04-24 Merck & Co., Inc. Antihypercholesterolemic compounds
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Also Published As

Publication number Publication date
SI1536796T1 (sl) 2008-08-31
EG25699A (en) 2012-05-22
HRP20050103A2 (en) 2006-09-30
KR20050026483A (ko) 2005-03-15
CN101165053A (zh) 2008-04-23
NO329308B1 (no) 2010-09-27
TWI342775B (en) 2011-06-01
ES2301873T3 (es) 2008-07-01
PA8579901A1 (es) 2005-03-03
IL166795A0 (en) 2006-01-15
UA79300C2 (en) 2007-06-11
US20060040989A1 (en) 2006-02-23
CN101165052B (zh) 2012-04-18
DE60319097D1 (de) 2008-03-27
EP1536796A1 (en) 2005-06-08
NO20050563L (no) 2005-01-31
US20090156623A1 (en) 2009-06-18
CA2494208A1 (en) 2004-03-04
JP4559856B2 (ja) 2010-10-13
IS2726B (is) 2011-03-15
TW200412954A (en) 2004-08-01
PL212405B1 (pl) 2012-09-28
PL373379A1 (en) 2005-08-22
CA2494208C (en) 2011-05-10
EA200500348A1 (ru) 2005-08-25
AU2003250215A1 (en) 2004-03-11
HK1083451A1 (en) 2006-07-07
NZ538680A (en) 2006-01-27
US8258304B2 (en) 2012-09-04
PT1536796E (pt) 2008-05-13
BR0313377A (pt) 2005-07-12
AU2003250215B2 (en) 2009-01-22
CN101165052A (zh) 2008-04-23
ATE385796T1 (de) 2008-03-15
IS7622A (is) 2004-12-29
MXPA05001712A (es) 2005-04-19
EP1536796B1 (en) 2008-02-13
DE60319097T2 (de) 2009-06-04
WO2004017969A1 (en) 2004-03-04
EA008061B1 (ru) 2007-02-27
KR101052204B1 (ko) 2011-07-29
HRP20050103B1 (hr) 2013-09-30
DK1536796T3 (da) 2008-06-09
MY136632A (en) 2008-11-28
AR040968A1 (es) 2005-04-27
CN100366252C (zh) 2008-02-06
CN1674900A (zh) 2005-09-28
JP2006500371A (ja) 2006-01-05
IL166795A (en) 2010-11-30
CY1107945T1 (el) 2013-09-04

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