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MA26762A1 - Derives de pyrrolidine- antagonistes du recepteur ccr-3 - Google Patents

Derives de pyrrolidine- antagonistes du recepteur ccr-3

Info

Publication number
MA26762A1
MA26762A1 MA26199A MA26199A MA26762A1 MA 26762 A1 MA26762 A1 MA 26762A1 MA 26199 A MA26199 A MA 26199A MA 26199 A MA26199 A MA 26199A MA 26762 A1 MA26762 A1 MA 26762A1
Authority
MA
Morocco
Prior art keywords
ccr
receptor antagonists
pyrrolidine derivatives
pyrrolidine
derivatives
Prior art date
Application number
MA26199A
Other languages
English (en)
Inventor
Daniel Harry Roger
John Saunders
John Patrick Williams
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of MA26762A1 publication Critical patent/MA26762A1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/06—Antiasthmatics
    • 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
    • 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
    • C07D207/08—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 hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
    • C07D207/09—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pulmonology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyrrole Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
MA26199A 1998-11-20 2001-05-17 Derives de pyrrolidine- antagonistes du recepteur ccr-3 MA26762A1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US10929798P 1998-11-20 1998-11-20

Publications (1)

Publication Number Publication Date
MA26762A1 true MA26762A1 (fr) 2004-12-20

Family

ID=22326918

Family Applications (1)

Application Number Title Priority Date Filing Date
MA26199A MA26762A1 (fr) 1998-11-20 2001-05-17 Derives de pyrrolidine- antagonistes du recepteur ccr-3

Country Status (27)

Country Link
US (1) US6166015A (fr)
EP (1) EP1131288A1 (fr)
JP (1) JP3593037B2 (fr)
KR (1) KR20010086045A (fr)
CN (1) CN1158256C (fr)
AR (1) AR023707A1 (fr)
AU (1) AU763960B2 (fr)
BR (1) BR9915520A (fr)
CA (1) CA2350903A1 (fr)
CO (1) CO5140119A1 (fr)
CZ (1) CZ20011760A3 (fr)
DE (1) DE19955794A1 (fr)
ES (1) ES2158814B1 (fr)
FR (1) FR2786185A1 (fr)
GB (1) GB2343893B (fr)
HU (1) HUP0104364A2 (fr)
ID (1) ID29067A (fr)
IL (1) IL143226A0 (fr)
IT (1) IT1307900B1 (fr)
MA (1) MA26762A1 (fr)
NO (1) NO20012411D0 (fr)
PE (1) PE20001403A1 (fr)
PL (1) PL348375A1 (fr)
TR (1) TR200101398T2 (fr)
UY (1) UY25811A1 (fr)
WO (1) WO2000031032A1 (fr)
ZA (1) ZA200103942B (fr)

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US7390830B1 (en) * 1999-05-18 2008-06-24 Teijin Limited Remedies or prophylactics for diseases in association with chemokines
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WO2001042208A1 (fr) * 1999-12-08 2001-06-14 Teijin Limited Antagonistes du recepteur ccr5 de la cycloamine
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MXPA03005581A (es) 2000-12-19 2003-10-06 Hoffmann La Roche Pirrolidinas substituidas como antagonistas del receptor ccr-3.
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EP1427696A1 (fr) * 2001-09-13 2004-06-16 F. Hoffmann-La Roche Ag Antagonistes v du recepteur ccr-3
US7067549B2 (en) * 2001-12-31 2006-06-27 Actelion Pharmaceuticals Ag Pyrrolidone carboxamides
GB0207439D0 (en) * 2002-03-28 2002-05-08 Glaxo Group Ltd Novel compounds
GB0207432D0 (en) 2002-03-28 2002-05-08 Glaxo Group Ltd Novel compounds
GB0207443D0 (en) * 2002-03-28 2002-05-08 Glaxo Group Ltd Novel compounds
GB0207436D0 (en) * 2002-03-28 2002-05-08 Glaxo Group Ltd Novel compounds
GB0212355D0 (en) * 2002-05-29 2002-07-10 Glaxo Group Ltd Novel compounds
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DK1531822T3 (da) 2002-06-12 2009-12-07 Chemocentryx Inc 1-aryl-4-substituerede piperazin derivater til anvendelse som CCR1 antagonister til behandlingen af inflammation og immunforstyrrelser
US7842693B2 (en) 2002-06-12 2010-11-30 Chemocentryx, Inc. Substituted piperazines
WO2004004731A1 (fr) * 2002-07-02 2004-01-15 F. Hoffmann-La Roche Ag Derives de pyrimidine a substitution 2, 5 utilises en tant qu'antagonistes ix du recepteur ccr-3
WO2004028530A1 (fr) * 2002-09-26 2004-04-08 Bristol-Myers Squibb Company Amines heterocycliques n-substituees, utilisees comme modulateurs de l'activite des recepteurs des chimiokines
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US7514562B2 (en) 2003-03-07 2009-04-07 Glaxo Group Limited Urea derivatives and their use as vanilloid receptor antagonists in the treatment of pain
GB0305426D0 (en) * 2003-03-08 2003-04-16 Glaxo Group Ltd Novel compounds
MXPA05009771A (es) 2003-03-14 2005-10-26 Ono Pharmaceutical Co Derivados heterociclicos que contienen nitrogeno y medicamentos que los contienen como el ingrediente activo.
JP4710606B2 (ja) 2003-04-18 2011-06-29 小野薬品工業株式会社 スピロピペリジン化合物およびその医薬用途
AU2004283842A1 (en) * 2003-10-24 2005-05-06 F. Hoffmann-La Roche Ag CCR3 receptor antagonists
JP4845873B2 (ja) 2004-03-03 2011-12-28 ケモセントリックス インコーポレーティッド 二環式および架橋した窒素複素環
US7435831B2 (en) 2004-03-03 2008-10-14 Chemocentryx, Inc. Bicyclic and bridged nitrogen heterocycles
RU2530889C2 (ru) * 2004-05-14 2014-10-20 Эмисфире Текнолоджис, Инк. Соединения и составы для доставки активных веществ
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JPWO2006129679A1 (ja) 2005-05-31 2009-01-08 小野薬品工業株式会社 スピロピペリジン化合物およびその医薬用途
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HUP0500886A2 (en) * 2005-09-23 2007-05-29 Sanofi Aventis Amide derivatives as ccr3 receptor ligands, process for producing them, pharmaceutical compositions containing them and their use
HUP0500877A2 (en) * 2005-09-22 2007-05-29 Sanofi Aventis Amide derivatives as ccr3 receptor ligands, process for producing them, pharmaceutical compositions containing them and their use and intermediates
BRPI0616150A2 (pt) * 2005-09-22 2011-06-07 Sanofi Aventis derivados de amino-alquil-amida como lìquidos receptores de ccr3
WO2007049771A1 (fr) 2005-10-28 2007-05-03 Ono Pharmaceutical Co., Ltd. Compose contenant un groupe basique et son utilisation
WO2007058322A1 (fr) 2005-11-18 2007-05-24 Ono Pharmaceutical Co., Ltd. Composé contenant un groupe basique et son utilisation
WO2007105637A1 (fr) 2006-03-10 2007-09-20 Ono Pharmaceutical Co., Ltd. Derive heterocyclique azote et agent pharmaceutique comprenant le derive en tant que principe actif
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Also Published As

Publication number Publication date
WO2000031032A1 (fr) 2000-06-02
CA2350903A1 (fr) 2000-06-02
DE19955794A1 (de) 2000-05-31
JP2002530374A (ja) 2002-09-17
CN1331677A (zh) 2002-01-16
FR2786185A1 (fr) 2000-05-26
ID29067A (id) 2001-07-26
ZA200103942B (en) 2002-08-15
PL348375A1 (en) 2002-05-20
CN1158256C (zh) 2004-07-21
JP3593037B2 (ja) 2004-11-24
PE20001403A1 (es) 2000-12-15
IT1307900B1 (it) 2001-11-19
GB2343893B (en) 2002-01-09
TR200101398T2 (tr) 2001-09-21
GB9927227D0 (en) 2000-01-12
AU763960B2 (en) 2003-08-07
ES2158814B1 (es) 2002-03-16
NO20012411L (no) 2001-05-16
EP1131288A1 (fr) 2001-09-12
US6166015A (en) 2000-12-26
AU1382500A (en) 2000-06-13
NO20012411D0 (no) 2001-05-16
CZ20011760A3 (cs) 2001-12-12
UY25811A1 (es) 2001-07-31
CO5140119A1 (es) 2002-03-22
HUP0104364A2 (hu) 2002-04-29
ITTO991009A0 (it) 1999-11-19
ITTO991009A1 (it) 2001-05-19
BR9915520A (pt) 2001-07-17
ES2158814A1 (es) 2001-09-01
KR20010086045A (ko) 2001-09-07
GB2343893A (en) 2000-05-24
AR023707A1 (es) 2002-09-04
IL143226A0 (en) 2002-04-21

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