CA2194397A1 - Acide (-)-(3r)-3-methyl-4-{4-[4-(4-pyridyl)piperazin-1-yl]phenoxy}butyrique inhibiteur d'adhesion cellulaire - Google Patents

Acide (-)-(3r)-3-methyl-4-{4-[4-(4-pyridyl)piperazin-1-yl]phenoxy}butyrique inhibiteur d'adhesion cellulaire

Info

Publication number
CA2194397A1
CA2194397A1 CA002194397A CA2194397A CA2194397A1 CA 2194397 A1 CA2194397 A1 CA 2194397A1 CA 002194397 A CA002194397 A CA 002194397A CA 2194397 A CA2194397 A CA 2194397A CA 2194397 A1 CA2194397 A1 CA 2194397A1
Authority
CA
Canada
Prior art keywords
optically active
pharmaceutically
ester
active compound
amide
Prior art date
Legal status (The legal status 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 status listed.)
Abandoned
Application number
CA002194397A
Other languages
English (en)
Inventor
Stuart Dennett Mills
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Syngenta Ltd
Original Assignee
Individual
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
Priority claimed from US08/457,538 external-priority patent/US5652242A/en
Priority claimed from GBGB9518188.9A external-priority patent/GB9518188D0/en
Application filed by Individual filed Critical Individual
Publication of CA2194397A1 publication Critical patent/CA2194397A1/fr
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D213/72Nitrogen atoms
    • C07D213/74Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Diabetes (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Hematology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)

Abstract

La présente invention se rapporte à l'acide (-)-(3R)-3-méthyl-4-{4-[4-(4-pyridyl)pipérazin-1-yl]phénoxy}butyrique, nouveau composé doté d'une activité optique, ainsi qu'à ses sels, esters, amides, ou solvates pharmaceutiquement acceptables. Cette invention concerne également des procédés de préparation de ce composé, des compositions pharmaceutiques contenant ce composé et l'utilisation de ce composé comme inhibiteur de l'adhésion cellulaire, et notamment de l'agrégation plaquettaire.
CA002194397A 1995-06-01 1996-05-28 Acide (-)-(3r)-3-methyl-4-{4-[4-(4-pyridyl)piperazin-1-yl]phenoxy}butyrique inhibiteur d'adhesion cellulaire Abandoned CA2194397A1 (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US08/457,538 US5652242A (en) 1993-03-29 1995-06-01 Heterocyclic derivatives
US08/457538 1995-06-01
GB9518188.9 1995-09-07
GBGB9518188.9A GB9518188D0 (en) 1995-09-07 1995-09-07 Optically active derivative

Publications (1)

Publication Number Publication Date
CA2194397A1 true CA2194397A1 (fr) 1996-12-05

Family

ID=26307696

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002194397A Abandoned CA2194397A1 (fr) 1995-06-01 1996-05-28 Acide (-)-(3r)-3-methyl-4-{4-[4-(4-pyridyl)piperazin-1-yl]phenoxy}butyrique inhibiteur d'adhesion cellulaire

Country Status (31)

Country Link
EP (1) EP0796247A1 (fr)
JP (1) JP2885941B2 (fr)
KR (1) KR100245957B1 (fr)
AT (1) AT406675B (fr)
AU (1) AU710105B2 (fr)
BE (1) BE1009520A5 (fr)
BR (1) BR9606409A (fr)
CA (1) CA2194397A1 (fr)
CH (1) CH691808A5 (fr)
CZ (1) CZ26997A3 (fr)
DE (1) DE19680509T1 (fr)
DK (1) DK10697A (fr)
ES (1) ES2137886B1 (fr)
FI (1) FI970393A (fr)
GB (1) GB2304340B (fr)
GR (1) GR1002702B (fr)
HU (1) HUP9700274A3 (fr)
IE (1) IE960405A1 (fr)
IL (1) IL118477A0 (fr)
IT (1) IT1290839B1 (fr)
LU (1) LU90008B1 (fr)
MC (1) MC2418A1 (fr)
MX (1) MX9700379A (fr)
NL (1) NL1003243C2 (fr)
NO (1) NO307460B1 (fr)
NZ (1) NZ308597A (fr)
PL (1) PL318440A1 (fr)
SE (1) SE510812C2 (fr)
SK (1) SK13097A3 (fr)
TR (1) TR199700020T1 (fr)
WO (1) WO1996038416A1 (fr)

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0100158A3 (fr) * 1982-07-28 1985-03-27 The Upjohn Company Hétéroalkysylalkanoles 3-pyridinyliques, leurs acides alkanoiques et leurs esters
GB8609630D0 (en) * 1986-04-19 1986-05-21 Pfizer Ltd Anti-arrhythmia agents
DK0825184T3 (da) * 1993-03-29 2001-09-10 Astrazeneca Ab Heterocykliske derivater som blodpladeaggregeringsinhibitorer
IL109145A0 (en) * 1993-03-29 1994-06-24 Zeneca Ltd Heterocyclic compounds

Also Published As

Publication number Publication date
GB2304340B (en) 1998-07-29
WO1996038416A1 (fr) 1996-12-05
AU710105B2 (en) 1999-09-16
KR970704689A (ko) 1997-09-06
FI970393A0 (fi) 1997-01-30
HUP9700274A3 (en) 2000-02-28
PL318440A1 (en) 1997-06-09
IE960405A1 (en) 1996-12-11
ITMI961113A1 (it) 1997-12-01
BR9606409A (pt) 1997-09-30
KR100245957B1 (ko) 2000-04-01
ATA900596A (de) 1999-12-15
HUP9700274A2 (hu) 1999-06-28
SE9700203L (sv) 1997-01-24
HU9700274D0 (en) 1997-04-28
BE1009520A5 (fr) 1997-04-01
AT406675B (de) 2000-07-25
EP0796247A1 (fr) 1997-09-24
ITMI961113A0 (it) 1996-05-31
SE510812C2 (sv) 1999-06-28
IL118477A0 (en) 1996-09-12
GR1002702B (el) 1997-05-22
CZ26997A3 (en) 1997-08-13
MX9700379A (es) 1997-04-30
JP2885941B2 (ja) 1999-04-26
TR199700020T1 (tr) 1997-04-22
FI970393A (fi) 1997-01-30
SE9700203D0 (sv) 1997-01-24
DE19680509T1 (de) 1997-12-04
NO970437D0 (no) 1997-01-31
LU90008B1 (fr) 1997-04-16
NO307460B1 (no) 2000-04-10
NZ308597A (en) 1998-11-25
AU5827296A (en) 1996-12-18
JPH09512836A (ja) 1997-12-22
NL1003243C2 (nl) 1996-12-04
CH691808A5 (de) 2001-10-31
ES2137886B1 (es) 2000-08-16
IT1290839B1 (it) 1998-12-14
SK13097A3 (en) 1997-08-06
DK10697A (da) 1997-04-01
ES2137886A1 (es) 1999-12-16
GB9627127D0 (en) 1997-02-19
MC2418A1 (fr) 1997-05-23
GB2304340A (en) 1997-03-19
NO970437L (no) 1997-02-20

Similar Documents

Publication Publication Date Title
EP0478328B1 (fr) Antagonistes de récepteur du fibrinogène
AU698705B2 (en) Thrombin inhibitors
CA2390231A1 (fr) Inhibiteurs de la dipeptidyl peptidase iv; methodes de fabrication et d'utilisation desdits inhibiteurs
SK63194A3 (en) Peptide derivatives
WO1992016549A1 (fr) Derives de phenylalanine substitues en position para
CA2268621A1 (fr) Derive d'acide 2-pipirazinone-1-acetique, production et utilisation de celui-ci
JPH01503063A (ja) 抗炎症組成物
US11434198B2 (en) Compounds and methods for the treatment of neurodegenerative diseases
JPH072820A (ja) 不可逆ヒト免疫不全ウイルス(hiv)プロテアーゼ阻害剤、その中間体、組成物およびその製法
CA2022112A1 (fr) Certains composes d'imidazole comme inhibiteurs de la transglutaminase
CN101790528A (zh) 氨基酰基前药
FR2758329A1 (fr) Derives d'imidazole-4-butane boronique, leur preparation et leur utilisation en therapeutique
CA2070983A1 (fr) Inhibiteurs cycliques de la renine
CA2194397A1 (fr) Acide (-)-(3r)-3-methyl-4-{4-[4-(4-pyridyl)piperazin-1-yl]phenoxy}butyrique inhibiteur d'adhesion cellulaire
SK281025B6 (sk) (1-fenyl-1-heterocyklyl)alkánové deriváty, spôsoby ich prípravy, medziprodukty na ich prípravu, farmaceutické prostriedky s ich obsahom a ich použitie
JPH10175967A (ja) 新規なn−ベンジルピペラジン化合物、その製造法及びそれを含有する医薬組成物
HU205951B (en) Process for producing amino-acid derivatives and pharmaceutical compositions containing them
CA2887420A1 (fr) Inhibiteurs de metalloproteinases matricielles et methodes de traitement de la douleur et d'autres maladies
NZ306451A (en) Substituted phenyl amidines, medicaments containing these compounds and process for producing them
CN102924567B (zh) 一类肽化合物、其制备方法及用途
CA2022110A1 (fr) Composes d'azole et leur utilisation comme inhibiteurs de la transglutaminase
CA2230445C (fr) Antagonistes de recepteur de fibrinogene, et preparation medicinale contenant ces antagonistes en tant qu'ingredient actif
US5817680A (en) Hemoregulatory compounds
CH677610A5 (fr)
FR2734818A1 (fr) Acide (-)-(3r)-3-methyl-4-{4-[4-(4-pyridyl)piperazine-1-yl- phenoxy}-butyrique, procede pour sa preparation et composition pharmaceutique le contenant

Legal Events

Date Code Title Description
FZDE Discontinued