NO302572B1 - Piperidinforbindelser, og farmasöytiske preparater inneholdende slike - Google Patents

Piperidinforbindelser, og farmasöytiske preparater inneholdende slike

Info

Publication number
NO302572B1
NO302572B1 NO931166A NO931166A NO302572B1 NO 302572 B1 NO302572 B1 NO 302572B1 NO 931166 A NO931166 A NO 931166A NO 931166 A NO931166 A NO 931166A NO 302572 B1 NO302572 B1 NO 302572B1
Authority
NO
Norway
Prior art keywords
group
hydrogen atom
alkyl group
alkyl
substituted
Prior art date
Application number
NO931166A
Other languages
English (en)
Norwegian (no)
Other versions
NO931166D0 (no
NO931166L (no
Inventor
Gilbert Lassalle
Thomas Purcell
Daniel Galtier
Paul Howard Williams
Frederic Galli
Original Assignee
Synthelabo
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 Synthelabo filed Critical Synthelabo
Publication of NO931166D0 publication Critical patent/NO931166D0/no
Publication of NO931166L publication Critical patent/NO931166L/no
Publication of NO302572B1 publication Critical patent/NO302572B1/no

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/64Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
    • 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
    • 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
    • C07D401/06Heterocyclic 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 linked by a carbon chain containing only aliphatic carbon atoms
    • 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
    • C07D401/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links
    • 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
    • C07D401/14Heterocyclic 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 three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06Dipeptides
    • C07K5/06139Dipeptides with the first amino acid being heterocyclic

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
NO931166A 1992-03-30 1993-03-29 Piperidinforbindelser, og farmasöytiske preparater inneholdende slike NO302572B1 (no)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR9203828A FR2689130B1 (fr) 1992-03-30 1992-03-30 Derives de 1-[2 (arylsulfonylamino)ethyl-1-oxo] piperidine, leur preparation et leur application en therapeutique.

Publications (3)

Publication Number Publication Date
NO931166D0 NO931166D0 (no) 1993-03-29
NO931166L NO931166L (no) 1993-10-01
NO302572B1 true NO302572B1 (no) 1998-03-23

Family

ID=9428242

Family Applications (2)

Application Number Title Priority Date Filing Date
NO931166A NO302572B1 (no) 1992-03-30 1993-03-29 Piperidinforbindelser, og farmasöytiske preparater inneholdende slike
NO975664A NO975664D0 (no) 1992-03-30 1997-12-05 Imidazolderivater som er nyttige som syntesemellomprodukter

Family Applications After (1)

Application Number Title Priority Date Filing Date
NO975664A NO975664D0 (no) 1992-03-30 1997-12-05 Imidazolderivater som er nyttige som syntesemellomprodukter

Country Status (21)

Country Link
US (1) US5453430A (ja)
EP (2) EP0565396B1 (ja)
JP (2) JP2550276B2 (ja)
KR (1) KR930019664A (ja)
CN (1) CN1076928A (ja)
AT (1) ATE161839T1 (ja)
AU (1) AU655876B2 (ja)
CA (1) CA2092867A1 (ja)
CZ (1) CZ52893A3 (ja)
DE (1) DE69316068T2 (ja)
FI (1) FI931413A (ja)
FR (1) FR2689130B1 (ja)
HU (1) HUT64758A (ja)
IL (1) IL105028A0 (ja)
MX (1) MX9301783A (ja)
NO (2) NO302572B1 (ja)
NZ (1) NZ247277A (ja)
PL (1) PL298299A1 (ja)
SK (1) SK26393A3 (ja)
TW (1) TW234717B (ja)
ZA (1) ZA932228B (ja)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2689130B1 (fr) 1992-03-30 1994-05-27 Synthelabo Derives de 1-[2 (arylsulfonylamino)ethyl-1-oxo] piperidine, leur preparation et leur application en therapeutique.
JPH06329627A (ja) * 1993-05-03 1994-11-29 Bristol Myers Squibb Co グアニジニル−またはアミジニル−置換ヘテロ環トロンビンインヒビター
FR2710061B1 (fr) * 1993-09-14 1995-12-29 Synthelabo Acides et chlorures d'acides 1,2,3, 4-tétrahydroquinoléine-8-sulfoniques, et leur utilisation comme intermédiaires de synthèse.
FR2710066B1 (fr) * 1993-09-14 1995-10-20 Synthelabo Dérivés de 1-[2-amino-5-[1-(triphénylméthyl-1H-imidazol-4-yl]-1-oxopentyl]piperidine, leur préparation et leur utilisation comme intermédiaires de synthèse.
FR2718443B1 (fr) * 1994-04-12 1996-05-10 Synthelabo Dérivés de 1-[2-[[(3-méthyl-1, 2, 3, 4-tétrahydroquinoléin-8-yl)sulfonyl] amino]-1-oxo-5-(1H-imidazol-4-yl)pentyl]pipéridine, leur préparation et leur application en thérapeutique.
FR2718439B3 (fr) * 1994-04-12 1996-02-09 Synthelabo Dérivés de l'acide pipécolique, leur préparation et leur utilisation comme intermédiaires de synthèse.
FR2718442B1 (fr) * 1994-04-12 1996-05-10 Synthelabo Dérivés de 5-(1H-imidazol-4-yl)-1-oxopentylpipéridine, leur préparation et leur application en thérapeutique.
FR2718444B1 (fr) * 1994-04-12 1996-05-10 Synthelabo Dérivés de (3-méthyl-1, 2, 3, 4-tétrahydroquinoléin-8-yl)sulfonyle, leur préparation et leur application en thérapeutique.
DE4424828A1 (de) * 1994-07-14 1996-01-18 Thomae Gmbh Dr K Neue substituierte Arylsulfonamide, ihre Herstellung und ihre Verwendung als Arzneimittel
FR2727413B1 (fr) * 1994-11-25 1996-12-20 Synthelabo Derives de 5-(1h-imidazol-4-yl)-1-oxo-2-(phenylsulfonamino)- pentylpiperidine, leur preparation et leur application en therapeutique
FR2728570B1 (fr) * 1994-12-23 1997-04-11 Synthelabo Derives de 1-oxo-2-(phenylsulfonylamino)pentylpiperidine, leur preparation et leur application en therapeutique
GB9505538D0 (en) * 1995-03-18 1995-05-03 Ciba Geigy Ag New compounds
US5811402A (en) * 1996-03-22 1998-09-22 Eli Lilly And Company Antithrombotic diamides
FR2747677B1 (fr) * 1996-04-22 1998-06-05 Synthelabo Derives de propargylglycine, leur preparation et leur utilisation comme intermediaires de synthese
IL125918A0 (en) * 1996-04-22 1999-04-11 Synthelabo Propargylgycine derivatives preparation and utilisation thereof as synthesis intermediates
FR2747676B1 (fr) * 1996-04-22 1998-06-05 Synthelabo Derives de [1-oxo-2-(sulfonylamino)ethyl] piperidine, leur preparation et leur application en therapeutique
US5840733A (en) * 1996-07-01 1998-11-24 Redcell, Canada, Inc. Methods and compositions for producing novel conjugates of thrombin inhibitors and endogenous carriers resulting in anti-thrombins with extended lifetimes
FR2756285B1 (fr) * 1996-11-22 1998-12-18 Synthelabo Derives de n-(imidazolylbutyle)benzenesulfonamide, leur preparation et leur application en therapeutique
US5773089A (en) * 1996-12-18 1998-06-30 E. I. Du Pont De Nemours And Company Process for treating aramid surfaces to be plated
FR2765220B1 (fr) * 1997-06-25 1999-07-30 Synthelabo Derives de 1-oxo-2-(phenylsulfonyl)aminopentyle, leur preparation et leur application en therapeutique
FR2771094B1 (fr) * 1997-11-19 2000-02-04 Synthelabo Derives de piperidine-2-carboxylate, leur preparation et leur application en therapeutique
CA2609161A1 (en) * 2005-05-18 2006-11-23 Siegfried Wurster Peptidomimetics selective for the somatostatin receptor subtypes 1 and/or 4
KR101682259B1 (ko) * 2008-12-22 2016-12-05 포라 가세이 고교 가부시키가이샤 멜라닌 생산 억제제
CN101794567B (zh) * 2010-02-10 2014-01-01 中兴通讯股份有限公司 图片加载的方法及终端
CN104098647B (zh) * 2014-06-24 2017-12-08 安徽省逸欣铭医药科技有限公司 阿加曲班类似物及其制备方法和医药用途
CN118724766A (zh) * 2023-03-28 2024-10-01 南京华狮新材料有限公司 一种氨基酸衍生物及其制备方法和作为中间体合成l-草铵膦的方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IE48623B1 (en) * 1978-08-31 1985-03-20 Mitsubishi Chem Ind Alpha-(n-arylsulfonyl-l-argininamides,processes for their preparation and pharmaceutical compositions containing these substances
EP0008596A1 (fr) * 1978-09-04 1980-03-19 DEVINTER Europe S.A. Société anonyme dite: Procédé de préparation de dérivés du type 4-hydroxyméthyl imidazole à partir d'esters d'acides 4-imidazole carboxyliques correspondants
SE8203887D0 (sv) * 1982-06-23 1982-06-23 Kabivitrum Ab Nya trombininhiberande foreningar
DE3771376D1 (de) 1986-03-17 1991-08-22 Glaxo Group Ltd Indol-derivate, verfahren zu ihrer herstellung und diese enthaltende pharmazeutische zusammensetzungen.
CA2043741C (en) * 1990-06-07 2003-04-01 Kiyofumi Ishikawa Endothelin antagonistic peptide derivatives
FR2689130B1 (fr) 1992-03-30 1994-05-27 Synthelabo Derives de 1-[2 (arylsulfonylamino)ethyl-1-oxo] piperidine, leur preparation et leur application en therapeutique.

Also Published As

Publication number Publication date
SK26393A3 (en) 1993-12-08
FI931413A (fi) 1993-10-01
KR930019664A (ko) 1993-10-18
HU9300915D0 (en) 1993-06-28
JPH0798807B2 (ja) 1995-10-25
US5453430A (en) 1995-09-26
ZA932228B (en) 1993-10-28
MX9301783A (es) 1994-02-28
DE69316068D1 (de) 1998-02-12
HUT64758A (en) 1994-02-28
NO931166D0 (no) 1993-03-29
TW234717B (en) 1994-11-21
NZ247277A (en) 1995-07-26
EP0579277A1 (fr) 1994-01-19
JPH06199807A (ja) 1994-07-19
PL298299A1 (en) 1993-10-18
IL105028A0 (en) 1993-07-08
FI931413A0 (fi) 1993-03-29
ATE161839T1 (de) 1998-01-15
FR2689130B1 (fr) 1994-05-27
CN1076928A (zh) 1993-10-06
AU655876B2 (en) 1995-01-12
NO975664D0 (no) 1997-12-05
NO975664L (no) 1993-10-01
JP2550276B2 (ja) 1996-11-06
NO931166L (no) 1993-10-01
CA2092867A1 (fr) 1993-10-01
DE69316068T2 (de) 1998-08-13
CZ52893A3 (en) 1994-02-16
JPH06157514A (ja) 1994-06-03
EP0565396A1 (fr) 1993-10-13
AU3556093A (en) 1993-10-07
FR2689130A1 (fr) 1993-10-01
EP0565396B1 (fr) 1998-01-07

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