ES2150489T3 - 1-amidinofenil-pirrolidonas, -piperidinonas, -azetinonas como inhibidores de la agregacion de plaquetas. - Google Patents

1-amidinofenil-pirrolidonas, -piperidinonas, -azetinonas como inhibidores de la agregacion de plaquetas.

Info

Publication number
ES2150489T3
ES2150489T3 ES94913308T ES94913308T ES2150489T3 ES 2150489 T3 ES2150489 T3 ES 2150489T3 ES 94913308 T ES94913308 T ES 94913308T ES 94913308 T ES94913308 T ES 94913308T ES 2150489 T3 ES2150489 T3 ES 2150489T3
Authority
ES
Spain
Prior art keywords
pct
aggregation
pirrolidonas
piperidinonas
azetinonas
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.)
Expired - Lifetime
Application number
ES94913308T
Other languages
English (en)
Inventor
Norman Anthony Abood
Daniel Lee Flynn
Robert Bruce Garland
Lori Ann Schretzman
Kenneth Williams
Jeffery Alan Zablocki
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.)
GD Searle LLC
Original Assignee
GD Searle LLC
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 GD Searle LLC filed Critical GD Searle LLC
Application granted granted Critical
Publication of ES2150489T3 publication Critical patent/ES2150489T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • C07D207/18—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 one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22—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 one double bond between ring members or between a ring member and a non-ring member 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
    • C07D207/24—Oxygen or sulfur atoms
    • C07D207/26—2-Pyrrolidones
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
    • C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
    • C07D205/06—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D205/08—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with one oxygen atom directly attached in position 2, e.g. beta-lactams
    • C07D205/085—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with one oxygen atom directly attached in position 2, e.g. beta-lactams with a nitrogen atom directly attached in position 3
    • 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
    • C07D207/18—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 one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22—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 one double bond between ring members or between a ring member and a non-ring member 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
    • C07D207/24—Oxygen or sulfur atoms
    • C07D207/26—2-Pyrrolidones
    • C07D207/273—2-Pyrrolidones 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 other ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/68—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D211/72—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D211/74—Oxygen atoms
    • C07D211/76—Oxygen atoms attached in position 2 or 6
    • 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
    • C07D405/12—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 chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/0803—Compounds with Si-C or Si-Si linkages
    • C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
    • C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring

Landscapes

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

Abstract

ESTA INVENCION SE REFIERE A COMPUESTOS QUE TIENEN LA FORMULA (I) O A SALES FARMACEUTICAMENTE ACEPTABLES DE LOS MISMOS QUE SON UTILES PARA INHIBIR LA AGREGACION DE PLAQUETAS, A COMPOSICIONES FARMACEUTICAS DE TALES DERIVADOS DE FENILAMIDINAS Y A UN METODO PARA INHIBIR LA AGREGACION DE PLAQUETAS EN MAMIFEROS MEDIANTE LA ADMINISTRACION DE TALES COMPUESTOS Y COMPOSICIONES.
ES94913308T 1993-03-31 1994-03-30 1-amidinofenil-pirrolidonas, -piperidinonas, -azetinonas como inhibidores de la agregacion de plaquetas. Expired - Lifetime ES2150489T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US4143393A 1993-03-31 1993-03-31

Publications (1)

Publication Number Publication Date
ES2150489T3 true ES2150489T3 (es) 2000-12-01

Family

ID=21916489

Family Applications (1)

Application Number Title Priority Date Filing Date
ES94913308T Expired - Lifetime ES2150489T3 (es) 1993-03-31 1994-03-30 1-amidinofenil-pirrolidonas, -piperidinonas, -azetinonas como inhibidores de la agregacion de plaquetas.

Country Status (16)

Country Link
US (1) US5721366A (es)
EP (1) EP0691953B1 (es)
JP (1) JP3034046B2 (es)
KR (1) KR100257837B1 (es)
CN (1) CN1054842C (es)
AT (1) ATE195117T1 (es)
AU (1) AU681396B2 (es)
CA (1) CA2159450C (es)
DE (1) DE69425431T2 (es)
DK (1) DK0691953T3 (es)
ES (1) ES2150489T3 (es)
FI (1) FI111007B (es)
GR (1) GR3034520T3 (es)
NO (1) NO305950B1 (es)
PT (1) PT691953E (es)
WO (1) WO1994022820A1 (es)

Families Citing this family (39)

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US5314902A (en) * 1993-01-27 1994-05-24 Monsanto Company Urea derivatives useful as platelet aggregation inhibitors
AU6395094A (en) * 1993-03-15 1994-10-11 G.D. Searle & Co. Urea derivatives useful as platelet aggregation inhibitors
US5610296A (en) * 1994-12-05 1997-03-11 G. D. Searle & Co. Process for the preparation of amidino phenyl pyrrolidine beta-alanine urea analogs
TW448172B (en) * 1996-03-08 2001-08-01 Pharmacia & Upjohn Co Llc Novel hydroxamic acid derivatives useful for the treatment of diseases related to connective tissue degradation
ES2166996T3 (es) * 1996-05-15 2002-05-01 Searle & Co Metodo y reactivo para controlar los niveles en sangre de compuestos antiplaquetarios.
KR20040084945A (ko) * 1996-07-25 2004-10-06 바이오겐 아이덱 엠에이 인코포레이티드 세포 유착 억제제
US5872122A (en) * 1997-10-16 1999-02-16 Monsanto Company Pyrimidinylamidino β-amino acid derivatives useful as inhibitors of platelet aggregation
US5986107A (en) * 1998-04-08 1999-11-16 G. D. Searle & Co. Process for the preparation of a 2-oxopyrrolidine compound
ID28658A (id) 1998-04-16 2001-06-21 Texas Biotechnology Corp Senyawa yang menghambat pengikatan integrin pada reseptornya
DE19822912A1 (de) * 1998-05-22 1999-11-25 Degussa Verfahren zur Herstellung von 3-Amino-2-oxo-pyrrolidinen, neue Zwischenprodukte und deren Verwendung
US6025358A (en) * 1998-06-11 2000-02-15 G. D. Searle & Co. Double prodrugs of potent GP IIb/IIIa antagonists
US6335324B1 (en) 1998-06-25 2002-01-01 Bristol-Myers Squibb Co. Beta lactam compounds and their use as inhibitors of tryptase
CA2338878A1 (en) * 1998-08-13 2000-02-24 Merck & Co., Inc. Integrin receptor antagonists
DE19841895A1 (de) * 1998-09-11 2000-03-23 Degussa Neues Verfahren zur Herstellung von 3-Amino-2-oxo-pyrrolidinen, neue Zwischenprodukte und deren Verwendung
US6037365A (en) * 1998-09-25 2000-03-14 G.D. Searle & Co. Aminobenzamidinosuccinyl lactone derivatives useful as inhibitors of platelet aggregation
EP1165546A2 (en) * 1999-04-02 2002-01-02 Du Pont Pharmaceuticals Company Novel lactam inhibitors of matrix metalloproteinases, tnf-alpha, and aggrecanase
RU2263109C2 (ru) * 1999-05-07 2005-10-27 Тексэс Байотекнолоджи Копэрейшн ПРОИЗВОДНЫЕ КАРБОНОВЫХ КИСЛОТ (ВАРИАНТЫ), ФАРМАЦЕВТИЧЕСКАЯ КОМПОЗИЦИЯ И СПОСОБ СЕЛЕКТИВНОГО ИНГИБИРОВАНИЯ СВЯЗЫВАНИЯ α4β1 ИНТЕГРИНА У МЛЕКОПИТАЮЩЕГО
US6723711B2 (en) 1999-05-07 2004-04-20 Texas Biotechnology Corporation Propanoic acid derivatives that inhibit the binding of integrins to their receptors
AU782616B2 (en) * 1999-05-07 2005-08-11 Encysive Pharmaceuticals Inc. Carboxylic acid derivatives that inhibit the binding of integrins to their receptors
US6972296B2 (en) * 1999-05-07 2005-12-06 Encysive Pharmaceuticals Inc. Carboxylic acid derivatives that inhibit the binding of integrins to their receptors
US6849639B2 (en) * 1999-12-14 2005-02-01 Amgen Inc. Integrin inhibitors and their methods of use
SI21096B (sl) * 2001-10-09 2012-05-31 Encysive Pharmaceuticals Inc Derivati karboksilne kisline ki inhibirajo vezavo integrinov na njihove receptorje
CN103073476B (zh) * 2013-01-29 2015-03-04 西北师范大学 一种n-芳基-5-三氟甲基-2-吡咯烷酮和n-芳基-6-三氟甲基-2-吡啶烷酮的合成方法
CN103356679A (zh) * 2013-06-24 2013-10-23 丁圣雨 Houttuynoid A在抗血小板聚集药物中的应用
CN103381176B (zh) * 2013-06-24 2015-04-29 丁圣雨 Houttuynoid C在制备治疗动脉粥样硬化药物中的应用
CN103356682B (zh) * 2013-06-24 2015-08-19 丁圣雨 Houttuynoid D在制备抗血小板聚集药物中的应用
CN103356669B (zh) * 2013-06-24 2015-08-19 丁圣雨 Houttuynoid A在制备治疗或预防急性心衰的药物中的应用
CN103381179B (zh) * 2013-06-24 2015-08-19 丁圣雨 Houttuynoid D在制备治疗缺血性脑损伤药物中的应用
CN103356678A (zh) * 2013-06-24 2013-10-23 丁圣雨 Houttuynoid C在抗血小板聚集药物中的应用
CN103356674A (zh) * 2013-06-24 2013-10-23 丁圣雨 Houttuynoid E在抗缺氧药物中的应用
CN103381174B (zh) * 2013-06-24 2015-08-19 丁圣雨 Houttuynoid E在制备治疗缺血性脑损伤药物中的应用
CN103393704B (zh) * 2013-06-24 2015-08-19 丁圣雨 Houttuynoid E在制备治疗动脉粥样硬化药物中的应用
CN103356672B (zh) * 2013-06-24 2015-08-19 丁圣雨 Houttuynoid B在制备扩血管药物中的应用
CN103462967A (zh) * 2013-09-22 2013-12-25 南京广康协生物医药技术有限公司 Incarviatone A在抗疱疹病毒的药物中的应用
DE102014108210A1 (de) 2014-06-11 2015-12-17 Dietrich Gulba Rodentizid
CN105130965A (zh) * 2015-10-08 2015-12-09 侯方杰 一种可用于制备治疗心血管疾病药物的化合物及其制备方法、用途
WO2019200202A1 (en) * 2018-04-12 2019-10-17 Morphic Therapeutic, Inc. Antagonists of human integrin (alpha4)(beta7)
WO2021076902A1 (en) 2019-10-16 2021-04-22 Morphic Therapeutic, Inc. INHIBITING HUMAN INTEGRIN α 4 β 7
EP4070658A1 (de) 2021-04-06 2022-10-12 BIORoxx GmbH Verwendung von blutgerinnungshemmenden verbindungen als rodentizide

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ATE230398T1 (de) * 1991-10-15 2003-01-15 Searle & Co Substituierte heterocyklische derivate, verwendbar als plättchenaggregationshemmstoffe
DE4213919A1 (de) * 1992-04-28 1993-11-04 Thomae Gmbh Dr K Cyclische iminoderivate, verfahren zu ihrer herstellung und diese verbindungen enthaltende arzneimittel
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Also Published As

Publication number Publication date
EP0691953B1 (en) 2000-08-02
DK0691953T3 (da) 2000-09-04
FI954609A0 (fi) 1995-09-28
JP3034046B2 (ja) 2000-04-17
US5721366A (en) 1998-02-24
NO953844L (no) 1995-11-20
FI954609A (fi) 1995-10-23
DE69425431D1 (en) 2000-09-07
GR3034520T3 (en) 2000-12-29
ATE195117T1 (de) 2000-08-15
JPH08508732A (ja) 1996-09-17
CN1124957A (zh) 1996-06-19
DE69425431T2 (de) 2001-02-08
NO953844D0 (no) 1995-09-28
CN1054842C (zh) 2000-07-26
AU681396B2 (en) 1997-08-28
CA2159450C (en) 2002-01-08
KR100257837B1 (ko) 2000-07-01
FI111007B (fi) 2003-05-15
NO305950B1 (no) 1999-08-23
EP0691953A1 (en) 1996-01-17
CA2159450A1 (en) 1994-10-13
WO1994022820A1 (en) 1994-10-13
PT691953E (pt) 2001-01-31
AU6552294A (en) 1994-10-24

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