FI115051B - Uusi amidinonaftyylijohdannainen tai sen suola - Google Patents

Uusi amidinonaftyylijohdannainen tai sen suola Download PDF

Info

Publication number
FI115051B
FI115051B FI972326A FI972326A FI115051B FI 115051 B FI115051 B FI 115051B FI 972326 A FI972326 A FI 972326A FI 972326 A FI972326 A FI 972326A FI 115051 B FI115051 B FI 115051B
Authority
FI
Finland
Prior art keywords
group
methyl
oxy
piperidyl
phenyl
Prior art date
Application number
FI972326A
Other languages
English (en)
Finnish (fi)
Swedish (sv)
Other versions
FI972326A0 (fi
FI972326A (fi
Inventor
Yuzo Matsumoto
Isao Yanagisawa
Hiroyuki Koshio
Fukushi Hirayama
Tomihisa Kawasaki
Seiji Kaku
Original Assignee
Yamanouchi Pharma Co Ltd
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 Yamanouchi Pharma Co Ltd filed Critical Yamanouchi Pharma Co Ltd
Publication of FI972326A0 publication Critical patent/FI972326A0/fi
Publication of FI972326A publication Critical patent/FI972326A/fi
Application granted granted Critical
Publication of FI115051B publication Critical patent/FI115051B/fi

Links

Classifications

    • 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
    • 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
    • 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
    • C07D211/40Oxygen atoms
    • C07D211/44Oxygen atoms attached in position 4
    • C07D211/46Oxygen atoms attached in position 4 having a hydrogen atom as the second substituent in position 4
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12Heterocyclic 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Hydrogenated Pyridines (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
FI972326A 1994-12-02 1997-06-02 Uusi amidinonaftyylijohdannainen tai sen suola FI115051B (fi)

Applications Claiming Priority (8)

Application Number Priority Date Filing Date Title
JP29996394 1994-12-02
JP29996394 1994-12-02
JP10520595 1995-04-28
JP10520595 1995-04-28
JP19881695 1995-08-03
JP19881695 1995-08-03
PCT/JP1995/002458 WO1996016940A1 (fr) 1994-12-02 1995-12-01 Nouveau derive d'amidinonaphtyle ou sel de celui-ci
JP9502458 1995-12-01

Publications (3)

Publication Number Publication Date
FI972326A0 FI972326A0 (fi) 1997-06-02
FI972326A FI972326A (fi) 1997-06-02
FI115051B true FI115051B (fi) 2005-02-28

Family

ID=27310425

Family Applications (1)

Application Number Title Priority Date Filing Date
FI972326A FI115051B (fi) 1994-12-02 1997-06-02 Uusi amidinonaftyylijohdannainen tai sen suola

Country Status (20)

Country Link
US (1) US5869501A (hu)
EP (1) EP0798295B1 (hu)
JP (1) JP3004362B2 (hu)
KR (1) KR100383161B1 (hu)
CN (1) CN1087736C (hu)
AT (1) ATE233240T1 (hu)
AU (1) AU688628B2 (hu)
CA (1) CA2206532C (hu)
DE (1) DE69529770T2 (hu)
ES (1) ES2193202T3 (hu)
FI (1) FI115051B (hu)
HU (1) HUT77313A (hu)
MX (1) MX9704059A (hu)
NO (1) NO309566B1 (hu)
NZ (1) NZ296210A (hu)
PL (1) PL184824B1 (hu)
PT (1) PT798295E (hu)
RU (1) RU2154633C2 (hu)
TW (1) TW300888B (hu)
WO (1) WO1996016940A1 (hu)

Families Citing this family (64)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK0813525T3 (da) 1995-03-10 2004-02-16 Berlex Lab Benzamidinderivater, deres fremstilling og anvendelse som antikoagulanter
SE9602646D0 (sv) 1996-07-04 1996-07-04 Astra Ab Pharmaceutically-useful compounds
EP0842941A1 (de) * 1996-11-16 1998-05-20 Roche Diagnostics GmbH Neue Phosphonate, Verfahren zu ihrer Herstellung und Arzneimittel
AU7808198A (en) 1997-06-03 1998-12-21 Biocryst Pharmaceuticals, Inc. Novel compounds useful in the complement, coagulat and kallikrein pathways and method for their preparation
CA2293824A1 (en) * 1997-06-19 1998-12-23 Mimi Lifen Quan (amidino)6-membered aromatics as factor xa inhibitors
US6060491A (en) * 1997-06-19 2000-05-09 Dupont Pharmaceuticals 6-membered aromatics as factor Xa inhibitors
ZA986594B (en) * 1997-07-25 1999-01-27 Abbott Lab Urokinase inhibitors
US6258822B1 (en) 1997-08-06 2001-07-10 Abbott Laboratories Urokinase inhibitors
WO1999011617A1 (fr) * 1997-09-01 1999-03-11 Yamanouchi Pharmaceutical Co., Ltd. Nouveaux derives de naphtamide et sels de ces derives
US6686364B2 (en) 1997-12-08 2004-02-03 Berlex Laboratories, Inc. Benzamidine derivatives and their use as anti-coagulants
DE19754490A1 (de) * 1997-12-09 1999-06-10 Boehringer Ingelheim Pharma Durch einen Aminocarbonylrest substituierte Bicyclen, ihre Herstellung und ihre Verwendung als Arzneimittel
WO1999033805A1 (fr) * 1997-12-26 1999-07-08 Mochida Pharmaceutical Co., Ltd. Composes aromatiques presentant des groupements amino cycliques ou leur sels
AU2074699A (en) * 1998-01-26 1999-08-09 Yamanouchi Pharmaceutical Co., Ltd. Novel benzene-fused heterocyclic derivatives or salts thereof
EP0937723A1 (de) * 1998-02-18 1999-08-25 Roche Diagnostics GmbH Neue Sulfonamide, Verfahren zu ihrer Herstellung sowie diese enthaltende Arzneimittel
EP1066272A4 (en) * 1998-03-27 2002-03-13 Biocryst Pharm Inc NEW CONNECTIONS USEFUL IN THE COMPLEMENT, COAGULATE AND KALLIKREIN REACTION WAY AND METHOD FOR THEIR PRODUCTION
EP1070714B1 (en) 1998-04-10 2004-08-04 Japan Tobacco Inc. Amidine compounds
US6284796B1 (en) 1998-08-06 2001-09-04 Abbott Laboratories Ukokinase inhibitors
US6504031B1 (en) 1998-08-06 2003-01-07 Milan Bruncko Naphthamidine urokinase inhibitors
US6262088B1 (en) 1998-11-19 2001-07-17 Berlex Laboratories, Inc. Polyhydroxylated monocyclic N-heterocyclic derivatives as anti-coagulants
AU3127900A (en) 1998-12-23 2000-07-31 Du Pont Pharmaceuticals Company Thrombin or factor xa inhibitors
MXPA01007038A (es) 1999-01-13 2002-07-30 Genentech Inc Inhibidores de proteasa serina.
WO2000043041A1 (fr) * 1999-01-22 2000-07-27 Yamanouchi Pharmaceutical Co., Ltd. Compositions medicamenteuses presentant une meilleure absorption orale
US6395897B1 (en) 1999-03-02 2002-05-28 Boehringer Ingelheim Pharmaceuticals, Inc. Nitrile compounds useful as reversible inhibitors of #9 cathepsin 5
FR2793247B1 (fr) * 1999-05-04 2001-06-22 Synthelabo Derives de 6-[[(aryl et heteroaryl)oxy]methyl]naphtalene-2- carboximidamide, leur preparation et leur application en therapeutique
US6858599B2 (en) 1999-06-30 2005-02-22 Mochida Pharmaceutical Co., Ltd. Tricyclic compound having spiro union
WO2001002356A1 (fr) * 1999-07-01 2001-01-11 Sankyo Company, Limited Dérivés d'indoline ou tétrahydroquinoline
US6350761B1 (en) * 1999-07-30 2002-02-26 Berlex Laboratories, Inc. Benzenamine derivatives as anti-coagulants
US6420364B1 (en) 1999-09-13 2002-07-16 Boehringer Ingelheim Pharmaceuticals, Inc. Compound useful as reversible inhibitors of cysteine proteases
RU2222529C2 (ru) 1999-10-28 2004-01-27 Санкио Компани, Лимитед Производные бензамидина
EP1095933A1 (en) * 1999-10-30 2001-05-02 Aventis Pharma Deutschland GmbH Novel N-guanidinoalkylamides, their preparation, their use, and pharmaceutical preparations comprising them
WO2001056989A2 (en) * 2000-02-01 2001-08-09 Cor Therapeutics, Inc. Inhibitors of factor xa
EP1259485B1 (en) 2000-02-29 2005-11-30 Millennium Pharmaceuticals, Inc. BENZAMIDES AND RELATED INHIBITORS OF FACTOR Xa
US6548517B2 (en) * 2000-03-24 2003-04-15 Millennium Pharmaceuticals, Inc. Oxindole inhibitors of factor Xa
AU776053B2 (en) * 2000-03-31 2004-08-26 Astellas Pharma Inc. Diazepan derivatives or salts thereof
US6495562B1 (en) 2000-04-25 2002-12-17 Abbott Laboratories Naphthamidine urokinase inhibitors
US6838479B2 (en) 2000-09-11 2005-01-04 Genentech, Inc. Amidine inhibitors of serine proteases
AU2406402A (en) 2000-11-22 2002-06-03 Yamanouchi Pharma Co Ltd Substituted benzene derivatives or salts thereof
JP2004520438A (ja) 2001-03-09 2004-07-08 オーソ−マクニール・フアーマシユーチカル・インコーポレーテツド セリンプロテアーゼインヒビターとしてのアミノピロリジンスルホンアミド
US6710061B2 (en) 2001-03-09 2004-03-23 Ortho-Mcneil Pharamceutical, Inc. Aminopyrrolidine sulfonamides as serine protease inhibitors
US7312235B2 (en) 2001-03-30 2007-12-25 Millennium Pharmaceuticals, Inc. Benzamide inhibitors of factor Xa
MXPA03009097A (es) 2001-04-05 2004-02-12 Sankyo Co Derivados de benzamidina.
CN100410236C (zh) 2002-01-29 2008-08-13 雪兰诺实验室有限公司 作为蛋白酪氨酸磷酸酶调节剂的取代亚甲基酰胺衍生物
WO2004048363A1 (ja) 2002-11-22 2004-06-10 Takeda Pharmaceutical Company Limited イミダゾール誘導体、その製造法および用途
DK1569912T3 (en) 2002-12-03 2015-06-29 Pharmacyclics Inc 2- (2-hydroxybiphenyl-3-yl) -1h-benzoimidazole-5-carboxamidine derivatives as factor VIIa inhibitors.
AU2003292748A1 (en) * 2002-12-24 2004-07-22 Daiichi Pharmaceutical Co., Ltd. Novel ethylenediamine derivatives
JP2007505160A (ja) 2003-05-20 2007-03-08 ジェネンテック・インコーポレーテッド 第VIIa因子のアシルスルファミド阻害剤
AU2004249671A1 (en) 2003-05-20 2004-12-29 Genentech, Inc. Benzofuran inhibitors of factor VIIa
CA2541809A1 (en) 2003-10-09 2005-04-21 Millennium Pharmaceuticals, Inc. Thioether-substituted benzamides as inhibitors of factor xa
TWI396686B (zh) 2004-05-21 2013-05-21 Takeda Pharmaceutical 環狀醯胺衍生物、以及其製品和用法
CN1968922A (zh) 2004-06-18 2007-05-23 米伦纽姆医药公司 因子xa抑制剂
WO2006055951A2 (en) 2004-11-19 2006-05-26 Portola Pharmaceuticals, Inc. Tetrahydroisoquinolines as factor xa inhibitors
WO2006063293A2 (en) * 2004-12-07 2006-06-15 Portola Pharmaceuticals, Inc. THIOUREAS AS FACTOR Xa INHIBITORS
US7678913B2 (en) 2004-12-07 2010-03-16 Portola Pharmaceuticals, Inc. Ureas as factor Xa inhibitors
EP1847527A4 (en) 2005-02-02 2009-04-08 Ajinomoto Kk NEW BENZAMIDINE DERIVATIVE
BRPI0618362A2 (pt) 2005-11-08 2011-08-30 Millennium Pharm Inc sais farmacêuticos inovadores e polimorfos de um inibidor de fator xa
JP2009531364A (ja) * 2006-03-28 2009-09-03 ノバルティス アクチエンゲゼルシャフト アミド誘導体およびgタンパク質関連疾患の処置のためのそれらの使用
AU2007307599A1 (en) * 2006-10-12 2008-04-17 Institute Of Medicinal Molecular Design. Inc. N-phenyloxamic acid derivatives
ES2382055T3 (es) 2006-11-02 2012-06-04 Millennium Pharmaceuticals, Inc. Métodos para sintetizar sales farmacéuticas de un inhibidor del factor Xa
US20110045028A1 (en) * 2006-11-30 2011-02-24 Takeda Pharmaceutical Company Limited Sustained release preparation
US8633245B2 (en) * 2008-04-11 2014-01-21 Institute Of Medicinal Molecular Design, Inc. PAI-1 inhibitor
EP2311810A4 (en) 2008-07-11 2012-04-04 Ajinomoto Kk AMIDINE DERIVATIVE
EA015918B1 (ru) 2010-03-03 2011-12-30 Дмитрий Геннадьевич ТОВБИН УРЕТАНЫ, МОЧЕВИНЫ, АМИДЫ И РОДСТВЕННЫЕ ИНГИБИТОРЫ ФАКТОРА Xa
WO2019241213A1 (en) * 2018-06-11 2019-12-19 The Regents Of The University Of Colorado, A Body Corporate 2-naphthimidamides, analogues thereof, and methods of treatment using same
CN117304076B (zh) * 2023-11-28 2024-02-20 苏州大学 一种n-磺酰基脒化合物的制备方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU527371B2 (en) * 1980-09-16 1983-03-03 Torii & Co., Ltd. Amidine
JPS59139357A (ja) * 1983-01-28 1984-08-10 Torii Yakuhin Kk アミジン誘導体
US4563527A (en) * 1984-07-19 1986-01-07 Torii & Co., Ltd. Amidine compounds
ZA928276B (en) * 1991-10-31 1993-05-06 Daiichi Seiyaku Co Aromatic amidine derivates and salts thereof.

Also Published As

Publication number Publication date
DE69529770T2 (de) 2003-12-24
FI972326A0 (fi) 1997-06-02
KR100383161B1 (ko) 2003-12-24
PL320486A1 (en) 1997-09-29
FI972326A (fi) 1997-06-02
TW300888B (hu) 1997-03-21
EP0798295A1 (en) 1997-10-01
EP0798295A4 (en) 1998-03-04
ES2193202T3 (es) 2003-11-01
CN1167484A (zh) 1997-12-10
ATE233240T1 (de) 2003-03-15
MX9704059A (es) 1997-08-30
PL184824B1 (pl) 2002-12-31
RU2154633C2 (ru) 2000-08-20
CN1087736C (zh) 2002-07-17
NZ296210A (en) 1998-05-27
NO972482L (no) 1997-08-01
JP3004362B2 (ja) 2000-01-31
HUT77313A (hu) 1998-03-30
NO309566B1 (no) 2001-02-19
AU3994295A (en) 1996-06-19
EP0798295B1 (en) 2003-02-26
NO972482D0 (no) 1997-05-30
CA2206532A1 (en) 1996-06-06
US5869501A (en) 1999-02-09
PT798295E (pt) 2003-07-31
AU688628B2 (en) 1998-03-12
DE69529770D1 (de) 2003-04-03
WO1996016940A1 (fr) 1996-06-06
CA2206532C (en) 2006-07-11

Similar Documents

Publication Publication Date Title
FI115051B (fi) Uusi amidinonaftyylijohdannainen tai sen suola
EP3328843B1 (en) 1,3,4-oxadiazole sulfonamide derivative compounds as histone deacetylase 6 inhibitor, and the pharmaceutical composition comprising the same
KR100637110B1 (ko) 세포 유착 억제제
RU2361861C2 (ru) Производное циклического амида, его получение и применение
EP2876105A1 (en) 1-(cycloalkyl-carbonyl)proline derivative
US9920034B2 (en) Crystalline forms of a factor XIa inhibitor
KR100739359B1 (ko) 디아제판 유도체 또는 이의 염
AU2016371014A1 (en) Polycyclic TLR7/8 antagonists and use thereof in the treatment of immune disorders
EP1695961A1 (en) Urea derivative, process for producing the same, and use
WO2002006234A1 (fr) Derives de sulfonate, procede de production et utilisation de ces derives
EP1950199A1 (en) Proline derivatives and use thereof as drugs
EP0562599A1 (en) Condensed thiadiazole derivative, method of its production, and use thereof
AU759488B2 (en) Amino acid derivatives and drugs containing the same as the active ingredient
JPH02290841A (ja) 新規化合物、その製法及びそれを含む医薬組成物
KR20050121681A (ko) 면역조절 헤테로고리 화합물
CA3196061A1 (en) Cftr modulator compounds, compositions, and uses thereof
EP1852431A1 (en) Optically active tetrahydronaphthalene derivative
JP4250423B2 (ja) アリール置換脂環式化合物及びそれを含有する医薬組成物
WO2007055183A1 (ja) ベンゼン誘導体又はその塩
WO1997002245A1 (fr) Derives de benzamidoxime et leur utilisation a des fins medicinales
JPH04128291A (ja) 新規なヘテロ環化合物およびその製造法
JP2842302B2 (ja) チアゾリン誘導体
JP4214524B2 (ja) アミノ酸誘導体およびそれらを有効成分として含有する薬剤
JP2004155774A (ja) イミダゾピリジン誘導体、その製造法および用途
JPH1045584A (ja) 血小板凝集抑制剤

Legal Events

Date Code Title Description
FG Patent granted

Ref document number: 115051

Country of ref document: FI

PC Transfer of assignment of patent

Owner name: ASTELLAS PHARMA INC.

Free format text: ASTELLAS PHARMA INC.

MA Patent expired