ES2104887T3 - Derivados de acridina. - Google Patents

Derivados de acridina.

Info

Publication number
ES2104887T3
ES2104887T3 ES92901861T ES92901861T ES2104887T3 ES 2104887 T3 ES2104887 T3 ES 2104887T3 ES 92901861 T ES92901861 T ES 92901861T ES 92901861 T ES92901861 T ES 92901861T ES 2104887 T3 ES2104887 T3 ES 2104887T3
Authority
ES
Spain
Prior art keywords
group
4alkoxy
4alkyl
hydrogen atom
atom
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
ES92901861T
Other languages
English (en)
Inventor
Bernard Andre Dumaitre
Nerina Dodic
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.)
Laboratoire Glaxo Wellcome SA
Original Assignee
Laboratoires Glaxo SA
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 GB919100637A external-priority patent/GB9100637D0/en
Priority claimed from GB919100628A external-priority patent/GB9100628D0/en
Priority claimed from GB919115981A external-priority patent/GB9115981D0/en
Priority claimed from GB919115956A external-priority patent/GB9115956D0/en
Application filed by Laboratoires Glaxo SA filed Critical Laboratoires Glaxo SA
Application granted granted Critical
Publication of ES2104887T3 publication Critical patent/ES2104887T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C205/00Compounds containing nitro groups bound to a carbon skeleton
    • C07C205/07Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by halogen atoms
    • C07C205/11Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by halogen atoms having nitro groups bound to carbon atoms of six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C205/00Compounds containing nitro groups bound to a carbon skeleton
    • C07C205/13Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups
    • C07C205/26Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups and being further substituted by halogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C205/00Compounds containing nitro groups bound to a carbon skeleton
    • C07C205/27Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups
    • C07C205/35Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
    • C07C205/36Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system
    • C07C205/37Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system the oxygen atom of at least one of the etherified hydroxy groups being further bound to an acyclic carbon atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C205/00Compounds containing nitro groups bound to a carbon skeleton
    • C07C205/49Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups
    • C07C205/56Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups having nitro groups bound to carbon atoms of six-membered aromatic rings and carboxyl groups bound to acyclic carbon atoms of the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D219/00Heterocyclic compounds containing acridine or hydrogenated acridine ring systems
    • C07D219/04Heterocyclic compounds containing acridine or hydrogenated acridine ring systems 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 carbon atoms of the ring system
    • C07D219/06Oxygen atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
  • Laminated Bodies (AREA)
  • Soft Magnetic Materials (AREA)
  • Paper (AREA)
  • Dry Shavers And Clippers (AREA)

Abstract

SE PRESENTAN COMPUESTOS DE LA FORMULA GENERAL (I), EN LA QUE A REPRESENTA UN ATOMO DE OXIGENO O DE AZUFRE, UN ENLACE O UN GRUPO (CH2)LNR9 (EN DONDE L REPRESENTA 0 O 1 Y R9 REPRESENTA UN ATOMO DE HIDROGENO O UN GRUPO DE METIL); B REPRESENTA UNA CADENA DE ALQUILENO C1-C4 OPCIONALMENTE SUSTITUIDA CON UN GRUPO DE HIDROXIL, CON LA EXCEPCION DE QUE EL GRUPO DE HIDROXIL Y LA MOLECULA A NO PUEDEN ESTAR UNIDAS AL MISMO ATOMO DE CARBONO CUANDO A REPRESENTE UN ATOMO DE OXIGENO O AZUFRE O UN GRUPO (CH2)LNR9 O CUANDO A REPRESENTE UN ENLACE B PUEDE TAMBIEN REPRESENTAR UNA CADENA DE ALQUENILENO C2-C4; R3 REPRESENTA UN ATOMO DE HIDROGENO O UN GRUPO DE ALQUIL C1-C4; M REPRESENTA 1 O 2; R7 REPRESENTA UN ATOMO DE HIDROGENO O R3 Y R7 JUNTAS FORMAN UN GRUPO -(CH2)N OS DE LA FORMULA I PUEDEN SENSIBILIZAR LAS CELULAS CANCEROSAS RESISTENTES A LAS DROGAS A LOS AGENTES QUIMIOTERAPEUTICOS Y PUEDE FORMULARSE PARA SU USO EN TERAPIAS, PARTICULARMENTE PARA MEJORAR O INCREMENTAR LA EFICACIA DE DROGAS ANTITUMORALES.
ES92901861T 1991-01-11 1992-01-07 Derivados de acridina. Expired - Lifetime ES2104887T3 (es)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
GB919100637A GB9100637D0 (en) 1991-01-11 1991-01-11 Chemical compounds
GB919100628A GB9100628D0 (en) 1991-01-11 1991-01-11 Chemical compounds
GB919115981A GB9115981D0 (en) 1991-07-24 1991-07-24 Chemical compounds
GB919115956A GB9115956D0 (en) 1991-07-24 1991-07-24 Chemical compounds

Publications (1)

Publication Number Publication Date
ES2104887T3 true ES2104887T3 (es) 1997-10-16

Family

ID=27450605

Family Applications (1)

Application Number Title Priority Date Filing Date
ES92901861T Expired - Lifetime ES2104887T3 (es) 1991-01-11 1992-01-07 Derivados de acridina.

Country Status (25)

Country Link
US (1) US5604237A (es)
EP (2) EP0569380B1 (es)
JP (1) JP2783680B2 (es)
KR (1) KR100220538B1 (es)
AT (1) ATE153660T1 (es)
AU (1) AU652996B2 (es)
CA (1) CA2100258C (es)
CZ (1) CZ283038B6 (es)
DE (1) DE69220037T2 (es)
DK (1) DK0569380T3 (es)
ES (1) ES2104887T3 (es)
FI (1) FI103888B1 (es)
GE (1) GEP20002210B (es)
GR (1) GR3024525T3 (es)
HU (2) HUT68856A (es)
IE (1) IE920083A1 (es)
IL (1) IL100631A (es)
MX (1) MX9200109A (es)
NO (1) NO300267B1 (es)
NZ (1) NZ241278A (es)
PL (1) PL168202B1 (es)
RU (1) RU2119482C1 (es)
SG (1) SG45403A1 (es)
SK (1) SK280864B6 (es)
WO (1) WO1992012132A1 (es)

Families Citing this family (40)

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HUT68856A (en) * 1991-01-11 1995-08-28 Glaxo Lab Sa Acridine derivatives, pharmaceutical compositions comprising the same compouds as effective substances and a process for producing the compounds and the pharmaceutical compositions
TR28930A (tr) * 1992-05-07 1997-07-21 Zeneca Ltd Alkil sübstitüentli nitrotoluen türevleri
GB9209872D0 (en) * 1992-05-07 1992-06-24 Ici Plc Alkyl substituted nitrotoluene derivatives
JP2718830B2 (ja) * 1992-07-10 1998-02-25 ラボラトワール、グラクソ、ソシエテ、アノニム アニリド誘導体
RU2036198C1 (ru) * 1993-04-01 1995-05-27 Товарищество с ограниченной ответственностью "Полисан" N-МЕТИЛ-N-( α,D -ГЛЮКОПИРАНОЗИЛ) АММОНИЯ-2-(АКРИДОН-9-ОН-10-ИЛ)АЦЕТАТ(ЦИКЛОФЕРОН), ОБЛАДАЮЩИЙ ИНТЕРФЕРОНОГЕННОЙ, ПРОТИВОВИРУСНОЙ, В ТОМ ЧИСЛЕ АНТИВИЧ, АНТИПАРАЗИТАРНОЙ, АНТИПРОМОТОРНОЙ И РАДИОПРОТЕКТИВНОЙ АКТИВНОСТЬЮ
US5387685A (en) * 1993-07-16 1995-02-07 American Cyanamid Co MDR reversal agents
DE4422517A1 (de) * 1994-06-28 1996-01-04 Dresden Arzneimittel Neue (2-(3,4-Dimethoxy-phenyl)-ethyl)-(2-phenoxy-ethyl)-amine, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
CA2196672A1 (en) * 1994-08-04 1996-02-15 You Sup Chung Amine derivatives, processes for producing same, and use thereof as antiarrhythmic drugs
EP0784474A2 (en) * 1994-10-05 1997-07-23 Glaxo Wellcome Inc. Parenteral pharmaceutical compositions containing gf120918a
FR2726267B1 (fr) * 1994-10-26 1998-01-02 Smithkline Beecham Lab Nouveaux agents anti-arythmiques, compositions pharmaceutiques les contenant, et procede pour les preparer
US6395770B1 (en) 1995-10-26 2002-05-28 Baker Norton Pharmaceuticals, Inc. Method and compositions for administering taxanes orally to human patients
US6245805B1 (en) 1995-10-26 2001-06-12 Baker Norton Pharmaceuticals, Inc. Method, compositions and kits for increasing the oral bioavailability of pharmaceutical agents
AU1597197A (en) * 1996-02-01 1997-08-22 Byk Gulden Lomberg Chemische Fabrik Gmbh Thienoquinolines
US6713517B1 (en) 1996-03-08 2004-03-30 Oxigene, Inc. Use of aryl N-substituted carboxamides directly and as radio-and chemosensitizers for killing tumor and cancer cells and novel compounds for such use
RU2118532C1 (ru) * 1996-04-10 1998-09-10 Олег Викторович Травкин Противоинфекционное, противовоспалительное и противоопухолевое лекарственное средство
GB9708805D0 (en) 1997-05-01 1997-06-25 Smithkline Beecham Plc Compounds
GB9710612D0 (en) * 1997-05-23 1997-07-16 Glaxo Group Ltd Synthesis of acridine derivatives
BR9809694A (pt) * 1997-05-27 2000-10-03 Baker Norton Pharma Processo e composição para administração de taxanos oralmente a pacientes humanos
GB9718903D0 (en) * 1997-09-05 1997-11-12 Glaxo Group Ltd Method,compositions and kits for increasing the oral bioavailability of pharmaceutical agents
GB9810876D0 (en) 1998-05-20 1998-07-22 Smithkline Beecham Plc Compounds
GB9812189D0 (en) * 1998-06-05 1998-08-05 Glaxo Group Ltd Methods and compositions for increasing penetration of HIV protease inhibitors
AU4698299A (en) * 1998-06-30 2000-01-17 Du Pont Pharmaceuticals Company 5-HT7 receptor antagonists
ATE316969T1 (de) 1998-10-08 2006-02-15 Smithkline Beecham Plc Tetrahydrobenzazepin-derivate verwendbar als dopamin-d3-rezeptor-modulatoren (antipsychotische mittel)
EP1189637B1 (en) * 1999-05-17 2006-08-23 Cancer Research Ventures Limited Compositions for improving bioavailability of orally administered drugs
WO2001024763A2 (en) 1999-10-01 2001-04-12 Immunogen, Inc. Compositions and methods for treating cancer using immunoconjugates and chemotherapeutic agents
US6521635B1 (en) 2000-01-20 2003-02-18 The United States Of America As Represented By The Department Of Health And Human Services Inhibition of MXR transport by acridine derivatives
DK1261325T3 (da) * 2000-02-18 2010-12-20 New York Medical College Tumorinhiberende sammensætninger, der indeholder nitroacridiner
PT1274687E (pt) 2000-03-14 2005-04-29 Actelion Pharmaceuticals Ltd Derivados de 1,2,3,4-tetra-hidroisoquinolina
CA2408343A1 (en) 2000-05-11 2002-11-07 Banyu Pharmaceutical Co., Ltd. N-acyltetrahydroisoquinoline derivatives
EA200300473A1 (ru) * 2000-10-16 2003-08-28 Неофарм, Инк. Терапевтическая композиция на основе митоксантрона (варианты) и липидный препарат, способ его получения и способ лечения заболевания млекопитающего с его использованием
WO2003095447A1 (en) * 2002-05-14 2003-11-20 Xenova Limited Process for the preparation of a hydrate of an anthranilic acid derivative
WO2004039795A2 (en) * 2002-10-29 2004-05-13 Fujisawa Pharmaceutical Co., Ltd. Amide compounds for the treatment of hyperlipidemia
US7763638B2 (en) 2004-03-01 2010-07-27 Actelion Pharmaceuticals Ltd. Substituted 1,2,3,4-tetrahydroisoquinoline derivatives
RU2346692C2 (ru) * 2007-03-29 2009-02-20 Ефаг АО Применение 9-оксоакридин-10-уксусной кислоты, ее солей и сложных эфиров в комбинированной терапии рака яичников, способ лечения и наборы
SE531698C2 (sv) * 2007-07-12 2009-07-07 Respiratorius Ab Nya bronkdilaterande a,b-omättade amider
WO2015142670A1 (en) * 2014-03-15 2015-09-24 Medisyn Technologies, Inc. Anti-diabetic compounds, pharmaceutical compositions containing them, and method to treat diabetes
WO2015018380A2 (en) 2014-07-03 2015-02-12 Cspc Zhongqi Pharmaceutical Technology(Shijiazhuang)Co., Ltd. Therapeutic nanoparticles and the preparation methods thereof
MX2020009563A (es) * 2018-03-21 2020-10-05 Izumi Tech Llc Analogos deuterados del elacridar.
CN115385847B (zh) * 2021-06-15 2023-09-29 山东第一医科大学(山东省医学科学院) 多取代二芳基类化合物及其制备方法和应用
CN115252613B (zh) * 2022-08-09 2024-01-12 北京清华长庚医院 药物组合物及其在逆转仑伐替尼耐药性中的用途

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US4021551A (en) * 1972-06-07 1977-05-03 Boehringer Ingelheim Gmbh 3,6-Bis-(heterocyclic aminoacyl-amino)-acridines and salts thereof
US4127573A (en) * 1972-09-06 1978-11-28 Burroughs Wellcome Co. Ditetrazole substituted acridone compounds
EP0048898B1 (en) * 1980-09-30 1985-04-17 Bayer Ag Method for the production of an antithrombin-heparin complex and pharmaceutical compositions containing the complex
NZ198115A (en) * 1981-08-21 1985-05-31 New Zealand Dev Finance 9-anilinoacridines;pharmaceutical compositions
NZ201084A (en) * 1982-06-25 1985-10-11 New Zealand Dev Finance 4-carboxamidoacridine derivatives and pharmaceutical compositions containing such
IN164921B (es) * 1986-07-22 1989-07-08 Hoechst India
US5104858A (en) * 1988-09-29 1992-04-14 Yale University Sensitizing multidrug resistant cells to antitumor agents
CA1340821C (en) * 1988-10-06 1999-11-16 Nobuyuki Fukazawa Heterocyclic compounds and anticancer-drug reinforcing agents containing them as effective components
JPH04506072A (ja) * 1989-06-19 1992-10-22 ザ・ウエルカム・ファウンデーション・リミテッド 癌治療に有用であり、かつ抗ヒスタミン特性を有する医薬
HUT68856A (en) * 1991-01-11 1995-08-28 Glaxo Lab Sa Acridine derivatives, pharmaceutical compositions comprising the same compouds as effective substances and a process for producing the compounds and the pharmaceutical compositions
US5296602A (en) * 1991-03-18 1994-03-22 Sloan-Kettering Institute For Cancer Research Multisubstituted 1-hydroxy-9-acridones with anticancer activity
US5240936A (en) * 1992-05-14 1993-08-31 Texas A&M University System Treating or preventing ocular inflammation or systemic imflammatory disease

Also Published As

Publication number Publication date
AU1154392A (en) 1992-08-17
SK280864B6 (en) 2000-08-14
WO1992012132A1 (en) 1992-07-23
EP0569380B1 (en) 1997-05-28
JP2783680B2 (ja) 1998-08-06
IL100631A0 (en) 1992-09-06
EP0569380A1 (en) 1993-11-18
FI103888B (fi) 1999-10-15
NO932512L (no) 1993-09-09
DE69220037T2 (de) 1997-11-06
RU2119482C1 (ru) 1998-09-27
MX9200109A (es) 1992-09-01
EP0494623A1 (en) 1992-07-15
DE69220037D1 (de) 1997-07-03
NO932512D0 (no) 1993-07-09
GR3024525T3 (en) 1997-11-28
HUT68856A (en) 1995-08-28
FI933149A0 (fi) 1993-07-09
AU652996B2 (en) 1994-09-15
CA2100258A1 (en) 1992-07-12
CA2100258C (en) 1999-12-14
KR100220538B1 (ko) 1999-09-15
CZ137893A3 (en) 1994-02-16
DK0569380T3 (da) 1997-12-22
FI933149A (fi) 1993-07-09
CZ283038B6 (cs) 1997-12-17
NZ241278A (en) 1994-05-26
IL100631A (en) 1996-09-12
IE920083A1 (en) 1992-07-15
NO300267B1 (no) 1997-05-05
FI103888B1 (fi) 1999-10-15
SK73093A3 (en) 1994-01-12
HU9301989D0 (en) 1993-10-28
JPH06506440A (ja) 1994-07-21
HU211623A9 (en) 1995-12-28
US5604237A (en) 1997-02-18
SG45403A1 (en) 1998-01-16
GEP20002210B (en) 2000-08-25
ATE153660T1 (de) 1997-06-15
PL168202B1 (pl) 1996-01-31

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