SG45403A1 - Acridine derivatives - Google Patents

Acridine derivatives

Info

Publication number
SG45403A1
SG45403A1 SG1996006197A SG1996006197A SG45403A1 SG 45403 A1 SG45403 A1 SG 45403A1 SG 1996006197 A SG1996006197 A SG 1996006197A SG 1996006197 A SG1996006197 A SG 1996006197A SG 45403 A1 SG45403 A1 SG 45403A1
Authority
SG
Singapore
Prior art keywords
group
4alkoxy
4alkyl
hydrogen atom
atom
Prior art date
Application number
SG1996006197A
Other languages
English (en)
Inventor
Bernard Andre Dumaitre
Nerina Dodic
Original Assignee
Glaxo Lab 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 Glaxo Lab Sa filed Critical Glaxo Lab Sa
Publication of SG45403A1 publication Critical patent/SG45403A1/en

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)
  • Soft Magnetic Materials (AREA)
  • Paper (AREA)
  • Laminated Bodies (AREA)
  • Dry Shavers And Clippers (AREA)
SG1996006197A 1991-01-11 1992-01-07 Acridine derivatives SG45403A1 (en)

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
SG45403A1 true SG45403A1 (en) 1998-01-16

Family

ID=27450605

Family Applications (1)

Application Number Title Priority Date Filing Date
SG1996006197A SG45403A1 (en) 1991-01-11 1992-01-07 Acridine derivatives

Country Status (25)

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

Families Citing this family (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2783680B2 (ja) * 1991-01-11 1998-08-06 ラボラトワール、グラクソ、ソシエテ、アノニム アクリジン誘導体
GB9209872D0 (en) * 1992-05-07 1992-06-24 Ici Plc Alkyl substituted nitrotoluene derivatives
TR28930A (tr) * 1992-05-07 1997-07-21 Zeneca Ltd Alkil sübstitüentli nitrotoluen türevleri
US5663179A (en) * 1992-07-10 1997-09-02 Laboratoires Glaxo Sa Certain isoquinoline derivatives having anti-tumor properties
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
CN1134410C (zh) * 1994-08-04 2004-01-14 C&C新药研究所 胺衍生物,制备它们的方法和它们作为抗心律失常药的应用
CZ104197A3 (en) * 1994-10-05 1997-09-17 Glaxo Wellcome Inc Pharmaceutical preparation
FR2726267B1 (fr) * 1994-10-26 1998-01-02 Smithkline Beecham Lab Nouveaux agents anti-arythmiques, compositions pharmaceutiques les contenant, et procede pour les preparer
US6245805B1 (en) 1995-10-26 2001-06-12 Baker Norton Pharmaceuticals, Inc. Method, compositions and kits for increasing the oral bioavailability of pharmaceutical agents
US6395770B1 (en) 1995-10-26 2002-05-28 Baker Norton Pharmaceuticals, Inc. Method and compositions for administering taxanes orally to human patients
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
PL337064A1 (en) * 1997-05-27 2000-07-31 Baker Norton Pharma Method of and compositions for orally administering taxanes to human beings
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
WO2000000472A1 (en) * 1998-06-30 2000-01-06 Du Pont Pharmaceuticals Company 5-ht7 receptor antagonists
MA26696A1 (fr) 1998-10-08 2004-12-20 Smithkline Beecham Plc Derives de tetrahydrobenzazepine nouveaux, procede pour leur preparation et compositions pharmaceutiques les contenant
DK1189637T3 (da) * 1999-05-17 2006-12-11 Cancer Res Ventures Ltd Produkter til forbedring af biotilgængeligheden for oralt indgivne medikamenter
CA2385528C (en) 1999-10-01 2013-12-10 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
AU2001238499A1 (en) 2000-02-18 2001-08-27 New York Medical College Nitroacridine/tumor inhibitor compositions
ES2234840T3 (es) 2000-03-14 2005-07-01 Actelion Pharmaceuticals Ltd. Derivados de 1,2,3,4- tetrahidroisoquinolina.
AU779266B2 (en) 2000-05-11 2005-01-13 Banyu Pharmaceutical Co., Ltd. N-acyltetrahydroisoquinoline derivatives
HUP0303719A2 (hu) * 2000-10-16 2004-03-01 Neopharm, Inc. Mitoxantron hatóanyag-tartalmú liposzómás gyógyszerkészítmények és eljárás az előállításukra
CA2485430C (en) * 2002-05-14 2011-12-06 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
CA2557163C (en) 2004-03-01 2011-08-16 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
CN104434808A (zh) 2014-07-03 2015-03-25 石药集团中奇制药技术(石家庄)有限公司 一种治疗性纳米粒子及其制备方法
IL277335B2 (en) * 2018-03-21 2024-03-01 Izumi Tech Llc Analogues of alcridar with deuterium
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
CN117414367A (zh) * 2022-08-09 2024-01-19 北京清华长庚医院 一种逆转仑伐替尼耐药的药物组合物及其用途

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4250182A (en) * 1972-02-24 1981-02-10 Burroughs Wellcome Co. Pharmaceutical composition containing acridone compounds and method of using same
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
DE3170001D1 (en) * 1980-09-30 1985-05-23 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 (pl) * 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
NZ234110A (en) * 1989-06-19 1993-01-27 Wellcome Found Dibenzoazepine, -oxepine and -cycloheptane substituted alkylidene amines; pharmaceutical compositions containing such compounds or various other aryl substituted amines
JP2783680B2 (ja) * 1991-01-11 1998-08-06 ラボラトワール、グラクソ、ソシエテ、アノニム アクリジン誘導体
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
DE69220037T2 (de) 1997-11-06
WO1992012132A1 (en) 1992-07-23
HUT68856A (en) 1995-08-28
CZ283038B6 (cs) 1997-12-17
HU211623A9 (en) 1995-12-28
IE920083A1 (en) 1992-07-15
DE69220037D1 (de) 1997-07-03
GEP20002210B (en) 2000-08-25
IL100631A (en) 1996-09-12
NO932512L (no) 1993-09-09
DK0569380T3 (da) 1997-12-22
CA2100258C (en) 1999-12-14
JP2783680B2 (ja) 1998-08-06
NO300267B1 (no) 1997-05-05
ES2104887T3 (es) 1997-10-16
ATE153660T1 (de) 1997-06-15
SK73093A3 (en) 1994-01-12
GR3024525T3 (en) 1997-11-28
HU9301989D0 (en) 1993-10-28
AU1154392A (en) 1992-08-17
FI933149A (fi) 1993-07-09
CZ137893A3 (en) 1994-02-16
MX9200109A (es) 1992-09-01
RU2119482C1 (ru) 1998-09-27
PL168202B1 (pl) 1996-01-31
FI103888B (fi) 1999-10-15
NZ241278A (en) 1994-05-26
AU652996B2 (en) 1994-09-15
NO932512D0 (no) 1993-07-09
EP0569380B1 (en) 1997-05-28
FI103888B1 (fi) 1999-10-15
FI933149A0 (fi) 1993-07-09
SK280864B6 (en) 2000-08-14
US5604237A (en) 1997-02-18
KR100220538B1 (ko) 1999-09-15
CA2100258A1 (en) 1992-07-12
EP0569380A1 (en) 1993-11-18
JPH06506440A (ja) 1994-07-21
EP0494623A1 (en) 1992-07-15
IL100631A0 (en) 1992-09-06

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