HK1059895A1 - Use of pyridoindolone derivatives for preparing anticancer medicines - Google Patents

Use of pyridoindolone derivatives for preparing anticancer medicines

Info

Publication number
HK1059895A1
HK1059895A1 HK04102775A HK04102775A HK1059895A1 HK 1059895 A1 HK1059895 A1 HK 1059895A1 HK 04102775 A HK04102775 A HK 04102775A HK 04102775 A HK04102775 A HK 04102775A HK 1059895 A1 HK1059895 A1 HK 1059895A1
Authority
HK
Hong Kong
Prior art keywords
preparing anticancer
anticancer medicines
pyridoindolone derivatives
pyridoindolone
derivatives
Prior art date
Application number
HK04102775A
Other languages
English (en)
Inventor
Bernard Bourrie
Pierre Casellas
Jean-Marie Derocq
Original Assignee
Sanofi Aventis
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 Sanofi Aventis filed Critical Sanofi Aventis
Publication of HK1059895A1 publication Critical patent/HK1059895A1/xx

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
HK04102775A 2001-04-27 2004-04-20 Use of pyridoindolone derivatives for preparing anticancer medicines HK1059895A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR0105843A FR2823975B1 (fr) 2001-04-27 2001-04-27 Nouvelle utilisation de pyridoindolone
PCT/FR2002/001449 WO2002087574A2 (fr) 2001-04-27 2002-04-26 Utilisation de derives de pyridoindolone pour la preparation de medicaments anticancereux

Publications (1)

Publication Number Publication Date
HK1059895A1 true HK1059895A1 (en) 2004-07-23

Family

ID=8862882

Family Applications (2)

Application Number Title Priority Date Filing Date
HK04102775A HK1059895A1 (en) 2001-04-27 2004-04-20 Use of pyridoindolone derivatives for preparing anticancer medicines
HK04103103A HK1060066A1 (en) 2001-04-27 2004-05-03 Pharmaceutical combinations based on pyridoindolone derivatives and anticancer agents

Family Applications After (1)

Application Number Title Priority Date Filing Date
HK04103103A HK1060066A1 (en) 2001-04-27 2004-05-03 Pharmaceutical combinations based on pyridoindolone derivatives and anticancer agents

Country Status (34)

Country Link
US (3) US6967203B2 (sh)
EP (2) EP1385513B1 (sh)
JP (2) JP2004531538A (sh)
KR (1) KR100847413B1 (sh)
CN (2) CN1505511A (sh)
AR (1) AR034313A1 (sh)
AT (2) ATE338548T1 (sh)
BG (2) BG108260A (sh)
BR (1) BR0209138A (sh)
CA (2) CA2443012C (sh)
CY (1) CY1105813T1 (sh)
CZ (2) CZ295224B6 (sh)
DE (2) DE60214533T2 (sh)
DK (2) DK1385513T3 (sh)
EA (1) EA005930B1 (sh)
EE (2) EE200300465A (sh)
ES (2) ES2271264T3 (sh)
FR (1) FR2823975B1 (sh)
HK (2) HK1059895A1 (sh)
HU (2) HUP0400744A2 (sh)
IL (4) IL158266A0 (sh)
IS (1) IS2441B (sh)
MX (1) MXPA03009639A (sh)
NO (2) NO20034785L (sh)
NZ (1) NZ528671A (sh)
PL (2) PL366910A1 (sh)
PT (2) PT1385512E (sh)
RS (2) RS50790B (sh)
RU (1) RU2292888C9 (sh)
SK (2) SK13252003A3 (sh)
TW (1) TWI252104B (sh)
UA (1) UA74876C2 (sh)
WO (2) WO2002087574A2 (sh)
ZA (1) ZA200307785B (sh)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2823975B1 (fr) * 2001-04-27 2003-05-30 Sanofi Synthelabo Nouvelle utilisation de pyridoindolone
US7456193B2 (en) * 2002-10-23 2008-11-25 Sanofi-Aventis Pyridoindolone derivatives substituted in the 3-position by a heterocyclic group, their preparation and their application in therapeutics
FR2846329B1 (fr) * 2002-10-23 2004-12-03 Sanofi Synthelabo Derives de pyridoindolone substitues en -3 par un phenyle, leur preparation et leur application en therapeutique
FR2869316B1 (fr) * 2004-04-21 2006-06-02 Sanofi Synthelabo Derives de pyridoindolone substitues en -6, leur preparation et leur application en therapeutique.
FR2892416B1 (fr) * 2005-10-20 2008-06-27 Sanofi Aventis Sa Derives de 6-heteroarylpyridoindolone, leur preparation et leur application en therapeutique

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1268772A (en) * 1968-03-15 1972-03-29 Glaxo Lab Ltd NOVEL alpha-CARBOLINE DERIVATIVES, THE PREPARATION THEREOF AND COMPOSITIONS CONTAINING THE SAME
US4263304A (en) * 1978-06-05 1981-04-21 Sumitomo Chemical Company, Limited 7 H-indolo[2,3-c]isoquinolines
SU833971A1 (ru) * 1979-07-10 1981-05-30 Ленинградский Химико-Фармацевтическийинститут Способ получени 3-фенил-2-оксо- - КАРбОлиНОВ
SU833972A1 (ru) 1979-10-26 1981-05-30 Институт Физико-Органической Химиии Углехимии Ah Украинской Ccp Имидазо(4,5-с)пиридиний иодиды вКАчЕСТВЕ пРОМЕжуТОчНыХ пРОдуКТОВ дл СиНТЕзА фуНгицидОВ
FR2595701B1 (fr) * 1986-03-17 1988-07-01 Sanofi Sa Derives du pyrido-indole, leur application a titre de medicaments et les compositions les renfermant
US5035252A (en) * 1990-12-14 1991-07-30 Mondre Steven J Nicotine-containing dental floss
WO1995028493A1 (en) * 1994-04-13 1995-10-26 The Rockefeller University Aav-mediated delivery of dna to cells of the nervous system
DE19502753A1 (de) * 1995-01-23 1996-07-25 Schering Ag Neue 9H-Pyrido[3,4-b]indol-Derivate
US6486177B2 (en) * 1995-12-04 2002-11-26 Celgene Corporation Methods for treatment of cognitive and menopausal disorders with D-threo methylphenidate
FR2765582B1 (fr) * 1997-07-03 1999-08-06 Synthelabo Derives de 3-alkyl-1,9-dihydro-2h-pyrido[2,3-b]indol-2-one leur preparation et leur application en therapeutique
FR2765581B1 (fr) * 1997-07-03 1999-08-06 Synthelabo Derives de 3-aryl-1,9-dihydro-2h-pyrido[2,3-b]indol-2-one, leur preparation et leur application en therapeutique
EP1068205A1 (en) * 1998-04-02 2001-01-17 Neurogen Corporation Aminoalkyl substituted 5,6,7,8-tetrahydro-9h pyrimidino 2,3-b]indole and 5,6,7,8-tetrahydro-9h-pyrimidino 4,5-b]indole derivatives: crf1 specific ligands
IT1313592B1 (it) 1999-08-03 2002-09-09 Novuspharma Spa Derivati di 1h-pirido 3,4-b indol-1-one.
US20020156016A1 (en) * 2001-03-30 2002-10-24 Gerald Minuk Control of cell growth by altering cell membrane potentials
FR2823975B1 (fr) * 2001-04-27 2003-05-30 Sanofi Synthelabo Nouvelle utilisation de pyridoindolone
FR2846329B1 (fr) 2002-10-23 2004-12-03 Sanofi Synthelabo Derives de pyridoindolone substitues en -3 par un phenyle, leur preparation et leur application en therapeutique
FR2846330B1 (fr) 2002-10-23 2004-12-03 Sanofi Synthelabo Derives de pyridoindolone substitues en -3 par groupe heterocyclique, leur preparation et leur application en therapeutique
US6958347B2 (en) 2002-12-18 2005-10-25 Pfizer Inc. Aminophenanthridinone and aminophenanthridine as NPY-5 antagonists
FR2869316B1 (fr) 2004-04-21 2006-06-02 Sanofi Synthelabo Derives de pyridoindolone substitues en -6, leur preparation et leur application en therapeutique.
FR2892416B1 (fr) 2005-10-20 2008-06-27 Sanofi Aventis Sa Derives de 6-heteroarylpyridoindolone, leur preparation et leur application en therapeutique

Also Published As

Publication number Publication date
US7524857B2 (en) 2009-04-28
HUP0400744A2 (hu) 2004-06-28
YU83903A (sh) 2006-08-17
NO20034787D0 (no) 2003-10-24
AR034313A1 (es) 2004-02-18
CZ299465B6 (cs) 2008-08-06
IS6984A (is) 2003-10-09
US20040122027A1 (en) 2004-06-24
IL158312A (en) 2009-09-01
EP1385513A1 (fr) 2004-02-04
ES2254683T3 (es) 2006-06-16
IL158312A0 (en) 2004-05-12
CN1505510A (zh) 2004-06-16
US6967203B2 (en) 2005-11-22
PL366910A1 (en) 2005-02-07
ZA200307785B (en) 2004-10-06
MXPA03009639A (es) 2004-06-30
BR0209138A (pt) 2004-06-08
NO20034785L (no) 2003-12-23
RU2292888C9 (ru) 2007-06-20
EE200300466A (et) 2003-12-15
HUP0400745A2 (hu) 2004-08-30
FR2823975A1 (fr) 2002-10-31
ES2271264T3 (es) 2007-04-16
DK1385512T3 (da) 2006-05-22
EA005930B1 (ru) 2005-08-25
IL158266A (en) 2009-09-01
CZ295224B6 (cs) 2005-06-15
IS2441B (is) 2008-11-15
UA74876C2 (en) 2006-02-15
DE60208365D1 (de) 2006-02-02
IL158266A0 (en) 2004-05-12
WO2002087574A3 (fr) 2003-02-13
ATE338548T1 (de) 2006-09-15
BG108261A (bg) 2004-12-30
CN1240382C (zh) 2006-02-08
NO20034785D0 (no) 2003-10-24
NZ528671A (en) 2004-06-25
SK13242003A3 (sk) 2004-03-02
SK13252003A3 (sk) 2004-03-02
NO20034787L (no) 2003-12-23
PL366916A1 (en) 2005-02-07
RS50791B (sr) 2010-08-31
CA2444334A1 (fr) 2002-11-07
EE200300465A (et) 2003-12-15
US20040122036A1 (en) 2004-06-24
JP2004528343A (ja) 2004-09-16
CZ20032910A3 (en) 2004-07-14
ATE314070T1 (de) 2006-01-15
EA200301062A1 (ru) 2004-04-29
DE60214533D1 (de) 2006-10-19
RU2292888C2 (ru) 2007-02-10
KR20040015138A (ko) 2004-02-18
EP1385512B1 (fr) 2005-12-28
TWI252104B (en) 2006-04-01
WO2002087574A2 (fr) 2002-11-07
CA2443012C (fr) 2009-07-28
EP1385512A2 (fr) 2004-02-04
FR2823975B1 (fr) 2003-05-30
CZ20032909A3 (en) 2004-06-16
CY1105813T1 (el) 2011-02-02
EP1385513B1 (fr) 2006-09-06
DE60208365T2 (de) 2006-09-07
WO2002087575A1 (fr) 2002-11-07
DE60214533T2 (de) 2007-06-21
US20050272760A1 (en) 2005-12-08
KR100847413B1 (ko) 2008-07-18
BG108260A (bg) 2004-12-30
HK1060066A1 (en) 2004-07-30
RS50790B (sr) 2010-08-31
PT1385513E (pt) 2007-01-31
PT1385512E (pt) 2006-05-31
YU83403A (sh) 2006-08-17
CA2443012A1 (en) 2002-11-07
CN1505511A (zh) 2004-06-16
DK1385513T3 (da) 2007-01-15
JP2004531538A (ja) 2004-10-14
US7160895B2 (en) 2007-01-09
RU2003130376A (ru) 2005-04-10

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Legal Events

Date Code Title Description
CHPA Change of a particular in the register (except of change of ownership)
PC Patent ceased (i.e. patent has lapsed due to the failure to pay the renewal fee)

Effective date: 20100426