TNSN98088A1 - INHIBITEURS DE FARNESYL- TRANSFERASE EN ASSOCIATION AVEC DES INHIBITEURS DE HMG-CoA-REDUCTASE POUR LE TRAITEMENT DU CANCER. - Google Patents

INHIBITEURS DE FARNESYL- TRANSFERASE EN ASSOCIATION AVEC DES INHIBITEURS DE HMG-CoA-REDUCTASE POUR LE TRAITEMENT DU CANCER.

Info

Publication number
TNSN98088A1
TNSN98088A1 TNTNSN98088A TNSN98088A TNSN98088A1 TN SN98088 A1 TNSN98088 A1 TN SN98088A1 TN TNSN98088 A TNTNSN98088 A TN TNSN98088A TN SN98088 A TNSN98088 A TN SN98088A TN SN98088 A1 TNSN98088 A1 TN SN98088A1
Authority
TN
Tunisia
Prior art keywords
inhibitors
hmg
coa
cancer
treatment
Prior art date
Application number
TNTNSN98088A
Other languages
English (en)
Inventor
Mohamed Kajiji Shama
Original Assignee
Pfizer Prod Inc
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 Pfizer Prod Inc filed Critical Pfizer Prod Inc
Publication of TNSN98088A1 publication Critical patent/TNSN98088A1/fr

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404—Indoles, e.g. pindolol
    • A61K31/405—Indole-alkanecarboxylic acids; Derivatives thereof, e.g. tryptophan, indomethacin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs 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)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

L’INVENTION CONCERNE L’UTILISATION D’UN INHIBITEUR DE FTase EN ASSOCIATION AVEC UN INHIBITEUR DE HMG-COA- REDUCTASE POUR LA PREPARATION D’UN MEDICAMENT. ELLE CONCERNE EGALEMENT DE COMPOSITIONS PHARMACEUTIQUES CONTENANT CES COMPOSES. APPLICATION :TRAITEMENT DU CANCER CHEZ UN MAMMIFIERE.
TNTNSN98088A 1997-06-16 1998-06-15 INHIBITEURS DE FARNESYL- TRANSFERASE EN ASSOCIATION AVEC DES INHIBITEURS DE HMG-CoA-REDUCTASE POUR LE TRAITEMENT DU CANCER. TNSN98088A1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US4963897P 1997-06-16 1997-06-16

Publications (1)

Publication Number Publication Date
TNSN98088A1 true TNSN98088A1 (fr) 2005-03-15

Family

ID=21960890

Family Applications (1)

Application Number Title Priority Date Filing Date
TNTNSN98088A TNSN98088A1 (fr) 1997-06-16 1998-06-15 INHIBITEURS DE FARNESYL- TRANSFERASE EN ASSOCIATION AVEC DES INHIBITEURS DE HMG-CoA-REDUCTASE POUR LE TRAITEMENT DU CANCER.

Country Status (37)

Country Link
EP (1) EP0986387B1 (fr)
JP (1) JP3713051B2 (fr)
KR (1) KR100392573B1 (fr)
CN (1) CN1259868A (fr)
AP (1) AP9801261A0 (fr)
AR (1) AR013090A1 (fr)
AT (1) ATE235905T1 (fr)
BG (1) BG103946A (fr)
BR (1) BR9810616A (fr)
CA (1) CA2294399C (fr)
CO (1) CO4950607A1 (fr)
DE (1) DE69812933T2 (fr)
DK (1) DK0986387T3 (fr)
DZ (1) DZ2518A1 (fr)
EA (1) EA199901043A1 (fr)
ES (1) ES2196559T3 (fr)
GT (1) GT199800081A (fr)
HN (1) HN1998000091A (fr)
HR (1) HRP980328B1 (fr)
HU (1) HUP0004624A3 (fr)
ID (1) ID23014A (fr)
IL (1) IL132765A0 (fr)
IS (1) IS5259A (fr)
MA (1) MA24569A1 (fr)
NO (1) NO996206L (fr)
NZ (1) NZ500662A (fr)
OA (1) OA11231A (fr)
PA (1) PA8453601A1 (fr)
PE (1) PE82899A1 (fr)
PL (1) PL337651A1 (fr)
PT (1) PT986387E (fr)
SK (1) SK169699A3 (fr)
TN (1) TNSN98088A1 (fr)
TR (1) TR199903074T2 (fr)
UA (1) UA57081C2 (fr)
WO (1) WO1998057633A1 (fr)
ZA (1) ZA985182B (fr)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ID27933A (id) 1998-05-12 2001-05-03 Warner Lambert Co Gabungan protein farnesiltransferase dan inhibitor hmg-coa reduktase serta penggunaannya untuk mengobati kanker
WO2000016778A1 (fr) * 1998-09-24 2000-03-30 Merck & Co., Inc. Procede de traitement du cancer
EP1006113A1 (fr) 1998-12-02 2000-06-07 Pfizer Products Inc. Dérivés de 2-(2-oxo-éthylidène)-imidazolidin-4-one et leur utilisation pour inhiber la croissance anormale des cellules
WO2000067737A2 (fr) * 1999-05-07 2000-11-16 The Brigham And Women's Hospital, Inc. UTILISATION D'INHIBITEURS DE HMGCoA REDUCTASE POUR LA PREVENTION DE MALADIES DONT LA PATHOGENESE DEPEND D'UNE NEOFORMATION DE VAISSEAUX SANGUINS
US6710058B2 (en) 2000-11-06 2004-03-23 Bristol-Myers Squibb Pharma Company Monocyclic or bicyclic carbocycles and heterocycles as factor Xa inhibitors
JP2004516287A (ja) 2000-12-19 2004-06-03 ファイザー・プロダクツ・インク ６−［（４−クロロ−フェニル）−ヒドロキシ−（３−メチル−３ｈ−イミダゾール−４−イル）−メチル］−４−（３−エチニル−フェニル）−１−メチル−１ｈ−キノリン−２−オン，２，３−ジヒドロキシブタン二酸塩の結晶形および製造方法
JP4092203B2 (ja) 2000-12-21 2008-05-28 ニトロメッド，インク． 新規のシクロオキシゲナーゼ２選択的阻害剤としての置換アリール化合物、組成物、および使用方法
US20020151563A1 (en) * 2001-03-29 2002-10-17 Pfizer Inc. Farnesyl transferase inhibitors in combination with HMG CoA reductase inhibitors for the inhibition of abnormal cell growth
US6740757B2 (en) 2001-08-29 2004-05-25 Pfizer Inc Enantiomers of 6-[(4-chloro-phenyl)-hydroxy-(3-methyl-3h-imidazol-4-yl)-methyl]-4-[3-(3-hydroxy-3-methyl-but-1-ynyl)-phenyl]-1-methyl-1h-quinolin-2-one and salts thereof, useful in the treatment of cancer
TWI297606B (en) * 2004-01-16 2008-06-11 Nat Health Research Institutes Cancer therapy
US8168667B2 (en) 2006-05-31 2012-05-01 Galapagos Nv Imidazolidine derivatives, uses therefor, preparation thereof and compositions comprising such
GB2463514C (en) 2008-09-11 2018-09-26 Galapagos Nv Imidazolidine compounds and uses therefor

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997005902A1 (fr) * 1995-08-09 1997-02-20 Banyu Pharmaceutical Co., Ltd. Composition medicinale

Also Published As

Publication number Publication date
CO4950607A1 (es) 2000-09-01
ES2196559T3 (es) 2003-12-16
IL132765A0 (en) 2001-03-19
NZ500662A (en) 2001-10-26
PT986387E (pt) 2003-06-30
OA11231A (en) 2003-05-26
GT199800081A (es) 1999-12-07
AU7445998A (en) 1999-01-04
HUP0004624A3 (en) 2002-11-28
ID23014A (id) 1999-12-30
PA8453601A1 (es) 2000-05-24
SK169699A3 (en) 2000-06-12
CA2294399C (fr) 2004-03-16
ATE235905T1 (de) 2003-04-15
MA24569A1 (fr) 1998-12-31
UA57081C2 (uk) 2003-06-16
HRP980328A2 (en) 1999-04-30
IS5259A (is) 1999-11-19
EP0986387B1 (fr) 2003-04-02
DZ2518A1 (fr) 2003-02-01
NO996206L (no) 2000-02-15
CN1259868A (zh) 2000-07-12
NO996206D0 (no) 1999-12-15
JP2000513031A (ja) 2000-10-03
HN1998000091A (es) 1999-09-29
DE69812933T2 (de) 2003-11-06
DK0986387T3 (da) 2003-07-14
JP3713051B2 (ja) 2005-11-02
BR9810616A (pt) 2000-09-12
BG103946A (bg) 2000-07-31
KR20010013839A (ko) 2001-02-26
AP9801261A0 (en) 1999-12-11
DE69812933D1 (de) 2003-05-08
EP0986387A1 (fr) 2000-03-22
PL337651A1 (en) 2000-08-28
WO1998057633A1 (fr) 1998-12-23
EA199901043A1 (ru) 2000-06-26
HRP980328B1 (en) 2002-06-30
CA2294399A1 (fr) 1998-12-23
HUP0004624A2 (hu) 2001-10-28
AR013090A1 (es) 2000-12-13
TR199903074T2 (xx) 2000-05-22
KR100392573B1 (ko) 2003-07-23
PE82899A1 (es) 1999-08-26
ZA985182B (en) 1999-12-17
AU724676B2 (en) 2000-09-28

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