PE82899A1 - INHIBIDORES DE LA FARNESIL TRANSFERASA COMBINADOS CON INHIBIDORES DE LA HMG CoA REDUCTASA PARA EL TRATAMIENTO DEL CANCER - Google Patents

INHIBIDORES DE LA FARNESIL TRANSFERASA COMBINADOS CON INHIBIDORES DE LA HMG CoA REDUCTASA PARA EL TRATAMIENTO DEL CANCER

Info

Publication number
PE82899A1
PE82899A1 PE1998000500A PE00050098A PE82899A1 PE 82899 A1 PE82899 A1 PE 82899A1 PE 1998000500 A PE1998000500 A PE 1998000500A PE 00050098 A PE00050098 A PE 00050098A PE 82899 A1 PE82899 A1 PE 82899A1
Authority
PE
Peru
Prior art keywords
halo
alkyl
coa reductase
hmg coa
optionally replaced
Prior art date
Application number
PE1998000500A
Other languages
English (en)
Inventor
Shama Mohammed Kajiji
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 PE82899A1 publication Critical patent/PE82899A1/es

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
    • A61K31/40Heterocyclic 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
    • 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
    • A61K31/40Heterocyclic 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
    • A61K31/403Heterocyclic 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
    • A61K31/404Indoles, e.g. pindolol
    • A61K31/405Indole-alkanecarboxylic acids; Derivatives thereof, e.g. tryptophan, indomethacin
    • 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
    • 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
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • 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)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (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)
  • Oncology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Hematology (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

SE REFIERE A UNA COMPOSICION FARMACEUTICA QUE COMPRENDE UN INHIBIDOR DE LA ENZIMA FARNESIL TRANSFERASA (FTASA) COMO a)UN COMPUESTO (I), DONDE R1 Y R2 SON -(CH2)p(HETEROCICLO DE 5-10 MIEMBROS), ALILO: OPCIONALMENTE SUSTITUIDOS POR 1-3 R9 o HALO; p ES 0-3; R3 ES -(CH2)m(1- o 2-ADAMANTILO), -(CH2)m(CICLOALQUILO C3-C10), ENTRE OTROS; m ES 0-6; R4 ES ARILO C6-C10, HETEROCICLO DE 5-10 MIEMBROS O ALQUILO C1-C6; OPCIONALMENTE SUSTITUIDOS POR 1-3 R5; R5 ES HALO, SO2NR6R7, NR6R8, ENTRE OTROS; R6 Y R7 SON H o ALQUILO C1-C4; R8 ES R6 U -OR6; b)COMPUESTOS IIA Y IIB, DONDE R1 ES H, HALO, CN, ENTRE OTROS; R2 ES -(CH2)nY U -OCOR5; R3 ES PIRIDILO, PIRIMIDILO, ENTRE OTROS; Y ES H, OH, NH2, ENTRE OTROS; R5 ES ALQUILO C1-C4, FENILO O BENCILO OPCIONALMENTE SUSTITUIDO; W ES HALO, R5, OH, ENTRE OTROS; m ES 0-2; n ES 1-7; p ES 0-1; E1 Y E2 SON H, HALO, ALQUILO C1-C3, ENTRE OTROS; HET` Y HET'' SON HETEROCICLOS DE 6 MIEMBROS CON 1-4 N, SUSTITUIDOS OPCIONALMENTE. LA COMPOSICION COMPRENDE TAMBIEN UN INHIBIDOR DE HIDROXIMETILGLUTARIL COENZIMA A REDUCTASA (HMG CoA REDUCTASA) SELECCIONADO DE ATORVASTATINA, PRAVASTATINA, LOVASTATINA, ENTRE OTROS. LA COMPOSICION INHIBE EL DESARROLLO ANORMAL DE CELULAS POR LO QUE PUEDE SER UTIL EN EL TRATAMIENTO DEL CANCER O TRASTORNO PROLIFERATIVO BENIGNO
PE1998000500A 1997-06-16 1998-06-12 INHIBIDORES DE LA FARNESIL TRANSFERASA COMBINADOS CON INHIBIDORES DE LA HMG CoA REDUCTASA PARA EL TRATAMIENTO DEL CANCER PE82899A1 (es)

Applications Claiming Priority (1)

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

Publications (1)

Publication Number Publication Date
PE82899A1 true PE82899A1 (es) 1999-08-26

Family

ID=21960890

Family Applications (1)

Application Number Title Priority Date Filing Date
PE1998000500A PE82899A1 (es) 1997-06-16 1998-06-12 INHIBIDORES DE LA FARNESIL TRANSFERASA COMBINADOS CON INHIBIDORES DE LA HMG CoA REDUCTASA PARA EL TRATAMIENTO DEL CANCER

Country Status (37)

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

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EA003860B1 (ru) * 1998-05-12 2003-10-30 Варнер-Ламберт Компани КОМБИНАЦИИ ИНГИБИТОРОВ ПРОТЕИН ФАРНЕЗИЛТРАНСФЕРАЗЫ И HMG KoA РЕДУКТАЗЫ И ИХ ПРИМЕНЕНИЕ ДЛЯ ЛЕЧЕНИЯ РАКА
AU6256499A (en) * 1998-09-24 2000-04-10 Merck & Co., Inc. A method of treating cancer
EP1006113A1 (en) * 1998-12-02 2000-06-07 Pfizer Products Inc. Derivatives of 2-(2-oxo-ethylidene)-imidazolidin-4-one and their use to inhibit abnormal cell growth
AU4988100A (en) * 1999-05-07 2000-11-21 Brigham And Women's Hospital Use of hmgcoa reductase inhibitors in the prevention of diseases whose pathogenesis is dependent on neovascularization
US6710058B2 (en) 2000-11-06 2004-03-23 Bristol-Myers Squibb Pharma Company Monocyclic or bicyclic carbocycles and heterocycles as factor Xa inhibitors
CA2432137C (en) 2000-12-19 2010-12-21 Pfizer Products Inc. Crystal forms of 6-[(4-chloro-phenyl)-hydroxy-(3-methyl-3h-imidazol-4-yl)-methyl]-4-(3-ethynyl-phenyl)-1-methyl-1h-quinolin-2-one, 2,3-dihydroxybutanedioate salts and method of production
DE60122939T2 (de) 2000-12-21 2007-01-11 Nitromed, Inc., Bedford Substituierte arylverbindungen als neue, cyclooxygenase-2-selektive inhibitoren, zusammensetzungen und verwendungsverfahren
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
EP0856315B1 (en) * 1995-08-09 2005-08-24 Banyu Pharmaceutical Co., Ltd. Protein-farnesyltransferase inhibitors in combination with hmgcoa-reductase-inhibitors for the treatment of aids

Also Published As

Publication number Publication date
JP3713051B2 (ja) 2005-11-02
HUP0004624A2 (hu) 2001-10-28
JP2000513031A (ja) 2000-10-03
NO996206L (no) 2000-02-15
CO4950607A1 (es) 2000-09-01
GT199800081A (es) 1999-12-07
SK169699A3 (en) 2000-06-12
BG103946A (bg) 2000-07-31
AU724676B2 (en) 2000-09-28
PL337651A1 (en) 2000-08-28
ZA985182B (en) 1999-12-17
HN1998000091A (es) 1999-09-29
AR013090A1 (es) 2000-12-13
OA11231A (en) 2003-05-26
IS5259A (is) 1999-11-19
MA24569A1 (fr) 1998-12-31
NO996206D0 (no) 1999-12-15
CN1259868A (zh) 2000-07-12
HRP980328B1 (en) 2002-06-30
ID23014A (id) 1999-12-30
DE69812933T2 (de) 2003-11-06
PA8453601A1 (es) 2000-05-24
BR9810616A (pt) 2000-09-12
ATE235905T1 (de) 2003-04-15
TNSN98088A1 (fr) 2005-03-15
KR100392573B1 (ko) 2003-07-23
ES2196559T3 (es) 2003-12-16
EP0986387A1 (en) 2000-03-22
HUP0004624A3 (en) 2002-11-28
UA57081C2 (uk) 2003-06-16
WO1998057633A1 (en) 1998-12-23
CA2294399C (en) 2004-03-16
TR199903074T2 (xx) 2000-05-22
AP9801261A0 (en) 1999-12-11
DK0986387T3 (da) 2003-07-14
PT986387E (pt) 2003-06-30
KR20010013839A (ko) 2001-02-26
NZ500662A (en) 2001-10-26
AU7445998A (en) 1999-01-04
EA199901043A1 (ru) 2000-06-26
EP0986387B1 (en) 2003-04-02
HRP980328A2 (en) 1999-04-30
CA2294399A1 (en) 1998-12-23
DZ2518A1 (fr) 2003-02-01
IL132765A0 (en) 2001-03-19
DE69812933D1 (de) 2003-05-08

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FG Grant, registration
FD Application declared void or lapsed