OA11231A - Farnesyl transferase inhibtors in combinatin with hmg coa reductase inhibitors for the treatment of cancer - Google Patents

Farnesyl transferase inhibtors in combinatin with hmg coa reductase inhibitors for the treatment of cancer Download PDF

Info

Publication number
OA11231A
OA11231A OA9900276A OA9900276A OA11231A OA 11231 A OA11231 A OA 11231A OA 9900276 A OA9900276 A OA 9900276A OA 9900276 A OA9900276 A OA 9900276A OA 11231 A OA11231 A OA 11231A
Authority
OA
OAPI
Prior art keywords
alkyl
phenyl
halo
amino
hydroxy
Prior art date
Application number
OA9900276A
Other languages
English (en)
Inventor
Shama Mohammed Kajiiji
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 OA11231A publication Critical patent/OA11231A/en

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)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Epidemiology (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
OA9900276A 1997-06-16 1999-12-10 Farnesyl transferase inhibtors in combinatin with hmg coa reductase inhibitors for the treatment of cancer OA11231A (en)

Applications Claiming Priority (1)

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

Publications (1)

Publication Number Publication Date
OA11231A true OA11231A (en) 2003-05-26

Family

ID=21960890

Family Applications (1)

Application Number Title Priority Date Filing Date
OA9900276A OA11231A (en) 1997-06-16 1999-12-10 Farnesyl transferase inhibtors in combinatin with hmg coa reductase inhibitors for the treatment of 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
ID27933A (id) 1998-05-12 2001-05-03 Warner Lambert Co Gabungan protein farnesiltransferase dan inhibitor hmg-coa reduktase serta penggunaannya untuk mengobati kanker
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
WO2000067737A2 (en) * 1999-05-07 2000-11-16 The Brigham And Women's Hospital, Inc. 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
EP1395577A1 (en) 2000-12-19 2004-03-10 Pfizer Products Inc. Crystal forms of 6- (4-chloro-phenyl)-hydroxy-(-3-methyl-3h-imidaol-4-yl)-methyl]-4-(3-ethynyl-phenyl)-1-methyl-1h-quinolin-2-one, 2,3-dihydroxybutanedioate salts and method of production
CA2432642A1 (en) 2000-12-21 2002-08-08 Subhash P. Khanapure Substituted aryl compounds as novel cyclooxygenase-2 selective inhibitors, compositions and methods of use
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
JP2005200419A (ja) * 2004-01-16 2005-07-28 National Health Research Inst 癌治療法
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
DE69635114T2 (de) * 1995-08-09 2006-03-02 Banyu Pharmaceutical Co., Ltd. Proteinfarnesyltransferase-inhibitoren in kombination mit hmgcoa-reduktase-inhibitoren zur behandlung von aids

Also Published As

Publication number Publication date
HN1998000091A (es) 1999-09-29
AP9801261A0 (en) 1999-12-11
HUP0004624A2 (hu) 2001-10-28
GT199800081A (es) 1999-12-07
DE69812933T2 (de) 2003-11-06
WO1998057633A1 (en) 1998-12-23
SK169699A3 (en) 2000-06-12
PL337651A1 (en) 2000-08-28
KR20010013839A (ko) 2001-02-26
CO4950607A1 (es) 2000-09-01
JP2000513031A (ja) 2000-10-03
DE69812933D1 (de) 2003-05-08
ATE235905T1 (de) 2003-04-15
JP3713051B2 (ja) 2005-11-02
DK0986387T3 (da) 2003-07-14
UA57081C2 (uk) 2003-06-16
CN1259868A (zh) 2000-07-12
PE82899A1 (es) 1999-08-26
NO996206D0 (no) 1999-12-15
NO996206L (no) 2000-02-15
CA2294399C (en) 2004-03-16
TR199903074T2 (xx) 2000-05-22
IL132765A0 (en) 2001-03-19
PA8453601A1 (es) 2000-05-24
KR100392573B1 (ko) 2003-07-23
EP0986387B1 (en) 2003-04-02
MA24569A1 (fr) 1998-12-31
ID23014A (id) 1999-12-30
TNSN98088A1 (fr) 2005-03-15
BR9810616A (pt) 2000-09-12
ZA985182B (en) 1999-12-17
AU7445998A (en) 1999-01-04
AU724676B2 (en) 2000-09-28
DZ2518A1 (fr) 2003-02-01
PT986387E (pt) 2003-06-30
IS5259A (is) 1999-11-19
NZ500662A (en) 2001-10-26
EA199901043A1 (ru) 2000-06-26
CA2294399A1 (en) 1998-12-23
HUP0004624A3 (en) 2002-11-28
HRP980328A2 (en) 1999-04-30
EP0986387A1 (en) 2000-03-22
BG103946A (bg) 2000-07-31
HRP980328B1 (en) 2002-06-30
ES2196559T3 (es) 2003-12-16
AR013090A1 (es) 2000-12-13

Similar Documents

Publication Publication Date Title
US20050014783A1 (en) Use of Rho-kinase inhibitors in the treatment of aneurysm and cardiac hypertrophy
MA27703A1 (fr) Derives de diazepino-indole servant d'inhibiteurs de kinases
CA2294399C (en) Farnesyl transferase inhibitors in combination with hmg coa reductase inhibitors for the treatment of cancer
TWI786723B (zh) 噠嗪并吲哚衍生物及其用途
Ory et al. Blocking HSP90 addiction inhibits tumor cell proliferation, metastasis development, and synergistically acts with zoledronic acid to delay osteosarcoma progression
EP2182941B1 (en) Multikinase inhibitors for use in the treatment of cancer
Lin et al. Combretastatin A4-induced differential cytotoxicity and reduced metastatic ability by inhibition of AKT function in human gastric cancer cells
US20190151289A1 (en) Identification of Small Molecule Inhibitors of Jumonji AT-Rich Interactive Domain 1A (JARID1A) Histone Demethylase
KR101354237B1 (ko) 골수종 치료를 위한 hdac 저해제의 용도
Tamanoi et al. Recent progress in developing small molecule inhibitors designed to interfere with ras membrane association: toward inhibiting K-Ras and N-Ras functions
RS56699B1 (sr) Stabilizovani amorfni oblik agomelatina, postupak za njegovu izradu i farmaceutske kompozicije koje ga sadrže
AU724676C (en) Farnesyl transferase inhibitors in combination with hmg CoA reductase inhibitors for the treatment of cancer
KR19990082064A (ko) 피페라진 옥시란 유도체를 사용하여 신생 세포의 사멸을유도하는 방법
JP2007063288A (ja) エンドセリンアンタゴニストを用いる癌及び癌関連痛の治療方法
US20030114503A1 (en) Farnesyl transferase inhibitors in combination with HMG CoA reductase inhibitors for the treatment of cancer
US20060178348A1 (en) Compositions and therapeutic methods utilizing a combination of a protein extravasation inhibitor and an NSAID
US20020151563A1 (en) Farnesyl transferase inhibitors in combination with HMG CoA reductase inhibitors for the inhibition of abnormal cell growth
MXPA99011798A (es) Inhibidores de la farnesil transferasa combinados con inhibidores de la hmg coa reductasa para el tratamiento del cancer
CZ448699A3 (cs) Inhibitory farnesyltransferasy v kombinaci s inhibitory HMG CoA reduktasy pro léčení rakoviny
US10196378B2 (en) Inhibitors of BCR-ABL mutants and use thereof
WO2005105078A1 (en) Indole derivatives useful for treating resistance to antitumour agents
Fan et al. Sodium salicylate acts through direct inhibition of phosphoinositide 3-kinase-like kinases to modulate topoisomerase-mediated DNA damage responses
WO2021086912A1 (en) Combined pikfyve and p38 map kinase inhibition for treating cancer
HK1027972A (en) Farnesyl transferase inhibitors in combination with hmg coa reductase inhibitors for the treatment of cancer
WO2002002116A2 (en) Therapeutic treatment of cancer with a protein kinase c inhibitor