AU2002214056A1 - Farnesyl transferase inhibiting benzoheterocyclic derivatives - Google Patents

Farnesyl transferase inhibiting benzoheterocyclic derivatives

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Publication number
AU2002214056A1
AU2002214056A1 AU2002214056A AU1405602A AU2002214056A1 AU 2002214056 A1 AU2002214056 A1 AU 2002214056A1 AU 2002214056 A AU2002214056 A AU 2002214056A AU 1405602 A AU1405602 A AU 1405602A AU 2002214056 A1 AU2002214056 A1 AU 2002214056A1
Authority
AU
Australia
Prior art keywords
sup
farnesyl transferase
transferase inhibiting
benzoheterocyclic derivatives
benzoheterocyclic
Prior art date
Legal status (The legal status 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 status listed.)
Abandoned
Application number
AU2002214056A
Inventor
Patrick Rene Angibaud
Virginie Sophie Poncelet
Marc Gaston Venet
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Janssen Pharmaceutica NV
Original Assignee
Janssen Pharmaceutica NV
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 Janssen Pharmaceutica NV filed Critical Janssen Pharmaceutica NV
Publication of AU2002214056A1 publication Critical patent/AU2002214056A1/en
Abandoned legal-status Critical Current

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    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P35/00—Antineoplastic agents
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    • A61P35/00—Antineoplastic agents
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P37/02—Immunomodulators
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/08—Antiallergic agents
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms

Abstract

This invention comprises the novel compounds of formula (I) wherein r, s, t, X, Z, R<SUP>1</SUP>, R<SUP>2</SUP>, R<SUP>3</SUP>, R<SUP>4</SUP>, R<SUP>5</SUP>, R<SUP>6 </SUP>and R<SUP>7 </SUP>have defined meanings, having farnesyl transferase inhibiting activity; their preparation, compositions containing them and their use as a medicine.
AU2002214056A 2000-11-21 2001-11-15 Farnesyl transferase inhibiting benzoheterocyclic derivatives Abandoned AU2002214056A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP00204149 2000-11-21
EP00204149 2000-11-21
PCT/EP2001/013317 WO2002042296A1 (en) 2000-11-21 2001-11-15 Farnesyl transferase inhibiting benzoheterocyclic derivatives

Publications (1)

Publication Number Publication Date
AU2002214056A1 true AU2002214056A1 (en) 2002-06-03

Family

ID=8172314

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2002214056A Abandoned AU2002214056A1 (en) 2000-11-21 2001-11-15 Farnesyl transferase inhibiting benzoheterocyclic derivatives

Country Status (8)

Country Link
US (1) US7153958B2 (en)
EP (1) EP1339709B1 (en)
JP (1) JP4348080B2 (en)
AT (1) ATE434615T1 (en)
AU (1) AU2002214056A1 (en)
DE (1) DE60139080D1 (en)
ES (1) ES2328225T3 (en)
WO (1) WO2002042296A1 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005111217A2 (en) 2004-04-29 2005-11-24 U.S. Smokeless Tobacco Company Nicotiana nucleic acid molecules and uses thereof
US8232402B2 (en) 2008-03-12 2012-07-31 Link Medicine Corporation Quinolinone farnesyl transferase inhibitors for the treatment of synucleinopathies and other indications
BRPI0920927A2 (en) 2008-11-13 2019-09-24 Link Medicine Corp azaquinolinone derivatives and uses thereof
CN113072509B (en) * 2021-03-01 2022-11-25 中国科学院成都有机化学有限公司 Method for synthesizing 7-amino clonazepam compound

Family Cites Families (20)

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Publication number Priority date Publication date Assignee Title
US3682892A (en) * 1970-12-23 1972-08-08 Hoffmann La Roche 7-hydroxy lower alkyl benzodiazepines
IL42416A (en) 1972-07-13 1976-06-30 Sparamedica Ag 6-phenyl-4h-s-triazolo(4,3-alpha)(1,4)benzodiazepine and n-oxide derivatives,their preparation and pharmaceutical compositions containing them
DE3610848A1 (en) * 1986-04-01 1987-10-15 Boehringer Ingelheim Kg NEW 1,4-DIAZEPINE
JP2742053B2 (en) 1986-07-31 1998-04-22 オーエン ハント，アンソニー Flexible coupling
CA2002864C (en) * 1988-11-29 1999-11-16 Eddy J. E. Freyne (1h-azol-1-ylmethyl) substituted quinoline, quinazoline or quinoxaline derivatives
MX9704683A (en) 1994-12-23 1997-09-30 Pfizer Naphthyl-benzoxazepines or -benzothiazepines as squalene synthetase inhibitors.
TW316902B (en) * 1994-12-28 1997-10-01 Janssen Pharmaceutica Nv
TW349948B (en) 1995-10-31 1999-01-11 Janssen Pharmaceutica Nv Farnesyl transferase inhibiting 2-quinolone derivatives
PT1162201E (en) * 1995-12-08 2006-08-31 Janssen Pharmaceutica Nv (IMIDAZOL-5-IL) METHYL-2-KINOLINONE DERIVATIVES AS FARNESIL PROTEIN INHIBITORS TRANSFERASE
US6011029A (en) * 1996-02-26 2000-01-04 Bristol-Myers Squibb Company Inhibitors of farnesyl protein transferase
TW591030B (en) 1997-03-10 2004-06-11 Janssen Pharmaceutica Nv Farnesyl transferase inhibiting 1,8-annelated quinolinone derivatives substituted with N- or C-linked imidazoles
ES2289783T3 (en) 1997-04-25 2008-02-01 Janssen Pharmaceutica N.V. QUINAZOLINONAS THAT INHIBIT THE FARNESILTRANSFERASA.
DK0988038T3 (en) 1997-06-02 2002-12-02 Janssen Pharmaceutica Nv Use of (imidazol-5-yl) methyl-2-quinolinone derivatives to inhibit smooth muscle cell proliferation
CZ300968B6 (en) 1998-07-06 2009-09-30 Janssen Pharmaceutica N. V. Pharmaceutical composition having radiosensitive properties and comprising farnesyl-protein transferase inhibitor
TR200003882T2 (en) 1998-07-06 2001-06-21 Janssen Pharmaceutica N.V. Farnesyl protein transferase inhibitors for the treatment of arthropathies.
AP2001002079A0 (en) 1998-08-27 2001-03-31 Pfizer Prod Inc Alkynyl-substituted quinolin-2-one derivatives useful as anticancer agents.
JP3494409B2 (en) 1998-08-27 2004-02-09 ファイザー・プロダクツ・インク Alkynyl-substituted quinolin-2-one derivatives useful as anticancer agents
ATE240327T1 (en) * 1998-12-23 2003-05-15 Janssen Pharmaceutica Nv 1,2-ANNELATED QUINOLINE DERIVATIVES
WO2000047574A1 (en) 1999-02-11 2000-08-17 Pfizer Products Inc. Heteroaryl-substituted quinolin-2-one derivatives useful as anticancer agents
HN2000000266A (en) 2000-01-21 2001-05-21 Pfizer Prod Inc ANTI-TARGET COMPOUND AND METHOD OF SEPARATION OF ENANTIOMERS USEFUL TO SYNTHEIZE SUCH COMPOUND.

Also Published As

Publication number Publication date
EP1339709A1 (en) 2003-09-03
US7153958B2 (en) 2006-12-26
ES2328225T3 (en) 2009-11-11
US20040034218A1 (en) 2004-02-19
JP4348080B2 (en) 2009-10-21
WO2002042296A1 (en) 2002-05-30
EP1339709B1 (en) 2009-06-24
DE60139080D1 (en) 2009-08-06
JP2004514677A (en) 2004-05-20
ATE434615T1 (en) 2009-07-15

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