WO2001081316A2 - Inhibiteurs de phenyle farnesyltransferase substitues - Google Patents

Inhibiteurs de phenyle farnesyltransferase substitues Download PDF

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Publication number
WO2001081316A2
WO2001081316A2 PCT/US2001/013678 US0113678W WO0181316A2 WO 2001081316 A2 WO2001081316 A2 WO 2001081316A2 US 0113678 W US0113678 W US 0113678W WO 0181316 A2 WO0181316 A2 WO 0181316A2
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WIPO (PCT)
Prior art keywords
methyl
imidazol
group
desired product
compound according
Prior art date
Application number
PCT/US2001/013678
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English (en)
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WO2001081316A3 (fr
Inventor
Wei-Bo Wang
Michael L. Curtin
Stephen A. Fakhoury
Stephen L. Ii Gwaltney
Lisa A. Hasvold
Charles W. Hutchins
Qui Li
Nan-Horng Lin
Lissa Taka Jennings Nelson
Stephen J. O'connor
Hing L. Sham
Gerald M. Sullivan
Gary T. Wang
Xilu Wang
Original Assignee
Abbott Laboratories
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Publication date
Application filed by Abbott Laboratories filed Critical Abbott Laboratories
Priority to JP2001578410A priority Critical patent/JP2004509064A/ja
Priority to AU2001259218A priority patent/AU2001259218A1/en
Priority to CA002407093A priority patent/CA2407093A1/fr
Priority to EP01932712A priority patent/EP1276726A2/fr
Priority to MXPA02010608A priority patent/MXPA02010608A/es
Publication of WO2001081316A2 publication Critical patent/WO2001081316A2/fr
Publication of WO2001081316A3 publication Critical patent/WO2001081316A3/fr
Priority to HK03104500.2A priority patent/HK1053833A1/zh

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/28Radicals substituted by singly-bound oxygen or sulphur atoms
    • C07D213/30Oxygen atoms
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P27/00Drugs for disorders of the senses
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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  • Chemical & Material Sciences (AREA)
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  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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  • Animal Behavior & Ethology (AREA)
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  • Bioinformatics & Cheminformatics (AREA)
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  • Immunology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Dermatology (AREA)
  • Transplantation (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Pyridine Compounds (AREA)

Abstract

L'invention concerne des composés de formule (I) ou des sels correspondants acceptables pharmaceutiquement qui inhibent la farnésyltransférase. Cette invention concerne également des méthodes de fabrication des composés, des compositions pharmaceutiques renfermant les composés, et des méthodes de traitement utilisant les composés.
PCT/US2001/013678 2000-04-27 2001-04-25 Inhibiteurs de phenyle farnesyltransferase substitues WO2001081316A2 (fr)

Priority Applications (6)

Application Number Priority Date Filing Date Title
JP2001578410A JP2004509064A (ja) 2000-04-27 2001-04-25 置換フェニルファルネシルトランスフェラーゼ阻害剤
AU2001259218A AU2001259218A1 (en) 2000-04-27 2001-04-25 Substituted phenyl farnesyltransferase inhibitors
CA002407093A CA2407093A1 (fr) 2000-04-27 2001-04-25 Inhibiteurs de phenyle farnesyltransferase substitues
EP01932712A EP1276726A2 (fr) 2000-04-27 2001-04-25 Inhibiteurs de phenyle farnesyltransferase substitues
MXPA02010608A MXPA02010608A (es) 2000-04-27 2001-04-25 Inhibidores de farnesiltransferasa sustituidos con fenilo.
HK03104500.2A HK1053833A1 (zh) 2000-04-27 2003-06-23 取代苯基法呢基轉移酶抑制劑

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US56325600A 2000-04-27 2000-04-27
US09/563,256 2000-04-27
US82220501A 2001-04-02 2001-04-02
US09/822,205 2001-04-02

Publications (2)

Publication Number Publication Date
WO2001081316A2 true WO2001081316A2 (fr) 2001-11-01
WO2001081316A3 WO2001081316A3 (fr) 2002-05-23

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ID=27073227

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Application Number Title Priority Date Filing Date
PCT/US2001/013678 WO2001081316A2 (fr) 2000-04-27 2001-04-25 Inhibiteurs de phenyle farnesyltransferase substitues

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EP (1) EP1276726A2 (fr)
JP (1) JP2004509064A (fr)
AU (1) AU2001259218A1 (fr)
CA (1) CA2407093A1 (fr)
HK (1) HK1053833A1 (fr)
MX (1) MXPA02010608A (fr)
PE (1) PE20011318A1 (fr)
WO (1) WO2001081316A2 (fr)

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003051366A2 (fr) 2001-12-13 2003-06-26 Abbott Laboratories Inhibiteurs de kinase
WO2004037791A1 (fr) 2002-10-21 2004-05-06 Chiron Corporation Inhibiteurs de glycogene synthase kinase 3
JP2005511790A (ja) * 2001-12-19 2005-04-28 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ ファルネシルトランスフェラーゼ阻害剤としての炭素連結トリアゾールで置換されている1,8−アネル化キノリン誘導体
EP1734957A2 (fr) * 2004-04-01 2006-12-27 Pfizer Products Inc. Composes de thiazole sulfamide utiles pour le traitement des maladies neurodegeneratives
US7179827B2 (en) 2004-03-31 2007-02-20 Lexicon Genetics Incorporated Thiazoles and methods of their use
US7745638B2 (en) 2003-07-22 2010-06-29 Astex Therapeutics Limited 3,4-disubstituted 1H-pyrazole compounds and their use as cyclin dependent kinase and glycogen synthase kinase-3 modulators
US8013163B2 (en) 2005-01-21 2011-09-06 Astex Therapeutics Limited 4-(2,6-dichloro-benzoylamino)-1H-pyrazole-3-carboxylic acid piperidin-4-ylamide acid addition salts as kinase inhibitors
US8404718B2 (en) 2005-01-21 2013-03-26 Astex Therapeutics Limited Combinations of pyrazole kinase inhibitors
US8710043B2 (en) 2011-06-24 2014-04-29 Amgen Inc. TRPM8 antagonists and their use in treatments
US8778941B2 (en) 2011-06-24 2014-07-15 Amgen Inc. TRPM8 antagonists and their use in treatments
US8952161B2 (en) 2007-04-06 2015-02-10 Neurocrine Biosciences, Inc. Gonadotropin-releasing hormone receptor antagonists and methods relating thereto
US8952009B2 (en) 2012-08-06 2015-02-10 Amgen Inc. Chroman derivatives as TRPM8 inhibitors
US11299467B2 (en) 2017-07-21 2022-04-12 Antabio Sas Chemical compounds

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW200806284A (en) * 2006-03-31 2008-02-01 Alcon Mfg Ltd Prenyltransferase inhibitors for ocular hypertension control and the treatment of glaucoma
JP2021527125A (ja) * 2018-06-07 2021-10-11 ディサーム・セラピューティクス・インコーポレイテッドDisarm Therapeutics, Inc. Sarm1阻害剤

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0079191A1 (fr) * 1981-11-06 1983-05-18 Imperial Chemical Industries Plc Dérivés d'amide
WO1998029199A1 (fr) * 1996-12-31 1998-07-09 Wayne Pigment Corp. Composition pigmentaire inhibant les taches
WO1999017777A1 (fr) * 1997-10-08 1999-04-15 Merck & Co., Inc. Inhibiteurs de transferase de prenyl-proteine
WO2000001382A1 (fr) * 1998-07-02 2000-01-13 Merck & Co., Inc. Inhibiteurs de prenyl-proteine transferase

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2868883B2 (ja) * 1990-10-15 1999-03-10 株式会社トクヤマ ジオキソラン誘導体

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0079191A1 (fr) * 1981-11-06 1983-05-18 Imperial Chemical Industries Plc Dérivés d'amide
WO1998029199A1 (fr) * 1996-12-31 1998-07-09 Wayne Pigment Corp. Composition pigmentaire inhibant les taches
WO1999017777A1 (fr) * 1997-10-08 1999-04-15 Merck & Co., Inc. Inhibiteurs de transferase de prenyl-proteine
WO2000001382A1 (fr) * 1998-07-02 2000-01-13 Merck & Co., Inc. Inhibiteurs de prenyl-proteine transferase

Cited By (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003051366A2 (fr) 2001-12-13 2003-06-26 Abbott Laboratories Inhibiteurs de kinase
WO2003051366A3 (fr) * 2001-12-13 2004-03-25 Abbott Lab Inhibiteurs de kinase
US6831175B2 (en) 2001-12-13 2004-12-14 Abbott Laboratories Kinase inhibitors
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JP2004509064A (ja) 2004-03-25
HK1053833A1 (zh) 2003-11-07
WO2001081316A3 (fr) 2002-05-23
PE20011318A1 (es) 2002-01-08
AU2001259218A1 (en) 2001-11-07
MXPA02010608A (es) 2003-05-14
CA2407093A1 (fr) 2001-11-01
EP1276726A2 (fr) 2003-01-22

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