WO2012037299A3 - Fatty acid synthase inhibitors - Google Patents

Fatty acid synthase inhibitors Download PDF

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Publication number
WO2012037299A3
WO2012037299A3 PCT/US2011/051672 US2011051672W WO2012037299A3 WO 2012037299 A3 WO2012037299 A3 WO 2012037299A3 US 2011051672 W US2011051672 W US 2011051672W WO 2012037299 A3 WO2012037299 A3 WO 2012037299A3
Authority
WO
WIPO (PCT)
Prior art keywords
fatty acid
acid synthase
synthase inhibitors
relates
triazolethiones
Prior art date
Application number
PCT/US2011/051672
Other languages
French (fr)
Other versions
WO2012037299A2 (en
Inventor
Nicholas D. Adams
Christopher Joseph Aquino
Jonathan M. Ghergurovich
David Lee Musso
Cynthia A. Parrish
Alexander Joseph Reif
Original Assignee
Glaxosmithkline Intellectual Property Development Limited
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 Glaxosmithkline Intellectual Property Development Limited filed Critical Glaxosmithkline Intellectual Property Development Limited
Priority to JP2013529311A priority Critical patent/JP2014508097A/en
Priority to EP11825905.0A priority patent/EP2616071A2/en
Priority to US13/824,000 priority patent/US20130172384A1/en
Publication of WO2012037299A2 publication Critical patent/WO2012037299A2/en
Publication of WO2012037299A3 publication Critical patent/WO2012037299A3/en

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • 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
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/05—Isotopically modified compounds, e.g. labelled

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

This invention relates to the use of triazolone and triazolethione derivatives for the modulation, notably the inhibition of the activity or function of fatty acid synthase (FAS). Suitably, the present invention relates to the use of triazolones and triazolethiones in the treatment of cancer.
PCT/US2011/051672 2010-09-17 2011-09-15 Fatty acid synthase inhibitors WO2012037299A2 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP2013529311A JP2014508097A (en) 2010-09-17 2011-09-15 Fatty acid synthase inhibitor
EP11825905.0A EP2616071A2 (en) 2010-09-17 2011-09-15 Fatty acid synthase inhibitors
US13/824,000 US20130172384A1 (en) 2010-09-17 2011-09-15 Fatty acid synthase inhibitors

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US38377410P 2010-09-17 2010-09-17
US61/383,774 2010-09-17

Publications (2)

Publication Number Publication Date
WO2012037299A2 WO2012037299A2 (en) 2012-03-22
WO2012037299A3 true WO2012037299A3 (en) 2014-03-27

Family

ID=45832231

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2011/051672 WO2012037299A2 (en) 2010-09-17 2011-09-15 Fatty acid synthase inhibitors

Country Status (4)

Country Link
US (1) US20130172384A1 (en)
EP (1) EP2616071A2 (en)
JP (1) JP2014508097A (en)
WO (1) WO2012037299A2 (en)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9505728B2 (en) 2012-03-09 2016-11-29 Inception 2, Inc. Triazolone compounds and uses thereof
EP2892892B1 (en) * 2012-09-07 2017-05-31 Janssen Pharmaceutica NV Imidazolin-5-one derivatives useful as fatty acid synthase (fasn) inhibitors for the treatment of cancer
MX2015007433A (en) * 2012-12-20 2015-12-07 Inception 2 Inc Triazolone compounds and uses thereof.
EP2943484B1 (en) * 2013-01-10 2017-10-25 Glaxosmithkline Intellectual Property (No. 2) Limited Fatty acid synthase inhibitors
PE20160122A1 (en) 2013-03-13 2016-02-12 Forma Therapeutics Inc NOBLE COMPOUNDS AND COMPOSITIONS FOR INHIBITION OF FASN
WO2015035059A1 (en) 2013-09-06 2015-03-12 Inception 2, Inc. Triazolone compounds and uses thereof
CA2934257C (en) * 2013-12-17 2022-06-07 Janssen Pharmaceutica Nv Imidazolin-5-one derivative useful as fasn inhibitors for the treatment of cancer
TW201722958A (en) * 2015-09-15 2017-07-01 葛蘭素史克智慧財產（第二）有限公司 Chemical compounds
TWI767148B (en) 2018-10-10 2022-06-11 美商弗瑪治療公司 Inhibiting fatty acid synthase (fasn)
CN113382633A (en) 2018-10-29 2021-09-10 福马治疗股份有限公司 Solid forms of (4- (2-fluoro-4- (1-methyl-1H-benzo [ d ] imidazol-5-yl) benzoyl) piperazin-1-yl) (1-hydroxycyclopropyl) methanone
CN111777593A (en) * 2019-04-03 2020-10-16 南京天印健华医药科技有限公司 Novel compounds as inhibitors of rearrangement kinase during transfection

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040116491A1 (en) * 2002-10-07 2004-06-17 King Bryan W. Triazolone and triazolethione derivatives as inhibitors of matrix metalloproteinases and/or TNF-alpha converting enzyme
US20100022540A1 (en) * 2006-05-18 2010-01-28 Hans-Michael Eggenweiler Triazole derivatives ii

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040116491A1 (en) * 2002-10-07 2004-06-17 King Bryan W. Triazolone and triazolethione derivatives as inhibitors of matrix metalloproteinases and/or TNF-alpha converting enzyme
US20100022540A1 (en) * 2006-05-18 2010-01-28 Hans-Michael Eggenweiler Triazole derivatives ii

Also Published As

Publication number Publication date
EP2616071A2 (en) 2013-07-24
JP2014508097A (en) 2014-04-03
WO2012037299A2 (en) 2012-03-22
US20130172384A1 (en) 2013-07-04

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