WO2008036967A3 - Novel heterocyclic compounds as lasy activators - Google Patents

Novel heterocyclic compounds as lasy activators Download PDF

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Publication number
WO2008036967A3
WO2008036967A3 PCT/US2007/079286 US2007079286W WO2008036967A3 WO 2008036967 A3 WO2008036967 A3 WO 2008036967A3 US 2007079286 W US2007079286 W US 2007079286W WO 2008036967 A3 WO2008036967 A3 WO 2008036967A3
Authority
WO
WIPO (PCT)
Prior art keywords
lasy
activators
heterocyclic compounds
novel heterocyclic
compound
Prior art date
Application number
PCT/US2007/079286
Other languages
French (fr)
Other versions
WO2008036967A2 (en
Inventor
Dumbala Srinivas Reddy
Indira Padmalayam
Debnath Bhuniya
Sivaram Pillarisetti
Ranjan Chakrabarti
Original Assignee
Reddy Us Therapeutics Inc
Dumbala Srinivas Reddy
Indira Padmalayam
Debnath Bhuniya
Sivaram Pillarisetti
Ranjan Chakrabarti
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 Reddy Us Therapeutics Inc, Dumbala Srinivas Reddy, Indira Padmalayam, Debnath Bhuniya, Sivaram Pillarisetti, Ranjan Chakrabarti filed Critical Reddy Us Therapeutics Inc
Publication of WO2008036967A2 publication Critical patent/WO2008036967A2/en
Publication of WO2008036967A3 publication Critical patent/WO2008036967A3/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/10Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/12Radicals substituted by oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/10Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/18Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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 two hetero rings
    • C07D401/06Heterocyclic 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 two hetero rings linked by a carbon chain containing only aliphatic carbon atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

This invention provides a compound of formula (I), which is a free species and/or a pharmaceutically-acceptable salt or a stereoisomer of the compound of formula (I). Another aspect of the present invention provides the compound of the formula (I) as a Lipoic acid synthase (LASY) inducer
PCT/US2007/079286 2006-09-22 2007-09-24 Novel heterocyclic compounds as lasy activators WO2008036967A2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US84649906P 2006-09-22 2006-09-22
US60/846,499 2006-09-22

Publications (2)

Publication Number Publication Date
WO2008036967A2 WO2008036967A2 (en) 2008-03-27
WO2008036967A3 true WO2008036967A3 (en) 2008-09-18

Family

ID=39201359

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2007/079286 WO2008036967A2 (en) 2006-09-22 2007-09-24 Novel heterocyclic compounds as lasy activators

Country Status (1)

Country Link
WO (1) WO2008036967A2 (en)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2477279C2 (en) * 2007-06-05 2013-03-10 Санофи-Авентис Substituted benzoylaminoindan-2-carboxylic acids and related compounds
ES2647664T3 (en) 2011-01-04 2017-12-26 Novartis Ag Indole compounds or analogs thereof useful for the treatment of age-related macular degeneration (AMD)
EP2567959B1 (en) 2011-09-12 2014-04-16 Sanofi 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
JP6273274B2 (en) 2012-06-28 2018-01-31 ノバルティス アーゲー Complement pathway modulators and uses thereof
JP6209605B2 (en) 2012-06-28 2017-10-04 ノバルティス アーゲー Pyrrolidine derivatives and their use as complement pathway regulators
ES2712190T3 (en) 2012-06-28 2019-05-09 Novartis Ag Modulators of the complement pathway and its uses
US9468661B2 (en) 2012-06-28 2016-10-18 Novartis Ag Pyrrolidine derivatives and their use as complement pathway modulators
JP6154897B2 (en) 2012-06-28 2017-06-28 ノバルティス アーゲー Pyrrolidine derivatives and their use as complement pathway regulators
KR20150036481A (en) 2012-07-12 2015-04-07 노파르티스 아게 Complement pathway modulators and uses thereof
BR112016022785B8 (en) 2014-04-04 2020-09-15 Iomet Pharma Ltd tryptophan-2,3-dioxigenase (tdo) and / or indoleamine-2,3-dioxigenase (acid) inhibitor compound, pharmaceutical composition, and use of tryptophan-2,3-dioxigenase (tdo) inhibitor and / or indoleamine-2,3dioxigenase (acid) or a pharmaceutically acceptable salt thereof for the manufacture of a medicinal product
WO2017123826A1 (en) 2016-01-14 2017-07-20 Beth Israel Deaconess Medical Center, Inc. Mast-cell modulators and uses thereof
US10858319B2 (en) 2016-10-03 2020-12-08 Iomet Pharma Ltd. Indole derivatives for use in medicine
GB201704476D0 (en) 2017-03-21 2017-05-03 Antabio Sas Chemical compounds
AU2021215709A1 (en) 2020-02-04 2022-09-01 Mindset Pharma Inc. 3-pyrrolidine-indole derivatives as serotonergic psychedelic agents for the treatment of CNS disorders

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7196111B2 (en) * 2002-06-04 2007-03-27 Schering Corporation Pyrazolo[1,5a]pyrimidine compounds as antiviral agents

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7196111B2 (en) * 2002-06-04 2007-03-27 Schering Corporation Pyrazolo[1,5a]pyrimidine compounds as antiviral agents

Also Published As

Publication number Publication date
WO2008036967A2 (en) 2008-03-27

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