Design and synthesis of a novel series of [1-(4-hydroxy-benzyl)-1H-indol-5-yloxy]-acetic acid compounds as potent, selective, thyroid hormone receptor β agonists.
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| Title: | Design and synthesis of a novel series of [1-(4-hydroxy-benzyl)-1H-indol-5-yloxy]-acetic acid compounds as potent, selective, thyroid hormone receptor β agonists. |
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| Authors: | Burkholder TP; Discovery Chemistry Research and Technology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA., Cunningham BE; Discovery Chemistry Research and Technology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA., Clayton JR; Discovery Chemistry Research and Technology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA., Lander PA; Discovery Chemistry Research and Technology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA., Brown ML; Discovery Chemistry Research and Technology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA., Doti RA; Discovery Chemistry Research and Technology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA., Durst GL; Discovery Chemistry Research and Technology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA., Montrose-Rafizadeh C; Lead Optimization Biology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA., King C; Lead Optimization Biology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA., Osborne HE; Lead Optimization Biology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA., Amos RM; Lead Optimization Biology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA., Zink RW; Lead Optimization Biology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA., Stramm LE; Lead Optimization Biology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA., Burris TP; Bone and Inflammation Therapeutic Area, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA., Cardona G; Bone and Inflammation Therapeutic Area, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA., Konkol DL; Diabetes Therapeutic Area, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA., Reidy C; Diabetes Therapeutic Area, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA., Christe ME; Diabetes Therapeutic Area, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA., Genin MJ; Discovery Chemistry Research and Technology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA. Electronic address: geninmi@lilly.com. |
| Source: | Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2015 Apr 01; Vol. 25 (7), pp. 1377-80. Date of Electronic Publication: 2015 Mar 03. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Elsevier Science Ltd Country of Publication: England NLM ID: 9107377 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1464-3405 (Electronic) Linking ISSN: 0960894X NLM ISO Abbreviation: Bioorg Med Chem Lett Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 25752984 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Design and synthesis of a novel series of [1-(4-hydroxy-benzyl)-1H-indol-5-yloxy]-acetic acid compounds as potent, selective, thyroid hormone receptor β agonists. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Burkholder+TP%22">Burkholder TP</searchLink>; Discovery Chemistry Research and Technology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.<br /><searchLink fieldCode="AU" term="%22Cunningham+BE%22">Cunningham BE</searchLink>; Discovery Chemistry Research and Technology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.<br /><searchLink fieldCode="AU" term="%22Clayton+JR%22">Clayton JR</searchLink>; Discovery Chemistry Research and Technology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.<br /><searchLink fieldCode="AU" term="%22Lander+PA%22">Lander PA</searchLink>; Discovery Chemistry Research and Technology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.<br /><searchLink fieldCode="AU" term="%22Brown+ML%22">Brown ML</searchLink>; Discovery Chemistry Research and Technology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.<br /><searchLink fieldCode="AU" term="%22Doti+RA%22">Doti RA</searchLink>; Discovery Chemistry Research and Technology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.<br /><searchLink fieldCode="AU" term="%22Durst+GL%22">Durst GL</searchLink>; Discovery Chemistry Research and Technology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.<br /><searchLink fieldCode="AU" term="%22Montrose-Rafizadeh+C%22">Montrose-Rafizadeh C</searchLink>; Lead Optimization Biology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.<br /><searchLink fieldCode="AU" term="%22King+C%22">King C</searchLink>; Lead Optimization Biology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.<br /><searchLink fieldCode="AU" term="%22Osborne+HE%22">Osborne HE</searchLink>; Lead Optimization Biology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.<br /><searchLink fieldCode="AU" term="%22Amos+RM%22">Amos RM</searchLink>; Lead Optimization Biology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.<br /><searchLink fieldCode="AU" term="%22Zink+RW%22">Zink RW</searchLink>; Lead Optimization Biology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.<br /><searchLink fieldCode="AU" term="%22Stramm+LE%22">Stramm LE</searchLink>; Lead Optimization Biology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.<br /><searchLink fieldCode="AU" term="%22Burris+TP%22">Burris TP</searchLink>; Bone and Inflammation Therapeutic Area, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.<br /><searchLink fieldCode="AU" term="%22Cardona+G%22">Cardona G</searchLink>; Bone and Inflammation Therapeutic Area, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.<br /><searchLink fieldCode="AU" term="%22Konkol+DL%22">Konkol DL</searchLink>; Diabetes Therapeutic Area, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.<br /><searchLink fieldCode="AU" term="%22Reidy+C%22">Reidy C</searchLink>; Diabetes Therapeutic Area, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.<br /><searchLink fieldCode="AU" term="%22Christe+ME%22">Christe ME</searchLink>; Diabetes Therapeutic Area, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.<br /><searchLink fieldCode="AU" term="%22Genin+MJ%22">Genin MJ</searchLink>; Discovery Chemistry Research and Technology, Lilly Research Laboratories, A Division of Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA. Electronic address: geninmi@lilly.com. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229107377%22">Bioorganic & medicinal chemistry letters</searchLink> [Bioorg Med Chem Lett] 2015 Apr 01; Vol. 25 (7), pp. 1377-80. <i>Date of Electronic Publication: </i>2015 Mar 03. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Elsevier+Science+Ltd%22">Elsevier Science Ltd </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9107377 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1464-3405 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%220960894X%22">0960894X </searchLink><i>NLM ISO Abbreviation: </i>Bioorg Med Chem Lett <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=25752984 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.bmcl.2015.02.062 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 1377 Titles: – TitleFull: Design and synthesis of a novel series of [1-(4-hydroxy-benzyl)-1H-indol-5-yloxy]-acetic acid compounds as potent, selective, thyroid hormone receptor β agonists. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Burkholder TP – PersonEntity: Name: NameFull: Cunningham BE – PersonEntity: Name: NameFull: Clayton JR – PersonEntity: Name: NameFull: Lander PA – PersonEntity: Name: NameFull: Brown ML – PersonEntity: Name: NameFull: Doti RA – PersonEntity: Name: NameFull: Durst GL – PersonEntity: Name: NameFull: Montrose-Rafizadeh C – PersonEntity: Name: NameFull: King C – PersonEntity: Name: NameFull: Osborne HE – PersonEntity: Name: NameFull: Amos RM – PersonEntity: Name: NameFull: Zink RW – PersonEntity: Name: NameFull: Stramm LE – PersonEntity: Name: NameFull: Burris TP – PersonEntity: Name: NameFull: Cardona G – PersonEntity: Name: NameFull: Konkol DL – PersonEntity: Name: NameFull: Reidy C – PersonEntity: Name: NameFull: Christe ME – PersonEntity: Name: NameFull: Genin MJ IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 04 Text: 2015 Apr 01 Type: published Y: 2015 Identifiers: – Type: issn-electronic Value: 1464-3405 Numbering: – Type: volume Value: 25 – Type: issue Value: 7 Titles: – TitleFull: Bioorganic & medicinal chemistry letters Type: main |
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