Home Fluorides 660868-91-7
660868-91-7,MFCD09971143
Catalog No.:AA00FBX8

660868-91-7 | GW843682, 5-(5,6-Dimethoxy-1H-benzimidazol-1-yl)-3-{[2-(trifluoromethyl)-benzyl]oxy}thiophene-2-carboxamide

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1mg
≥98%
in stock  
$82.00   $57.00
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5mg
≥98%
in stock  
$188.00   $132.00
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10mg
≥98%
in stock  
$281.00   $197.00
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25mg
≥98%
in stock  
$532.00   $373.00
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50mg
≥98%
in stock  
$897.00   $628.00
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100mg
≥98%
in stock  
$1,177.00   $824.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00FBX8
Chemical Name:
GW843682, 5-(5,6-Dimethoxy-1H-benzimidazol-1-yl)-3-{[2-(trifluoromethyl)-benzyl]oxy}thiophene-2-carboxamide
CAS Number:
660868-91-7
Molecular Formula:
C22H18F3N3O4S
Molecular Weight:
477.4562
MDL Number:
MFCD09971143
SMILES:
COc1cc2c(cc1OC)ncn2c1cc(c(s1)C(=O)N)OCc1ccccc1C(F)(F)F
Properties
Properties
 
Form:
Solid  

Computed Properties
 
Complexity:
688  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
33  
Hydrogen Bond Acceptor Count:
9  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
7  
XLogP3:
4.6  

Downstream Synthesis Route
660868-91-7   
5-(5,6-dimethoxy-1H-benzimidazol-1-yl)-3-2-(trifluoromethyl)benzyloxy}thiophene-2-carbothioamide 

[1]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-WO2004/14899,2004,A1Locationinpatent:Page178

[2]Locationinpatent:schemeortableEmmitte,KyleA.;Andrews,C.Webb;Badiang,JenniferG.;Davis-Ward,RondaG.;Dickson,HamiltonD.;Drewry,DavidH.;Emerson,HollyK.;Epperly,AndreaH.;Hassler,DanielF.;Knick,VictoriaB.;Kuntz,KevinW.;Lansing,TimothyJ.;Linn,JamesA.;MookJr.,RobertA.;Nailor,KristenE.;Salovich,JamesM.;Spehar,GlennM.;Cheung,Mui[BioorganicandMedicinalChemistryLetters,2009,vol.19,#3,p.1018-1021]

[1]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-WO2004/14899,2004,A1Locationinpatent:Page179

[2]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-WO2005/75465,2005,A1Locationinpatent:Page/Pagecolumn31-32

[3]Locationinpatent:schemeortableEmmitte,KyleA.;Andrews,C.Webb;Badiang,JenniferG.;Davis-Ward,RondaG.;Dickson,HamiltonD.;Drewry,DavidH.;Emerson,HollyK.;Epperly,AndreaH.;Hassler,DanielF.;Knick,VictoriaB.;Kuntz,KevinW.;Lansing,TimothyJ.;Linn,JamesA.;MookJr.,RobertA.;Nailor,KristenE.;Salovich,JamesM.;Spehar,GlennM.;Cheung,Mui[BioorganicandMedicinalChemistryLetters,2009,vol.19,#3,p.1018-1021]

methyl5-(5,6-dimethoxy-1H-benzimidazol-1-yl)-3-(2-trifluoromethylbenzyl)oxythiophene-2-carboxylate 
  660868-91-7 

[1]Locationinpatent:schemeortableEmmitte,KyleA.;Andrews,C.Webb;Badiang,JenniferG.;Davis-Ward,RondaG.;Dickson,HamiltonD.;Drewry,DavidH.;Emerson,HollyK.;Epperly,AndreaH.;Hassler,DanielF.;Knick,VictoriaB.;Kuntz,KevinW.;Lansing,TimothyJ.;Linn,JamesA.;MookJr.,RobertA.;Nailor,KristenE.;Salovich,JamesM.;Spehar,GlennM.;Cheung,Mui[BioorganicandMedicinalChemistryLetters,2009,vol.19,#3,p.1018-1021]

Literature

Title: Identification of potent Yes1 kinase inhibitors using a library screening approach.

Journal: Bioorganic & medicinal chemistry letters 20130801

Title: Raptor, a positive regulatory subunit of mTOR complex 1, is a novel phosphoprotein of the rDNA transcription machinery in nucleoli and chromosomal nucleolus organizer regions (NORs).

Journal: Cell cycle (Georgetown, Tex.) 20110915

Title: An in-vitro evaluation of the polo-like kinase inhibitor GW843682X against paediatric malignancies.

Journal: Anti-cancer drugs 20110701

Title: Targeting Plk1 in cutaneous T-cell lymphomas (CTCLs).

Journal: Cell cycle (Georgetown, Tex.) 20110515

Title: Polo-like kinase 1 (Plk1) is expressed by cutaneous T-cell lymphomas (CTCLs), and its downregulation promotes cell cycle arrest and apoptosis.

Journal: Cell cycle (Georgetown, Tex.) 20110415

Title: Polo-like kinase 1 regulates activation of AMP-activated protein kinase (AMPK) at the mitotic apparatus.

Journal: Cell cycle (Georgetown, Tex.) 20110415

Title: Polo-like kinase 1 enhances survival and mutagenesis after genotoxic stress in normal cells through cell cycle checkpoint bypass.

Journal: Carcinogenesis 20100501

Title: Polo-like kinase guides cytokinesis in Trypanosoma brucei through an indirect means.

Journal: Eukaryotic cell 20100501

Title: A novel treatment strategy targeting polo-like kinase 1 in hematological malignancies.

Journal: Leukemia 20090901

Title: Design of potent thiophene inhibitors of polo-like kinase 1 with improved solubility and reduced protein binding.

Journal: Bioorganic & medicinal chemistry letters 20090315

Title: Discovery of thiophene inhibitors of polo-like kinase.

Journal: Bioorganic & medicinal chemistry letters 20090201

Title: Evaluation of Polo-like Kinase 1 inhibition on the G2/M checkpoint in Acute Myelocytic Leukaemia.

Journal: European journal of pharmacology 20080904

Title: In vitro biological activity of a novel small-molecule inhibitor of polo-like kinase 1.

Journal: Molecular cancer therapeutics 20070201

Title: Lansing TJ, et al. In vitro biological activity of a novel small-molecule inhibitor of polo-like kinase 1. Mol Cancer Ther. 2007 Feb;6(2):450-9. Epub 2007 Jan 31.

Title: Didier C, et al. Evaluation of Polo-like Kinase 1 inhibition on the G2/M checkpoint in Acute Myelocytic Leukaemia. Eur J Pharmacol. 2008 Sep 4;591(1-3):102-5.

Title: Ikezoe T, et al. A novel treatment strategy targeting polo-like kinase 1 in hematological malignancies. Leukemia. 2009 Sep;23(9):1564-76.

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SDS
Tags:660868-91-7 Molecular Formula|660868-91-7 MDL|660868-91-7 SMILES|660868-91-7 GW843682, 5-(5,6-Dimethoxy-1H-benzimidazol-1-yl)-3-{[2-(trifluoromethyl)-benzyl]oxy}thiophene-2-carboxamide