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Author Smyth, L.A.; Matthews, T.P.; Collins, I. openurl 
  Title (up) Type Journal Article
  Year Publication Abbreviated Journal Bioorganic & medicinal chemistry  
  Volume Issue Pages  
  Keywords Binding Sites Computer Simulation Drug Design Humans Indoles/chemistry Protein Kinase Inhibitors/chemical synthesis/*chemistry/pharmacology Protein Kinases/*chemistry/metabolism Pyridones/chem  
  Abstract A lead-like kinase inhibitor screening library containing new 3-aminopyrazolopyridinones and closely related compounds was designed that contained hydrogen-bond donor-acceptor motifs and substitution vectors inspired by the natural product kinase inhibitor indirubin. The solubility of the 3-aminopyrazolopyridinone scaffold was more than 1000-fold greater than that of indirubin itself, and solubility was enhanced by reduction of the proportion of lipophilic aryl substituents or the introduction of basic groups. Several components of the library showed kinase inhibitory activity. A subset of diaryl-substituted analogues preferentially inhibited tyrosine kinases with low micromolar activity and good ligand efficiency, and showed cellular antiproliferative activity. The evaluation of the library shows that new, non-natural compounds with relevant biological activity and improved physicochemical properties can be generated from the natural product indirubin, providing compounds that may be useful for kinase inhibitor drug discovery.  
  Address Cancer Research UK Cancer Therapeutics Unit, The Institute of Cancer Research, Belmont, Surrey SM2 5NG, UK.  
  Corporate Author Thesis  
  Publisher Place of Publication Editor  
  Language Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN ISBN Medium  
  Area Expedition Conference  
  Notes Approved no  
  Call Number refbase @ user @ Serial 12903  
Permanent link to this record
 

 
Author Smyth, L.A.; Matthews, T.P.; Collins, I. openurl 
  Title (up) Type Journal Article
  Year Publication Abbreviated Journal Bioorganic & medicinal chemistry  
  Volume Issue Pages  
  Keywords Binding Sites Computer Simulation Drug Design Humans Indoles/chemistry Protein Kinase Inhibitors/chemical synthesis/*chemistry/pharmacology Protein Kinases/*chemistry/metabolism Pyridones/chem  
  Abstract A lead-like kinase inhibitor screening library containing new 3-aminopyrazolopyridinones and closely related compounds was designed that contained hydrogen-bond donor-acceptor motifs and substitution vectors inspired by the natural product kinase inhibitor indirubin. The solubility of the 3-aminopyrazolopyridinone scaffold was more than 1000-fold greater than that of indirubin itself, and solubility was enhanced by reduction of the proportion of lipophilic aryl substituents or the introduction of basic groups. Several components of the library showed kinase inhibitory activity. A subset of diaryl-substituted analogues preferentially inhibited tyrosine kinases with low micromolar activity and good ligand efficiency, and showed cellular antiproliferative activity. The evaluation of the library shows that new, non-natural compounds with relevant biological activity and improved physicochemical properties can be generated from the natural product indirubin, providing compounds that may be useful for kinase inhibitor drug discovery.  
  Address Cancer Research UK Cancer Therapeutics Unit, The Institute of Cancer Research, Belmont, Surrey SM2 5NG, UK.  
  Corporate Author Thesis  
  Publisher Place of Publication Editor  
  Language Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN ISBN Medium  
  Area Expedition Conference  
  Notes Approved no  
  Call Number refbase @ user @ Serial 12942  
Permanent link to this record
 

 
Author openurl 
  Title (up) Type Book Whole
  Year 1978 Publication Abbreviated Journal  
  Volume Issue Pages  
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  Corporate Author Thesis  
  Publisher Crkva u svijetu Place of Publication Split Editor  
  Language Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN ISBN Medium  
  Area Expedition Conference  
  Notes Approved no  
  Call Number refbase @ admin @ Serial 13116  
Permanent link to this record
 

 
Author openurl 
  Title (up) Type Conference Article
  Year 1977 Publication Abbreviated Journal  
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  Address  
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  Publisher Republièka konferencija SSRN BiH Place of Publication Sarajevo Editor  
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  Notes Proceedings Title: Socijalistièki savez radnog naroda Bosne i Hercegovine u ostvarivanju politike u odnosu na religiju i djelovanje vjerskih zajednica. Savjetovanje predsjednika opštinskih, Gradske i meðuopštinskih konferencija Socijalistièkog saveza radnog naroda Bosne i Hercegovine, Sarajevo, 1977 Approved no  
  Call Number refbase @ admin @ Serial 13148  
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Author openurl 
  Title (up) Type Conference Article
  Year 1986 Publication Abbreviated Journal  
  Volume Issue Pages  
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  Address  
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  Publisher Kršæanska sadašnjost. Place of Publication Zagreb Editor  
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  Notes Proceedings Title: Evangelizirati “sekulariziranu Evropu” : šesti simpozij evropskih biskupa, Rim, 7-11. listopada 1985 Approved no  
  Call Number refbase @ admin @ Serial 13149  
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