956105-76-3Relevant articles and documents
Discovery of novel FabF ligands inspired by platensimycin by integrating structure-based design with diversity-oriented synthetic accessibility
Fisher, Martin,Basak, Ramkrishna,Kalverda, Arnout P.,Fishwick, Colin W. G.,Bruce Turnbull,Nelson, Adam
, p. 486 - 494 (2014/01/06)
An approach for designing bioactive small molecules has been developed in which de novo structure-based ligand design (SBLD) was focused on regions of chemical space accessible using a diversity-oriented synthetic approach. The approach was exploited in the design and synthesis of a focused library of platensimycin analogues in which the complex bridged ring system was replaced with a series of alternative ring systems. The affinity of the resulting compounds for the C163Q mutant of FabF was determined using a WaterLOGSY competition binding assay. Several compounds had significantly improved affinity for the protein relative to a reference ligand. The integration of synthetic accessibility with ligand design enabled focus to be placed on synthetically-accessible regions of chemical space that were relevant to the target protein under investigation.
An efficient entry to amino-substituted resorcylic acid derivatives for the synthesis of platensimycin and analogues
Heretsch, Philipp,Giannis, Athanassios
, p. 2614 - 2616 (2008/02/13)
An efficient entry to protected amino-substituted resorcylic acid derivatives, methyl 3- or 5-amino-2,4-bis(methoxymethoxy)benzoate, is reported. Both derivatives can be used for the synthesis of platensimycin and its analogues. Georg Thieme Verlag Stuttg
