114998-55-9Relevant articles and documents
Optimisation of the P2 pharmacophore in a series of thrombin inhibitors: Ion-dipole interactions with lysine 60G
Ambler, John,Brown, Lyndon,Cockcroft, Xiao-Ling,Gruetter, Markus,Hayler, Judy,Janus, Diana,Jones, Darryl,Kane, Peter,Menear, Keith,Priestle, John,Smith, Garrick,Talbot, Mark,Walker V, Clive,Wathey, Bernard
, p. 1317 - 1322 (2007/10/03)
The optimisation of the P2 pharmacophore in a series of thrombin inhibitors is described. The interaction of a number of piperidine P2 functionalities with lysine 60G of thrombin is explored with reference to the crystal structure of inhibitor enzyme complexes. A primary ion-dipole interaction between the terminal P2 side chain group and lysine 60G is evoked to explain the SAR in this series.