1199810-63-3Relevant academic research and scientific papers
High-affinity inhibitors of tRNA-guanine transglycosylase replacing the function of a structural water cluster
Kohler, Philipp C.,Ritschel, Tina,Bernd Schweizer,Klebe, Gerhard,Diederich, Francois
, p. 10809 - 10817 (2009)
The tRNA-modifying enzyme tRNA-guanine transglycosylase (TGT) is essential for the pathogenic mechanism of Shigella flexneri, the causing agent of the bacterial diarrheal disease shigellosis. Herein, the synthesis of a new class of rationally designed 6-amino-imidazo[4,5-g]quinazolin-8(7H)-one- (lim-benzoguanine) based inhibitors of TGT are reported. In order to accommodate a small hydrophobic crevice opening near the binding site of ribose-34, 2-aminoethyl substituents were introduced in position 4 of the heterocyclic scaffold. For this purpose, a synthetic sequence consisting of iodination, Suzuki cross-coupling, hydroboration, Mitsunobu reaction, and Gabriel synthesis was employed, furnishing a primary amine that served as a common intermediate for the preparation of a series of derivatives. The resulting ligands displayed very low inhibition constants, down to Ki = 2nM. Substantial additional inhibitory potency is gained by interaction of terminal lipophilic groups attached to the substituent at position 4 with the hydrophobic crevice shaped by Val45 and Leu68. At the same time, the secondary ammonium center in the substituent displaces a cluster of water molecules, solvating the catalytic residues Asp102 and Asp280, without loss in binding affinity. In addition, a synthetic intermediate with an unusual 3,6,7,8,9,10-hexahydroimidazo[4,5-g][1,3] benzodiazepine core, as confirmed by X-ray analysis, is reported.
