Please use this identifier to cite or link to this item: http://repositorio.unifesp.br/handle/11600/34797
Title: A tellurium-based cathepsin B inhibitor: Molecular structure, modelling, molecular docking and biological evaluation
Authors: Caracelli, Ignez
Vega-Teijido, Mauricio
Zukerman-Schpector, Julio
Cezari, Maria H. S. [UNIFESP]
Lopes, Jose G. S.
Juliano, Luiz [UNIFESP]
Santos, Paulo S.
Comasseto, Joao V.
Cunha, Rodrigo L. O. R. [UNIFESP]
Tiekink, Edward R. T.
Universidade Federal de São Carlos (UFSCar)
Universidade de São Paulo (USP)
Universidade Federal de São Paulo (UNIFESP)
Univ Fed Juiz de Fora
Universidade Federal do ABC (UFABC)
Univ Malaya
Keywords: Tellurium
Cathepsin B
X-ray crystal structure
Molecular modelling
Docking
Structure-activity relationships
Issue Date: 11-Apr-2012
Publisher: Elsevier B.V.
Citation: Journal of Molecular Structure. Amsterdam: Elsevier B.V., v. 1013, p. 11-18, 2012.
Abstract: The crystallographically determined structure of biologically active 4,4-dichloro-1,3-diphenyl-4-telluraoct-2-en-1-one, 3, shows the coordination geometry for Te to be distorted psi-pentagonal bipyramidal based on a C2OCl3(lone pair) donor set. Notable is the presence of an intramolecular axial Te center dot center dot center dot O (carbonyl) interaction, a design element included to reduce hydrolysis. Raman and molecular modelling studies indicate the persistence of the Te center dot center dot center dot O(carbonyl) interaction in the solution (CHCl3) and gasphases, respectively. Docking studies of 3' (i.e. original 3 less one chloride) with Cathepsin B reveals a change in the configuration about the vinyl C = C bond. i.e. to E from Z (crystal structure). This isomerism allows the optimisation of interactions in the complex which features a covalent Te-SGCys29 bond. Crucially, the E configuration observed for 3' allows for the formation of a hypervalent Te center dot center dot center dot O interaction as well as an O center dot center dot center dot H-O hydrogen bond with the Gly27 and Glu122 residues, respectively. Additional stabilisation is afforded by a combination of interactions spanning the S1, S2, S1' and S2' sub-sites of Cathepsin B. the greater experimental inhibitory activity of 3 compared with analogues is rationalised by the additional interactions formed between 3' and the His110 and His111 residues in the occluding loop, which serve to hinder the entrance to the active site. (C) 2012 Elsevier B.V. All rights reserved.
URI: http://repositorio.unifesp.br/handle/11600/34797
ISSN: 0022-2860
Other Identifiers: http://dx.doi.org/10.1016/j.molstruc.2012.01.008
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