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A tellurium-based cathepsin B inhibitor: Molecular structure, modelling, molecular docking and biological evaluation
  • Universidade Federal de São Carlos (UFSCar)
  • Universidade Estadual Paulista (UNESP)
  • Universidade Federal de São Paulo (UNIFESP)
  • Universidade Federal de Juiz de Fora (UFJF)
  • Universidade de São Paulo (USP)
  • Universidade Federal do ABC (UFABC)
  • Univ Malaya
  • Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
  • Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
  • Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
  • Ministry of Higher Education (Malaysia)
Sponsorship Process Number: 
  • CAPES: 808/2009
  • CNPq: 308116/2010-0
  • CNPq: 306532/2009-3
  • FAPESP: 06/56078-4
  • FAPESP: 07/52734-7
  • Ministry of Higher Education (Malaysia): UM.C/HIR/MOHE/SC/12
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.
Issue Date: 
Journal of Molecular Structure. Amsterdam: Elsevier B.V., v. 1013, p. 11-18, 2012.
Elsevier B.V.
  • Tellurium
  • Cathepsin B
  • X-ray crystal structure
  • Molecular modelling
  • Docking
  • Structure-activity relationships
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Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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