Crystallographic and docking (Cathepsins B, K, L and S) studies on bioactive halotelluroxetanes
| Autor: | Mauricio Vega-Teijido, Ignez Caracelli, Stella H. Maganhi, Josiane de Oliveira Cardoso, Rodrigo L. O. R. Cunha, Julio Zukerman-Schpector, Edward R. T. Tiekink |
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| Rok vydání: | 2017 |
| Předmět: |
0301 basic medicine
biology 010405 organic chemistry Chemistry Supramolecular chemistry Halide Condensed Matter Physics 01 natural sciences 0104 chemical sciences Inorganic Chemistry Cathepsin L 03 medical and health sciences Crystallography 030104 developmental biology Docking (molecular) Covalent bond X-ray crystallography Halogen biology.protein General Materials Science Cysteine |
| Zdroj: | Zeitschrift für Kristallographie - Crystalline Materials. 233:113-124 |
| ISSN: | 2196-7105 2194-4946 |
| DOI: | 10.1515/zkri-2017-2079 |
| Popis: | The molecular structures of the halotelluroxetanes p-MeOC6H4Te(X)[C(=C(H)X′)C(CH2)nO], X=X′=Cl and n=6 (1) and X=Cl, X′=Br and n=5 (4), show similar binuclear aggregates sustained by {· · ·Te–O}2 cores comprising covalent Te–O and secondary Te· · ·O interactions. The resulting C2ClO2(lone-pair) sets define pseudo-octahedral geometries. In each structure, C–X· · ·π(arene) interactions lead to supramolecular layers. Literature studies have shown these and related compounds (i.e. 2: X=X′=Cl and n=5; 3: X=X′=Br and n=5) to inhibit Cathepsins B, K, L and S to varying extents. Molecular docking calculations have been conducted on ligands (i.e. cations derived by removal of the tellurium-bound X atoms) 1′–3′ (note 3′=4′) enabling correlations between affinity for sub-sites and inhibition. The common feature of all docked complexes was the formation of a Te–S covalent bond with cysteine residues, the relative stability of the ligands with an E-configuration and the formation of a C–O· · ·π interaction with the phenyl ring; for 1′ the Te–S covalent bond was weak, a result correlating with its low inhibition profile. At the next level differences are apparent, especially with respect to the interactions formed by the organic-ligand-bound halides. While these atoms do not form specific interactions in Cathepsins B and K, in Cathepsin L, these halides are involved in C–O· · ·X halogen bonds. |
| Databáze: | OpenAIRE |
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