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Eur J Med Chem. 2009 Mar;44(3):1230-9. doi: 10.1016/j.ejmech.2008.09.018. Epub 2008 Sep 24.

Natural polyprenylated benzophenones inhibiting cysteine and serine proteases.

Author information

1
Department of Exact Science, Federal University of Alfenas, Rua Gabriel Monteiro da Silva 714, Alfenas, MG 37130-000, Brazil. felipetmartins@yahoo.com.br

Abstract

We have investigated the in vitro inhibition of papain, trypsin, and cathepsins B and G by five benzophenone-type compounds, three natural ones isolated from Garcinia brasiliensis and two synthetic derivatives. The activities of pentaprenylated trihydroxy-substituted benzophenone guttiferone A (1) on all assayed enzymes were approximately 2-69 folds higher than that manifested by mono-hydroxylated tetraprenylated and triprenylated compounds epiclusianone (2) and garciniaphenone (3), respectively, the other natural benzophenones that also inhibited significantly the four enzymes. Differently, the synthetic derivatives 2,2',4-trihydroxybenzophenone (4) and diphenylmethanone (5) have inhibited weakly the studied proteases. Furthermore, compound 1 has bonded preferentially to cathepsin G, once its IC(50) value (2.7+/-0.1 microM) on such peptidase is quite similar to that of the classical inhibitor of serine proteases, chymostatin (2.1+/-0.1 microM). Interesting structure-activity relationships (SARs) were confirmed by flexible docking simulations, likewise the potential usefulness of natural compound 1 as antitumoral drug is strengthened by our results concerning the antiproteolytic activity.

PMID:
18995931
DOI:
10.1016/j.ejmech.2008.09.018
[Indexed for MEDLINE]

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