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1.
Biochem Biophys Res Commun ; 466(3): 418-25, 2015 Oct 23.
Article in English | MEDLINE | ID: mdl-26365353

ABSTRACT

Dihydroxynaphthyl aryl ketones 1-5 have been evaluated for their abilities to inhibit microtubule assembly and the binding to tubulin. Compounds 3, 4 and 5 displayed competitive inhibition against colchicine binding, and docking analysis showed that they bind to the tubulin colchicine-binding pocket inducing sheets instead of microtubules. Remarkable differences in biological activity observed among the assayed compounds seem to be related to the structure and position of the aryl substituent bonded to the carbonyl group. Compounds 2, 3 and 4, which contain a heterocyclic ring, presented higher affinity for tubulin compared to the carbocyclic analogue 5. Compound 4 showed the best affinity of the series, with an IC50 value of 2.1 µM for microtubule polymerization inhibition and a tubulin dissociation constant of 1.0 ± 0.2 µM, as determined by thermophoresis. Compound 4 was more efficacious in disrupting microtubule assembly in vitro than compound 5 although it contains the trimethoxyphenyl ring present in colchicine. Hydrogen bonds with Asn101 of α-tubulin seem to be responsible for the higher affinity of compound 4 respects to the others.


Subject(s)
Colchicine/metabolism , Ketones/metabolism , Microtubules/metabolism , Tubulin/metabolism , Animals , Binding Sites , Binding, Competitive , Chickens , Colchicine/pharmacology , Hydrogen Bonding , Ketones/chemistry , Ketones/pharmacology , Kinetics , Microtubules/drug effects , Models, Molecular , Molecular Dynamics Simulation , Protein Binding , Structure-Activity Relationship , Tubulin Modulators/metabolism , Tubulin Modulators/pharmacology
2.
Nat Prod Commun ; 7(5): 611-4, 2012 May.
Article in English | MEDLINE | ID: mdl-22799089

ABSTRACT

Parastrephia lepidophylla, family Asteraceae, has ancient use in traditional medicine in the region of Tarapacá, Chile. Bioguided fractionation of extracts of this plant was undertaken in the search for compounds with analgesic and antioxidant activity. Two benzofuran derivatives were isolated as the major components of this plant, identified as tremetone 1 and methoxytremetone 6. Remarkably, neither of these showed antioxidant activity, but tremetone 1 exhibited a morphine-like analgesic property. Reduction of this analgesic effect by naloxone suggests a direct effect on opiate receptors as a possible signaling pathway. However, both the low diffusion across lipid membranes (PAMPA assay) and the lipophilicity (Log P) shown by tremetone 1 make elusive the mechanism explaining its induced analgesia.


Subject(s)
Analgesics/pharmacology , Asteraceae/chemistry , Benzofurans/pharmacology , Plant Extracts/pharmacology , Animals , Benzofurans/isolation & purification , Chile , Humans , Male , Medicine, Traditional , Rats , Rats, Sprague-Dawley
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