Literature DB >> 20025647

Evaluation of mutagenic and antimutagenic properties of some bioactive xanthone derivatives using Vibrio harveyi test.

K Słoczyńska1, E Pekala, A Wajda, G Wegrzyn, H Marona.   

Abstract

AIMS: Drug safety evaluation plays an important role in the early phase of drug development, especially in the preclinical identification of compounds' biological activity. The Vibrio harveyi assay was used to assess mutagenic and antimutagenic activity of some aminoalkanolic derivatives of xanthone (1-5), which were synthesized and evaluated for their anticonvulsant and hemodynamic activities. METHODS AND
RESULTS: A novel V. harveyi assay was used to assess mutagenic and antimutagenic activity of derivatives of xanthone 1-5. Two V. harveyi strains were used: BB7 (natural isolate) and BB7M (BB7 derivative containing mucA and mucB genes on a plasmid pAB91273, products of these genes enhance error-prone DNA repair). According to the results obtained, the most beneficial mutagenic and antimutagenic profiles were observed for compounds 2 and 3. A modification of the chemical structure of compound 2 by the replacement of the hydroxy group by a chloride improved considerably the antimutagenic activity of the compound. Thus, antimutagenic potency reached a maximum with the presence of tertiary amine and chloride atom in the side chain.
CONCLUSIONS: Among the newly synthesized aminoalkanolic derivatives of xanthone with potential anticonvulsant properties, there are some compounds exhibiting in vitro antimutagenic activity. In addition, it appears that the V. harveyi assay can be applied for primary mutagenicity and antimutagenicity assessment of compounds. SIGNIFICANCE AND IMPACT OF THE STUDY: The obtained preliminary mutagenicity and antimutagenicity results encourage further search in the group of amino derivatives of xanthone as the potential antiepileptic drugs also presenting some antimutagenic potential. Furthermore, V. harveyi test may be a useful tool for compounds safety evaluation.

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Year:  2009        PMID: 20025647     DOI: 10.1111/j.1472-765X.2009.02781.x

Source DB:  PubMed          Journal:  Lett Appl Microbiol        ISSN: 0266-8254            Impact factor:   2.858


  5 in total

1.  Preliminary Safety Assessment of New Azinesulfonamide Analogs of Aripiprazole using Prokaryotic Models.

Authors:  Beata Powroźnik; Karolina Słoczyńska; Krzysztof Marciniec; Paweł Zajdel; Elżbieta Pękala
Journal:  Adv Pharm Bull       Date:  2016-09-25

2.  Preliminary mutagenicity and genotoxicity evaluation of selected arylsulfonamide derivatives of (aryloxy)alkylamines with potential psychotropic properties.

Authors:  Beata Powroźnik; Karolina Słoczyńska; Vittorio Canale; Katarzyna Grychowska; Paweł Zajdel; Elżbieta Pękala
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Review 3.  Antimutagenic compounds and their possible mechanisms of action.

Authors:  Karolina Słoczyńska; Beata Powroźnik; Elżbieta Pękala; Anna M Waszkielewicz
Journal:  J Appl Genet       Date:  2014-03-11       Impact factor: 3.240

4.  In Vitro Biotransformation, Safety, and Chemopreventive Action of Novel 8-Methoxy-Purine-2,6-Dione Derivatives.

Authors:  Małgorzata Anna Marć; Enrique Domínguez-Álvarez; Karolina Słoczyńska; Paweł Żmudzki; Grażyna Chłoń-Rzepa; Elżbieta Pękala
Journal:  Appl Biochem Biotechnol       Date:  2017-06-17       Impact factor: 2.926

5.  Evaluation of anticonvulsant and antinociceptive properties of new N-Mannich bases derived from pyrrolidine-2,5-dione and 3-methylpyrrolidine-2,5-dione.

Authors:  Anna Rapacz; Sabina Rybka; Jolanta Obniska; Kinga Sałat; Beata Powroźnik; Elżbieta Pękala; Barbara Filipek
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2015-12-09       Impact factor: 3.000

  5 in total

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