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Computerized Prediction, Synthesis, and Antimicrobial Activity of New Amino-Acid Derivatives of 2-Chloro-N-(9,10-Dioxo-9,10-Dihydroanthracen-1-Yl)Acetamide

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An Erratum to this article was published on 08 January 2015

Interaction of 2-chloro-N-(9,10-dioxo-9,10-dihydroanthracen-1-yl)acetamide with α-, β- and ω-amino acids was used to synthesize new amino-acid derivatives of 9,10-anthraquinone. Experimental testing of the antimicrobial actions of the compounds synthesized demonstrated antibacterial activity against Mycobacterium luteum and antifungal activity against Aspergillus niger and Candida tenuis. These results from experimental testing of biological activity are consistent with results obtained by predictions using the computer program PASS. The prediction identified the need for further study of the antitumor and antioxidant actions of the newly synthesized amino acid derivatives.

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Authors and Affiliations

  1. L’vov Polytechnic National University, S. Bander Street, 79013, L’vov-13, Ukraine

    V. I. Zvarich, M. V. Stasevich, O. V. Stan’ko, E. Z. Komarovskaya-Porokhnyavets & V. P. Novikov

  2. V. N. Orekhovich Science Research Institute of Biomedical Chemistry, Russian Academy of Medical Sciences, 10 Pogodinskaya Street, 119121, Moscow, Russia

    V. V. Poroikov, A. V. Rudik & A. A. Lagunin

  3. Institute of Organic Chemistry, Ukrainian National Academy of Sciences, 5 Murmanskaya Street, 02660, Kiev-94, Ukraine

    M. V. Vovk

Authors
  1. V. I. Zvarich
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  2. M. V. Stasevich
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  3. O. V. Stan’ko
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  4. E. Z. Komarovskaya-Porokhnyavets
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  5. V. V. Poroikov
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  6. A. V. Rudik
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  7. A. A. Lagunin
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  8. M. V. Vovk
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  9. V. P. Novikov
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Corresponding author

Correspondence to V. P. Novikov.

Additional information

Translated from Khimiko-Farmatsevticheskii Zhurnal, Vol. 48, No. 9, pp. 20 – 24, September, 2014.

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Zvarich, V.I., Stasevich, M.V., Stan’ko, O.V. et al. Computerized Prediction, Synthesis, and Antimicrobial Activity of New Amino-Acid Derivatives of 2-Chloro-N-(9,10-Dioxo-9,10-Dihydroanthracen-1-Yl)Acetamide. Pharm Chem J 48, 582–586 (2014). https://doi.org/10.1007/s11094-014-1154-z

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  • DOI: https://doi.org/10.1007/s11094-014-1154-z

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