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Bioorg Med Chem. 2017 Jan 1;25(1):132-137. doi: 10.1016/j.bmc.2016.10.019. Epub 2016 Oct 17.

Antibacterial profiling of abietane-type diterpenoids.

Author information

1
Centre for Drug Research, Division of Pharmaceutical Biosciences, Faculty of Pharmacy, Viikinkaari 5 E (PO Box 56), FI-00014 University of Helsinki, Helsinki, Finland.
2
Division of Pharmaceutical Chemistry and Technology, Faculty of Pharmacy, Viikinkaari 5 E (PO Box 56), FI-00014 University of Helsinki, Helsinki, Finland.
3
Pharmacognosy Department, Faculty of Pharmacy, Anadolu University, 26470 Eskişehir, Turkey.
4
Division of Pharmaceutical Chemistry and Technology, Faculty of Pharmacy, Viikinkaari 5 E (PO Box 56), FI-00014 University of Helsinki, Helsinki, Finland. Electronic address: vania.moreira@helsinki.fi.
5
Centre for Drug Research, Division of Pharmaceutical Biosciences, Faculty of Pharmacy, Viikinkaari 5 E (PO Box 56), FI-00014 University of Helsinki, Helsinki, Finland. Electronic address: paivi.tammela@helsinki.fi.

Abstract

Abietic and dehydroabietic acid are interesting diterpenes with a highly diverse repertoire of associated bioactivities. They have, among others, shown antibacterial and antifungal activity, potentially valuable in the struggle against the increasing antimicrobial resistance and imminent antibiotic shortage. In this paper, we describe the synthesis of a set of 9 abietic and dehydroabietic acid derivatives containing amino acid side chains and their in vitro antimicrobial profiling against a panel of human pathogenic microbial strains. Furthermore, their in vitro cytotoxicity against mammalian cells was evaluated. The experimental results showed that the most promising compound was 10 [methyl N-(abiet-8,11,13-trien-18-yl)-d-serinate], with an MIC90 of 60μg/mL against Staphylococcus aureus ATCC 25923, and 8μg/mL against methicillin-resistant S. aureus, Staphylococcus epidermidis and Streptococcus mitis. The IC50 value for compound 10 against Balb/c 3T3 cells was 45μg/mL.

KEYWORDS:

Abietic acid; Amino acid derivative; Bacteria; Cytotoxicity; Dehydroabietic acid; Fungi

PMID:
27793449
DOI:
10.1016/j.bmc.2016.10.019
[Indexed for MEDLINE]

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