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Medicinal Chemistry

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ISSN (Print): 1573-4064
ISSN (Online): 1875-6638

Research Article

Antibacterial Evaluation of Novel Substituted Cycloheptaindoles in Staphylococcus and Enterococcus Strains

Author(s): Andreas Hilgeroth*, Kaveh Yasrebi, Sibel Suzen, Tobias Hertlein, Knut Ohlsen and Michael Lalk

Volume 15, Issue 8, 2019

Page: [833 - 839] Pages: 7

DOI: 10.2174/1573406415666190208170126

Price: $65

Abstract

Background: Due to emerging resistances against antibiotics there is a strong need to find novel antibacterial agents with a novel structure to prevent early resistance developments.

Objective: Bisindole compounds with antibacterial activities which formally result from the reaction of an aldehyde with indole motivated to investigate the reaction of a dialdehyde and indole to give novel structures with potential antibacterial activities.

Methods: Compounds were yielded by chemical synthesis and purified using column chromatography. The antibacterial activity was determined as minimal inhibitory growth activity in cultures of Gram-positive strains of Staphylococcus aureus and Enterococcus species.

Results: Cyclohepta[2,3-b]indoles have been yielded in a one-step reaction procedure with indole substitutions at the cycloheptane central core matching a solution for achieving fused novel cycloalkane indoles with functionalized residues of promising biological activity. So far fused cycloalkane indoles have not been available in a one-step procedure and moreover, core functionalizations have been additional challenges. Various indole substitutions have been done to provide a first set of compounds.

Conclusion: Substituent-dependent effects have been suggested to influence the antibacterial activity and first compounds were identified with specific Staphylococcus activities and Enterococcus species effects towards Enterococcus faecalis as critical pathogens in the hospital with upcoming resistances against standard antibiotics.

Keywords: One-step procedure, fused indole, structure-activity relationships, antibacterial, Staphylococcus aureus, Enterococcus.

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[1]
Buckland, D. Antimicrobial resistance and the race to find new antibiotics. Prescriber, 2017, 28, 12-15.
[http://dx.doi.org/10.1002/psb.1528]
[2]
Ventola, C.L. The antibiotic resistance crisis: Part 1: Causes and threats. P T, 2015, 40(4), 277-283.
[PMID: 25859123]
[3]
Michael, C.A.; Dominey-Howes, D.; Labbate, M. The antimicrobial resistance crisis: Causes, consequences, and management. Front. Public Health, 2014, 2, 145.
[http://dx.doi.org/10.3389/fpubh.2014.00145] [PMID: 25279369]
[4]
Gothwal, R.; Thatikonda, S. Role of environmental pollution in prevalence of antibiotic resistant bacteria in aquatic environment of river: case of Musi river, South India. Water Envir. J., 2017, 31, 456-462.
[5]
Center For Disease Control and Prevention, Office of Infectious Disease.. Antibiotic resistance threats in the United States Available at: http://www.cdc.gov/drugresistance/threat-report-20132018.
[6]
Bartlett, J.G.; Gilbert, D.N.; Spellberg, B. Seven ways to preserve the miracle of antibiotics. Clin. Infect. Dis., 2013, 56(10), 1445-1450.
[http://dx.doi.org/10.1093/cid/cit070] [PMID: 23403172]
[7]
Imhoff, J.F. Natural Products from Marine Fungi--Still an Underrepresented Resource. Mar. Drugs, 2016, 14(1), 19.
[http://dx.doi.org/10.3390/md14010019] [PMID: 26784209]
[8]
Biswas, K.; Paul, D.; Sinha, S.N. Marine Bacteria: A Potential Tool for Antibacterial Activity. J. Appl. Envir. Microbiol., 2016, 4, 25-29.
[9]
Paudel, A.; Hamamoto, H.; Kobayashi, Y.; Yokoshima, S.; Fukuyama, T.; Sekimizu, K. Identification of novel deoxyribofuranosyl indole antimicrobial agents. J. Antibiot. (Tokyo), 2012, 65(2), 53-57.
[http://dx.doi.org/10.1038/ja.2011.110] [PMID: 22167161]
[10]
Cushnie, T.P.T.; Cushnie, B.; Lamb, A.J. Alkaloids: An overview of their antibacterial, antibiotic-enhancing and antivirulence activities. Int. J. Antimicrob. Agents, 2014, 44(5), 377-386.
[http://dx.doi.org/10.1016/j.ijantimicag.2014.06.001] [PMID: 25130096]
[11]
Silver, L.L. Challenges of antibacterial discovery. Clin. Microbiol. Rev., 2011, 24(1), 71-109.
[http://dx.doi.org/10.1128/CMR.00030-10] [PMID: 21233508]
[12]
Fernandes, P.; Martens, E. Antibiotics in late clinical development. Biochem. Pharmacol., 2017, 133, 152-163.
[http://dx.doi.org/10.1016/j.bcp.2016.09.025] [PMID: 27687641]
[13]
Veluri, R.; Oka, I.; Wagner-Döbler, I.; Laatsch, H. New indole alkaloids from the North Sea bacterium Vibrio parahaemolyticus Bio249. J. Nat. Prod., 2003, 66(11), 1520-1523.
[http://dx.doi.org/10.1021/np030288g] [PMID: 14640534]
[14]
Gillespie, D.E.; Brady, S.F.; Bettermann, A.D.; Cianciotto, N.P.; Liles, M.R.; Rondon, M.R.; Clardy, J.; Goodman, R.M.; Handelsman, J. Isolation of antibiotics turbomycin a and B from a metagenomic library of soil microbial DNA. Appl. Environ. Microbiol., 2002, 68(9), 4301-4306.
[http://dx.doi.org/10.1128/AEM.68.9.4301-4306.2002] [PMID: 12200279]
[15]
Xiu, J.; Wenbin, Y. Radical-based regioselective cross-coupling of indoles and cycloalkanes. Catal. Sci. Technol., 2016, 6, 998-1002.
[http://dx.doi.org/10.1039/C5CY01907A]
[16]
Huang, Y.; Yang, Y.; Song, H.; Liu, Y.; Wang, Q. Synthesis of Structurally Diverse 2,3-Fused Indoles via Microwave-Assisted AgSbF6-Catalysed Intramolecular Difunctionalization of o-Alkynylanilines. Sci. Rep., 2015, 5, 13516.
[http://dx.doi.org/10.1038/srep13516] [PMID: 26310858]
[17]
Xia, G.; Han, X.; Lu, X. Pd(II)-catalyzed one-step construction of cycloalkane-fused indoles and its application in formal synthesis of. Aspidospermidine. Org. Lett., 2014, 16, 2058-2061.
[http://dx.doi.org/10.1021/ol500662f] [PMID: 24650163]
[19]
Assis, L.M.; Nedeljković, M.; Dessen, A. New strategies for targeting and treatment of multi-drug resistant Staphylococcus aureus. Drug Resist. Updat., 2017, 31, 1-14.
[http://dx.doi.org/10.1016/j.drup.2017.03.001] [PMID: 28867240]
[20]
Diekema, D.J.; Pfaller, M.A.; Schmitz, F.J.; Smayevsky, J.; Bell, J.; Jomes, R.N.; Beach, M.; Group, S.P. Survey of infections due to Staphylococcus species: Frequency of occurrence and antimicrobial susceptibility of isolates collected in the United States, Canada, Latin America, Europe, and the Western Pacific region for the SENTRY Antimicrobial Surveillance Program., 2001, 32, S114-S132.
[21]
von Eiff, C.; Jansen, B.; Kohnen, W.; Becker, K. Infections associated with medical devices: pathogenesis, management and prophylaxis. Drugs, 2005, 65(2), 179-214.
[http://dx.doi.org/10.2165/00003495-200565020-00003] [PMID: 15631541]
[22]
Garzoni, C.; Kelley, W.L. Return of the Trojan horse: Intracellular phenotype switching and immune evasion by Staphylococcus aureus. EMBO Mol. Med., 2011, 3(3), 115-117.
[http://dx.doi.org/10.1002/emmm.201100123] [PMID: 21365763]
[23]
David, M.Z.; Dryden, M.; Gottlieb, T.; Tattevin, P.; Gould, I.M. Recently approved antibacterials for methicillin-resistant Staphylococcus aureus (MRSA) and other Gram-positive pathogens: the shock of the new. Int. J. Antimicrob. Agents, 2017, 50(3), 303-307.
[http://dx.doi.org/10.1016/j.ijantimicag.2017.05.006] [PMID: 28666751]
[24]
Nunez, N.; Derré-Bobillot, A.; Gaubert, S.; Herry, J-M.; Deschamps, J.; Wei, Y.; Baranek, T.; Si-Tahar, M.; Briandet, R.; Serror, P.; Archambaud, C. Exploration of the role of the virulence factor ElrA during Enterococcus faecalis cell infection. Sci. Rep., 2018, 8(1), 1749.
[http://dx.doi.org/10.1038/s41598-018-20206-6] [PMID: 29379180]
[25]
Sievert, D.M.; Ricks, P.; Edwards, J.R.; Schneider, A.; Patel, J.; Srinivasan, A.; Kallen, A.; Limbago, B.; Fridkin, S. Antimicrobial-resistant pathogens associated with healthcare-associated infections: Summary of data reported to the National Healthcare Safety Network at the Centers for Disease Control and Prevention, 2009-2010. Infect. Control Hosp. Epidemiol., 2013, 34(1), 1-14.
[http://dx.doi.org/10.1086/668770] [PMID: 23221186]
[26]
Goh, H.M.S.; Yong, M.H.A.; Chong, K.K.L.; Kline, K.A. Model systems for the study of Enterococcal colonization and infection. Virulence, 2017, 8(8), 1525-1562.
[http://dx.doi.org/10.1080/21505594.2017.1279766] [PMID: 28102784]

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