Antimicrobial Potential of Wild Edible Herbaceous Species

Antimicrobial potential, antioxidant activity and total phenolic contents of EtOH extract of aerial part from Korean mint (Agustache rugosa) germplasm

Planta Medica ◽

10.1055/s-0032-1320324 ◽

2012 ◽

Vol 78 (11) ◽

Author(s):

MJ Kang ◽

HC Ko ◽

NY Ro ◽

OS Hur ◽

JH Rhee ◽

...

Keyword(s):

Antioxidant Activity ◽

Aerial Part ◽

Total Phenolic ◽

Phenolic Contents ◽

Etoh Extract ◽

Total Phenolic Contents ◽

Antimicrobial Potential

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BATTLE OF THE GIANTS: PRIMARY AND SECONDARY INVASIONS BY LARGE HERBACEOUS SPECIES

Biology & Environment Proceedings of the Royal Irish Academy ◽

10.3318/bioe.2011.14 ◽

2012 ◽

Vol 111 (3) ◽

pp. 1-17 ◽

Cited By ~ 5

Author(s):

Margherita Gioria ◽

Burkart Dieterich ◽

Bruce Osborne

Keyword(s):

Herbaceous Species

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ANTIMICROBIAL POTENTIAL OF ENDOPHYTIC ACTINOBACTERIA FROM MEDICINAL PLANTS

Bulletin of Orenburg State University ◽

10.25198/1814-6457-209-106 ◽

2017 ◽

Vol 209 (09) ◽

pp. 106-110

Author(s):

G.O.O. Hassan ◽

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I.R. Yagudina ◽

N.S. Karamova ◽

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...

Keyword(s):

Medicinal Plants ◽

Antimicrobial Potential ◽

Endophytic Actinobacteria

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Antimicrobial Potential of Benzamides and Derived Nanosystems for Controlling in vitro Biofilm Development on Medical Devices

Current Organic Chemistry ◽

10.2174/1385272811317020013 ◽

2013 ◽

Vol 17 (2) ◽

pp. 162-175 ◽

Cited By ~ 2

Author(s):

Carmen Limban ◽

Alexandru Mihai Grumezescu ◽

Mariana Chirea ◽

Lilia Matei ◽

Mariana Carmen Chifiriuc

Keyword(s):

Medical Devices ◽

Antimicrobial Potential ◽

Biofilm Development

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Synthesis, Characterization, Antimicrobial and Antioxidant Potential of Diazenyl Chalcones

Current Topics in Medicinal Chemistry ◽

10.2174/1568026618666180626095714 ◽

2018 ◽

Vol 18 (10) ◽

pp. 844-856 ◽

Cited By ~ 5

Author(s):

Harmeet Kaur ◽

Balasubramanian Narasimhan

Keyword(s):

Radical Scavenging Activity ◽

Radical Scavenging ◽

Antioxidant Potential ◽

Dilution Method ◽

Dpph Assay ◽

Antimicrobial Potential ◽

Structural Conformation ◽

Uv Visible ◽

Tube Dilution Method

A series of diazenyl chalcones was prepared by base catalyzed Claisen-Schmidt condensation of synthesized hydroxy substituted acetophenone azo dye with various substituted aromatic/ heteroaromatic aldehydes. The structural conformation of synthesized chalcones was done by a number of physicochemical and spectral means like FTIR, UV-visible, mass, NMR spectroscopy and CHNS/O analysis. These diazenyl chalcones were assessed for their in vitro antimicrobial potential against several Gram-negative, Gram-positive bacterial and fungal strains by serial tube dilution method. The fluconazole and cefadroxil were used as standard drugs. The target compounds were also evaluated for their antioxidant potential by DPPH assay. (2E)-3-(2,4-Dichlorophenyl)-1-(4-((2,6- dihydroxyphenyl)diazenyl)phenyl)prop-2-en-1-one (C-7) had shown very good antimicrobial potential with MIC ranges from 3.79 to 15.76 μg/ml against most of the tested microorganisms. Most of the synthesized diazenyl chalcones were found to be active against B. subtilis. The (2E)-1-(5-((2-Chloro- 4-nitrophenyl)diazenyl)-2-hydroxyphenyl)-3-(2-hydroxynaphthalen-1-yl)prop-2-en-1-one (C-10) had shown high free radical-scavenging activity when compared with the ascorbic acid as the reference antioxidant.

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