2014
DOI: 10.1002/cbdv.201300366
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Volatile Oils from the Aerial Parts of Eremophila maculata and Their Antimicrobial Activity

Abstract: The essential oils isolated from the fresh flowers, fresh leaves, and both fresh and air-dried stems of Eremophila maculata (Scrophulariaceae) were characterized by GC-FID and GC/MS analyses. Sabinene was the major component in most of the oils, followed by limonene, α-pinene, benzaldehyde, (Z)-β-ocimene, and spathulenol. The leaf and flower essential oils showed antibacterial and antifungal activity against five Gram-positive and four Gram-negative bacterial strains, multi-resistant clinical isolates from pat… Show more

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Cited by 28 publications
(26 citation statements)
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“…Mean of 3 independent runs was used to calculate areas under the peaks (AUP) using an SRI Instrument (Torrance, CA, USA) and the total area was considered as 100%. Wiley Registry of Mass Spectral Data 8th edition, National Institute of Standards and Technology (NIST) Mass Spectral Library (December 2005), and the literature were used to compare and identify the active constituent of spectral data [ 29 , 30 ].…”
Section: Methodsmentioning
confidence: 99%
“…Mean of 3 independent runs was used to calculate areas under the peaks (AUP) using an SRI Instrument (Torrance, CA, USA) and the total area was considered as 100%. Wiley Registry of Mass Spectral Data 8th edition, National Institute of Standards and Technology (NIST) Mass Spectral Library (December 2005), and the literature were used to compare and identify the active constituent of spectral data [ 29 , 30 ].…”
Section: Methodsmentioning
confidence: 99%
“…2.4 (Shimadzu Corporation, Kyoto, Japan) was used for recording and integrating the chromatograms. Volatile components were identified by comparing their retention indices (RI) and mass spectra with those built in libraries (NIST Mass Spectral Library (December 2005), Wiley Registry of Mass Spectral Data 8th edition) and literature [ 22 , 23 ].…”
Section: Methodsmentioning
confidence: 99%
“…Anhydrous Na 2 SO 4 was used to dehydrate the prepared essential oils, yielding 0.4, 0.7, 0.3, 0.3, 0.8 and 0.5 % v/w of dry weight for Fc, Fk, Fp, Fs, Ft and Fv, respectively. Then the various oil samples were maintained at −30 • C in dark-colored stoppered glasses until their analyses [26,27].…”
Section: Preparation Of Essential Oil Samplesmentioning
confidence: 99%