Publications by authors named "Ekundayo Olusegun"

Article Synopsis
  • Bacterial resistance is a growing global issue, leading to difficulties in treating infectious diseases, prompting the exploration of natural products like plant secondary metabolites to help address the problem.
  • Two fruit essential oils were extracted using hydrodistillation and analyzed, revealing significant antibacterial and antifungal properties along with a detailed breakdown of their chemical composition.
  • The essential oils showed strong antibacterial effects against specific bacteria at low concentrations, while demonstrating limited antifungal activity, and no significant toxicity to human cancer cells was found, highlighting their potential as alternative antimicrobial agents.
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Unlabelled: (turmeric) has been used in Chinese traditional medicine and Ayurvedic medicine for many years.

Methods: The leaf essential oil of from southern Nigeria was obtained by hydrodistillation and analyzed by gas chromatography-mass spectrometry (GC-MS). The essential oil was screened for antibacterial, antifungal, and cytotoxic activities.

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In West Africa and Nigeria in particular, many virgin plants are still waiting to be evaluated for their medicinal importance. Claims of plants with folk medicinal applications need to be evaluated and verified. Gomphrena celosioides (family - Amaranthaceae) is a weed grown in lawns and the biological activity of the extract had earlier been established.

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The concentrations and distributions of organochlorine pesticides (OCPs) in some higher plant samples collected from oil exploration areas of the Niger Delta, Nigeria were examined. The concentrations of Σ(25)OCP ranged from 82 to 424, 44 to 200 , 34 to 358, 33 to 106 and 16 to 75 ng/g in Olomoro, Oginni, Uzere, Irri and Calabar plants, respectively. The compositional profiles of the analysed OCPs in most of the plants showed no fresh inputs in the area.

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The chemical composition of the essential oil from the whole plant of Acalypha segetalis Muell. Arg. was analyzed by GC and GC/MS.

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Japodagrin (1) and japodagrone (2), two macrocylic diterpenoids possessing lathyrane and jatrophane skeletons, respectively, have been isolated from the root of Jatropha podagrica Hook. Four other diterpenoids (3-6) were also isolated from this plant. The structures of these compounds were elucidated on the basis of NMR and HRMS analysis, and by spectral comparisons.

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GC-MS of the essential oil prepared by hydrodistillation of the green parts of a specimen of Solidago canadensis collected near Katowice, Poland, revealed two new sesquiterpene hydrocarbons. Their EI mass spectra resembled the mass spectrum of beta-ylangene (1) but the retention indices of the new compounds differed markedly from this known compound. After isolation of the new compounds by preparative GC their investigation by one- and two-dimensional NMR techniques resulted in the identification of 6-epi-alpha-cubebene (2) (minor constituent, 1.

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