Personal Chair
- 51cg
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- Email Address
- r.ebel@abdn.ac.uk
- Telephone Number
- +44 (0)1224 272930
- Office Address
- School/Department
- School of Natural and Computing Sciences
Internal Memberships
Safety Adviser for the Chemistry Department, Member of the University Health & Safety Committee
Latest Publications
2-((((R)-3-(((9E,17Z)-18-Bromooctadeca-9,17-dien-7,15-diynoyl)oxy)-2-hydroxypropoxy)(hydroxy)phosphoryl)oxy)-N,N,N-trimethylethan-1-aminium
MolBank, vol. 2026, no. 3, M2188Contributions to Journals: Articles- [ONLINE] DOI:
- [OPEN ACCESS]
- [ONLINE]
An Exploratory LC-HRMS Metabolomics Study of Culture Medium-Dependent Metabolic Variation and Bioactivity in Ten Fungal Strains
International Journal of Molecular Sciences, vol. 27, no. 9, 3866Contributions to Journals: Articles- [ONLINE] DOI:
- [OPEN ACCESS]
- [ONLINE]
New Compounds from the Deep-sea Sponge Mycale lingua
Chemistry & Biodiversity, vol. 23, no. 2, e03519Contributions to Journals: Articles- [ONLINE] DOI:
- [OPEN ACCESS]
Deep-Sea Marine Metabolites as Promising Anti-Tubercular Agents: CADD-Guided Targeting of the F420-Dependent Oxidoreductase
Marine Drugs, vol. 24, no. 2, 58Contributions to Journals: Articles- [ONLINE] DOI:
- [OPEN ACCESS]
- [ONLINE]
Virtual screening of azoles libraries: the search for potential anti-mucormycotic agents using computational tools
Network Modeling Analysis in Health Informatics and Bioinformatics, vol. 14, no. 1, 23Contributions to Journals: Articles- [ONLINE] DOI:
- [OPEN ACCESS]
- Research
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Research Overview
Biologically Active Natural Products
- Structure elucidation of biologically active marine and terrestrial-derived natural products with the aid of modern spectroscopic methods, including one- and two-dimensional NMR spectroscopy and various mass spectrometric techniques.
- Characterisation of natural products with regard to biological activity in pharmacologically relevant assay systems.
An endophytic fungus is a fungus that spends the whole or part of its life cycle colonizing inside the healthy tissue of the host plant, typically without causing any apparent symptoms of disease, but forming a relationship between latent phytopathogenesis to mutualistic symbiosis.
Endophytic fungi associated with plants represent a potential new source of novel chemistry and biology to assist in solving not only human, but also animal and plant health problems.
Current research of our group explores endophytes isolated from different medicinal plants and mangroves for pharmacologically active natural products which might prove to be suitable for specific medicinal or agrochemical applications. By the use of advanced cultivation and investigation procedures as well as chemical technology, novel natural product leads will be optimized on the basis of their biological activities to yield effective chemotherapeutic and other bioactive agents.
- Marine microbiology, especially cultivation of marine fungi for analysis of secondary metabolite profiles.
The marine environment serves as a source not only of untapped taxonomical diversity of fungi, but also unique chemical structures of novel fungal metabolites. Marine fungi have been gaining increased attention in recent decades because of their potential as producers of biologically active secondary metabolites with therapeutic potential. Moreover, the exploration of fungi could also solve the problem of supply of marine-derived pharmacologically active substances, which normally are produced in a limited amount. Cephalosporine C is a first classical example of a b-lactam antibiotic isolated from a marine derived fungus (Cephalosporium acremonium).
- Molecular taxonomy of marine-derived fungi as well as endophytic fungi
Isolation of endophytic or endosymbiontic fungi is limited by the phenomenon that more than 99.8 % of micro-organisms existing in nature are not amenable to currently available cultivation methods. Molecular biology techniques can be used to overcome these limitations. Fungi strains may be identified by total DNA isolation, amplification of the so-called ITS region, sequencing of the product and database search. Â Complex samples consisting of multiple fungi will result in a mixture of amplification products that cannot be sequenced together. Separation, traditionally performed by cloning, nowadays can be achieved by denaturing gradient gel electrophoresis that separates PCR products by their sequence-based melting behaviour.
- Structure elucidation of biologically active marine and terrestrial-derived natural products with the aid of modern spectroscopic methods, including one- and two-dimensional NMR spectroscopy and various mass spectrometric techniques.
- Teaching
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Programmes
- Undergraduate, 4 year, September start
- Undergraduate, 5 year, September start
Teaching Responsibilities
Professor Ebel teaches in the following courses:
- CM1020 Chemistry for the Life Sciences 1
- CM1021 Chemistry for the Physical Sciences 1
- CM1022 Elements of Chemistry 1CM1512 Chemistry for the Life Sciences 2
- CM1522 Elements Of Chemistry 2
- CM2016 Analytical Chemistry and Spectroscopy
- CM2514 Organic and Biological Chemistry
- CM3534 Organic and Biological Chemistry
- CM4537 Advanced Honours Chemistry, module "Natural Products"
- CM4538 Integrated Chemistry
- CM5003 MChem Chemistry Applications
- Publications
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Arabinofuranosyl Thymine Derivatives—Potential Candidates against Cowpox Virus: A Computational Screening Study
International Journal of Molecular Sciences, vol. 24, no. 2, 1751Contributions to Journals: Articles- [ONLINE] DOI:
- [OPEN ACCESS]
Antiparasitic Activities of Compounds Isolated from Aspergillus fumigatus Strain Discovered in Northcentral Nigeria
Antibiotics, vol. 12, no. 1, 109Contributions to Journals: Articles- [ONLINE] DOI:
- [OPEN ACCESS]
- [ONLINE]
Can Crude Oil Exploration Influence the Phytochemicals and Bioactivity of Medicinal Plants?: A Case of Nigerian Vernonia amygdalina and Ocimum gratissimum.
Molecules, vol. 27, no. 23, 8372Contributions to Journals: Articles- [ONLINE] DOI:
- [OPEN ACCESS]
Computational Repurposing of Mitoxantrone-Related Structures against Monkeypox Virus: A Molecular Docking and 3D Pharmacophore Study
International Journal of Molecular Sciences, vol. 23, no. 22, 14287Contributions to Journals: Articles- [ONLINE] DOI:
- [OPEN ACCESS]
Mutactimycin AP, a New Mutactimycin Isolated from an Actinobacteria from the Atacama Desert
Molecules, vol. 27, no. 21, 7185Contributions to Journals: Articles- [ONLINE] DOI:
- [OPEN ACCESS]
- [ONLINE]
A structure-activity relationship analysis of anthraquinones with antifouling activity against marine biofilm-forming bacteria
Frontiers in Natural Products, vol. 1, 990822Contributions to Journals: Articles- [ONLINE] DOI:
- [OPEN ACCESS]
Fosbergenone: 3-[2-(1,2,5,5-Tetramethyl-7-oxo-1,2,3,4,4a,5,6,7-octahydronaphthalen-1-yl)ethyl]-2,5-dihydrofuran-2-one
MolBank, vol. 2022, no. 2, M1391Contributions to Journals: Comments and Debates- [ONLINE] DOI:
- [OPEN ACCESS]
- [ONLINE]
Inhibition of the Quorum Sensing System, Elastase Production and Biofilm Formation in Pseudomonas aeruginosa by Psammaplin A and Bisaprasin
Molecules, vol. 27, no. 5, 1721Contributions to Journals: Articles- [ONLINE] DOI:
- [OPEN ACCESS]
ISOLATION WITH CHARACTERIZATION OF COLUMBIN AND NOVEL CLERODANE FURANO-DITERPENE WITH GC-MS AND ANTIMICROBIAL ANALYSES OF ESSENTIAL OILS FROM Sphenocentrum jollyanum Pierre
Journal of Chemical Society of Nigeria, vol. 46, no. 6, pp. 1084–1098Contributions to Journals: Articles- [ONLINE] DOI:
- [OPEN ACCESS]
Heavy metals, proximate analysis and brine shrimp lethality of Vernonia amygdalina and Ocimum gratissimum growing in crude oil-rich delta state, Nigeria
Foods, vol. 10, no. 12, 2913Contributions to Journals: Articles- [ONLINE] DOI:
- [OPEN ACCESS]
- [ONLINE]