FRSE, FRSC, CChem, BA Hons (Cantab), PhD (Dublin), ScD (Cantab)
Chair in Chemistry
- About
-
- Email Address
- m.jaspars@abdn.ac.uk
- Telephone Number
- +44 (0)1224 272895
- Office Address
Meston Building Room G21
- School/Department
- School of Natural and Computing Sciences
Biography
Previous Positions
- Head of the Department of Chemistry, University of Aberdeen 2016-2019
- Scientific Project Leader of the EU FP7 Project ‘PharmaSea’ (€ 9.5 M, 24 partners from 14 countries) 2012-2017
- Visiting Professor for Senior International Scientists of the Chinese Academy of Sciences 2012-2013
- Visiting Professor (20%) at the University of Tromsø, Norway to provide advice for their £14 M marine biodiscovery programme. 2007-2017
- Sabbatical at the Australian Institute of Marine Science, 2004
- Professor of Organic Chemistry, University of Aberdeen, 2003-
- Senior Lecturer in Organic Chemistry, University of Aberdeen, 2000-2003
- Lecturer in Organic Chemistry, University of Aberdeen, 1995-2000
- Post-Doc, Crews Lab, University of California, Santa Cruz, 1993-1995
- Post-Doc, Burgess Lab, Texas A & M University, 1992-1993
Qualifications
- BA Hons (Cantab) Natural Sciences (Chemistry)1987 - University of Cambridge
- PhD Organic Chemistry1992 - Trinity College, DublinElectrophilic Catalysis of the Sakurai Reaction
- ScD (Cantab) Organic Chemistry2018 - University of CambridgeInvestigating the Chemical Structures, Bioactivity and Biosynthesis of Marine and Desert Natural Products
External Memberships
On the Scientific Advisory Board of the Center for Microbial Secondary Metabolites, Danish Technical University, Copenhagen, Denmark 2018-
Management board of NPRONET, a BBSRC network in industrial biotechnology and biosciences. 2014-2018
Governing board member of Industrial Biotechnology Innovation Centre, Strathclyde 2014-2016
Policy Work:
Contributing author to “Science in Small Island Developing States: Capacity Challenges and Options relating to Marine Genetic Resources of Areas Beyond National Jurisdiction”
Co-author of Blue Paper on the Ocean Genome for the High Level Panel for a Sustainable Ocean Economy 2020
Co-author of study for the United Nations Convention on Biological Diversity on Digital Sequence Information on Genetic Resources: Concept, Scope and Current Use. CBD/DSI/AHTEG/2020/1/3 2020
Special advisor on Marine Genetic Resources to the International Union for the Conservation of Nature at the United Nations process on the Conservation and Sustainable Use of Biodiversity of Areas Beyond National Jurisdiction. Member of the Member of the IUCN World Council on Protected Areas 2019-
Co-lead of the Deep Sea Genetic Resources Working Group of the Deep Ocean Stewardship Initiative. 2018-
Member of Royal Society working group writing a policy briefing for the Government Office of Science entitled “Future Ocean Resources: Metal-Rich Minerals and Genetics” Released July 2017.
Chair of advisory panel of policy and legal experts (Part of the PharmaSea EU FP7 consortium lead by Marcel Jaspars 2012-17) bringing together policymakers (United Nations, European Commission) with NGOs (International Union for the Conservation of Nature, Convention on Biodiversity Secretariat, International Seabed Authority) with international marine biotechnology companies and academic and legal/policy experts to shape the policy debate on intellectual property derived from marine genetic resources in areas beyond national jurisdiction (United Nations process on the Conservation and Sustainable Use of Biodiversity of Areas Beyond National Jurisdiction). Contributions recorded on our BBNJ Page and our Song of the Ocean page
UK member of the Marine Biotechnology working group of the European Science Foundation’s Marine Board Marine Biotechnology Working Group to assist in the revision of the White Paper “Marine Biotechnology – A European Strategy” 2009-2010
Prizes and Awards
Biotechnology and Biological Sciences Research Council Research Development Fellow, 2006-2009
American Society of Pharmacognosy Matt Suffness Award for young investigators, 2003
Fellow of the Royal Society of Chemistry, Chartered Chemist
Fellow of the Royal Society of Edinburgh
Fellow of the Higher Education Academy
- Research
-
Research Overview
Tour the lab and find out what we do
Introduction:
My research involves the discovery of new compounds with potential pharmaceutical use from marine and desert environments, their structure determination and biosynthesis. Translation of bioactive natural compounds into preclinical evaluation is exemplified by with sponge derived compounds/analogues that have activity in animal models for Alzheimer’s disease or epilepsy or are able to deliver proteins into animal brains to generate a model of Alzheimer’s disease.
Natural Product Structure Determination:
Structural work involves the use of complementary NMR and theoretical methods to solve the relative stereochemistry of complex natural products, particularly the use of NOE data to constrain conformational searches and the comparison of predicted and experimental CD spectra. A combination of analytical and spectroscopic methods was used to define a metal complex present in the extract of a seasquirt, giving insight into its ecological role.Together with Leo Gross at IBM Research, I started original work on organic structure determination using a combination of spectroscopy and atomic force microscopy (AFM). First we showed how Ångstrom-resolution AFM images may be used to solve the structure of a simple planar molecule and how this process might be generalised. Subsequently we applied the combined methods to an unknown molecule with a NMR silent region (no H atoms). In a book chapter, we propose the developments needed so that AFM may become invaluable in the rapid structure determination of complex organic molecules in the future.
Biosynthesis:
The isolation and structural characterisation of modified cyclic peptides of marine origin was driven by an interest in their chemical structure in solution and their interaction with metal ions. A major problem with these bioactive cyclic compounds was a sustainable supply. In 2004, I worked together with Dr Paul Long at the London School of Pharmacy and scientists from the Australian Institute of Marine Science to effect the first shotgun cloning of the patellamide biosynthetic pathway resulting in low level production of these compounds.Subsequent collaboration with Professor Jim Naismith at St Andrews succeeded in overexpressing and structurally characterising the main enzymes involved in the biosynthesis of the patellamides and related cyanobactins. Working together, we defined the main proteases involved including the macrocyclase that circularises a linear peptide without inclusion of a signal sequence, thus making it a very exciting prospect for biotechnological application. We have defined a unique enzyme that forms the heterocycles – the first crystal structure of this type of enzyme. Engineering of this enzyme allowed short synthetic peptide sequences to be processed to form heterocycles in the chain. These enzymes are extremely permissive, and natural and non-natural substrates can be processed using them resulting in the formation milligram quantities of complex, modified cyclic peptides. The starting sequences may include non-natural amino acids and even non-amino acid segments such as fatty acids, aromatics and sugars, with a minimum of three residues required for this to work.
Research Areas
Chemistry
Research Specialisms
- Marine Chemistry
- Medicinal Chemistry
- Organic Chemistry
- Analytical Chemistry
- Applied Chemistry
Our research specialisms are based on the Higher Education Classification of Subjects (HECoS) which is HESA open data, published under the Creative Commons Attribution 4.0 International licence.
MARBLES EU Project
Harnessing marine microbes for drug discovery and sustainable production of fish and crops
Knowledge Exchange
Policy Work:
Protecting the Oceans Using Chemistry
Professor Marcel Jaspars has been advising the UN to develop a new law to protect marine biodiversity. The UN is working to conserve and sustainably use marine biodiversity in areas beyond national jurisdiction – about 60% of the oceans and 40% of the entire planet. The Song of the Oceans brings together science, the arts and humanities to publicise the urgent need to conserve the oceans.
Policy Input
Marcel provided scientific leadership for a large EU FP7 consortium ‘PharmaSea’, running from 2012-2017 with the contribution of 24 partners from 14 countries. Part of this project was to engage with stakeholders, NGOs and policy makers to provide sound scientific advice on major issues affecting the conservation and sustainable use of marine biodiversity. His major role was to translate scientific information and provide options on this topic to senior policy makers at the EU and UN, making visits to Brussels and New York to present information in a digestible format and answer questions, paying particular attention to the legal and policy requirements.
Marcel has been active at national and international levels to develop the science, its applications/industrial uptake and associated policy involved in marine biodiscovery and biotechnology. Since 2014 Marcel has been involved in the BBNJ process, providing scientific input and co-authoring the Mare Geneticum proposal which provides building blocks based on good scientific practice towards a solution for the MGR aspects of the BBNJ process. Also see our work to bring this to a wider audience with our 'Song of the Oceans'.
At EU level he was involved in coordinating the authoring the health section of a European Science Foundation position paper on the Future of Marine Biotechnology informing the blue growth agenda of the European Commission through a number of concrete and measurable recommendations. In 2017 he was a member of the UK Marine Foresight Committee’s Royal Society Working group that wrote a report entitled ‘Future Ocean Resources: Metal-Rich Minerals and Genetics’ on the UN BBNJ issue and he has since provided advice on this topic to the UK’s Foreign and Commonwealth Office. More recently he was a co-author on a report on the Ocean Genome for the High Level Panel for a Sustainable Ocean Economy and a lead author on a study for the United Nations Convention on Biological Diversity on Digital Sequence Information on Genetic Resources: Scope, Concept and Current Use.
Marcel Jaspars speaking at UN HQ in New York as advisor to the International Union for the Conservation of Nature at the Second Intergovernmental Conference on the UN process on the Conservation and Sustainable Use of Biodiversity in Areas Beyond National Jurisdiction
Funding and Grants
Grants in the last 5 years
05/2021
EU Horizon 2020
£561 K
MARBLES Project
08/2021
IBIOIC BBSRC DTP
£102 K
Downstream processing and structure confirmation of chemoenzymatically produced macrocycles
10/2021
EASTBio BBSRC DTP
£97 K
The role of sponge competition in cold-water coral reefs – ROV video analyses and secondary metabolite profiling in the search for compounds of medical and ecological relevance
10/2021
Commonwealth Scholarship Commission
£107 K
PhD scholarship
08/2022
DEFRA
£217 K
DEEPEND project
11/2022
EU Horizon Europe
£553 K
BlueRemediomics Project
01/2023
EU Horizon Europe
£265 K
HOTBIO Doctoral Training Network
04/2023
DEFRA
£166 K
DEEPEND 2 Project
- Teaching
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Courses
Non-course Teaching Responsibilities
Professor Jaspars is:
Year 3 Coordinator
Erasmus Officer for Chemistry
Coordinator for SX3002 'Science and Society'
- Publications
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Page 3 of 3 Results 201 to 272 of 272
Pore forming polyalkylpyridinium salts from marine sponges versus synthetic lipofection systems: distinct tools for intracellular delivery of cDNA and siRNA
BMC Biotechnology, vol. 6, 6Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1186/1472-6750-6-6
- [OPEN ACCESS] http://aura.abdn.ac.uk/bitstream/2164/3686/1/Pore_forming.pdf
A homologous series of eunicellin-based diterpenes from Acalycigorgia sp. characterised by tandem mass spectrometry
Tetrahedron, vol. 62, pp. 8770-8778Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/j.tet.2006.06.102
Acute actions of marine toxin latrunculin A on the electrophysiological properties of cultured dorsal root ganglion neurones
Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology, vol. 142, no. 1-2, pp. 19-29Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/j.cbpc.2005.09.006
Bioactivity of Hirsutanolol, Oregonin and Genkwanin, Isolated from the Seeds of Alnus glutinosa (Betulaceae)
Natural Product Communications, vol. 1, no. 8, pp. 641-644Contributions to Journals: ArticlesHederacine A and Hederacine B from Glechoma hederaceae Inhibit the growth of Colorectal Cancer Cells in vitro
Natural Product Communications, vol. 1, no. 1, pp. 33-35Contributions to Journals: ArticlesIdentification of novel inhibitors of UDP-Glc4/-epimerase, a validated drug target for african sleeping sickness
Bioorganic & Medicinal Chemistry, vol. 16, pp. 5744-5747Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/j.bmcl.2006.08.091
Inhibition of TNFa-induced activation of nuclear factor ¿B by kava (Piper methysticum) derivatives
Biochemical Pharmacology, vol. 71, no. 71, pp. 1206-1218Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/j.bcp.2005.12.032
Montamine, a unique dimeric indole alkaloid, from the seeds of Centaurea montana (Asteraceae), and its in vitro cytotoxic activity against the CaCo2 colon cancer cells
Tetrahedron, vol. 62, pp. 11172-11177Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/j.tet.2006.09.020
New Methods for Medicinal Chemistry - Universal Gene Cloning and Expression Systems for Production of Marine Bioactive Metabolites
Current Medicinal Chemistry, no. 13, pp. 697-710Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.2174/092986706776055643
Spontaneity in the patellamide biosynthetic pathway
Organic & Biomolecular Chemistry, no. 4, pp. 631-638Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1039/b515938e
Shotgun Cloning and Heterologous Expression of the Patellamide Gene Cluster as a Strategy to Achieving Sustained Metabolite Production
ChemBioChem, vol. 6, no. 6, pp. 1760-1765Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1002/cbic.200500210
4-Hydroxybenzoyl derivative from the aqueous extract of the hydroid Campanularia sp
Journal of Natural Products, vol. 68, no. 3, pp. 453-455Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1021/np049666n
Anticancer activities of constituents of kava (Piper methysticum)
The South Pacific Journal of Natural Science, vol. 23, pp. 26-29Contributions to Journals: ArticlesIsolation, structure elucidation and bioactivity of schischkiniin, a unique indole alkaloid from the seeds of Centaurea schischkinii
Tetrahedron, vol. 61, pp. 9001-9006Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/j.tet.2005.07.047
2D NMR spectroscopic analyses of archangelicin from the seeds of Angelica archangelica
Acta Pharmaceutica, vol. 54, no. 4, pp. 277-285Contributions to Journals: Articles- [ONLINE] View publication in Scopus
Dimethylarsinothioyl acetic acid identified in a biological sample: the first occurrence of a mammalian arsinothio(y)l metabolite
Angewandte Chemie International Edition, vol. 43, pp. 337-340Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1002/anie.200352740
Arsinothioyl-sugars produced by in vitro incubation of seaweed extract with liver cytosol analysed by HPLC coupled simultaneously to ES-MS and ICP-MS
Analyst, vol. 129, no. 129, pp. 1058-1064Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1039/b409661b
Bioactive Lignans from the Sees of Centaurea Macrocephala
DARU, vol. 12, no. 3, pp. 87-93Contributions to Journals: Articles- [ONLINE] http://journals.tums.ac.ir/abs/12
Cell membrane permeabilisation by alkylpyridinium sponge toxin preparations and their utilisation as novel transfection reagents
Neurotox' 2003: Neurotoxicological Targets from Functional: Chapter 5, pp. 51-58, 8 pagesChapters in Books, Reports and Conference Proceedings: ChaptersComparative studies on biological activities of Prunus padus and P-spinosa
Fitoterapia, vol. 75, pp. 77-80Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/j.fitote.2003.08.011
Epoxylignans from the seeds of Centaurea cyanus (Asteraceae)
Biochemical Systematics and Ecology, vol. 32, pp. 1201-1204Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/j.bse.2004.03.011
Isolation, structure elucidation, and biological activity of flavone 6-C-glycosides from Allaria petiolata
Chemistry of Natural Compounds, vol. 40, pp. 122-128Contributions to Journals: ArticlesSulfur-containing arsenical mistaken for dimethylarsinous acid (DMA(III)) and identified as a natural metabolite in urine: Major implications for studies on assenic metabolism and toxicity
Chemical Research in Toxicology, vol. 17, pp. 1086-1091Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1021/tx049978q
Irreversible and reversible pore formation by polymeric alkylpyridinium salts (poly-APS) from the sponge Reniera sarai
British Journal of Pharmacology, vol. 139, no. 8, pp. 1399-1408Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1038/sj.bjp.0705374
A mixed crystal of imperatorin and phellopterin, with C-H center dot center dot center dot O, C-H center dot center dot center dot pi and pi-pi interactions
Acta Crystallographica Section C, Crystal Structure Communications, vol. 59Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1107/S0108270103012459
A mixed crystal of imperatorin and phellopterin, with C¾H¼O, C¾H¼p and p-p interactions
Acta Crystallographica Section C, Crystal Structure Communications, vol. C59, pp. o520-o522Contributions to Journals: ArticlesAcid-induced dimerisation of 1,2-di(thien-2-yl)ethanone
Tetrahedron, no. 59, pp. 4153-4155Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/S0040-4020(03)00581-7
An anomalous racemate of naringenin at 120 K
Acta Crystallographica Section E: Structure Reports Online, vol. E59, pp. o46-o48Contributions to Journals: ArticlesBioactive flavonoid glycosides from the seeds of Rosa canina
Pharmaceutical Biology, vol. 41, pp. 237-242Contributions to Journals: ArticlesBioactivity of secoiridoid glycosides from Centaurium erythraea
Phytomedicine, vol. 10, pp. 344-347Contributions to Journals: ArticlesBiological Activity of Lignans from the Seeds of Centaurea scabiosa
Pharmaceutical Biology, vol. 41, no. 3, pp. 203-206Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1076/phbi.41.3.203.15099
Biological activity of Euonymous eoropaeus
Fitoterapia, vol. 74, pp. 305-307Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/S0367-326X(03)00022-4
Chlorinated C12 Fatty Acid Metabolites from the Red Alga Gracilaria verrucosa
Journal of Natural Products, no. 66, pp. 1509-1511Contributions to Journals: ArticlesClionasterol, a triterpenoid from the Kenyan marine green macroalga halimeda macroloba
Western Indian Ocean Journal of Marine Science, vol. 2, no. 2, pp. 157-161Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.4314/wiojms.v2i2.28436
- [OPEN ACCESS] http://aura.abdn.ac.uk/bitstream/2164/3995/1/Clionasterol.pdf
Cyanogenic glycosids from Prunus spinosa (Rosaceae)
Biochemical Systematics and Ecology, vol. 31, no. 31, pp. 1063-1065Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/S0305-1978(03)00063-2
Dibenzylbutyrolactone lignans and indole alkaloids from the seeds of Centaurea nigra (Asteraceae)
Biochemical Systematics and Ecology, vol. 31, no. 31, pp. 653-656Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/S0305-1978(02)00227-2
Elevated microcystin and nodularin levels in cyanobacteria growing in spent medium of Planktothrix agardhii
Archiv für Hydrobiologie, vol. 158, no. 158, pp. 541-550Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1127/0003-9136/2003/0158-0541
Further studies of [omega-(haloalkylstannyl)alkyl]phosphine oxides.: Structures of bis[2-(bromodimethylstannyl)ethyl]phenylphosphine oxide and t-butyl[3-(iododimethylstannyl)propyl]phenylphosphine oxide
Polyhedron, vol. 22, no. 22, pp. 3277-3288Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/S0277-5387(03)00470-4
Isolation, structure elucidation and biological activity of hederacine A and B, two unique alkaloids from Glechoma hederaceae
Tetrahedron, vol. 59, no. 59, pp. 6403-6407Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/S0040-4020(03)01093-7
Processes influencing surface interaction and photocatalytic destruction of microcystins on titanium dioxide photocatalysts
Journal of Catalysis, no. 213, pp. 109-113Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/S0021-9517(02)00049-0
Short Communication: Bioactivity of secoiridoid glycosides from Centaurium erythraea
Phytomedicine, no. 10, pp. 344-347Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1078/094471103322004857
The influence of alkyl pyridinium sponge toxins on membrane properties, cytotoxicity, transfection and protein expression in mammalian cells
Biochimica et Biophysica Acta (BBA) - Biomembranes, vol. 1614, no. 2, pp. 171-181Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/S0005-2736(03)00175-5
Novel activities of saliva from the octopus Eledone cirrhosa (Mollusca; Cephalopoda)
Toxicon, vol. 40, no. 6, pp. 677-683Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/S0041-0101(01)00254-9
Psammaplin A, a chitinase inhibitor isolated from the Fijian marine sponge Aplysinella rhax
Bioorganic and Medicinal Chemistry, vol. 10, no. 4, pp. 1123-1128Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/S0968-0896(01)00372-8
- [ONLINE] View publication in Scopus
Axinellin C, a proline-rich cyclic octapeptide isolated from the Fijian marine sponge Stylotella aurantium
Tetrahedron, vol. 58, pp. 7863-7868Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/S0040-4020(02)00898-0
Biological activity of Glechoma hederacea
Fitoterapia, vol. 73, pp. 721-723Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/S0367-326X(02)00237-X
Conformational change in the thiazole and oxazoline containing cyclic octapeptides, the patellamides. Part 1. Cu2+ and Zn2+ induced conformational change
Journal of the Chemical Society, Perkin Transactions 2, pp. 1072-1075Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1039/b202823n
Purealidin S and Purpuramine J, Bromotyrosine Alkaloids from the Fijian Marine Sponge Druinella sp.
Journal of Natural Products, vol. 65, pp. 1798-1801Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1021/np020275n
Screening seeds of Scottish plants for antibacterial activity
Journal of Ethnopharmacology, vol. 83, pp. 73-77Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/S0378-8741(02)00214-3
(R)-1,3-Thiazolidin-3-ium-4-carboxylate
Acta Crystallographica Section E: Structure Reports Online, vol. 57Contributions to Journals: ArticlesIndole alkaloids from the seeds of Centaurea cyanus (Asteraceae)
Phytochemistry, vol. 57, pp. 1273-1276Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/S0031-9422(01)00084-X
Metal binding of Lissclinum patella metabolites. Part 1: Patellamides A, C and ulithiacyclamide A
Tetrahedron, vol. 57, no. 15, pp. 3185-3197Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/S0040-4020(01)00177-6
Metal binding of Lissoclinum patella metabolites. Part 2: Lissoclinamides 9 and 10
Tetrahedron, vol. 57, no. 15, pp. 3199-3207Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/S0040-4020(01)00178-8
Potential Ecological Roles of Lissoclinum patella Metabolites
Gordon Research Conference on Inorganic Reaction MechanismsContributions to Conferences: PostersS-Benzyl-L-cysteine
Acta Crystallographica Section E: Structure Reports Online, vol. 57Contributions to Journals: ArticlesStelliferin Riboside, a Triterpene Monosaccharide Isolated from the Fijian Sponge Geodia globostellifera
Journal of Natural Products, vol. 64, pp. 813-815Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1021/np010019v
Wainunuamide, a histidine-containing proline-rich cyclic heptapeptide isolated from the Fijian marine sponge Stylotella aurantium
Tetrahedron Letters, vol. 42, pp. 9273-9276Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/S0040-4039(01)01993-1
Analysis of the structure and electrophysiological actions of halitoxins: 1,3 alkyl-pyridinium salts from Callyspongia ridleyi
Journal of Membrane Biology, vol. 176, pp. 119-131Contributions to Journals: ArticlesGlutathione-dependent conversion of N-ethylmaleimide to the maleamic acid by Escherichia coli: an intracellular detoxification process
Applied and Environmental Microbiology, vol. 66, pp. 1393-1399Contributions to Journals: ArticlesH-Bond Mediated Folding of Natural & Model Patellamides - Modified Cyclic Octapeptides from Lissoclinum Patella
Gordon Research Conference on Marine Natural ProductsContributions to Conferences: PostersRedox Properties of the Patellamides: Dicopper Complexing Modified Cyclic Octapeptides Isolated from the Seasquirt Lissoclinum patella
International Conference on Coordination ChemistryContributions to Conferences: PostersStructure determination and MSn analysis of two new lissoclinamides isolated from the Indo-Pacific ascidian Lissoclinum patella: NOE restrained molecular dynamics confirms the absolute stereochemistry derived by degradative methods
Tetrahedron, vol. 56, no. 42, pp. 8345-8353Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/S0040-4020(00)00746-8
- [ONLINE] View publication in Scopus
A bioactive modified peptide, aeruginosamide, isolated from the cyanobacterium Microcystis aeruginosa
Journal of Organic Chemistry, vol. 64, pp. 5329-5332Contributions to Journals: ArticlesComputer assisted structure elucidation of natural products using two-dimensional NMR spectroscopy
Natural Product Reports, vol. 16, pp. 241-247Contributions to Journals: Literature ReviewsConformational Studies on Free and Cu(II) Bound Patellamide C
2nd Euroconference on Marine Natural ProductsContributions to Conferences: PostersConformational Studies on Free and Cu(II) Bound Patellamide C
Biodiversity: A Source of New Leads for the Pharmaceutical and Agrochemical IndustriesContributions to Conferences: PostersDetoxification of microcystins (cyanobacterial hepatotoxins) using TiO2 photocatalytic oxidation
Environmental Science & Technology, vol. 33, pp. 771-775Contributions to Journals: ArticlesTesting the water
Structural Chemistry, pp. 51-55Contributions to Journals: ArticlesCyanobacteria - A novel source of pharmaceuticals
Current Opinion in Drug Discovery and Development, vol. 1, no. 1, pp. 77-84Contributions to Journals: Articles- [ONLINE] View publication in Scopus
Processes influencing the destruction of microcystin-LR by TiO2 photocatalysis
Journal of Photochemistry and Photobiology A: Chemistry, vol. 116, no. 3, pp. 215-219Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/S1010-6030(98)00312-8
- [ONLINE] View publication in Scopus
A bioactive secosterol with an unusual A- and B-ring oxygenation pattern isolated from an Indonesian soft coral Lobophytum sp.
Journal of Natural Products, vol. 61, no. 4, pp. 538-541Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1021/np9705118
- [ONLINE] View publication in Scopus
Syntheses and structures of 3-stannylcholest-5-ene species
Journal of the Chemical Society - Perkin Transactions 1, no. 24, pp. 3657-3664Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1039/a703596i
- [ONLINE] View publication in Scopus