A5010394693- Marine Sponges and Natural Products
- Microbial Natural Products and Biosynthesis
- Synthesis and Biological Activity
- Synthetic Organic Chemistry Methods
- Chemical synthesis and alkaloids
- Seaweed-derived Bioactive Compounds
- Fungal Biology and Applications
- Analytical Chemistry and Chromatography
- Beetle Biology and Toxicology Studies
- Natural product bioactivities and synthesis
- Marine Toxins and Detection Methods
- Asymmetric Synthesis and Catalysis
- Traditional and Medicinal Uses of Annonaceae
- Phytochemical compounds biological activities
- Plant Pathogens and Fungal Diseases
- Chemical Synthesis and Analysis
- Carbohydrate Chemistry and Synthesis
- Bioactive Compounds and Antitumor Agents
- Metabolomics and Mass Spectrometry Studies
- Biological Activity of Diterpenoids and Biflavonoids
- Molecular spectroscopy and chirality
- Synthesis and bioactivity of alkaloids
- Marine Biology and Environmental Chemistry
- Phytochemistry and Biological Activities
- Antimicrobial Peptides and Activities
University of Canterbury
2010-2023
Christ University
2015-2017
NHS Grampian
2015
Technical University of Denmark
2004-2010
Oregon Health & Science University
2010
University of California, Santa Barbara
2010
Rhodes University
2010
University of Auckland
2010
University of Bonn
2009
University of Colombo
2006-2009
ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTNodularin, microcystin, and the configuration of AddaKenneth L. Rinehart, Kenichi. Harada, Michio. Namikoshi, Choryu. Chen, Carl A. Harvis, Murray H. G. Munro, John W. Blunt, Paul E. Mulligan, Val R. Beasley, . et al.Cite this: J. Am. Chem. Soc. 1988, 110, 25, 8557–8558Publication Date (Print):December 1, 1988Publication History Published online1 May 2002Published inissue 1 December...
Covering: 2008. Previous review: Nat. Prod. Rep., 2009, 26, 170
ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTMycalamide A, an antiviral compound from a New Zealand sponge of the genus MycaleNigel B. Perry, John W. Blunt, Murray H. G. Munro, and Lewis K. PannellCite this: J. Am. Chem. Soc. 1988, 110, 14, 4850–4851Publication Date (Print):July 1, 1988Publication History Published online1 May 2002Published inissue 1 July 1988https://pubs.acs.org/doi/10.1021/ja00222a067https://doi.org/10.1021/ja00222a067research-articleACS PublicationsRequest reuse...
Summary Genetic techniques were employed to investigate the archaeal, bacterial and eukaryotic communities associated with Antarctic sponges Kirkpatrickia varialosa , Latrunculia apicalis Homaxinella balfourensis Mycale acerata Sphaerotylus antarcticus. The phylogenetic affiliation of sponge‐derived bacteria was assessed by 16S rRNA sequencing cloned DNA fragments. Denaturing gradient gel electrophoresis (DGGE) used determine stability associations within each sponge species across spatial...
ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTDiscorhabdin C, a highly cytotoxic pigment from sponge of the genus LatrunculiaNigel B. Perry, John W. Blunt, D. McCombs, and Murray H. G. MunroCite this: J. Org. Chem. 1986, 51, 26, 5476–5478Publication Date (Print):December 1, 1986Publication History Published online1 May 2002Published inissue 1 December 1986https://pubs.acs.org/doi/10.1021/jo00376a096https://doi.org/10.1021/jo00376a096research-articleACS PublicationsRequest reuse...
The use of an HPLC bioactivity profiling/microtiter plate technique in conjunction with capillary probe NMR instrumentation and access to appropriate databases effectively short-circuits conventional dereplication procedures, necessarily based on multimilligram extracts, a single, more rapid submilligram operation. This approach is illustrated using fungal or bacterial extracts that contain known compounds. In each case the steps were carried out microgram quantities extract demonstrate...
Abstract