ORCID Profile
0000-0001-7550-4607
Current Organisation
Murdoch University
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Publisher: Elsevier BV
Date: 05-2019
Publisher: Elsevier BV
Date: 03-2020
Publisher: Elsevier BV
Date: 04-2010
Publisher: Elsevier BV
Date: 05-2019
Publisher: American Chemical Society (ACS)
Date: 15-11-2013
DOI: 10.1021/ED400106M
Publisher: Elsevier BV
Date: 10-2020
Publisher: Elsevier BV
Date: 05-2011
Publisher: Frontiers Media SA
Date: 23-06-2016
Publisher: Elsevier BV
Date: 06-2017
Publisher: Elsevier BV
Date: 2020
Publisher: Elsevier BV
Date: 2019
Publisher: American Chemical Society (ACS)
Date: 27-02-2013
DOI: 10.1021/IE3024824
Publisher: Springer Science and Business Media LLC
Date: 24-08-2020
Publisher: Elsevier BV
Date: 05-2020
Publisher: Elsevier BV
Date: 08-2019
Publisher: American Chemical Society (ACS)
Date: 29-03-2007
DOI: 10.1021/NP060489V
Publisher: Elsevier BV
Date: 07-2012
Publisher: American Chemical Society (ACS)
Date: 15-09-2020
Publisher: Elsevier BV
Date: 10-2009
Publisher: Elsevier BV
Date: 02-2019
Publisher: American Chemical Society (ACS)
Date: 09-03-2007
DOI: 10.1021/NP060566M
Abstract: Chemical investigation of the Western Australian marine brown alga Cystophora harveyi resulted in the isolation of the new linearly fused 6,6,5-tricyclic compound pycnanthuquinone C (1), in addition to four previously reported geranyltoluquinol derivatives. Structures were elucidated by interpretation of spectrometric data. Compounds with the same cyclic skeleton as 1 have been reported to be useful drug leads for the treatment of type 2 diabetes, while compounds 4 and 7 are known constituents of Chinese medicinal herbs. A biosynthetic scheme encompassing all of the geranyltoluquinol derivatives isolated from C. harveyi is proposed.
Publisher: Elsevier BV
Date: 05-2006
DOI: 10.1016/J.PHYTOCHEM.2006.03.011
Abstract: Six cyclised tetraprenyltoluquinols and five stereoisomers with the previously reported amentol skeleton have been isolated from the lipophilic extract of the South African brown alga Cystophora fibrosa. Structures and relative stereochemistry were determined using spectrometric techniques, particularly 1D and 2D NMR, and molecular modelling experiments. The compounds isolated appear to be enantiomeric to compounds with the same skeleton isolated from brown algae of the genus Cystoseira collected in northern Africa and the Mediterranean Sea. The isolation of tetraprenyltoluquinols with the amentol skeleton from this alga suggests that C. fibrosa should be moved from the genus Cystophora into the Cystoseira.
Publisher: Elsevier BV
Date: 11-2017
Publisher: Elsevier BV
Date: 11-2020
No related grants have been discovered for Damian Laird.