Zobrazeno 1 - 10 of 82 pro vyhledávání: '"Dumdei BE"'
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Akademický článek
Cyanide and thiocyanate-derived functionality in marine organisms - structures, biosynthesis and ecology
Autor: Garson[xc*], M.J., Simpson, J.S., Flowers, A.E., Dumdei, E.J.
Publikováno v: In Studies in Natural Products Chemistry 2000 21 Part B:329-372
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2
A Lightweight Battery for Backpack Electrofishing
Autor: Gabriel T. Brooks, Stephen Achord, Nathan D. Dumdei, Eric E. Hockersmith
Publikováno v: North American Journal of Fisheries Management. 33:265-268
A lithium ion battery was modified to replace the conventional sealed lead acid battery used to operate a backpack electrofishing unit. Specifications and performance of the lithium ion battery were compared with those of a lead acid battery of simil
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::86cbfa6e1e4457988232ebd9f01e5356
https://doi.org/10.1080/02755947.2013.765526
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4
Cellular origin of chlorinated diketopiperazines in the dictyoceratid sponge Dysidea herbacea (Keller)
Autor: Mary J. Garson, Romila D. Charan, Richard I. Webb, Eric J. Dumdei, Andrew E. Flowers
Publikováno v: Cell and Tissue Research. 292:597-607
The tropical marine sponge Dysidea herbacea (Keller) contains the filamentous unicellular cyanobacterium Oscillatoria spongeliae (Schulze) Hauck as an endosymbiont, plus numerous bacteria, both intracellular and extracellular. Archaeocytes and choano
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94e7c82d4e018d28024ac51648f551ae
https://doi.org/10.1007/s004410051089
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5
Theonellapeptolide IIIe, a New Cyclic Peptolide from the New Zealand Deep Water Sponge, Lamellomorpha strongylata
Autor: Shangxiao Li, Murray H. G. Munro, John W. Blunt, Eric J. Dumdei, Ward T. Robinson, L. K. Pannell
Publikováno v: Journal of Natural Products. 61:724-728
The structure, stereochemistry, and conformation of theonellapeptolide IIIe (1), a new 36-membered ring cyclic peptolide from the New Zealand deep-water sponge Lamellomorpha strongylata, is described. The sequence of the cytotoxic peptolide was deter
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3bb40a7dd5206a754cb465e094f0163
https://doi.org/10.1021/np970417r
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6
The biosynthesis of sesquiterpene isocyanides and isothiocyanates in the marine sponge Acanthella cavernosa (Dendy); Evidence for dietary transfer to the dorid nudibranch Phyllidiella pustulosa
Autor: Eric J. Dumdei, Christopher J. Moore, Mary J. Garson, Andrew E. Flowers
Publikováno v: Comparative Biochemistry and Physiology Part A: Physiology. 118:1385-1392
The tropical marine sponge Acanthella cavernosa (Dendy) converts potassium [14C] cyanide to axisonitrile-3 (1); this precursor is also used for the synthesis of axisothiocyanate-3 (2) suggesting that isocyanides are precursors to isothiocyanates in A
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::123f4d17f5ae6830125f5d1dc010b23e
https://doi.org/10.1016/s0300-9629(97)00051-0
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7
New terpenoid metabolites from the skin extracts, an egg mass, and dietary sponges of the Northeastern Pacific dorid nudibranch Cadlinaluteomarginata
Autor: Raymond J. Andersen, Jorge Rios Steiner, Jana Pika, Eric J. Dumdei, John Coleman, Jon Clardy, Julia Kubanek
Publikováno v: Canadian Journal of Chemistry. 75:773-789
Chemical investigations of Cadlinaluteomarginata skin extracts, egg masses, and dietary sponges have led to the identification of the novel terpenoids cadlinaldehyde (30), spongian 32, seco-spongian 35, 20-acetoxy-12-marginatone (38), and lutenolide
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a00e65f6ecc4061bad6997316029da6b
https://doi.org/10.1139/v97-094
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8
MS/MS analysis of the products of toluene photooxidation and measurement of their mutagenic activity
Autor: Paul B. Shepson, Bruce E. Dumdei, Tadeusz E. Kleindienst, Chris M. Nero, Donald V. Kenny, Larry D. Claxton, Larry T. Cupitt
Publikováno v: Environmental sciencetechnology. 22(12)
Products of the photooxidation of toluene from an irradiated 5.1 ppm toluene/0.9 ppm NO/sub x/ mixture were identified by use of a triple-quadrupole MS/MS operated in an atmospheric pressure ionization mode. The reaction was carried out in a flow-mod
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01873a5b0da229bbb2bb8a21879c0316
https://pubmed.ncbi.nlm.nih.gov/22200479
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9
Acanthenes A to C: a chloro, isothiocyanate, formamide sesquiterpene triad isolated from the Northeastern Pacific marine sponge Acanthella sp. and the dorid nudibranch Cadlina luteomarginata
Autor: David L. Burgoyne, Eric J. Dumdei, Raymond J. Andersen
Publikováno v: Tetrahedron. 49:4503-4510
Acanthenes A (1) and B (2), two new eudesmane sesquiterpenoids, have been isolated from the marine sponge Acanthella. Acanthene C (3), the formamide analog of 1 and 2, has been isolated from the nudibranch Cadlina luteomarginata which feeds on Acanth
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::58fc99633b76729c863eab5b5ae5a606
https://doi.org/10.1016/s0040-4020(01)81280-1
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