@article {4857,
	title = {Geographic variation and tissue distribution of endogenous terpenoids in the Northeastern Pacific Ocean dorid nudibranch Cadlina luteomarginata: Implications for the regulation of de novo biosynthesis},
	journal = {Journal of Chemical Ecology},
	volume = {26},
	number = {2},
	year = {2000},
	note = {ISI Document Delivery No.: 285PTTimes Cited: 6Cited Reference Count: 14},
	month = {Feb},
	pages = {377-389},
	type = {Article},
	abstract = {Gas chromatography (GC) analyses of whole animal skin extracts and individual tissue extracts obtained from specimens of Cadlina luteo-marginata collected in British Columbia and southern California were used to determine if concentrations of the nudibranch{\textquoteright}s biosynthetic products-albicanyl acetate (1), cadlinaldehyde (2), and luteone (3)-vary significantly between two populations, among individuals of a population, and among body tissues of individual specimens. The major biosynthetic product, albicanyl acetate (1), has the same concentration in both British Columbia and California populations, while the British Columbia population contains greater total amounts of 2 and 3 than the California population. Within individuals from one population, the largest proportion of endogenous metabolites is in the dorsum, specifically in the mantle dermal formations and margins. The GC analyses show that across geographically separated populations and within geographically localized populations the concentration of endogenous metabolites is inversely correlated with availability of structurally similar compounds from dietary sources. This suggests that the de novo biosynthesis of defensive compounds might be regulated according to need.},
	keywords = {Cadlina luteomarginata, CHEMICAL DEFENSE, de novo biosynthesis, instraspecific variation, MOLLUSKS, nudibranch, opistobranch, terpenes},
	isbn = {0098-0331},
	url = {<Go to ISI>://000085398000005},
	author = {Kubanek, J. and Faulkner, D. J. and Andersen, R. J.}
}
@article {3946,
	title = {New terpenoid metabolites from the skin extracts, an egg mass, and dietary sponges of the Northeastern Pacific dorid nudibranch Cadlina luteomarginata},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {75},
	number = {6},
	year = {1997},
	note = {ISI Document Delivery No.: XL704Times Cited: 27Cited Reference Count: 26},
	month = {Jun},
	pages = {773-789},
	type = {Article},
	abstract = {Chemical investigations of Cadlina luteomarginata 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 (39) from the nudibranch skin extracts, the new drimane sesquiterpenoid 1 alpha,2 alpha-diacetoxyalbicanyl acetate (40) from the nudibranch{\textquoteright}s egg mass, and the new sesquiterpenoids O-methyl-9-oxofurodysininlactone (47), 2-oxomicrocionin-2-lactone (48), and O-methyl-2-oxomicrocionin-2-lactone (49), from the dietary sponge Pleraplysilla sp. The known terpenoids furodysinin (1), furodysin (16), marginatafuran (21), and 9,11-dihydrogracillin A (37), which have been frequently isolated from C. luteomarginata skin extracts, were found for the first time in extracts of the dietary sponges Pleraplysilla sp. and Aplysilla sp. One of the new terpenoids, cadlinaldehyde (30), has an unprecedented degraded sesterterpenoid skeleton.},
	keywords = {APLYSILLA-GLACIALIS, CHEMICAL DEFENSE, MOLLUSKS, nudibranch, SPONGE, structure elucidation, terpenoids},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1997XL70400025},
	author = {Dumdei, E. J. and Kubanek, J. and Coleman, J. E. and Pika, J. and Andersen, R. J. and Steiner, J. R. and Clardy, J.}
}
@article {7082,
	title = {CHROMODORANE DITERPENES FROM THE TROPICAL DORID NUDIBRANCH CHROMODORIS-CAVAE},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {69},
	number = {5},
	year = {1991},
	note = {ISI Document Delivery No.: FP799Times Cited: 9Cited Reference Count: 10},
	month = {May},
	pages = {768-771},
	type = {Article},
	abstract = {Two novel diterpenoids, chromodorolides A (1) and B (2), have been isolated from skin extracts of the tropical dorid nudibranch Chromodoris cavae. Complete NMR assignments are presented for chromodorolide A (1). The structure of chromodorolide B (2) has been solved by spectroscopic analysis. Chromodorolides A (1) and B (2) are the first examples of diterpenoids with the highly rearranged chromodorane carbon skeleton.},
	keywords = {CARBON SKELETON, CHROMODORANE, CHROMODORIS, DITERPENE, nudibranch},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1991FP79900002},
	author = {Morris, S. A. and De Silva, E. D. and Andersen, R. J.}
}
