@article {4589,
	title = {Evidence for de novo biosynthesis of the polyketide fragment of diaulusterol a by the northeastern Pacific Dorid nudibranch Diaulula sandiegensis},
	journal = {Journal of Natural Products},
	volume = {62},
	number = {5},
	year = {1999},
	note = {ISI Document Delivery No.: 201YPTimes Cited: 2Cited Reference Count: 16},
	month = {May},
	pages = {777-779},
	type = {Article},
	abstract = {Stable isotope incorporation experiments using sodium [1,2-C-13(2)]acetate have demonstrated that the 3-hydroxybutyrate substituent of diaulusterol A (1) is biosynthesized de novo by the dorid nudibranch Diaulula sandiegensis. There was no evidence for acetate incorporation into the steroid portion of 1, nor were radiolabeled mevalonate or cholesterol incorporated.},
	keywords = {DEFENSE, ISOTOPE INCORPORATION EVIDENCE, MARINE MOLLUSKS, TRIOPHAMINE},
	isbn = {0163-3864},
	url = {<Go to ISI>://000080625100030},
	author = {Kubanek, J. and Andersen, R. J.}
}
@article {3682,
	title = {Stable isotope incorporation evidence for a polyacetate origin of the acyl residues in triophamine, a diacylguanidine metabolite obtained from the dorid nudibranch Triopha catalinae},
	journal = {Chemical Communications},
	number = {20},
	year = {1996},
	note = {ISI Document Delivery No.: VP467Times Cited: 11Cited Reference Count: 16},
	month = {Oct},
	pages = {2377-2378},
	type = {Article},
	abstract = {Biosynthetic feeding experiments with sodium [1,2-(13)-C-2]-acetate have shown that the acyl residues of triophamine 1 are formed de novo in Triopha catalinae from five intact acetate units.},
	keywords = {biosynthesis, DEFENSE, MARINE NATURAL-PRODUCTS, MOLLUSKS},
	isbn = {1359-7345},
	url = {<Go to ISI>://A1996VP46700036},
	author = {Graziani, E. I. and Andersen, R. J.}
}
