Issue 20, 1996

Stable isotope incorporation evidence for a polyacetate origin of the acyl residues in triophamine, a diacylguanidine metabolite obtained from the dorid nudibranch Triopha catalinae

Abstract

Biosynthetic feeding experiments with sodium [1,2-13C2]-acetate have shown that the acyl residues of triophamine 1 are formed de novo in Triopha catalinae from five intact acetate units.

Article information

Article type
Paper

Chem. Commun., 1996, 2377-2378

Stable isotope incorporation evidence for a polyacetate origin of the acyl residues in triophamine, a diacylguanidine metabolite obtained from the dorid nudibranch Triopha catalinae

E. I. Graziani and R. J. Andersen, Chem. Commun., 1996, 2377 DOI: 10.1039/CC9960002377

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