Complanine

Complanine

Names
IUPAC name 4-{[(2R,5Z,8Z)-2-Hydroxy-5,8-undecadien-1-yl]amino}-N,N,N-trimethyl-4-oxo-1-butanaminium
Other names (−)-Complanine (R)-(−)-Complanine
Identifiers
CAS Number	1042688-43-6
3D model (Jmol)	Interactive image
ChemSpider	25047857
InChI InChI=1S/C18H34N2O2/c1-5-6-7-8-9-10-11-13-17(21)16-19-18(22)14-12-15-20(2,3)4/h6-7,9-10,17,21H,5,8,11-16H2,1-4H3/p+1/b7-6-,10-9-/t17-/m1/s1 Key: QYFDYRHORFAECH-SVCKQPKZSA-O InChI=1/C18H34N2O2/c1-5-6-7-8-9-10-11-13-17(21)16-19-18(22)14-12-15-20(2,3)4/h6-7,9-10,17,21H,5,8,11-16H2,1-4H3/p+1/b7-6-,10-9-/t17-/m1/s1 Key: QYFDYRHORFAECH-SKOIHYTMBD
SMILES CC/C=C\C/C=C\CC[C@H](CNC(=O)CCC[N+](C)(C)C)O
Properties
Chemical formula	C11H22NO
Molar mass	184.30 g·mol^−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Eurythoe complanata

Complanine is an quaternary ammonium compound isolated from the marine fireworm Eurythoe complanata. It causes an inflammatory effect upon contact with the skin or mucous membranes.

Occurrence

It was previously known that handling the fireworm caused it to release a chemical that induces inflammation of the skin of marine predators and mammals (including humans). Complanine was the first compound isolated from the fireworm which causes these effects. The chemical structure of Complanine was determined by spectroscopical methods^[1] and the absolute configuration was confirmed with a total synthesis.^[2]

It is presumed that this compound's function is to deter predators of the fireworm.

References

1. Kazuhiko Nakamura; Yu Tachikawa; Makoto Kitamura; Osamu Ohno; Masami Suganuma; Daisuke Uemura (2008). "Complanine, an inflammation-inducing substance isolated from the marine fireworm Eurythoe complanata". Org. Biomol. Chem. 6 (12): 2058–2060. doi:10.1039/b803107j. PMID 18528565.
2. Nakamura, Kazuhiko; Tachikawa, Yu; Uemura, Daisuke (2009). "(−)-Complanine, an inflammatory substance of marine fireworm: a synthetic study". Beilstein Journal of Organic Chemistry. 5. doi:10.3762/bjoc.5.12.