Vaccenyl acetate

11-*cis*-Vaccenyl acetate
Names
	IUPAC name (Z)-octadec-11-enyl acetate
Identifiers
CAS Number	6186-98-7 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:46274 ;
ChemSpider	4515653 ;
PubChem CID	5363286;
CompTox Dashboard (EPA)	DTXSID401028467 ;
	InChI InChI=1S/C20H38O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-22-20(2)21/h8-9H,3-7,10-19H2,1-2H3/b9-8- Key: QSZKEDWVAOAFQY-HJWRWDBZSA-N ; InChI=1/C20H38O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-22-20(2)21/h8-9H,3-7,10-19H2,1-2H3/b9-8- Key: QSZKEDWVAOAFQY-HJWRWDBZBI;
	SMILES CCCCCC/C=C\CCCCCCCCCCOC(=O)C;
Properties
Chemical formula	C20H38O2
Molar mass	310.51 g/mol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

11-cis-Vaccenyl acetate (cVA) is a volatile chemical compound that acts as a pheromone in Drosophila and at least one species of longhorn beetle. It is the acetate ester of vaccenyl alcohol.

The odorant receptor subunit Or67d was shown to be necessary for detection of cVA.^[1] Males that are mutant for Or67d start courting other males, whereas females that lack Or67d become less receptive towards males courting them.^[2] The sensory neurons expressing Or67d send projections to the glomerulus DA1.^[3] DA1 is one of the three glomeruli that is bigger in males than in females. Moreover, the projection neurons that connect to DA1 have sexually dimorphic arborizations in the higher brain centers (esp. lateral horn).

References

^ Ha, TS, Smith DP J. Neurosci. 26:8727-8733 (2006).
^ A. Kurtovic, A. Widmer, B. J. Dickson, Nature 446, 542 (2007).
^ Couto A, Alenius M, Dickson BJ.; Curr Biol. 2005 Sep 6;15(17):1535-47.

A Ray, A Zunic, RL Alten, JS McElfresh, LM Hanks, JG Millar. 2011. J. Chem. Ecol. 37:173-178.

[1] Ha, TS, Smith DP J. Neurosci. 26:8727-8733 (2006).

[2] A. Kurtovic, A. Widmer, B. J. Dickson, Nature 446, 542 (2007).

[3] Couto A, Alenius M, Dickson BJ.; Curr Biol. 2005 Sep 6;15(17):1535-47.

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