Lunularin

Lunularin
Names
	IUPAC name 3-[2-(4-hydroxyphenyl)ethyl]phenol
Identifiers
CAS Number	37116-80-6;
3D model (JSmol)	Interactive image;
ChemSpider	157893;
KEGG	C10269;
PubChem CID	181511;
CompTox Dashboard (EPA)	DTXSID20190614 ;
	InChI InChI=1S/C14H14O2/c15-13-8-6-11(7-9-13)4-5-12-2-1-3-14(16)10-12/h1-3,6-10,15-16H,4-5H2 Key: ILEYXPCRQKRNIJ-UHFFFAOYSA-N; InChI=1/C14H14O2/c15-13-8-6-11(7-9-13)4-5-12-2-1-3-14(16)10-12/h1-3,6-10,15-16H,4-5H2 Key: ILEYXPCRQKRNIJ-UHFFFAOYAQ;
	SMILES c1cc(cc(c1)O)CCc2ccc(cc2)O;
Properties
Chemical formula	C14H14O2
Molar mass	214.26 g/mol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Lunularin is a dihydrostilbenoid found in common celery. It has also been found in the roots of Hydrangea macrophylla.[1]

A lunularic acid decarboxylase has been detected from the liverwort Conocephalum conicum.[2] It converts lunularic acid into lunularin.

References

Lunularic acid and related compounds in liverworts, algae and Hydrangea. John Gorham, Phytochemistry, 1977, Volume 16, Issue 2, Pages 249–253, doi:10.1016/S0031-9422(00)86795-3
Lunularic acid decarboxylase from the liverwort Conocephalum conicum. Robert J. Pryce and Linda Linton, Phytochemistry, November 1974, Volume 13, Issue 11, Pages 2497–2501, doi:10.1016/S0031-9422(00)86926-5

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Dihydrostilbenoids and their glycosides
Dihydrostilbenoids	Batatasin-III (3,3′-dihydroxy-5-methoxybibenzyl) Combretastatin and combretastatin B-1 Dihydro-resveratrol Isonotholaenic acid Lunularic acid Lunularin Notholaenic acid Tyrolobibenzyl A, B and C
Oligomeric forms	Bis(bibenzyls): 13,13'-O-Isoproylidenericcardin D Marchantin B and E Neomarchantin A Plagiochin E Riccardin H Macrocyclic bis(benzyls): Marchantin A and C Riccardin B and C Cyclic bibenzyl-dihydrophenanthrene derivative: Cavicularin