Lunularin - Misplaced Pages

Lunularin
Names

Preferred IUPAC name 3-phenol
Identifiers
CAS Number	37116-80-6
3D model (JSmol)	Interactive image
ChemSpider	157893
KEGG	C10269
PubChem CID	181511
UNII	AXG9EP247C
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,4-5H2Key: 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,4-5H2Key: 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 , 100 kPa). Infobox references

Chemical compound

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

A lunularic acid decarboxylase has been detected from the liverwort Conocephalum conicum. 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

v t e 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

Dihydrostilbenoids and their glycosides

Oligomeric forms

This article about an aromatic compound is a stub. You can help Misplaced Pages by expanding it.