Herniarin

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Herniarin

IUPAC name 7-Methoxychromen-2-one
Other names 7-O-Methylumbelliferone 7-Methoxycoumarin Ayapanin Herniarine Methyl umbelliferyl ether
Identifiers
CAS number	531-59-9^Y=
PubChem	10748
ChemSpider	10295^N
ChEMBL	CHEMBL49732^N
Jmol-3D images	Image 1
SMILES O=C/2Oc1cc(OC)ccc1\C=C\2
InChI InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3^N Key: LIIALPBMIOVAHH-UHFFFAOYSA-N^N InChI=1/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3 Key: LIIALPBMIOVAHH-UHFFFAOYAW
Properties
Molecular formula	C₁₀H₈O₃
Molar mass	176.17 g mol⁻¹
N (verify) (what is: Y/N?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

Herniarin is a natural chemical compound. Chemically, it can be considered a methoxy derivative of coumarin or a methyl derivative of umbelliferone.

Herniarin is found in Herniaria glabra,^[1] Ayapana triplinervis and in species of the genus Prunus (P. mahaleb, P. pensylvanica, and P. maximowiczii).^[2]

References

↑ "Herniarin". liberherbarum.com.
↑ Santamour F. S. and Riedel L. G. H. (1994). "Distribution and inheritance of scopolin and herniarin in some Prunus species". Biochemical systematics and ecology 22 (2): 197–201.

Types of coumarins

O-Methylated	Fraxetin Herniarin (7-O-Methylumbelliferone) Osthol Scopoletin (6-Methoxyumbelliferone)

derivatives

Aglycones

O-Methylated	Bergapten (5-methoxypsoralen) Isopimpinellin (5,8-Dimethoxypsoralene) Methoxsalen (8-Methoxypsoralen) Trioxsalen (2,5,9-Trimethylpsoralen)

Furanocoumarin glycosides

Meroterpene furanocoumarin ether

Oligomers

Synthetic

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