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Herniarin

From Wikipedia, the free encyclopedia
Herniarin
Chemical structure of herniarin
Chemical structure of herniarin
Names
Preferred IUPAC name
7-Methoxy-2H-1-benzopyran-2-one
Other names
7-O-Methylumbelliferone
7-Methoxycoumarin
Ayapanin
Herniarine
Methyl umbelliferyl ether
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard100.007.741Edit this at Wikidata
UNII
  • 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
  • O=C/2Oc1cc(OC)ccc1\C=C\2
Properties
C10H8O3
Molar mass176.171 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

Herniarin is a natural chemical compound. Chemically, it can be considered amethoxyderivative ofcoumarin or amethyl derivative ofumbelliferone.

Herniarin is found inHerniaria glabra,[1]Ayapana triplinervis and in species of the genusPrunus (P. mahaleb,P. pensylvanica, andP. maximowiczii).[2]

References

[edit]
  1. ^"Herniarin". liberherbarum.com.
  2. ^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.Bibcode:1994BioSE..22..197S.doi:10.1016/0305-1978(94)90008-6.
Types ofcoumarins
Aglycones
O-Methylated
Glycosides
Derivatives
Furanocoumarins
Aglycones
O-Methylated
Furanocoumarin glycosides
Meroterpene furanocoumarin ether
Oligomers
Synthetic


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