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Obovatol

From Wikipedia, the free encyclopedia
Obovatol
Names
Preferred IUPAC name
5-(Prop-2-en-1-yl)-3-[4-(prop-2-en-1-yl)phenoxy]benzene-1,2-diol
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
  • InChI=1S/C18H18O3/c1-3-5-13-7-9-15(10-8-13)21-17-12-14(6-4-2)11-16(19)18(17)20/h3-4,7-12,19-20H,1-2,5-6H2
    Key: OPGPFZQBCIAFLI-UHFFFAOYSA-N
  • C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)CC=C
Properties
C18H18O3
Molar mass282.339 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Obovatol is a biphenolicanti-inflammatory,anxiolytic, andnootropicisolated from the bark ofMagnolia obovata.[1] It is a biphenyllignan.[2]

References

[edit]
  1. ^Choi, DY; Lee, JW; Peng, J; Lee, YJ; Han, JY; Lee, YH; Choi, IS; Han, SB; Jung, JK; Lee, WS; Lee, SH; Kwon, BM; Oh, KW; Hong, JT (2012)."Obovatol improves cognitive functions in animal models for Alzheimer's disease".Journal of Neurochemistry.120 (6):1048–59.doi:10.1111/j.1471-4159.2011.07642.x.PMID 22212065.S2CID 25896721.
  2. ^Obovatol andobovatal, novel biphenyl ether lignans from the leaves ofMagnolia obovata Thunb. K Ito, T Iida, K Ichino, M Tsunezuka and M Hattori, … and Pharmaceutical Bulletin, 1982
Alcohols
Barbiturates
Benzodiazepines
Carbamates
Flavonoids
Imidazoles
Kava constituents
Monoureides
Neuroactive steroids
Nonbenzodiazepines
Phenols
Piperidinediones
Pyrazolopyridines
Quinazolinones
Volatiles/gases
Others/unsorted
Types oflignans
Lignans
Lignanglycosides
Mammalian lignans (enterolignans)
Neolignans
Flavonolignans


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