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1 References  














Oxyresveratrol






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From Wikipedia, the free encyclopedia
 


Oxyresveratrol
Names
Preferred IUPAC name

4-[(E)-2-(3,5-Dihydroxyphenyl)ethen-1-yl]benzene-1,3-diol

Other names

2,3',4,5'-Tetrahydroxy-trans-stilbene

Identifiers

CAS Number

3D model (JSmol)

ChemSpider
ECHA InfoCard 100.108.380 Edit this at Wikidata
KEGG
MeSH C034912

PubChem CID

UNII

CompTox Dashboard (EPA)

  • InChI=1S/C14H12O4/c15-11-4-3-10(14(18)8-11)2-1-9-5-12(16)7-13(17)6-9/h1-8,15-18H/b2-1+

    Key: PDHAOJSHSJQANO-OWOJBTEDSA-N

  • C1=CC(=C(C=C1O)O)C=CC2=CC(=CC(=C2)O)O

Properties

Chemical formula

C14H12O4
Molar mass 244.24 g/mol

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Infobox references

Oxyresveratrol is a stilbenoid. It is found in the heartwood of Artocarpus lakoocha and in the traditional drug 'Puag-Haad' made from it.[1] It is also the aglycone of mulberroside A, a compound found in Morus alba, the white mulberry.[2]

Oxyresveratrol is a potent tyrosinase inhibitor.[2]

References[edit]

  1. ^ Maneechai, S; Likhitwitayawuid, K; Sritularak, B; Palanuvej, C; Ruangrungsi, N; Sirisa-Ard, P (2009). "Quantitative analysis of oxyresveratrol content in Artocarpus lakoocha and 'Puag-Haad'". Medical Principles and Practice. 18 (3): 223–7. doi:10.1159/000204354. PMID 19349726. S2CID 29232919.
  • ^ a b Kim, JK; Kim, M; Cho, SG; Kim, MK; Kim, SW; Lim, YH (2010). "Biotransformation of mulberroside a from Morus alba results in enhancement of tyrosinase inhibition". Journal of Industrial Microbiology & Biotechnology. 37 (6): 631–7. doi:10.1007/s10295-010-0722-9. PMID 20411402. S2CID 21236818.

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  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Oxyresveratrol&oldid=1184045699"

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    This page was last edited on 8 November 2023, at 00:46 (UTC).

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