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Details

Stereochemistry ACHIRAL
Molecular Formula C14H12O4
Molecular Weight 244.2427
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of HYDROXYRESVERATROL

SMILES

OC1=CC(O)=C(\C=C\C2=CC(O)=CC(O)=C2)C=C1

InChI

InChIKey=PDHAOJSHSJQANO-OWOJBTEDSA-N
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+

HIDE SMILES / InChI

Molecular Formula C14H12O4
Molecular Weight 244.2427
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Hydroxyresveratrol (Oxyresveratrol) is a major active compound in the heartwood of Artocarpus lacucha. It was first isolated from the heartwood of Artocarpus lakoocha, and has also been found in various plants, including Smilax China, Morus alba, Varatrum nigrum, Scirpus maritinus, and Maclura pomifera. Oxyresveratrol, an aglycone of mulberroside A, has been produced by microbial biotransformation or enzymatic hydrolysis of a glycosylated stilbene mulberroside A, which is one of the major compounds of the roots of M. alba. Oxyresveratrol plays an important role in anti-tyrosinase, antioxidant, anti-inflammatory, antiviral and neuroprotective properties. There are many A. lacucha commercial products available on the market for skin whitening and anti-aging effects. OxyResvenox™ is the registered trademark of Oxyresveratrol from Sabinsa. Oxyresveratrol is an analog of Resveratrol and is of synthetic origin. The hydroxystilbene compounds including oxyresveratrol and resveratrol showed the potent inhibitory effect on tyrosinase activity. Oxyresveratrol is also naturally present in Morus alba L., Morus bombycis. Oxyresveratrol exhibits a potent inhibitory effect on dopa oxidase activity of tyrosinase which catalyzes rate-limiting steps of melanin biosynthesis. Oxyresveratrol showed superoxide scavenging effects with the IC50 values 3.81 ± 0.5 uM, Oxyresveratrol exhibited a DPPH free radical scavenging effect (IC50 = 23.4 ± 1.5 uM). Oxyresveratrol also showed hepatoprotective effects with EC50 values 32.3 ± 2.62 uM, on tacrine-induced cytotoxicity in human liver-derived Hep G2 cells. Oxyresveratrol significantly inhibited LPS-evoked nuclear translocation of NF-kappaB and cyclooxygenase-2 (COX-2) activity in RAW 264.7 cells. The results suggest that the anti-inflammatory properties of oxyresveratrol might be correlated with inhibition of the iNOS expression through down-regulation of NF-kappaB binding activity and significant inhibition of COX-2 activity. Oxyresveratrol revealed a dose-dependent neuroprotective effect in an in vivo stroke model. This may prove to be beneficial for a therapeutic strategy to limit brain injury in acute brain ischemia.

Approval Year

TargetsConditions
PubMed

PubMed

TitleDatePubMed
Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: Humans: topical - Recommended usage level in cosmetic and personal care applications is 0.05 – 0.2% w/w of the composition. http://www.esbalabs.com/assets/images/Bump-and-Blemish/Oxyresvenox-skin-brightener.pdf
Rats: Oxyresveratrol (10 or 20 mg/kg) significantly reduced the brain infarct volume by approximately 54% and 63%, respectively, when compared to vehicle-treated MCAO rats. Oxyresveratrol (2, 10, 20 and 30 mg/kg body weight in a total volume of 1 ml in 30% ethanol) or equal volumes of the vehicle were administered intraperitoneally (i.p.) in animals twice: at the time of occlusion and at the time of reperfusion.
Route of Administration: Intraperitoneal
Oxyresveratrol with 0.3 to 5 uM exhibited potent and dose-dependent inhibitions (25 to 84%) on the tyrosinase enzyme activity, where 50% of inhibition was shown at the concentration of about 1 uM.
Substance Class Chemical
Created
by admin
on Sat Dec 16 20:02:11 GMT 2023
Edited
by admin
on Sat Dec 16 20:02:11 GMT 2023
Record UNII
6V071CP5CR
Record Status Validated (UNII)
Record Version
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Name Type Language
HYDROXYRESVERATROL
INCI  
INCI  
Official Name English
TRANS-STILBENE-2,4,3',5'-TETROL
Systematic Name English
1,3-BENZENEDIOL, 4-(2-(3,5-DIHYDROXYPHENYL)ETHENYL)-, (E)-
Common Name English
HYDROXYRESVERATROL [INCI]
Common Name English
2,3',4,5'-STILBENETETROL, (E)-
Systematic Name English
TRANS-2,3',4,5'-TETRAHYDROXYSTILBENE
Systematic Name English
OXYRESVENOX
Brand Name English
1,3-BENZENEDIOL, 4-((1E)-2-(3,5-DIHYDROXYPHENYL)ETHENYL)-
Systematic Name English
Code System Code Type Description
FDA UNII
6V071CP5CR
Created by admin on Sat Dec 16 20:02:11 GMT 2023 , Edited by admin on Sat Dec 16 20:02:11 GMT 2023
PRIMARY
EPA CompTox
DTXSID801030442
Created by admin on Sat Dec 16 20:02:11 GMT 2023 , Edited by admin on Sat Dec 16 20:02:11 GMT 2023
PRIMARY
PUBCHEM
5281717
Created by admin on Sat Dec 16 20:02:11 GMT 2023 , Edited by admin on Sat Dec 16 20:02:11 GMT 2023
PRIMARY
MESH
C515052
Created by admin on Sat Dec 16 20:02:11 GMT 2023 , Edited by admin on Sat Dec 16 20:02:11 GMT 2023
PRIMARY
CAS
29700-22-9
Created by admin on Sat Dec 16 20:02:11 GMT 2023 , Edited by admin on Sat Dec 16 20:02:11 GMT 2023
PRIMARY
DAILYMED
6V071CP5CR
Created by admin on Sat Dec 16 20:02:11 GMT 2023 , Edited by admin on Sat Dec 16 20:02:11 GMT 2023
PRIMARY
WIKIPEDIA
Oxyresveratrol
Created by admin on Sat Dec 16 20:02:11 GMT 2023 , Edited by admin on Sat Dec 16 20:02:11 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> ACTIVE CONSTITUENT ALWAYS PRESENT
Activity against BACE-1 with Ki value of 5.4 x 10-6M and IC50 of 7.6 x 10-5M.