Chemodex

Oxyresveratrol

Product Code:
 
CDX-O0035
Product Group:
 
Inhibitors and Activators
Supplier:
 
Chemodex
Regulatory Status:
 
RUO
Shipping:
 
AMBIENT
Storage:
 
-20°C
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Chemical Structure
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Chemical Structure

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CodeSizePrice
CDX-O0035-M100100 mg£157.00
Quantity:
CDX-O0035-G0011 g£1,048.00
Quantity:
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This product comes from: Switzerland.
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Further Information

Alternate Names/Synonyms:
trans-2',3,4',5-Tetramethoxystilbene
Appearance:
White to off-white powder.
CAS:
29700-22-9
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Handling Advice:
Keep cool and dry.Protect from light and moisture.
Hazards:
H319
InChi:
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-
InChiKey:
PDHAOJSHSJQANO-UPHRSURJSA-N
Long Description:
Chemical. CAS: 29700-22-9. Formula: C14H12O4. MW: 244.2. Synthetic. Naturallly occuring analog of resveratrol. Potent antioxidant and free-radical scavenger. Shown to have neuroprotective activity against cerebral ischemia and against traumatic injury. Apoptosis inhibitor in transient cerebral ischemia. Inhibits viral DNA replication and late viral protein synthesis of African Swine fever virus. Has depigmenting effects by effectively inhibiting tyrosinase activity, which catalyzes the rate-limiting step in synthesizing melanin pigments. Has anti-inflammatory properties based on inhibition of iNOS expression through down-regulation of NF-kB binding activity and significant inhibition of COX-2 activity. Antihyperlipidemic agent.
MDL:
MFCD11974969
Molecular Formula:
C14H12O4
Molecular Weight:
244.2
Package Type:
Vial
Precautions:
P305, P351, P338
Product Description:
Naturallly occuring analog of resveratrol. Potent antioxidant and free-radical scavenger. Shown to have neuroprotective activity against cerebral ischemia and against traumatic injury. Apoptosis inhibitor in transient cerebral ischemia. Inhibits viral DNA replication and late viral protein synthesis of African Swine fever virus. Has depigmenting effects by effectively inhibiting tyrosinase activity, which catalyzes the rate-limiting step in synthesizing melanin pigments. Has anti-inflammatory properties based on inhibition of iNOS expression through down-regulation of NF-kB binding activity and significant inhibition of COX-2 activity. Antihyperlipidemic agent.
Purity:
>98% (HPLC)
Signal word:
Warning
SMILES:
OC1=CC(O)=C(C=CC2=CC(O)=CC(O)=C2)C=C1
Solubility Chemicals:
Soluble in chloroform.
Source / Host:
Synthetic.
Transportation:
Non-hazardous
UNSPSC Category:
Biochemical Reagents
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.

References

(1) Y.M. Kim, et al.; J. Biol. Chem. 277, 16340 (2002) | (2) P. Lorenz, et al.; Nitric Oxide 9, 64 (2003) | (3) K.-O. Chung, et al.; J. Pharm. Pharmacol. 55, 1695 (2003) | (4) S.A. Andrabi, et al.; Brain Res. 1017, 98 (2004) | (5) I. Galindo, et al.; Antiviral Res. 91, 57 (2011) | (6) M. Chatsumpun, et al.; Nat. Prod. Commun. 6, 41 (2011) | (7) J.T. Weber, et al.; Eur. J. Pharmacol. 680, 55 (2012) | (8) S.-P. Jo, et al.; Food Chem. Toxicol. 65, 213 (2014)