Oxyresveratrol

SKU: O0035

Category: Phytochemicals

Synonyms: trans-2',3,4',5-Tetramethoxystilbene; 29700-22-9
CAS-Number: C₁₄H₁₂O₄
Molecular Formula: 244.2
Molecular Weight

Product Data
Handling
Safety Information
Details

Specifications

Purity: ≥98% (HPLC)
Identity: 1H-NMR
Appearance: White to off-white powder

Properties

Solvents: chloroform

Handling Advice: Protect from light and moisture.
Use / Stability: Stable for at least 2 years after receipt when stored at -20°C.
Long Term Storage: -20°C
Short Term Storage: +4°C
Shipping: AMBIENT

Transportation: Not dangerous goods
Signal word: Warning
GHS Symbol: GHS07
Precautionary statements: P305 + P351 + P338
Hazard statements: H319

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.
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-
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)
InChi Key: PDHAOJSHSJQANO-UPHRSURJSA-N
Smiles: OC1=CC(O)=C(C=CC2=CC(O)=CC(O)=C2)C=C1

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.

SKU: O0035 Category: Phytochemicals

Additional information

Additional information

Synonyms	trans-2',3,4',5-Tetramethoxystilbene
Purity	≥98% (HPLC)
Appearance	White to off-white powder
CAS-Number	29700-22-9
Molecular Formula	C14H12O4
Molecular Weight	244.2
Identity	1H-NMR
Solvents	chloroform
Smiles	OC1=CC(O)=C(C=CC2=CC(O)=CC(O)=C2)C=C1
InChi Key	PDHAOJSHSJQANO-UPHRSURJSA-N
Shipping	AMBIENT
Short Term Storage	+4°C
Long Term Storage	-20°C
Handling Advice	Protect from light and moisture.
Use / Stability	Stable for at least 2 years after receipt when stored at -20°C.
Hazard statements	H319
Precautionary statements	P305 + P351 + P338
GHS Symbol	GHS07
Signal word	Warning
Transportation	Not dangerous goods
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)
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-
Quantity	100 mg, 1 g, Bulk