Re: sell the bio-vine extract

Re: sell the bio-vine extract


[ PPPindia ] [ Technology Page ]

Posted by mary on July 25, 2005 at 05:59:40:

In Reply to: Re: Morinda root extract/Radix morindae officinalis extract posted by smile on July 05, 2005 at 21:56:59:

Organic Herb Inc.

Phone +86 731 4060828

Mobile +86 131 8709 3042

Fax +86 731 4023669
Email: mary@organic-herb.com


Website: http://www.organic-herb.com
Product Information of Bio-vine
Bio-vine: Grape Skin Extracted Resveratrol

Basic Info
Formal Name: [trans¨C3,4',5¨CTrihydroxystilbene
Molecular Formula C14H12O3
Molecular Weight 228.2 Daltons
Odor : Characteristic
Purity: No Less Than 98%
Stability: Refrigerate. Protect from light. This product is stable for 3 years as supplied
Solubility "DMSO and acetone (50 mg/mL)
"
Supplied as: A Off¨Cwhite solid. Packaged under an inert gas
UV/Vis: ¦Ëmax: 218, 235, 307, 321 nm

Laboratory Procedure

For long term storage£¬we suggest that Resveratrol be supplied at-20˚C£®It will be stable for at least three year.
Resveratrol is supplied as a crystalline solid.A stock solution may be made by dissolving the Resveratrol in an
organic solvent purged with an inert gas.Resveratrol is soluble in organic solvents such as ethanol,DMSO,and dimethyl
formamide.The solubility of Resveratrol in these solvents is at least 65mg/ml
Further dilutions of the stock solution into aqueous buffers or isotonic saline should be made prior to performing
biological experiments.Ensure that the residual amount of organic solvent is insignificant,since organic solvents may
have physiological effects at low concentrations.Organic solvent-free aqueous solutions of Resveratrol can be prepared
than 100ug/ml.We do not recommend storing the aqueous solution for more than one day.
Resveratrol is a selective inhibitor of cyclooxygenase-1(COX-1).¹ It inhibits cyclooxgenase and peroxidase
activities of COX-¹ with ED values of 15and 3.7uM,respectively.respectively.It also has antioxidant properties.

Reference
Jang, M., et al. 1997. Science 275, 218.
Chen, C.K., et al. 1996. Gen. Pharmacol. 27, 363





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