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Orsellinic acid

Free radical scavenger
ALX-350-391-M001 1 mg 142.00 USD
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Benzoic acid. Blocks PAF-mediated neuronal apoptosis. Shows free radical scavenging activity.

Product Specification

Alternative Name:2,4-Dihydroxy-6-methylbenzoic acid, Orsellic acid
Source:Isolated from fungus Chaetomium sp.
MI:14: 6881
Purity:≥97% (HPLC)
Identity:Identity determined by 1H-NMR and ESI-MS.
Solubility:Soluble in water, DMSO or 100% ethanol.
Long Term Storage:-20°C
Handling:Protect from light.
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Product Literature References

Radical-scavenging activity of orsellinates: T.I. Lopes, et al.; Chem. Pharm. Bull. (Tokyo) 56, 1551 (2008), Abstract; Full Text
Plant phenolics regulate neoplastic cell growth and survival: a quantitative structure-activity and biochemical analysis: C.S. Harris, et al.; Can. J. Physiol. Pharmacol. 85, 1124 (2007), Abstract;
Platelet activating factor-induced neuronal apoptosis is initiated independently of its G-protein coupled PAF receptor and is inhibited by the benzoate orsellinic acid: S.D. Ryan, et al.; J. Neurochem. 103, 88 (2007), Abstract; Full Text
Cytotoxic activity of orsellinates: A.T. Gomes, et al.; Z. Naturforsch. [C] 61, 653 (2006), Abstract;
Isolation and identification of orsellinic acid and penicillic acid produced by Penicillium fennelliae Stolk: G.W. van Eijk; Antonie Van Leeuwenhoek 35, 497 (1969), Abstract;
Studies on the biosynthesis of phenols in fungi. Conversion of [14C]orsellinic acid and [14C]orcinol into fumigatol by Aspergillus fumigatus I.M.I. 89353: N.M. Packter; Biochem. J. 98, 353 (1966), Abstract; Full Text
A Synthesis of Orsellinic Acid: R.A. Kloss & D.A. Clayton; J. Org. Chem. 30, 3566 (1965), Abstract;
Studies in the biochemistry of micro-organisms. 110. Production and biosynthesis of orsellinic acid by Penicillium madriti G. Smith: J.H. Birkinshaw & A. Gowlland; Biochem. J. 84, 342 (1962), Abstract; Full Text

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