A depsidone lichen metabolite
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Salazinic Acid

Item No. 29885

Technical Information
Formal Name
1,3-dihydro-1,4,10-trihydroxy-5-(hydroxymethyl)-8-methyl-3,7-dioxo-7H-isobenzofuro[4,5-b][1,4]benzodioxepin-11-carboxaldehyde
CAS Number
521-39-1
Synonyms
  • NSC 87509
Molecular Formula
C18H12O10
Formula Weight
Purity
≥95%
A solid
DMF: solubleDMSO: solubleEthanol: solubleMethanol: soluble
SMILES
O=CC1=C(O)C=C(C)C2=C1OC3=C(C(CO)=C(O)C4=C3C(O)OC4=O)OC2=O
InChi Code
InChI=1S/C18H12O10/c1-5-2-8(21)6(3-19)13-9(5)16(23)27-14-7(4-20)12(22)10-11(15(14)26-13)18(25)28-17(10)24/h2-3,18,20-22,25H,4H2,1H3
InChi Key
QQTKVXCQLZIJPP-UHFFFAOYSA-N
Origin
Fungus/Usnea sp.
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Salazinic acid is a depsidone lichen metabolite that has been found in P. sulcata.1 It is active against B. cereus, B. subtilis, S. aureus, P. aeruginosa, S. typhimurium, C. albicans, and A. niger in vitro (MICs = 3.9-30.8 mM). Salazinic acid is cytotoxic to MM98, A431, and HaCaT cells in crystal violet (EC50s = 159, 2,870, and 48 μM, respectively) and neutral red uptake assays (EC50s = 1,925, 1,913, and 907 μM, respectively).2 It increases the wound closure rate in scratch-wounded HaCaT monolayers and increases HaCaT cell migration in a transwell assay when used at a concentration of 30 μM.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Candan, M., Yilmaz, M., Tay, T., et alAntimicrobial activity of extracts of the lichen Parmelia sulcata and its salazinic acid constituent. Z. Naturforsch. C J. Biosci. 62(7-8), 619-621 (2007).

    2. Burlando, B., Ranzato, E., Volante, A., et alAntiproliferative effects on tumour cells and promotion of keratinocyte wound healing by different lichen compounds. Planta. Med. 75(6), 607-613 (2009).