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Revision as of 07:24, 25 July 2011 by CheMoBot (talk | contribs) (Updating {{chembox}} (changes to watched fields - updated 'UNII_Ref', 'ChemSpiderID_Ref', 'StdInChI_Ref', 'StdInChIKey_Ref', 'ChEMBL_Ref') per Chem/Drugbox validation (report [[Wikipedia_talk:Wik)(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff)meta-depside bond digalloyl ester | |
Names | |
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IUPAC name 3,4-dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxybenzoic acid | |
Other names
Digallate 3,4-dihydroxy-5-(3,4,5-trihydroxybenzoyloxy)benzoate m-digallic acid Digalloyl ester | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ECHA InfoCard | 100.007.842 |
PubChem CID | |
CompTox Dashboard (EPA) | |
SMILES
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Properties | |
Chemical formula | C14H10O9 |
Molar mass | 322.22 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is ?) Infobox references |
Digallic acid is a polyphenolic compound found in Pistacia lentiscus. Digallic acid is also present in the molecule of tannic acid. Digalloyl esters involve either -meta or -para depside bonds.
Tannase is an enzyme that uses digallate to produce gallic acid.
References
- Study of genotoxic, antigenotoxic and antioxidant activities of the digallic acid isolated from Pistacia lentiscus fruits. Wissem Bhouri, Safa Derbel, Ines Skandrani, Jihed Boubaker, Ines Bouhlel, Mohamed B. Sghaier, Soumaya Kilani, Anne M. Mariotte, Marie G. Dijoux-Franca, Kamel Ghedira and Leila Chekir-Ghedir, Toxicology in Vitro, Volume 24, Issue 2, March 2010, pp. 509-515, doi:10.1016/j.tiv.2009.06.024
- Analysis of gallic, digallic and trigallic acids in tannic acids by high-performance liquid chromatography. P. Delahaye and M. Verzele, Journal of Chromatography A, Volume 265, 1983, pp. 363-367, doi:10.1016/S0021-9673(01)96734-2
- Tannin chemistry, by Ann E. Hagerman
Types of gallotannins | |||||||||||||
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Aglycones | |||||||||||||
Galloylglucoses |
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Galloylquinic acids: |
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Galloylshikimic acids: | |||||||||||||
others |