Theogallin

Theogallin

Names
IUPAC name (1S,3R,4R,5R)-1,3,4-trihydroxy-5-(3,4,5-trihydroxybenzoyl)oxycyclohexane-1-carboxylic acid
Other names 3-O-Galloylquinic acid
Identifiers
CAS Number	17365-11-6
ChEBI	CHEBI:9522
ChemSpider	391291
Jmol interactive 3D	Image
PubChem	442988
InChI InChI=1S/C14H16O10/c15-6-1-5(2-7(16)10(6)18)12(20)24-9-4-14(23,13(21)22)3-8(17)11(9)19/h1-2,8-9,11,15-19,23H,3-4H2,(H,21,22)/t8-,9-,11-,14+/m1/s1 Key: LDPLFHGGZNSKDS-FTBFGRRBSA-N
SMILES O=C(O)[C@]2(O)C[C@@H](O)[C@@H](O)[C@H](OC(=O)c1cc(O)c(O)c(O)c1)C2
Properties
Chemical formula	C14H16O10
Molar mass	344.27 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Theogallin is a trihydroxybenzoic acid glycoside, a type of polyphenolic compound found in tea^[1] where it has been characterised as an umami enhancing compound.^[2] The compound can also be found in Arbutus unedo fruits.^[3]

In rats, theogallin, or its metabolite quinic acid, can move through the blood–brain barrier and can have cognition enhancing activities.^[4]

References

1. Cartwright, R. A.; Roberts, E. A. H. (1954). "Theogallin, a polyphenol occurring in tea". Journal of the Science of Food and Agriculture 5 (12): 593. doi:10.1002/jsfa.2740051207.
2. Kaneko, S; Kumazawa, K; Masuda, H; Henze, A; Hofmann, T (2006). "Flavour Science - Recent Advances and Trends". Developments in Food Science 43: 181. doi:10.1016/S0167-4501(06)80043-9. ISBN 978-0-444-52742-4. |chapter= ignored (help)
3. Pawlowska, A.M., De Leo, M., Braca, A. (2006). "Phenolics of Arbutus unedo L. (Ericaceae) fruits: identification of anthocyanins and gallic acid derivatives". J. Agric. Food Chem. 54 (26): 10234–8. doi:10.1021/jf062230o. PMID 17177565.
4. Dimpfel, Wilfried; Kler, Adolf; Kriesl, Erwin; Lehnfeld, Romanus (2007). "Theogallin and l-theanine as active ingredients in decaffeinated green tea extract: II. Characterization in the freely moving rat by means of quantitative field potential analysis". Journal of Pharmacy and Pharmacology 59 (10): 1397–403. doi:10.1211/jpp.59.10.0010. PMID 17910815.