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Preferred IUPAC name (1S,3R,4S,5R)-1-Hydroxy-3,4,5-triscyclohexane-1-carboxylic acid | |
Other names
TGQA (3R,5R)-1-Hydroxy-3,4,5-tris(3,4,5-trihydroxyphenylcarbonyloxy)cyclohexanecarboxylic acid | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ChEMBL | |
ChemSpider | |
PubChem CID | |
CompTox Dashboard (EPA) | |
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Properties | |
Chemical formula | C28H24O18 |
Molar mass | 648.482 g·mol |
Density | 1.98g/cm |
Boiling point | 1,114.4 °C (2,037.9 °F; 1,387.6 K) at 760mmHg |
Hazards | |
Flash point | 364.6 °C (688.3 °F; 637.8 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). N verify (what is ?) Infobox references |
3,4,5-Tri-O-galloylquinic acid is a hydrolysable tannin found in Lepidobotrys staudtii, in Guiera senegalensis or in the resurrection plant (Myrothamnus flabellifolius).
It is classified as a natural product with anti-HIV activity and a DNA polymerase inhibitor.
References
- ^ "3,4,5-tri-O-galloylquinic acid on home.ncifcrf.gov". Archived from the original on 2011-07-16. Retrieved 2010-07-05.
- Bouchet, N.; Levesque, J. L.; Bodo, B.; Pousset, J. L. (1998). "3,4,5-Tri-O-Galloylquinic Acid Ethyl Ester from Guiera senegalensis". Pharmaceutical Biology. 36: 63–65. doi:10.1076/phbi.36.1.63.4624.
- Westall, K. L.; Moore, J. P.; Ravenscroft, N.; Farrant, J. M.; Lindsey, G. G.; Brandt, W. F. (2005). "The predominant polyphenol in the leaves of the resurrection plant Myrothamnus flabellifolius, 3,4,5 tri-O-galloylquinic acid, protects membranes against desiccation and free radical-induced oxidation". Biochemical Journal. 385 (Pt 1): 301–308. doi:10.1042/BJ20040499. PMC 1134698. PMID 15355309.
- CID 127406 from PubChem
Types of gallotannins | |||||||||||||
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Aglycones | |||||||||||||
Galloylglucoses |
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Galloylquinic acids: |
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Galloylshikimic acids: | |||||||||||||
others |
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