| Weight | 192.167 g/mol |
|---|---|
| Formula | C7H12O6 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 5 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
quinic acid (77-95-2, 36413-60-2)
Quinate
Score:
#2214 in Biochemistry
,
#4487 in Biology
,
#5681 in Chemistry
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- Silencing of Hydroxycinnamoyl-Coenzyme A Shikimate/Quinate Hydroxycinnamoyltransferase Affects Phenylpropanoid Biosynthesis (The Plant Cell, 2004)
- Purification, cloning, and properties of an acyltransferase controlling shikimate and quinate ester intermediates in phenylpropanoid metabolism. (Journal of Biological Chemistry, 2003)
- AtMYB12 regulates caffeoyl quinic acid and flavonol synthesis in tomato: expression in fruit results in very high levels of both types of polyphenol (Plant Journal, 2008)
- Anti-hepatitis B virus activity of chlorogenic acid, quinic acid and caffeic acid in vivo and in vitro. (Antiviral Research, 2009)
- Four Di-O-caffeoyl Quinic Acid Derivatives from Propolis. Potent Hepatoprotective Activity in Experimental Liver Injury Models (Biological & Pharmaceutical Bulletin, 1996)
- Antioxidant activity of caffeoyl quinic acid derivatives from the roots of Dipsacus asper Wall (Journal of Ethnopharmacology, 2006)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Quinate
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SMILESC1C(C(C(CC1(C(=O)O)O)O)O)O
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InChIKeyAAWZDTNXLSGCEK-UHFFFAOYSA-N
- Pubchem - quinic acid
- Wikipedia - Quinic acid
Quinic acid is a cyclitol, a cyclic polyol, and a cyclohexanecarboxylic acid. It is a crystalline acid obtained from cinchona bark, coffee beans, and other plant products and made synthetically by hydrolysis of chlorogenic acid. Quinic acid is also implicated in the perceived acidity of coffee.
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quinic acid
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