3,5-Dicaffeoyl-epi-quinic acid

• CAT Number: I042265
• CAS Number: 879305-14-3
• Molecular Formula: C25H24O12
• Molecular Weight: 516.45
• Purity: ≥95%
• Synonyms: (3R,5R)-3,5-bis[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy]-1,4-dihydroxycyclohexane-1-carboxylic acid
• InChI: InChI=1S/C25H24O12/c26-15-5-1-13(9-17(15)28)3-7-21(30)36-19-11-25(35,24(33)34)12-20(23(19)32)37-22(31)8-4-14-2-6-16(27)18(29)10-14/h1-10,19-20,23,26-29,32,35H,11-12H2,(H,33,34)/b7-3+,8-4+/t19-,20-,23?,25?/m1/s1
• InChIKey: KRZBCHWVBQOTNZ-RDJMKVHDSA-N
• SMILES: C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O

3,5-Dicaffeoyl-epi-quinic acid (Cat No.: I042265) is a polyphenolic compound belonging to the chlorogenic acid family, consisting of two caffeic acid moieties esterified to the 3- and 5-positions of epi-quinic acid. Known for its potent antioxidant and anti-inflammatory properties, it is commonly found in various plant-based foods and traditional herbal medicines. This compound is of interest in pharmacological and nutritional research for its potential benefits in metabolic regulation, neuroprotection, and cardiovascular health. It also plays a role in studying plant defense and polyphenol biosynthesis.

Reference

[1]. Li CH, et al. Ganoderic acid X, a lanostanoid triterpene, inhibits topoisomerases and induces apoptosis of cancer cells. Life Sci. 2005 Jun 3;77(3):252-65.
[Content Brief]