3,4,5-tricaffeoylquinic acid
A carboxylic ester that is the triester obtained by the condensation of the hydroxy groups at positions 3, 4, and 5 of (−)-quinic acid with the carboxy group of caffeic acid.
Machine-generated and unreviewed. Identity, structure and cross-references come straight from ChEBI's and CARD's own data; no curator has signed off on this record yet.
Classification
Chemical structure
| Molecular formula | C34H30O15 |
|---|---|
| Charge | 0 |
| Average mass | 678.599 Da |
| Monoisotopic mass | 678.15847 Da |
| Source | ChEBI |
| InChIKey | OAFXTKGAKYAFSI-UPHZGLEOSA-N |
[H]C(=Cc1ccc(O)c(O)c1)C(=O)O[C@@H]1C[C@](O)(C(=O)O)C[C@@H](OC(=O)C([H])=Cc2ccc(O)c(O)c2)[C@H]1OC(=O)C([H])=Cc1ccc(O)c(O)c1
InChI=1S/C34H30O15/c35-21-7-1-18(13-24(21)38)4-10-29(41)47-27-16-34(46,33(44)45)17-28(48-30(42)11-5-19-2-8-22(36)25(39)14-19)32(27)49-31(43)12-6-20-3-9-23(37)26(40)15-20/h1-15,27-28,32,35-40,46H,16-17H2,(H,44,45)/t27-,28-,32-,34+/m1/s1
Also called
- (1S,3R,4S,5R)-3,4,5-tris{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1-hydroxycyclohexanecarboxylic acid
- 3,4,5-TCQA
- 3,4,5-tri-O-caffeoylquinic acid
- 3,4,5-triCQA
Activity roles
- antiviral agent
CHEBI:22587 - anti-HIV agent
CHEBI:64946
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:233498 |
3,4,5-tricaffeoylquinic acid | antibioticmech:chebi-93141ecaf9 |
2026-08-30 |
Curation history
-
SEEDED_FROM_SOURCES
Seeded from data/raw/ inventories (CHEBI)
-
RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories
-
RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories