L-quinate (BioCAD00000230959)
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Metabolite Card
Formula: C7H11O6 (191.0556)
SMILES: OC1CC(O)(CC(O)C1O)C([O-])=O
Synonyms [en]
L-Quinate; (-)-quinate; (1S,3R,4S,5R)-1,3,4,5-tetrahydroxycyclohexanecarboxylate; ; (3R,5R)-1,3,4,5-tetrahydroxycyclohexane-1-carboxylate; Acid, Quinic
Last reviewed on 2024-06-28.
Cite this Page
L-quinate. 数据之源，洞见之始. SMRUCC genomics institute, a synthetic life researcher from China.
https://biocad_registry.innovation.ac.cn/s/(-)-arctiin
(retrieved
2026-01-03) (CAD Registry RN: BioCAD00000230959). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Note
L-quinate, also known as L-quinic acid, belongs to quinic acids and derivatives class of compounds. Those are compounds containing a quinic acid moiety (or a derivative thereof), which is a cyclitol made up of a cyclohexane ring that bears four hydroxyl groups at positions 1,3.4, and 5, as well as a carboxylic acid at position 1. L-quinate is very soluble (in water) and a weakly acidic compound (based on its pKa). L-quinate can be found in a number of food items such as fireweed, yellow wax bean, japanese walnut, and black cabbage, which makes L-quinate a potential biomarker for the consumption of these food products. 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. It is a constituent of the tara tannins .
DBLinks
- CAS Registry Number:
- PubChem CID: 1560034
- ChEBI: 29751
- HMDB: HMDB0304404
- LipidMaps:
- KEGG:
- BioCyc: QUINATE
- NCBI MeSH: Quinic Acid
- Wikipedia:
Other DBLinks
- PubChem: 1560034
- ChEBI: ChEBI:29751
- HMDB: HMDB0304404
- BioCyc: QUINATE
- NCBI MeSH: Quinic Acid
Class / Ontology
| ID | EC Number | Name |
|---|---|---|
| Rhea:RHEA:15022 | 2.3.1.99 | L-quinate + (E)-feruloyl-CoA => 4-O-feruloyl-D-quinate + CoA |
| Rhea:RHEA:15023 | 2.3.1.99 | 4-O-feruloyl-D-quinate + CoA => L-quinate + (E)-feruloyl-CoA |
| Rhea:RHEA:15024 | 2.3.1.99 | L-quinate + (E)-feruloyl-CoA <=> 4-O-feruloyl-D-quinate + CoA |
| Rhea:RHEA:18426 | 1.1.1.282 | L-quinate + NADP+ => 3-dehydroquinate + NADPH + H+ |
| Rhea:RHEA:18427 | 1.1.1.282 | 3-dehydroquinate + NADPH + H+ => L-quinate + NADP+ |
| Rhea:RHEA:18428 | 1.1.1.282 | L-quinate + NADP+ <=> 3-dehydroquinate + NADPH + H+ |
| Rhea:RHEA:20690 | 3.1.1.42 | chlorogenate + H2O => L-quinate + (E)-caffeate + H+ |
| Rhea:RHEA:20691 | 3.1.1.42 | L-quinate + (E)-caffeate + H+ => chlorogenate + H2O |
| Rhea:RHEA:20692 | 3.1.1.42 | chlorogenate + H2O <=> L-quinate + (E)-caffeate + H+ |
| Rhea:RHEA:22365 | 1.1.1.24 | L-quinate + NAD+ => 3-dehydroquinate + NADH + H+ |
| Rhea:RHEA:22366 | 1.1.1.24 | 3-dehydroquinate + NADH + H+ => L-quinate + NAD+ |
| Rhea:RHEA:22367 | 1.1.1.24 | L-quinate + NAD+ <=> 3-dehydroquinate + NADH + H+ |
| Rhea:RHEA:23205 | 2.3.1.98 | chlorogenate + D-glucarate => 2-O-caffeoylglucarate + L-quinate |
| Rhea:RHEA:23206 | 2.3.1.98 | 2-O-caffeoylglucarate + L-quinate => chlorogenate + D-glucarate |
| Rhea:RHEA:23207 | 2.3.1.98 | chlorogenate + D-glucarate <=> 2-O-caffeoylglucarate + L-quinate |
| Rhea:RHEA:23673 | 1.1.5.8 | L-quinate + a quinone => 3-dehydroquinate + a quinol |
| Rhea:RHEA:23674 | 1.1.5.8 | 3-dehydroquinate + a quinol => L-quinate + a quinone |
| Rhea:RHEA:23675 | 1.1.5.8 | L-quinate + a quinone <=> 3-dehydroquinate + a quinol |
| Rhea:RHEA:35196 | L-quinate(in) => L-quinate(out) | |
| Rhea:RHEA:35197 | L-quinate(out) => L-quinate(in) |
Taxonomy Source
Pathway Synthetic
| pathway id | name |
|---|---|
| BioCyc:META_PWY-6040 | chlorogenic acid biosynthesis II |
| BioCyc:META_PWY-6954 | superpathway of aromatic compound degradation via 2-hydroxypentadienoate |
| BioCyc:ARA_PWY-361 | phenylpropanoid biosynthesis |
| BioCyc:THAPS_PWY-6673 | caffeoylglucarate biosynthesis |
| BioCyc:META_PWY-6039 | chlorogenic acid biosynthesis I |
| BioCyc:META_QUINATEDEG-PWY | quinate degradation I |
| BioCyc:META_PWY-6673 | caffeoylglucarate biosynthesis |
| BioCyc:ARA_PWY-6040 | chlorogenic acid biosynthesis II |
| BioCyc:SCO_QUINATEDEG-PWY | quinate degradation I |
| BioCyc:PCHR_PWY-6416 | quinate degradation II |
| BioCyc:META_PWY-2504 | superpathway of aromatic compound degradation via 3-oxoadipate |
| BioCyc:META_PWY-6416 | quinate degradation II |
| BioCyc:TRYPANO_QUINATEDEG-PWY | quinate degradation I |
| BioCyc:AGRO_QUINATEDEG-PWY | quinate degradation I |
| BioCyc:SCO_PWY-2504 | superpathway of aromatic compound degradation via 3-oxoadipate |
| BioCyc:CORYNE_PWY-6416 | quinate degradation II |
| BioCyc:META_PWY-6781 | chlorogenic acid degradation |
| BioCyc:META_PWY-361 | phenylpropanoid biosynthesis |
| BioCyc:ARA_PWY-6039 | chlorogenic acid biosynthesis I |
| BioCyc:ARA_PWY-6673 | caffeoylglucarate biosynthesis |