ChemFOnt: Showing chemical card for 6-{4-[2,3-dioxo-3-(2,4,6-trihydroxyphenyl)propyl]-2,3,6-trihydroxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid (CFc000105751)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:22:50 UTC

Chemfont ID

CFc000105751

Molecule Identification

Common Name

6-{4-[2,3-dioxo-3-(2,4,6-trihydroxyphenyl)propyl]-2,3,6-trihydroxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid

Definition

6-{4-[2,3-dioxo-3-(2,4,6-trihydroxyphenyl)propyl]-2,3,6-trihydroxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid is a predicted metabolite generated by BioTransformer¹ that is produced by the metabolism of 3-(2,3,4,5-tetrahydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)propane-1,2-dione. It is generated by UDP-glucuronosyltransferase 1-1 (P22309) enzyme via an aromatic-OH-glucuronidation reaction. This aromatic-OH-glucuronidation occurs in humans.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
6-{4-[2,3-dioxo-3-(2,4,6-trihydroxyphenyl)propyl]-2,3,6-trihydroxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylate	Generator

Chemical Formula

C₂₁H₂₀O₁₅

Average Molecular Weight

512.376

Monoisotopic Molecular Weight

512.080219944

IUPAC Name

6-{4-[2,3-dioxo-3-(2,4,6-trihydroxyphenyl)propyl]-2,3,6-trihydroxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid

Traditional Name

6-{4-[2,3-dioxo-3-(2,4,6-trihydroxyphenyl)propyl]-2,3,6-trihydroxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid

CAS Registry Number

None

SMILES

OC1C(O)C(OC2=C(O)C=C(CC(=O)C(=O)C3=C(O)C=C(O)C=C3O)C(O)=C2O)OC(C1O)C(O)=O

InChI Identifier

InChI=1S/C21H20O15/c22-6-3-7(23)11(8(24)4-6)13(28)9(25)1-5-2-10(26)18(15(30)12(5)27)35-21-17(32)14(29)16(31)19(36-21)20(33)34/h2-4,14,16-17,19,21-24,26-27,29-32H,1H2,(H,33,34)

InChI Key

FVKCEBQPRYNCHO-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavonoid o-glycosides. Flavonoid O-glycosides are compounds containing a carbohydrate moiety which is O-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid O-glycosides

Alternative Parents

Substituents

Flavonoid o-glycoside
2'-hydroxy-dihydrochalcone
Phenolic glycoside
Linear 1,3-diarylpropanoid
Cinnamylphenol
1-o-glucuronide
O-glucuronide
Glucuronic acid or derivatives
Ubiquinol skeleton
Hexose monosaccharide
Acylphloroglucinol derivative
Butyrophenone
Glycosyl compound
O-glycosyl compound
Benzenetriol
Phloroglucinol derivative
Hydroxyquinol derivative
Aryl ketone
Benzoyl
Phenoxy compound
Phenol ether
Beta-hydroxy acid
Phenol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Monocyclic benzene moiety
Pyran
Oxane
Hydroxy acid
Alpha-diketone
Monosaccharide
Vinylogous acid
Ketone
Secondary alcohol
Polyol
Carboxylic acid
Carboxylic acid derivative
Acetal
Oxacycle
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Carbonyl group
Organooxygen compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Endogenous (HMDB: HMDB0125342)

Plant

Plant (HMDB: HMDB0125342)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	3.61 g/L	ALOGPS
logP	1.23	ALOGPS
logP	0.88	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	2.74	ChemAxon
pKa (Strongest Basic)	-4.8	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	15	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	271.97 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	112.41 m³·mol⁻¹	ChemAxon
Polarizability	44.84 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

HMDB0125342

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB084256

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131831867

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

Showing chemical card for 6-{4-[2,3-dioxo-3-(2,4,6-trihydroxyphenyl)propyl]-2,3,6-trihydroxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid (CFc000105751)

MOL for CFc000105751 (6-{4-[2,3-dioxo-3-(2,4,6-trihydroxyphenyl)propyl]-2,3,6-trihydroxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D MOL for CFc000105751 (6-{4-[2,3-dioxo-3-(2,4,6-trihydroxyphenyl)propyl]-2,3,6-trihydroxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D SDF for CFc000105751 (6-{4-[2,3-dioxo-3-(2,4,6-trihydroxyphenyl)propyl]-2,3,6-trihydroxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D-SDF for CFc000105751 (6-{4-[2,3-dioxo-3-(2,4,6-trihydroxyphenyl)propyl]-2,3,6-trihydroxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

PDB for CFc000105751 (6-{4-[2,3-dioxo-3-(2,4,6-trihydroxyphenyl)propyl]-2,3,6-trihydroxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D PDB for CFc000105751 (6-{4-[2,3-dioxo-3-(2,4,6-trihydroxyphenyl)propyl]-2,3,6-trihydroxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

SMILES for CFc000105751 (6-{4-[2,3-dioxo-3-(2,4,6-trihydroxyphenyl)propyl]-2,3,6-trihydroxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

INCHI for CFc000105751 (6-{4-[2,3-dioxo-3-(2,4,6-trihydroxyphenyl)propyl]-2,3,6-trihydroxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

Structure for CFc000105751 (6-{4-[2,3-dioxo-3-(2,4,6-trihydroxyphenyl)propyl]-2,3,6-trihydroxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D Structure for CFc000105751 (6-{4-[2,3-dioxo-3-(2,4,6-trihydroxyphenyl)propyl]-2,3,6-trihydroxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)