ChemFOnt: Showing chemical card for 6-{4-[3-(3,4-dihydroxyphenyl)propanoyl]-3,5-dihydroxy-2,6-dimethoxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid (CFc000111164)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:30:45 UTC

Chemfont ID

CFc000111164

Molecule Identification

Common Name

6-{4-[3-(3,4-dihydroxyphenyl)propanoyl]-3,5-dihydroxy-2,6-dimethoxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid

Definition

6-{4-[3-(3,4-dihydroxyphenyl)propanoyl]-3,5-dihydroxy-2,6-dimethoxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid is a predicted metabolite generated by BioTransformer¹ that is produced by the metabolism of 3-(3,4-dihydroxyphenyl)-1-(2,4,6-trihydroxy-3,5-dimethoxyphenyl)propan-1-one. It is generated by 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-[3-(3,4-dihydroxyphenyl)propanoyl]-3,5-dihydroxy-2,6-dimethoxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylate	Generator

Chemical Formula

C₂₃H₂₆O₁₄

Average Molecular Weight

526.447

Monoisotopic Molecular Weight

526.132255517

IUPAC Name

6-{4-[3-(3,4-dihydroxyphenyl)propanoyl]-3,5-dihydroxy-2,6-dimethoxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid

Traditional Name

6-{4-[3-(3,4-dihydroxyphenyl)propanoyl]-3,5-dihydroxy-2,6-dimethoxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

COC1=C(O)C(C(=O)CCC2=CC(O)=C(O)C=C2)=C(O)C(OC)=C1OC1OC(C(O)C(O)C1O)C(O)=O

InChI Identifier

InChI=1S/C23H26O14/c1-34-18-13(27)12(10(25)6-4-8-3-5-9(24)11(26)7-8)14(28)19(35-2)21(18)37-23-17(31)15(29)16(30)20(36-23)22(32)33/h3,5,7,15-17,20,23-24,26-31H,4,6H2,1-2H3,(H,32,33)

InChI Key

CIKBEWNYFACWGR-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
Alkyl-phenylketone
Hexose monosaccharide
Butyrophenone
Glycosyl compound
O-glycosyl compound
Methoxyphenol
M-dimethoxybenzene
Dimethoxybenzene
4-alkoxyphenol
Phenylketone
Aryl alkyl ketone
Aryl ketone
Methoxybenzene
Resorcinol
Catechol
Anisole
Phenol ether
Phenoxy compound
Benzoyl
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
Phenol
Beta-hydroxy acid
Benzenoid
Hydroxy acid
Pyran
Monocyclic benzene moiety
Monosaccharide
Oxane
Vinylogous acid
Ketone
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Carboxylic acid
Acetal
Ether
Alcohol
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Endogenous (HMDB: HMDB0130755)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	1.8 g/L	ALOGPS
logP	1.44	ALOGPS
logP	1.33	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	2.72	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	232.9 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	120.63 m³·mol⁻¹	ChemAxon
Polarizability	49.9 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

HMDB0130755

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

Showing chemical card for 6-{4-[3-(3,4-dihydroxyphenyl)propanoyl]-3,5-dihydroxy-2,6-dimethoxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid (CFc000111164)

MOL for CFc000111164 (6-{4-[3-(3,4-dihydroxyphenyl)propanoyl]-3,5-dihydroxy-2,6-dimethoxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D MOL for CFc000111164 (6-{4-[3-(3,4-dihydroxyphenyl)propanoyl]-3,5-dihydroxy-2,6-dimethoxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D SDF for CFc000111164 (6-{4-[3-(3,4-dihydroxyphenyl)propanoyl]-3,5-dihydroxy-2,6-dimethoxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D-SDF for CFc000111164 (6-{4-[3-(3,4-dihydroxyphenyl)propanoyl]-3,5-dihydroxy-2,6-dimethoxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

PDB for CFc000111164 (6-{4-[3-(3,4-dihydroxyphenyl)propanoyl]-3,5-dihydroxy-2,6-dimethoxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D PDB for CFc000111164 (6-{4-[3-(3,4-dihydroxyphenyl)propanoyl]-3,5-dihydroxy-2,6-dimethoxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

SMILES for CFc000111164 (6-{4-[3-(3,4-dihydroxyphenyl)propanoyl]-3,5-dihydroxy-2,6-dimethoxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

INCHI for CFc000111164 (6-{4-[3-(3,4-dihydroxyphenyl)propanoyl]-3,5-dihydroxy-2,6-dimethoxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

Structure for CFc000111164 (6-{4-[3-(3,4-dihydroxyphenyl)propanoyl]-3,5-dihydroxy-2,6-dimethoxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D Structure for CFc000111164 (6-{4-[3-(3,4-dihydroxyphenyl)propanoyl]-3,5-dihydroxy-2,6-dimethoxyphenoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)