ChemFOnt: Showing chemical card for 6-{2-[4-(2-carboxy-2-oxoethyl)-2-(2-hydroxyethoxy)phenoxy]ethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid (CFc000122447)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:47:38 UTC

Chemfont ID

CFc000122447

Molecule Identification

Common Name

6-{2-[4-(2-carboxy-2-oxoethyl)-2-(2-hydroxyethoxy)phenoxy]ethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid

Definition

6-{2-[4-(2-carboxy-2-oxoethyl)-2-(2-hydroxyethoxy)phenoxy]ethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid is a predicted metabolite generated by BioTransformer¹ that is produced by the metabolism of 3-[3,4-bis(2-hydroxyethoxy)phenyl]-2-oxopropanoic acid. It is generated by UDP-glucuronosyltransferase 1-1 (P22309) enzyme via an alkyl-OH-glucuronidation reaction. This alkyl-OH-glucuronidation occurs in humans.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
6-{2-[4-(2-carboxy-2-oxoethyl)-2-(2-hydroxyethoxy)phenoxy]ethoxy}-3,4,5-trihydroxyoxane-2-carboxylate	Generator

Chemical Formula

C₁₉H₂₄O₁₃

Average Molecular Weight

460.388

Monoisotopic Molecular Weight

460.121690833

IUPAC Name

6-{2-[4-(2-carboxy-2-oxoethyl)-2-(2-hydroxyethoxy)phenoxy]ethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid

Traditional Name

6-{2-[4-(2-carboxy-2-oxoethyl)-2-(2-hydroxyethoxy)phenoxy]ethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

OCCOC1=C(OCCOC2OC(C(O)C(O)C2O)C(O)=O)C=CC(CC(=O)C(O)=O)=C1

InChI Identifier

InChI=1S/C19H24O13/c20-3-4-29-12-8-9(7-10(21)17(25)26)1-2-11(12)30-5-6-31-19-15(24)13(22)14(23)16(32-19)18(27)28/h1-2,8,13-16,19-20,22-24H,3-7H2,(H,25,26)(H,27,28)

InChI Key

AKUOSDYVGKLONL-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as o-glucuronides. These are glucuronides in which the aglycone is linked to the carbohydrate unit through an O-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glucuronides

Alternative Parents

Substituents

1-o-glucuronide
O-glucuronide
Hexose monosaccharide
Phenylpyruvate
Glycosyl compound
O-glycosyl compound
3-phenylpropanoic-acid
Phenoxy compound
Phenol ether
Alkyl aryl ether
Beta-hydroxy acid
Alpha-keto acid
Hydroxy acid
Keto acid
Dicarboxylic acid or derivatives
Pyran
Oxane
Benzenoid
Monocyclic benzene moiety
Monosaccharide
Alpha-hydroxy ketone
Ketone
Secondary alcohol
Acetal
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Carboxylic acid
Polyol
Ether
Primary alcohol
Carbonyl group
Hydrocarbon derivative
Alcohol
Organic oxide
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Endogenous (HMDB: HMDB0142038)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	1.82 g/L	ALOGPS
logP	-0.93	ALOGPS
logP	-1.2	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	2.53	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	209.51 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	100.5 m³·mol⁻¹	ChemAxon
Polarizability	43.73 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0142038

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-{2-[4-(2-carboxy-2-oxoethyl)-2-(2-hydroxyethoxy)phenoxy]ethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid (CFc000122447)

MOL for CFc000122447 (6-{2-[4-(2-carboxy-2-oxoethyl)-2-(2-hydroxyethoxy)phenoxy]ethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D MOL for CFc000122447 (6-{2-[4-(2-carboxy-2-oxoethyl)-2-(2-hydroxyethoxy)phenoxy]ethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D SDF for CFc000122447 (6-{2-[4-(2-carboxy-2-oxoethyl)-2-(2-hydroxyethoxy)phenoxy]ethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D-SDF for CFc000122447 (6-{2-[4-(2-carboxy-2-oxoethyl)-2-(2-hydroxyethoxy)phenoxy]ethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

PDB for CFc000122447 (6-{2-[4-(2-carboxy-2-oxoethyl)-2-(2-hydroxyethoxy)phenoxy]ethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D PDB for CFc000122447 (6-{2-[4-(2-carboxy-2-oxoethyl)-2-(2-hydroxyethoxy)phenoxy]ethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

SMILES for CFc000122447 (6-{2-[4-(2-carboxy-2-oxoethyl)-2-(2-hydroxyethoxy)phenoxy]ethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

INCHI for CFc000122447 (6-{2-[4-(2-carboxy-2-oxoethyl)-2-(2-hydroxyethoxy)phenoxy]ethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

Structure for CFc000122447 (6-{2-[4-(2-carboxy-2-oxoethyl)-2-(2-hydroxyethoxy)phenoxy]ethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D Structure for CFc000122447 (6-{2-[4-(2-carboxy-2-oxoethyl)-2-(2-hydroxyethoxy)phenoxy]ethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)