ChemFOnt: Showing chemical card for 2-{[(2E)-3-{3-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-4-hydroxyphenyl}prop-2-enoyl]oxy}-3-hydroxybutanedioic acid (CFc000122714)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:48:03 UTC

Chemfont ID

CFc000122714

Molecule Identification

Common Name

2-{[(2E)-3-{3-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-4-hydroxyphenyl}prop-2-enoyl]oxy}-3-hydroxybutanedioic acid

Definition

2-{[(2e)-3-{3-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-4-hydroxyphenyl}prop-2-enoyl]oxy}-3-hydroxybutanedioic acid is a predicted metabolite generated by BioTransformer¹ that is produced by the metabolism of 2-{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-3-hydroxybutanedioic acid. 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
2-{[(2E)-3-{3-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-4-hydroxyphenyl}prop-2-enoyl]oxy}-3-hydroxybutanedioate	Generator

Chemical Formula

C₁₉H₂₀O₁₅

Average Molecular Weight

488.354

Monoisotopic Molecular Weight

488.080219944

IUPAC Name

2-{[(2E)-3-{3-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-4-hydroxyphenyl}prop-2-enoyl]oxy}-3-hydroxybutanedioic acid

Traditional Name

2-{[(2E)-3-{3-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-4-hydroxyphenyl}prop-2-enoyl]oxy}-3-hydroxybutanedioic acid

CAS Registry Number

Not Available

SMILES

[H]\C(=C(\[H])C1=CC(OC2OC(C(O)C(O)C2O)C(O)=O)=C(O)C=C1)C(=O)OC(C(O)C(O)=O)C(O)=O

InChI Identifier

InChI=1S/C19H20O15/c20-7-3-1-6(2-4-9(21)33-15(18(30)31)13(25)16(26)27)5-8(7)32-19-12(24)10(22)11(23)14(34-19)17(28)29/h1-5,10-15,19-20,22-25H,(H,26,27)(H,28,29)(H,30,31)/b4-2+

InChI Key

GZORFRHUWLYASV-DUXPYHPUSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Phenolic glycosides

Alternative Parents

Substituents

Phenolic glycoside
O-glucuronide
1-o-glucuronide
Tetracarboxylic acid or derivatives
Glucuronic acid or derivatives
Cinnamic acid ester
Hydroxycinnamic acid or derivatives
Cinnamic acid or derivatives
Coumaric acid or derivatives
O-glycosyl compound
Phenoxy compound
Phenol ether
Styrene
Beta-hydroxy acid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Sugar acid
Fatty acid ester
Alpha-hydroxy acid
Monocyclic benzene moiety
Fatty acyl
Hydroxy acid
Benzenoid
Monosaccharide
Oxane
Pyran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Secondary alcohol
Organoheterocyclic compound
Acetal
Oxacycle
Carboxylic acid
Carboxylic acid derivative
Polyol
Hydrocarbon derivative
Alcohol
Organic oxide
Carbonyl group
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Endogenous (HMDB: HMDB0142305)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	1.79 g/L	ALOGPS
logP	0.45	ALOGPS
logP	-1.3	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	2.72	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	-3	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	257.81 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	101.75 m³·mol⁻¹	ChemAxon
Polarizability	43.47 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

HMDB0142305

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 2-{[(2E)-3-{3-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-4-hydroxyphenyl}prop-2-enoyl]oxy}-3-hydroxybutanedioic acid (CFc000122714)

MOL for CFc000122714 (2-{[(2E)-3-{3-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-4-hydroxyphenyl}prop-2-enoyl]oxy}-3-hydroxybutanedioic acid)

3D MOL for CFc000122714 (2-{[(2E)-3-{3-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-4-hydroxyphenyl}prop-2-enoyl]oxy}-3-hydroxybutanedioic acid)

3D SDF for CFc000122714 (2-{[(2E)-3-{3-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-4-hydroxyphenyl}prop-2-enoyl]oxy}-3-hydroxybutanedioic acid)

3D-SDF for CFc000122714 (2-{[(2E)-3-{3-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-4-hydroxyphenyl}prop-2-enoyl]oxy}-3-hydroxybutanedioic acid)

PDB for CFc000122714 (2-{[(2E)-3-{3-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-4-hydroxyphenyl}prop-2-enoyl]oxy}-3-hydroxybutanedioic acid)

3D PDB for CFc000122714 (2-{[(2E)-3-{3-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-4-hydroxyphenyl}prop-2-enoyl]oxy}-3-hydroxybutanedioic acid)

SMILES for CFc000122714 (2-{[(2E)-3-{3-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-4-hydroxyphenyl}prop-2-enoyl]oxy}-3-hydroxybutanedioic acid)

INCHI for CFc000122714 (2-{[(2E)-3-{3-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-4-hydroxyphenyl}prop-2-enoyl]oxy}-3-hydroxybutanedioic acid)

Structure for CFc000122714 (2-{[(2E)-3-{3-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-4-hydroxyphenyl}prop-2-enoyl]oxy}-3-hydroxybutanedioic acid)

3D Structure for CFc000122714 (2-{[(2E)-3-{3-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-4-hydroxyphenyl}prop-2-enoyl]oxy}-3-hydroxybutanedioic acid)