ChemFOnt: Showing chemical card for 2-(2,3,5-trihydroxy-4-methoxyphenyl)propanoic acid (CFc000105443)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:22:23 UTC

Chemfont ID

CFc000105443

Molecule Identification

Common Name

2-(2,3,5-trihydroxy-4-methoxyphenyl)propanoic acid

Definition

2-(2,3,5-trihydroxy-4-methoxyphenyl)propanoic acid is a predicted metabolite generated by BioTransformer¹ that is produced by the metabolism of 1-(2,4-dihydroxy-5-methoxyphenyl)-2-(2,3,5-trihydroxy-4-methoxyphenyl)propan-1-one. It is generated by unspecified-gutmicro enzyme via a keto-hydrolysis-pattern5 reaction. This keto-hydrolysis-pattern5 occurs in human gut microbiota.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
2-(2,3,5-Trihydroxy-4-methoxyphenyl)propanoate	Generator

Chemical Formula

C₁₀H₁₂O₆

Average Molecular Weight

228.2

Monoisotopic Molecular Weight

228.063388106

IUPAC Name

2-(2,3,5-trihydroxy-4-methoxyphenyl)propanoic acid

Traditional Name

2-(2,3,5-trihydroxy-4-methoxyphenyl)propanoic acid

CAS Registry Number

None

SMILES

COC1=C(O)C=C(C(C)C(O)=O)C(O)=C1O

InChI Identifier

InChI=1S/C10H12O6/c1-4(10(14)15)5-3-6(11)9(16-2)8(13)7(5)12/h3-4,11-13H,1-2H3,(H,14,15)

InChI Key

NPAKTTCKAUMAFO-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as ubiquinols. These are coenzyme Q derivatives containing a 5, 6-dimethoxy-3-methylbenzene-1,4-diol moiety to which an isoprenyl group is attached at ring position 2(or 6).

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Quinone and hydroquinone lipids

Direct Parent

Ubiquinols

Alternative Parents

Substituents

Ubiquinol skeleton
2-phenylpropanoic-acid
Methoxyphenol
Hydroxyquinol derivative
Anisole
Phenoxy compound
Phenol ether
Methoxybenzene
1-hydroxy-2-unsubstituted benzenoid
Phenol
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Polyol
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Ether
Carboxylic acid
Organic oxide
Organooxygen compound
Carbonyl group
Organic oxygen compound
Hydrocarbon derivative
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Route of exposure

Enteral

Ingestion (HMDB: HMDB0125034)

Source

Endogenous

Endogenous (HMDB: HMDB0125034)

Animal

Animal (HMDB: HMDB0125034)

Exogenous

Food

Food (HMDB: HMDB0125034)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0125034)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0125034)

Lipid metabolism pathway (HMDB: HMDB0125034)

Cellular process

Cell signaling (HMDB: HMDB0125034)

Biochemical process

Lipid transport (HMDB: HMDB0125034)

Role

Biological role

Energy source (HMDB: HMDB0125034)

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	4.21 g/L	ALOGPS
logP	1.42	ALOGPS
logP	1.09	ChemAxon
logS	-1.7	ALOGPS
pKa (Strongest Acidic)	3.29	ChemAxon
pKa (Strongest Basic)	-4.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	107.22 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	54.35 m³·mol⁻¹	ChemAxon
Polarizability	21.39 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0125034

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB083953

KNApSAcK ID

Not Available

Chemspider ID

74851611

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131831581

PDB ID

Not Available

ChEBI ID

169326

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

Showing chemical card for 2-(2,3,5-trihydroxy-4-methoxyphenyl)propanoic acid (CFc000105443)

MOL for CFc000105443 (2-(2,3,5-trihydroxy-4-methoxyphenyl)propanoic acid)

3D MOL for CFc000105443 (2-(2,3,5-trihydroxy-4-methoxyphenyl)propanoic acid)

3D SDF for CFc000105443 (2-(2,3,5-trihydroxy-4-methoxyphenyl)propanoic acid)

3D-SDF for CFc000105443 (2-(2,3,5-trihydroxy-4-methoxyphenyl)propanoic acid)

PDB for CFc000105443 (2-(2,3,5-trihydroxy-4-methoxyphenyl)propanoic acid)

3D PDB for CFc000105443 (2-(2,3,5-trihydroxy-4-methoxyphenyl)propanoic acid)

SMILES for CFc000105443 (2-(2,3,5-trihydroxy-4-methoxyphenyl)propanoic acid)

INCHI for CFc000105443 (2-(2,3,5-trihydroxy-4-methoxyphenyl)propanoic acid)

Structure for CFc000105443 (2-(2,3,5-trihydroxy-4-methoxyphenyl)propanoic acid)

3D Structure for CFc000105443 (2-(2,3,5-trihydroxy-4-methoxyphenyl)propanoic acid)