ChemFOnt: Showing chemical card for 3-(2,3,4-trimethoxyphenyl)propanoic acid (CFc000122483)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:47:42 UTC

Chemfont ID

CFc000122483

Molecule Identification

Common Name

3-(2,3,4-trimethoxyphenyl)propanoic acid

Definition

3-(2,3,4-trimethoxyphenyl)propanoic acid is a predicted metabolite generated by BioTransformer¹ that is produced by the metabolism of 3-(2,3,4-trimethoxyphenyl)prop-2-enoic acid. It is generated by abkar1 enzyme via a reduction-of-alpha-beta-unsaturated-compounds-pattern1 reaction. This reduction-of-alpha-beta-unsaturated-compounds-pattern1 occurs in humans and human gut microbiota.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
3-(2,3,4-Trimethoxyphenyl)propanoate	Generator

Chemical Formula

C₁₂H₁₆O₅

Average Molecular Weight

240.255

Monoisotopic Molecular Weight

240.099773615

IUPAC Name

3-(2,3,4-trimethoxyphenyl)propanoic acid

Traditional Name

3-(2,3,4-trimethoxyphenyl)propanoic acid

CAS Registry Number

None

SMILES

COC1=C(OC)C(OC)=C(CCC(O)=O)C=C1

InChI Identifier

InChI=1S/C12H16O5/c1-15-9-6-4-8(5-7-10(13)14)11(16-2)12(9)17-3/h4,6H,5,7H2,1-3H3,(H,13,14)

InChI Key

QOPNYPCVRBRZOP-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenylpropanoic acids. Phenylpropanoic acids are compounds with a structure containing a benzene ring conjugated to a propanoic acid.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Phenylpropanoic acids

Sub Class

Not Available

Direct Parent

Phenylpropanoic acids

Alternative Parents

Substituents

3-phenylpropanoic-acid
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Ether
Carboxylic acid
Organic oxygen compound
Organooxygen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Endogenous (HMDB: HMDB0142074)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.47 g/L	ALOGPS
logP	1.72	ALOGPS
logP	1.58	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	3.87	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	64.99 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	61.36 m³·mol⁻¹	ChemAxon
Polarizability	24.66 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

HMDB0142074

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB093331

KNApSAcK ID

Not Available

Chemspider ID

105822

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

118401

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

Showing chemical card for 3-(2,3,4-trimethoxyphenyl)propanoic acid (CFc000122483)

MOL for CFc000122483 (3-(2,3,4-trimethoxyphenyl)propanoic acid)

3D MOL for CFc000122483 (3-(2,3,4-trimethoxyphenyl)propanoic acid)

3D SDF for CFc000122483 (3-(2,3,4-trimethoxyphenyl)propanoic acid)

3D-SDF for CFc000122483 (3-(2,3,4-trimethoxyphenyl)propanoic acid)

PDB for CFc000122483 (3-(2,3,4-trimethoxyphenyl)propanoic acid)

3D PDB for CFc000122483 (3-(2,3,4-trimethoxyphenyl)propanoic acid)

SMILES for CFc000122483 (3-(2,3,4-trimethoxyphenyl)propanoic acid)

INCHI for CFc000122483 (3-(2,3,4-trimethoxyphenyl)propanoic acid)

Structure for CFc000122483 (3-(2,3,4-trimethoxyphenyl)propanoic acid)

3D Structure for CFc000122483 (3-(2,3,4-trimethoxyphenyl)propanoic acid)