ChemFOnt: Showing chemical card for 4-hydroxy-5-[4-hydroxy-3-(sulfooxy)phenyl]pentanoic acid (CFc000108155)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:26:21 UTC

Chemfont ID

CFc000108155

Molecule Identification

Common Name

4-hydroxy-5-[4-hydroxy-3-(sulfooxy)phenyl]pentanoic acid

Definition

4-hydroxy-5-[4-hydroxy-3-(sulfooxy)phenyl]pentanoic acid is a predicted metabolite generated by BioTransformer¹ that is produced by the metabolism of 5-(3,4-dihydroxyphenyl)-4-hydroxypentanoic acid. It is generated by Sulfotransferase 1A3 (P0DMM9) and Sulfotransferase enzymes via a -3-O-sulfation-of-phenolic-compound reaction. This -3-O-sulfation-of-phenolic-compound occurs in humans.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
4-Hydroxy-5-[4-hydroxy-3-(sulfooxy)phenyl]pentanoate	Generator
4-Hydroxy-5-[4-hydroxy-3-(sulphooxy)phenyl]pentanoate	Generator
4-Hydroxy-5-[4-hydroxy-3-(sulphooxy)phenyl]pentanoic acid	Generator
4-Hydroxy-5-(4'-hydroxyphenyl)valeric acid-3'-sulfate	HMDB
4-Hydroxy-5-(4-hydroxy-3-sulfooxyphenyl)pentanoic acid	HMDB
4-Hydroxy-5-(4-hydroxyphenyl)valeric acid-3-sulfate	HMDB

Chemical Formula

C₁₁H₁₄O₈S

Average Molecular Weight

306.29

Monoisotopic Molecular Weight

306.040938585

IUPAC Name

4-hydroxy-5-[4-hydroxy-3-(sulfooxy)phenyl]pentanoic acid

Traditional Name

4-hydroxy-5-[4-hydroxy-3-(sulfooxy)phenyl]pentanoic acid

CAS Registry Number

None

SMILES

OC(CCC(O)=O)CC1=CC(OS(O)(=O)=O)=C(O)C=C1

InChI Identifier

InChI=1S/C11H14O8S/c12-8(2-4-11(14)15)5-7-1-3-9(13)10(6-7)19-20(16,17)18/h1,3,6,8,12-13H,2,4-5H2,(H,14,15)(H,16,17,18)

InChI Key

HROSNTXKMPHTSL-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sulfated fatty acids. These are fatty acids containing linked to a sulfate group linked to its tail.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Sulfated fatty acids

Alternative Parents

Substituents

Phenylsulfate
Sulfated fatty acid
Arylsulfate
Medium-chain hydroxy acid
Phenoxy compound
Medium-chain fatty acid
1-hydroxy-2-unsubstituted benzenoid
Hydroxy fatty acid
Phenol
Monocyclic benzene moiety
Benzenoid
Sulfuric acid ester
Sulfuric acid monoester
Sulfate-ester
Organic sulfuric acid or derivatives
Secondary alcohol
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 32966057)

Excreta

Biofluid or Excreta

Urine (PMID: 32966057)

Cellular substructure

Cytoplasm (HMDB: HMDB0127746)
Cell membrane (HMDB: HMDB0127746)

Organelle

Adiposome (HMDB: HMDB0127746)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0127746)

Source

Endogenous

Endogenous (HMDB: HMDB0127746)

Animal

Animal (HMDB: HMDB0127746)

Exogenous

Food

Food (HMDB: HMDB0127746)

Cocoa and cocoa product

Cocoa and cocoa products (HMDB: HMDB0127746)

Tea

Tea products (HMDB: HMDB0127746)

Nut

Nuts (HMDB: HMDB0127746)

Beverage

Alcoholic beverage

Red wine (HMDB: HMDB0127746)

Fruit

Berries (HMDB: HMDB0127746)

Pome

Apple (HMDB: HMDB0127746)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0127746)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0127746)

Lipid metabolism pathway (HMDB: HMDB0127746)

Biochemical process

Lipid transport (HMDB: HMDB0127746)

Role

Biological role

Energy source (HMDB: HMDB0127746)

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	1.61 g/L	ALOGPS
logP	-0.89	ALOGPS
logP	-0.73	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	-2	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	141.36 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	66.79 m³·mol⁻¹	ChemAxon
Polarizability	27.88 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0127746

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB086607

KNApSAcK ID

Not Available

Chemspider ID

74851997

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131834075

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

Showing chemical card for 4-hydroxy-5-[4-hydroxy-3-(sulfooxy)phenyl]pentanoic acid (CFc000108155)

MOL for CFc000108155 (4-hydroxy-5-[4-hydroxy-3-(sulfooxy)phenyl]pentanoic acid)

3D MOL for CFc000108155 (4-hydroxy-5-[4-hydroxy-3-(sulfooxy)phenyl]pentanoic acid)

3D SDF for CFc000108155 (4-hydroxy-5-[4-hydroxy-3-(sulfooxy)phenyl]pentanoic acid)

3D-SDF for CFc000108155 (4-hydroxy-5-[4-hydroxy-3-(sulfooxy)phenyl]pentanoic acid)

PDB for CFc000108155 (4-hydroxy-5-[4-hydroxy-3-(sulfooxy)phenyl]pentanoic acid)

3D PDB for CFc000108155 (4-hydroxy-5-[4-hydroxy-3-(sulfooxy)phenyl]pentanoic acid)

SMILES for CFc000108155 (4-hydroxy-5-[4-hydroxy-3-(sulfooxy)phenyl]pentanoic acid)

INCHI for CFc000108155 (4-hydroxy-5-[4-hydroxy-3-(sulfooxy)phenyl]pentanoic acid)

Structure for CFc000108155 (4-hydroxy-5-[4-hydroxy-3-(sulfooxy)phenyl]pentanoic acid)

3D Structure for CFc000108155 (4-hydroxy-5-[4-hydroxy-3-(sulfooxy)phenyl]pentanoic acid)