ChemFOnt: Showing chemical card for {4-[(E)-2-(4-hydroxy-2-oxo-2H-pyran-6-yl)ethenyl]-2-methoxyphenyl}oxidanesulfonic acid (CFc000111619)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:31:25 UTC

Chemfont ID

CFc000111619

Molecule Identification

Common Name

{4-[(E)-2-(4-hydroxy-2-oxo-2H-pyran-6-yl)ethenyl]-2-methoxyphenyl}oxidanesulfonic acid

Definition

{4-[(e)-2-(4-hydroxy-2-oxo-2h-pyran-6-yl)ethenyl]-2-methoxyphenyl}oxidanesulfonic acid is a predicted metabolite generated by BioTransformer¹ that is produced by the metabolism of 4-hydroxy-6-[(e)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]-2h-pyran-2-one. It is generated by Sulfotransferase 1A3 (P0DMM9) and Sulfotransferase enzymes via a -4-O-sulfation-of-phenolic-compound reaction. This -4-O-sulfation-of-phenolic-compound occurs in humans.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
{4-[(e)-2-(4-hydroxy-2-oxo-2H-pyran-6-yl)ethenyl]-2-methoxyphenyl}oxidanesulfonate	Generator
{4-[(e)-2-(4-hydroxy-2-oxo-2H-pyran-6-yl)ethenyl]-2-methoxyphenyl}oxidanesulphonate	Generator
{4-[(e)-2-(4-hydroxy-2-oxo-2H-pyran-6-yl)ethenyl]-2-methoxyphenyl}oxidanesulphonic acid	Generator

Chemical Formula

C₁₄H₁₂O₈S

Average Molecular Weight

340.3

Monoisotopic Molecular Weight

340.02528852

IUPAC Name

{4-[(E)-2-(4-hydroxy-2-oxo-2H-pyran-6-yl)ethenyl]-2-methoxyphenyl}oxidanesulfonic acid

Traditional Name

{4-[(E)-2-(4-hydroxy-6-oxopyran-2-yl)ethenyl]-2-methoxyphenyl}oxidanesulfonic acid

CAS Registry Number

Not Available

SMILES

[H]\C(=C(\[H])C1=CC(OC)=C(OS(O)(=O)=O)C=C1)C1=CC(O)=CC(=O)O1

InChI Identifier

InChI=1S/C14H12O8S/c1-20-13-6-9(3-5-12(13)22-23(17,18)19)2-4-11-7-10(15)8-14(16)21-11/h2-8,15H,1H3,(H,17,18,19)/b4-2+

InChI Key

JYIJYBZKTVQXNR-DUXPYHPUSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenylsulfates. Phenylsulfates are compounds containing a sulfuric acid group conjugated to a phenyl group.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Organic sulfuric acids and derivatives

Sub Class

Arylsulfates

Direct Parent

Phenylsulfates

Alternative Parents

Substituents

Phenylsulfate
Phenoxy compound
Anisole
Phenol ether
Methoxybenzene
Styrene
Alkyl aryl ether
Pyranone
Monocyclic benzene moiety
Pyran
Sulfuric acid monoester
Sulfate-ester
Sulfuric acid ester
Benzenoid
Heteroaromatic compound
Vinylogous acid
Lactone
Oxacycle
Organoheterocyclic compound
Ether
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organic oxygen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Endogenous (HMDB: HMDB0131210)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.13 g/L	ALOGPS
logP	-0.04	ALOGPS
logP	1.59	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	-2.2	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	119.36 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	82.43 m³·mol⁻¹	ChemAxon
Polarizability	31.64 Å³	ChemAxon
Number of Rings	2	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

HMDB0131210

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 {4-[(E)-2-(4-hydroxy-2-oxo-2H-pyran-6-yl)ethenyl]-2-methoxyphenyl}oxidanesulfonic acid (CFc000111619)

MOL for CFc000111619 ({4-[(E)-2-(4-hydroxy-2-oxo-2H-pyran-6-yl)ethenyl]-2-methoxyphenyl}oxidanesulfonic acid)

3D MOL for CFc000111619 ({4-[(E)-2-(4-hydroxy-2-oxo-2H-pyran-6-yl)ethenyl]-2-methoxyphenyl}oxidanesulfonic acid)

3D SDF for CFc000111619 ({4-[(E)-2-(4-hydroxy-2-oxo-2H-pyran-6-yl)ethenyl]-2-methoxyphenyl}oxidanesulfonic acid)

3D-SDF for CFc000111619 ({4-[(E)-2-(4-hydroxy-2-oxo-2H-pyran-6-yl)ethenyl]-2-methoxyphenyl}oxidanesulfonic acid)

PDB for CFc000111619 ({4-[(E)-2-(4-hydroxy-2-oxo-2H-pyran-6-yl)ethenyl]-2-methoxyphenyl}oxidanesulfonic acid)

3D PDB for CFc000111619 ({4-[(E)-2-(4-hydroxy-2-oxo-2H-pyran-6-yl)ethenyl]-2-methoxyphenyl}oxidanesulfonic acid)

SMILES for CFc000111619 ({4-[(E)-2-(4-hydroxy-2-oxo-2H-pyran-6-yl)ethenyl]-2-methoxyphenyl}oxidanesulfonic acid)

INCHI for CFc000111619 ({4-[(E)-2-(4-hydroxy-2-oxo-2H-pyran-6-yl)ethenyl]-2-methoxyphenyl}oxidanesulfonic acid)

Structure for CFc000111619 ({4-[(E)-2-(4-hydroxy-2-oxo-2H-pyran-6-yl)ethenyl]-2-methoxyphenyl}oxidanesulfonic acid)

3D Structure for CFc000111619 ({4-[(E)-2-(4-hydroxy-2-oxo-2H-pyran-6-yl)ethenyl]-2-methoxyphenyl}oxidanesulfonic acid)