ChemFOnt: Showing chemical card for {3-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]-2-hydroxy-6-methoxyphenyl}oxidanesulfonic acid (CFc000115013)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:36:24 UTC

Chemfont ID

CFc000115013

Molecule Identification

Common Name

{3-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]-2-hydroxy-6-methoxyphenyl}oxidanesulfonic acid

Definition

{3-[(e)-2-(3,5-dihydroxyphenyl)ethenyl]-2-hydroxy-6-methoxyphenyl}oxidanesulfonic acid is a predicted metabolite generated by BioTransformer¹ that is produced by the metabolism of 3-[(e)-2-(3,5-dihydroxyphenyl)ethenyl]-6-methoxybenzene-1,2-diol. 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
{3-[(e)-2-(3,5-dihydroxyphenyl)ethenyl]-2-hydroxy-6-methoxyphenyl}oxidanesulfonate	Generator
{3-[(e)-2-(3,5-dihydroxyphenyl)ethenyl]-2-hydroxy-6-methoxyphenyl}oxidanesulphonate	Generator
{3-[(e)-2-(3,5-dihydroxyphenyl)ethenyl]-2-hydroxy-6-methoxyphenyl}oxidanesulphonic acid	Generator

Chemical Formula

C₁₅H₁₄O₈S

Average Molecular Weight

354.33

Monoisotopic Molecular Weight

354.040938585

IUPAC Name

{3-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]-2-hydroxy-6-methoxyphenyl}oxidanesulfonic acid

Traditional Name

{3-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]-2-hydroxy-6-methoxyphenyl}oxidanesulfonic acid

CAS Registry Number

None

SMILES

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

InChI Identifier

InChI=1S/C15H14O8S/c1-22-13-5-4-10(14(18)15(13)23-24(19,20)21)3-2-9-6-11(16)8-12(17)7-9/h2-8,16-18H,1H3,(H,19,20,21)/b3-2+

InChI Key

IFXREJSSLAQNJL-NSCUHMNNSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Stilbenes

Sub Class

Not Available

Direct Parent

Stilbenes

Alternative Parents

Substituents

Stilbene
Phenylsulfate
Methoxyphenol
Arylsulfate
Phenoxy compound
Phenol ether
Resorcinol
Styrene
Methoxybenzene
Anisole
1-hydroxy-4-unsubstituted benzenoid
Phenol
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Sulfate-ester
Sulfuric acid monoester
Sulfuric acid ester
Benzenoid
Monocyclic benzene moiety
Organic sulfuric acid or derivatives
Ether
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Endogenous (HMDB: HMDB0134604)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.26 g/L	ALOGPS
logP	0.63	ALOGPS
logP	3.12	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	-2.3	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	133.52 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	85.89 m³·mol⁻¹	ChemAxon
Polarizability	33.51 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

HMDB0134604

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB091605

KNApSAcK ID

Not Available

Chemspider ID

74853621

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131838319

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

Showing chemical card for {3-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]-2-hydroxy-6-methoxyphenyl}oxidanesulfonic acid (CFc000115013)

MOL for CFc000115013 ({3-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]-2-hydroxy-6-methoxyphenyl}oxidanesulfonic acid)

3D MOL for CFc000115013 ({3-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]-2-hydroxy-6-methoxyphenyl}oxidanesulfonic acid)

3D SDF for CFc000115013 ({3-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]-2-hydroxy-6-methoxyphenyl}oxidanesulfonic acid)

3D-SDF for CFc000115013 ({3-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]-2-hydroxy-6-methoxyphenyl}oxidanesulfonic acid)

PDB for CFc000115013 ({3-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]-2-hydroxy-6-methoxyphenyl}oxidanesulfonic acid)

3D PDB for CFc000115013 ({3-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]-2-hydroxy-6-methoxyphenyl}oxidanesulfonic acid)

SMILES for CFc000115013 ({3-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]-2-hydroxy-6-methoxyphenyl}oxidanesulfonic acid)

INCHI for CFc000115013 ({3-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]-2-hydroxy-6-methoxyphenyl}oxidanesulfonic acid)

Structure for CFc000115013 ({3-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]-2-hydroxy-6-methoxyphenyl}oxidanesulfonic acid)

3D Structure for CFc000115013 ({3-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]-2-hydroxy-6-methoxyphenyl}oxidanesulfonic acid)