ChemFOnt: Showing chemical card for [3-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-2-yl)-2,6-dihydroxyphenyl]oxidanesulfonic acid (CFc000112366)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:32:31 UTC

Chemfont ID

CFc000112366

Molecule Identification

Common Name

[3-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-2-yl)-2,6-dihydroxyphenyl]oxidanesulfonic acid

Definition

[3-(5,6-dihydroxy-7-methoxy-4-oxo-4h-chromen-2-yl)-2,6-dihydroxyphenyl]oxidanesulfonic acid is a predicted metabolite generated by BioTransformer¹ that is produced by the metabolism of 5,6-dihydroxy-7-methoxy-2-(2,3,4-trihydroxyphenyl)-4h-chromen-4-one. 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-(5,6-Dihydroxy-7-methoxy-4-oxo-4H-chromen-2-yl)-2,6-dihydroxyphenyl]oxidanesulfonate	Generator
[3-(5,6-Dihydroxy-7-methoxy-4-oxo-4H-chromen-2-yl)-2,6-dihydroxyphenyl]oxidanesulphonate	Generator
[3-(5,6-Dihydroxy-7-methoxy-4-oxo-4H-chromen-2-yl)-2,6-dihydroxyphenyl]oxidanesulphonic acid	Generator

Chemical Formula

C₁₆H₁₂O₁₁S

Average Molecular Weight

412.32

Monoisotopic Molecular Weight

412.01003238

IUPAC Name

[3-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-2-yl)-2,6-dihydroxyphenyl]oxidanesulfonic acid

Traditional Name

[3-(5,6-dihydroxy-7-methoxy-4-oxochromen-2-yl)-2,6-dihydroxyphenyl]oxidanesulfonic acid

CAS Registry Number

Not Available

SMILES

COC1=C(O)C(O)=C2C(=O)C=C(OC2=C1)C1=C(O)C(OS(O)(=O)=O)=C(O)C=C1

InChI Identifier

InChI=1S/C16H12O11S/c1-25-11-5-10-12(15(21)14(11)20)8(18)4-9(26-10)6-2-3-7(17)16(13(6)19)27-28(22,23)24/h2-5,17,19-21H,1H3,(H,22,23,24)

InChI Key

GUBHXVJSYPNSJL-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 7-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

O-methylated flavonoids

Direct Parent

7-O-methylated flavonoids

Alternative Parents

Substituents

7-methoxyflavonoid-skeleton
Hydroxyflavonoid
Flavone
4'-hydroxyflavonoid
5-hydroxyflavonoid
6-hydroxyflavonoid
Phenylsulfate
Chromone
1-benzopyran
Arylsulfate
Benzopyran
Phenoxy compound
Resorcinol
Anisole
1-hydroxy-2-unsubstituted benzenoid
Pyranone
1-hydroxy-4-unsubstituted benzenoid
Phenol
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Sulfuric acid ester
Sulfate-ester
Sulfuric acid monoester
Pyran
Vinylogous acid
Heteroaromatic compound
Organic sulfuric acid or derivatives
Ether
Oxacycle
Organoheterocyclic compound
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Endogenous (HMDB: HMDB0131957)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.7 g/L	ALOGPS
logP	1.07	ALOGPS
logP	2.77	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	-2.7	ChemAxon
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	180.05 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	93.33 m³·mol⁻¹	ChemAxon
Polarizability	36.68 Å³	ChemAxon
Number of Rings	3	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

HMDB0131957

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 [3-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-2-yl)-2,6-dihydroxyphenyl]oxidanesulfonic acid (CFc000112366)

MOL for CFc000112366 ([3-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-2-yl)-2,6-dihydroxyphenyl]oxidanesulfonic acid)

3D MOL for CFc000112366 ([3-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-2-yl)-2,6-dihydroxyphenyl]oxidanesulfonic acid)

3D SDF for CFc000112366 ([3-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-2-yl)-2,6-dihydroxyphenyl]oxidanesulfonic acid)

3D-SDF for CFc000112366 ([3-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-2-yl)-2,6-dihydroxyphenyl]oxidanesulfonic acid)

PDB for CFc000112366 ([3-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-2-yl)-2,6-dihydroxyphenyl]oxidanesulfonic acid)

3D PDB for CFc000112366 ([3-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-2-yl)-2,6-dihydroxyphenyl]oxidanesulfonic acid)

SMILES for CFc000112366 ([3-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-2-yl)-2,6-dihydroxyphenyl]oxidanesulfonic acid)

INCHI for CFc000112366 ([3-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-2-yl)-2,6-dihydroxyphenyl]oxidanesulfonic acid)

Structure for CFc000112366 ([3-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-2-yl)-2,6-dihydroxyphenyl]oxidanesulfonic acid)

3D Structure for CFc000112366 ([3-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-2-yl)-2,6-dihydroxyphenyl]oxidanesulfonic acid)