ChemFOnt: Showing chemical card for {[6-(5,7-dihydroxy-4-oxo-2-phenyl-4H-chromen-8-yl)-3,4,5-trihydroxyoxan-2-yl]methoxy}sulfonic acid (CFc000107581)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:25:31 UTC

Chemfont ID

CFc000107581

Molecule Identification

Common Name

{[6-(5,7-dihydroxy-4-oxo-2-phenyl-4H-chromen-8-yl)-3,4,5-trihydroxyoxan-2-yl]methoxy}sulfonic acid

Definition

{[6-(5,7-dihydroxy-4-oxo-2-phenyl-4h-chromen-8-yl)-3,4,5-trihydroxyoxan-2-yl]methoxy}sulfonic acid is a predicted metabolite generated by BioTransformer¹ that is produced by the metabolism of 5,7-dihydroxy-2-phenyl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4h-chromen-4-one. It is generated by Sulfotransferase family cytosolic 2B member 1 (O00204) and Sulfotransferase enzymes via a sulfation-of-primary-alcohol reaction. This sulfation-of-primary-alcohol occurs in humans.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
{[6-(5,7-dihydroxy-4-oxo-2-phenyl-4H-chromen-8-yl)-3,4,5-trihydroxyoxan-2-yl]methoxy}sulfonate	Generator
{[6-(5,7-dihydroxy-4-oxo-2-phenyl-4H-chromen-8-yl)-3,4,5-trihydroxyoxan-2-yl]methoxy}sulphonate	Generator
{[6-(5,7-dihydroxy-4-oxo-2-phenyl-4H-chromen-8-yl)-3,4,5-trihydroxyoxan-2-yl]methoxy}sulphonic acid	Generator

Chemical Formula

C₂₁H₂₀O₁₂S

Average Molecular Weight

496.44

Monoisotopic Molecular Weight

496.067547258

IUPAC Name

{[6-(5,7-dihydroxy-4-oxo-2-phenyl-4H-chromen-8-yl)-3,4,5-trihydroxyoxan-2-yl]methoxy}sulfonic acid

Traditional Name

[6-(5,7-dihydroxy-4-oxo-2-phenylchromen-8-yl)-3,4,5-trihydroxyoxan-2-yl]methoxysulfonic acid

CAS Registry Number

None

SMILES

OC1C(O)C(COS(O)(=O)=O)OC(C1O)C1=C(O)C=C(O)C2=C1OC(=CC2=O)C1=CC=CC=C1

InChI Identifier

InChI=1S/C21H20O12S/c22-10-6-11(23)16(20-15(10)12(24)7-13(32-20)9-4-2-1-3-5-9)21-19(27)18(26)17(25)14(33-21)8-31-34(28,29)30/h1-7,14,17-19,21-23,25-27H,8H2,(H,28,29,30)

InChI Key

YHSYPAINNSYJDR-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavonoid 8-c-glycosides. Flavonoid 8-C-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to 8-position of a 2-phenylchromen-4-one flavonoid backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid 8-C-glycosides

Alternative Parents

Substituents

Flavonoid-8-c-glycoside
5-hydroxyflavonoid
7-hydroxyflavonoid
Flavone
Hydroxyflavonoid
Phenolic glycoside
Hexose monosaccharide
C-glycosyl compound
Chromone
Glycosyl compound
Benzopyran
Monosaccharide sulfate
1-benzopyran
1-hydroxy-2-unsubstituted benzenoid
Pyranone
Sulfate-ester
Sulfuric acid monoester
Pyran
Alkyl sulfate
Sulfuric acid ester
Oxane
Monocyclic benzene moiety
Monosaccharide
Benzenoid
Organic sulfuric acid or derivatives
Vinylogous acid
Heteroaromatic compound
Secondary alcohol
Polyol
Organoheterocyclic compound
Dialkyl ether
Ether
Oxacycle
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Alcohol
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Endogenous (HMDB: HMDB0127172)

Plant

Plant (HMDB: HMDB0127172)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	5.25 g/L	ALOGPS
logP	0.12	ALOGPS
logP	-1.7	ChemAxon
logS	-2	ALOGPS
pKa (Strongest Acidic)	-2.2	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	200.28 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	114.04 m³·mol⁻¹	ChemAxon
Polarizability	45.99 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0127172

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB086037

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

131833540

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

Showing chemical card for {[6-(5,7-dihydroxy-4-oxo-2-phenyl-4H-chromen-8-yl)-3,4,5-trihydroxyoxan-2-yl]methoxy}sulfonic acid (CFc000107581)

MOL for CFc000107581 ({[6-(5,7-dihydroxy-4-oxo-2-phenyl-4H-chromen-8-yl)-3,4,5-trihydroxyoxan-2-yl]methoxy}sulfonic acid)

3D MOL for CFc000107581 ({[6-(5,7-dihydroxy-4-oxo-2-phenyl-4H-chromen-8-yl)-3,4,5-trihydroxyoxan-2-yl]methoxy}sulfonic acid)

3D SDF for CFc000107581 ({[6-(5,7-dihydroxy-4-oxo-2-phenyl-4H-chromen-8-yl)-3,4,5-trihydroxyoxan-2-yl]methoxy}sulfonic acid)

3D-SDF for CFc000107581 ({[6-(5,7-dihydroxy-4-oxo-2-phenyl-4H-chromen-8-yl)-3,4,5-trihydroxyoxan-2-yl]methoxy}sulfonic acid)

PDB for CFc000107581 ({[6-(5,7-dihydroxy-4-oxo-2-phenyl-4H-chromen-8-yl)-3,4,5-trihydroxyoxan-2-yl]methoxy}sulfonic acid)

3D PDB for CFc000107581 ({[6-(5,7-dihydroxy-4-oxo-2-phenyl-4H-chromen-8-yl)-3,4,5-trihydroxyoxan-2-yl]methoxy}sulfonic acid)

SMILES for CFc000107581 ({[6-(5,7-dihydroxy-4-oxo-2-phenyl-4H-chromen-8-yl)-3,4,5-trihydroxyoxan-2-yl]methoxy}sulfonic acid)

INCHI for CFc000107581 ({[6-(5,7-dihydroxy-4-oxo-2-phenyl-4H-chromen-8-yl)-3,4,5-trihydroxyoxan-2-yl]methoxy}sulfonic acid)

Structure for CFc000107581 ({[6-(5,7-dihydroxy-4-oxo-2-phenyl-4H-chromen-8-yl)-3,4,5-trihydroxyoxan-2-yl]methoxy}sulfonic acid)

3D Structure for CFc000107581 ({[6-(5,7-dihydroxy-4-oxo-2-phenyl-4H-chromen-8-yl)-3,4,5-trihydroxyoxan-2-yl]methoxy}sulfonic acid)