ChemFOnt: Showing chemical card for [2-(5,7-dihydroxy-2-methyl-4-oxo-4H-chromen-6-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid (CFc000163704)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 23:54:47 UTC

Chemfont ID

CFc000163704

Molecule Identification

Common Name

[2-(5,7-dihydroxy-2-methyl-4-oxo-4H-chromen-6-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid

Definition

[2-(5,7-dihydroxy-2-methyl-4-oxo-4H-chromen-6-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. Based on a literature review very few articles have been published on [2-(5,7-dihydroxy-2-methyl-4-oxo-4H-chromen-6-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
[2-(5,7-Dihydroxy-2-methyl-4-oxo-4H-chromen-6-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxidanesulfonate	Generator
[2-(5,7-Dihydroxy-2-methyl-4-oxo-4H-chromen-6-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxidanesulphonate	Generator
[2-(5,7-Dihydroxy-2-methyl-4-oxo-4H-chromen-6-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxidanesulphonic acid	Generator

Chemical Formula

C₁₆H₁₈O₁₂S

Average Molecular Weight

434.37

Monoisotopic Molecular Weight

434.051897194

IUPAC Name

[2-(5,7-dihydroxy-2-methyl-4-oxo-4H-chromen-6-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid

Traditional Name

[2-(5,7-dihydroxy-2-methyl-4-oxochromen-6-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid

CAS Registry Number

Not Available

SMILES

CC1=CC(=O)C2=C(O1)C=C(O)C(C1OC(CO)C(O)C(O)C1OS(O)(=O)=O)=C2O

InChI Identifier

InChI=1S/C16H18O12S/c1-5-2-6(18)10-8(26-5)3-7(19)11(13(10)21)15-16(28-29(23,24)25)14(22)12(20)9(4-17)27-15/h2-3,9,12,14-17,19-22H,4H2,1H3,(H,23,24,25)

InChI Key

UVUMLBNSDALOLP-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Phenolic glycosides

Alternative Parents

Substituents

Phenolic glycoside
Hexose monosaccharide
C-glycosyl compound
Chromone
Benzopyran
1-benzopyran
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Pyranone
Monosaccharide
Oxane
Pyran
Sulfuric acid monoester
Sulfate-ester
Alkyl sulfate
Sulfuric acid ester
Benzenoid
Organic sulfuric acid or derivatives
Heteroaromatic compound
Vinylogous acid
Secondary alcohol
Organoheterocyclic compound
Dialkyl ether
Ether
Oxacycle
Primary alcohol
Alcohol
Organic oxide
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Not Available

Not Available

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	24.7 g/L	ALOGPS
logP	-0.69	ALOGPS
logP	-2.8	ChemAxon
logS	-1.2	ALOGPS
pKa (Strongest Acidic)	-2.2	ChemAxon
pKa (Strongest Basic)	-3	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	4	ChemAxon
Refractivity	94.18 m³·mol⁻¹	ChemAxon
Polarizability	39.27 Å³	ChemAxon
Number of Rings	3	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

HMDB0183347

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 [2-(5,7-dihydroxy-2-methyl-4-oxo-4H-chromen-6-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid (CFc000163704)

MOL for CFc000163704 ([2-(5,7-dihydroxy-2-methyl-4-oxo-4H-chromen-6-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid)

3D MOL for CFc000163704 ([2-(5,7-dihydroxy-2-methyl-4-oxo-4H-chromen-6-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid)

3D SDF for CFc000163704 ([2-(5,7-dihydroxy-2-methyl-4-oxo-4H-chromen-6-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid)

3D-SDF for CFc000163704 ([2-(5,7-dihydroxy-2-methyl-4-oxo-4H-chromen-6-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid)

PDB for CFc000163704 ([2-(5,7-dihydroxy-2-methyl-4-oxo-4H-chromen-6-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid)

3D PDB for CFc000163704 ([2-(5,7-dihydroxy-2-methyl-4-oxo-4H-chromen-6-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid)

SMILES for CFc000163704 ([2-(5,7-dihydroxy-2-methyl-4-oxo-4H-chromen-6-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid)

INCHI for CFc000163704 ([2-(5,7-dihydroxy-2-methyl-4-oxo-4H-chromen-6-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid)

Structure for CFc000163704 ([2-(5,7-dihydroxy-2-methyl-4-oxo-4H-chromen-6-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid)

3D Structure for CFc000163704 ([2-(5,7-dihydroxy-2-methyl-4-oxo-4H-chromen-6-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid)