ChemFOnt: Showing chemical card for [4-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-3-yl)-2-methoxyphenyl]oxidanesulfonic acid (CFc000127946)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:56:05 UTC

Chemfont ID

CFc000127946

Molecule Identification

Common Name

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

Definition

[4-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-3-yl)-2-methoxyphenyl]oxidanesulfonic acid belongs to the class of organic compounds known as 7-o-methylisoflavones. These are isoflavones with methoxy groups attached to the C7 atom of the isoflavone backbone. Based on a literature review a significant number of articles have been published on [4-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-3-yl)-2-methoxyphenyl]oxidanesulfonic acid.

Structure

MOL SDF PDB SMILES InChI

Synonyms

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

Chemical Formula

C₁₇H₁₄O₁₀S

Average Molecular Weight

410.35

Monoisotopic Molecular Weight

410.030767825

IUPAC Name

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

Traditional Name

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

CAS Registry Number

Not Available

SMILES

COC1=C(O)C(O)=C2C(=O)C(=COC2=C1)C1=CC(OC)=C(OS(O)(=O)=O)C=C1

InChI Identifier

InChI=1S/C17H14O10S/c1-24-11-5-8(3-4-10(11)27-28(21,22)23)9-7-26-12-6-13(25-2)16(19)17(20)14(12)15(9)18/h3-7,19-20H,1-2H3,(H,21,22,23)

InChI Key

CYDSQKYXNYWBBZ-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 7-o-methylisoflavones. These are isoflavones with methoxy groups attached to the C7 atom of the isoflavone backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

O-methylated isoflavonoids

Direct Parent

7-O-methylisoflavones

Alternative Parents

Substituents

3p-methoxyisoflavone
7-o-methylisoflavone
Hydroxyisoflavonoid
Isoflavone
Chromone
Phenylsulfate
Arylsulfate
Benzopyran
1-benzopyran
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
Pyranone
Sulfuric acid monoester
Pyran
Monocyclic benzene moiety
Sulfate-ester
Benzenoid
Sulfuric acid ester
Organic sulfuric acid or derivatives
Vinylogous acid
Heteroaromatic compound
Oxacycle
Organoheterocyclic compound
Ether
Organic oxygen compound
Organic oxide
Organooxygen compound
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Exogenous (HMDB: HMDB0147537)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.36 g/L	ALOGPS
logP	1.12	ALOGPS
logP	2.29	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	-2.5	ChemAxon
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	148.82 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	94.6 m³·mol⁻¹	ChemAxon
Polarizability	37.91 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

HMDB0147537

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-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-3-yl)-2-methoxyphenyl]oxidanesulfonic acid (CFc000127946)

MOL for CFc000127946 ([4-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-3-yl)-2-methoxyphenyl]oxidanesulfonic acid)

3D MOL for CFc000127946 ([4-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-3-yl)-2-methoxyphenyl]oxidanesulfonic acid)

3D SDF for CFc000127946 ([4-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-3-yl)-2-methoxyphenyl]oxidanesulfonic acid)

3D-SDF for CFc000127946 ([4-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-3-yl)-2-methoxyphenyl]oxidanesulfonic acid)

PDB for CFc000127946 ([4-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-3-yl)-2-methoxyphenyl]oxidanesulfonic acid)

3D PDB for CFc000127946 ([4-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-3-yl)-2-methoxyphenyl]oxidanesulfonic acid)

SMILES for CFc000127946 ([4-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-3-yl)-2-methoxyphenyl]oxidanesulfonic acid)

INCHI for CFc000127946 ([4-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-3-yl)-2-methoxyphenyl]oxidanesulfonic acid)

Structure for CFc000127946 ([4-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-3-yl)-2-methoxyphenyl]oxidanesulfonic acid)

3D Structure for CFc000127946 ([4-(5,6-dihydroxy-7-methoxy-4-oxo-4H-chromen-3-yl)-2-methoxyphenyl]oxidanesulfonic acid)