ChemFOnt: Showing chemical card for (4-{5-hydroxy-8,8-dimethyl-2-oxo-4-phenyl-2H,8H-pyrano[2,3-f]chromen-6-yl}-2-methyl-4-oxobutoxy)sulfonic acid (CFc000112035)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:32:01 UTC

Chemfont ID

CFc000112035

Molecule Identification

Common Name

(4-{5-hydroxy-8,8-dimethyl-2-oxo-4-phenyl-2H,8H-pyrano[2,3-f]chromen-6-yl}-2-methyl-4-oxobutoxy)sulfonic acid

Definition

(4-{5-hydroxy-8,8-dimethyl-2-oxo-4-phenyl-2h,8h-pyrano[2,3-f]chromen-6-yl}-2-methyl-4-oxobutoxy)sulfonic acid is a predicted metabolite generated by BioTransformer¹ that is produced by the metabolism of 5-hydroxy-6-(4-hydroxy-3-methylbutanoyl)-8,8-dimethyl-4-phenyl-2h,8h-pyrano[2,3-f]chromen-2-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
(4-{5-hydroxy-8,8-dimethyl-2-oxo-4-phenyl-2H,8H-pyrano[2,3-F]chromen-6-yl}-2-methyl-4-oxobutoxy)sulfonate	Generator
(4-{5-hydroxy-8,8-dimethyl-2-oxo-4-phenyl-2H,8H-pyrano[2,3-F]chromen-6-yl}-2-methyl-4-oxobutoxy)sulphonate	Generator
(4-{5-hydroxy-8,8-dimethyl-2-oxo-4-phenyl-2H,8H-pyrano[2,3-F]chromen-6-yl}-2-methyl-4-oxobutoxy)sulphonic acid	Generator

Chemical Formula

C₂₅H₂₄O₉S

Average Molecular Weight

500.52

Monoisotopic Molecular Weight

500.114103527

IUPAC Name

(4-{5-hydroxy-8,8-dimethyl-2-oxo-4-phenyl-2H,8H-pyrano[2,3-f]chromen-6-yl}-2-methyl-4-oxobutoxy)sulfonic acid

Traditional Name

4-{5-hydroxy-8,8-dimethyl-2-oxo-4-phenylpyrano[2,3-f]chromen-6-yl}-2-methyl-4-oxobutoxysulfonic acid

CAS Registry Number

Not Available

SMILES

CC(COS(O)(=O)=O)CC(=O)C1=C2OC(C)(C)C=CC2=C2OC(=O)C=C(C3=CC=CC=C3)C2=C1O

InChI Identifier

InChI=1S/C25H24O9S/c1-14(13-32-35(29,30)31)11-18(26)21-22(28)20-17(15-7-5-4-6-8-15)12-19(27)33-23(20)16-9-10-25(2,3)34-24(16)21/h4-10,12,14,28H,11,13H2,1-3H3,(H,29,30,31)

InChI Key

GDXRCPQNIJSEDP-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as prenylated neoflavonoids. These are neoflavonoids that features a C5-isoprenoid substituent at any position of the A, B, or C ring. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Neoflavonoids

Sub Class

Prenylated neoflavonoids

Direct Parent

Prenylated neoflavonoids

Alternative Parents

Substituents

Prenylated neoflavonoid
Pyranoneoflavonoid
4-phenylcoumarin
Pyranocoumarin
Angular pyranocoumarin
Pyranochromene
2,2-dimethyl-1-benzopyran
Butyrophenone
Coumarin
Benzopyran
1-benzopyran
Aryl alkyl ketone
Aryl ketone
Alkyl aryl ether
Pyranone
Monocyclic benzene moiety
Pyran
Sulfuric acid monoester
Sulfate-ester
Alkyl sulfate
Sulfuric acid ester
Benzenoid
Organic sulfuric acid or derivatives
Vinylogous acid
Heteroaromatic compound
Lactone
Ketone
Organoheterocyclic compound
Oxacycle
Ether
Organooxygen compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Endogenous (HMDB: HMDB0131626)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.012 g/L	ALOGPS
logP	1.81	ALOGPS
logP	4.15	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	-2.3	ChemAxon
pKa (Strongest Basic)	-5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	136.43 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	137.5 m³·mol⁻¹	ChemAxon
Polarizability	50.2 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

HMDB0131626

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-hydroxy-8,8-dimethyl-2-oxo-4-phenyl-2H,8H-pyrano[2,3-f]chromen-6-yl}-2-methyl-4-oxobutoxy)sulfonic acid (CFc000112035)

MOL for CFc000112035 ((4-{5-hydroxy-8,8-dimethyl-2-oxo-4-phenyl-2H,8H-pyrano[2,3-f]chromen-6-yl}-2-methyl-4-oxobutoxy)sulfonic acid)

3D MOL for CFc000112035 ((4-{5-hydroxy-8,8-dimethyl-2-oxo-4-phenyl-2H,8H-pyrano[2,3-f]chromen-6-yl}-2-methyl-4-oxobutoxy)sulfonic acid)

3D SDF for CFc000112035 ((4-{5-hydroxy-8,8-dimethyl-2-oxo-4-phenyl-2H,8H-pyrano[2,3-f]chromen-6-yl}-2-methyl-4-oxobutoxy)sulfonic acid)

3D-SDF for CFc000112035 ((4-{5-hydroxy-8,8-dimethyl-2-oxo-4-phenyl-2H,8H-pyrano[2,3-f]chromen-6-yl}-2-methyl-4-oxobutoxy)sulfonic acid)

PDB for CFc000112035 ((4-{5-hydroxy-8,8-dimethyl-2-oxo-4-phenyl-2H,8H-pyrano[2,3-f]chromen-6-yl}-2-methyl-4-oxobutoxy)sulfonic acid)

3D PDB for CFc000112035 ((4-{5-hydroxy-8,8-dimethyl-2-oxo-4-phenyl-2H,8H-pyrano[2,3-f]chromen-6-yl}-2-methyl-4-oxobutoxy)sulfonic acid)

SMILES for CFc000112035 ((4-{5-hydroxy-8,8-dimethyl-2-oxo-4-phenyl-2H,8H-pyrano[2,3-f]chromen-6-yl}-2-methyl-4-oxobutoxy)sulfonic acid)

INCHI for CFc000112035 ((4-{5-hydroxy-8,8-dimethyl-2-oxo-4-phenyl-2H,8H-pyrano[2,3-f]chromen-6-yl}-2-methyl-4-oxobutoxy)sulfonic acid)

Structure for CFc000112035 ((4-{5-hydroxy-8,8-dimethyl-2-oxo-4-phenyl-2H,8H-pyrano[2,3-f]chromen-6-yl}-2-methyl-4-oxobutoxy)sulfonic acid)

3D Structure for CFc000112035 ((4-{5-hydroxy-8,8-dimethyl-2-oxo-4-phenyl-2H,8H-pyrano[2,3-f]chromen-6-yl}-2-methyl-4-oxobutoxy)sulfonic acid)