ChemFOnt: Showing chemical card for 6-({6-[(3,3-dimethyloxiran-2-yl)methyl]-7-hydroxy-2-oxo-4-phenyl-2H-chromen-5-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylic acid (CFc000111946)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:31:54 UTC

Chemfont ID

CFc000111946

Molecule Identification

Common Name

6-({6-[(3,3-dimethyloxiran-2-yl)methyl]-7-hydroxy-2-oxo-4-phenyl-2H-chromen-5-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylic acid

Definition

6-({6-[(3,3-dimethyloxiran-2-yl)methyl]-7-hydroxy-2-oxo-4-phenyl-2h-chromen-5-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylic acid is a predicted metabolite generated by BioTransformer¹ that is produced by the metabolism of 6-[(3,3-dimethyloxiran-2-yl)methyl]-5,7-dihydroxy-4-phenyl-2h-chromen-2-one. It is generated by UDP-glucuronosyltransferase 1-1 (P22309) enzyme via an aromatic-OH-glucuronidation reaction. This aromatic-OH-glucuronidation occurs in humans.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
6-({6-[(3,3-dimethyloxiran-2-yl)methyl]-7-hydroxy-2-oxo-4-phenyl-2H-chromen-5-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylate	Generator

Chemical Formula

C₂₆H₂₆O₁₁

Average Molecular Weight

514.483

Monoisotopic Molecular Weight

514.147511657

IUPAC Name

6-({6-[(3,3-dimethyloxiran-2-yl)methyl]-7-hydroxy-2-oxo-4-phenyl-2H-chromen-5-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylic acid

Traditional Name

6-({6-[(3,3-dimethyloxiran-2-yl)methyl]-7-hydroxy-2-oxo-4-phenylchromen-5-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC1(C)OC1CC1=C(OC2OC(C(O)C(O)C2O)C(O)=O)C2=C(OC(=O)C=C2C2=CC=CC=C2)C=C1O

InChI Identifier

InChI=1S/C26H26O11/c1-26(2)16(37-26)8-13-14(27)10-15-18(12(9-17(28)34-15)11-6-4-3-5-7-11)22(13)35-25-21(31)19(29)20(30)23(36-25)24(32)33/h3-7,9-10,16,19-21,23,25,27,29-31H,8H2,1-2H3,(H,32,33)

InChI Key

VBCHYSJWPUMTDK-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumarin glycosides. These are aromatic compounds containing a carbohydrate moiety glycosidically bound to a coumarin moiety.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Coumarins and derivatives

Sub Class

Coumarin glycosides

Direct Parent

Coumarin glycosides

Alternative Parents

Substituents

Coumarin-5-o-glycoside
Coumarin o-glycoside
Prenylated neoflavonoid
4-phenylcoumarin
Neoflavonoid skeleton
Phenolic glycoside
O-glucuronide
1-o-glucuronide
Glucuronic acid or derivatives
7-hydroxycoumarin
Hexose monosaccharide
Hydroxycoumarin
Glycosyl compound
O-glycosyl compound
1-benzopyran
Benzopyran
Beta-hydroxy acid
1-hydroxy-2-unsubstituted benzenoid
Pyranone
Monocyclic benzene moiety
Benzenoid
Hydroxy acid
Pyran
Monosaccharide
Oxane
Heteroaromatic compound
Lactone
Secondary alcohol
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Carboxylic acid
Oxacycle
Dialkyl ether
Oxirane
Acetal
Organoheterocyclic compound
Ether
Organic oxide
Organooxygen compound
Hydrocarbon derivative
Carbonyl group
Alcohol
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Endogenous (HMDB: HMDB0131537)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.44 g/L	ALOGPS
logP	1.77	ALOGPS
logP	1.41	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	2.93	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	175.51 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	134.16 m³·mol⁻¹	ChemAxon
Polarizability	49.66 Å³	ChemAxon
Number of Rings	5	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

HMDB0131537

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 6-({6-[(3,3-dimethyloxiran-2-yl)methyl]-7-hydroxy-2-oxo-4-phenyl-2H-chromen-5-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylic acid (CFc000111946)

MOL for CFc000111946 (6-({6-[(3,3-dimethyloxiran-2-yl)methyl]-7-hydroxy-2-oxo-4-phenyl-2H-chromen-5-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D MOL for CFc000111946 (6-({6-[(3,3-dimethyloxiran-2-yl)methyl]-7-hydroxy-2-oxo-4-phenyl-2H-chromen-5-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D SDF for CFc000111946 (6-({6-[(3,3-dimethyloxiran-2-yl)methyl]-7-hydroxy-2-oxo-4-phenyl-2H-chromen-5-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D-SDF for CFc000111946 (6-({6-[(3,3-dimethyloxiran-2-yl)methyl]-7-hydroxy-2-oxo-4-phenyl-2H-chromen-5-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

PDB for CFc000111946 (6-({6-[(3,3-dimethyloxiran-2-yl)methyl]-7-hydroxy-2-oxo-4-phenyl-2H-chromen-5-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D PDB for CFc000111946 (6-({6-[(3,3-dimethyloxiran-2-yl)methyl]-7-hydroxy-2-oxo-4-phenyl-2H-chromen-5-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

SMILES for CFc000111946 (6-({6-[(3,3-dimethyloxiran-2-yl)methyl]-7-hydroxy-2-oxo-4-phenyl-2H-chromen-5-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

INCHI for CFc000111946 (6-({6-[(3,3-dimethyloxiran-2-yl)methyl]-7-hydroxy-2-oxo-4-phenyl-2H-chromen-5-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

Structure for CFc000111946 (6-({6-[(3,3-dimethyloxiran-2-yl)methyl]-7-hydroxy-2-oxo-4-phenyl-2H-chromen-5-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D Structure for CFc000111946 (6-({6-[(3,3-dimethyloxiran-2-yl)methyl]-7-hydroxy-2-oxo-4-phenyl-2H-chromen-5-yl}oxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)