ChemFOnt: Showing chemical card for 2-{5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-2-ethenyl-7-hydroxy-4-oxo-4H-chromen-3-yl}propanedioic acid (CFc000148021)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 23:28:42 UTC

Chemfont ID

CFc000148021

Molecule Identification

Common Name

2-{5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-2-ethenyl-7-hydroxy-4-oxo-4H-chromen-3-yl}propanedioic acid

Definition

2-{5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-2-ethenyl-7-hydroxy-4-oxo-4H-chromen-3-yl}propanedioic 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-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-2-ethenyl-7-hydroxy-4-oxo-4H-chromen-3-yl}propanedioic acid.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
2-{5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-2-ethenyl-7-hydroxy-4-oxo-4H-chromen-3-yl}propanedioate	Generator

Chemical Formula

C₂₀H₁₈O₁₄

Average Molecular Weight

482.35

Monoisotopic Molecular Weight

482.06965526

IUPAC Name

2-{5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-2-ethenyl-7-hydroxy-4-oxo-4H-chromen-3-yl}propanedioic acid

Traditional Name

2-{5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-2-ethenyl-7-hydroxy-4-oxochromen-3-yl}propanedioic acid

CAS Registry Number

Not Available

SMILES

OC1C(O)C(OC2=CC(O)=CC3=C2C(=O)C(C(C(O)=O)C(O)=O)=C(O3)C=C)OC(C1O)C(O)=O

InChI Identifier

InChI=1S/C20H18O14/c1-2-6-10(11(17(26)27)18(28)29)12(22)9-7(32-6)3-5(21)4-8(9)33-20-15(25)13(23)14(24)16(34-20)19(30)31/h2-4,11,13-16,20-21,23-25H,1H2,(H,26,27)(H,28,29)(H,30,31)

InChI Key

VYMGVSUWCXHOTA-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
O-glucuronide
1-o-glucuronide
Glucuronic acid or derivatives
Chromone
O-glycosyl compound
Benzopyran
1-benzopyran
Tricarboxylic acid or derivatives
1-hydroxy-2-unsubstituted benzenoid
Beta-hydroxy acid
Pyranone
1,3-dicarbonyl compound
Pyran
Benzenoid
Monosaccharide
Oxane
Hydroxy acid
Heteroaromatic compound
Vinylogous ester
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Acetal
Carboxylic acid
Carboxylic acid derivative
Polyol
Alcohol
Carbonyl group
Hydrocarbon derivative
Organic oxide
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	1.81 g/L	ALOGPS
logP	0.28	ALOGPS
logP	-1.1	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	-2.5	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-4	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	237.58 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	104.41 m³·mol⁻¹	ChemAxon
Polarizability	43.06 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	Yes	ChemAxon

External Links

HMDB ID

HMDB0167613

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-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-2-ethenyl-7-hydroxy-4-oxo-4H-chromen-3-yl}propanedioic acid (CFc000148021)

MOL for CFc000148021 (2-{5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-2-ethenyl-7-hydroxy-4-oxo-4H-chromen-3-yl}propanedioic acid)

3D MOL for CFc000148021 (2-{5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-2-ethenyl-7-hydroxy-4-oxo-4H-chromen-3-yl}propanedioic acid)

3D SDF for CFc000148021 (2-{5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-2-ethenyl-7-hydroxy-4-oxo-4H-chromen-3-yl}propanedioic acid)

3D-SDF for CFc000148021 (2-{5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-2-ethenyl-7-hydroxy-4-oxo-4H-chromen-3-yl}propanedioic acid)

PDB for CFc000148021 (2-{5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-2-ethenyl-7-hydroxy-4-oxo-4H-chromen-3-yl}propanedioic acid)

3D PDB for CFc000148021 (2-{5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-2-ethenyl-7-hydroxy-4-oxo-4H-chromen-3-yl}propanedioic acid)

SMILES for CFc000148021 (2-{5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-2-ethenyl-7-hydroxy-4-oxo-4H-chromen-3-yl}propanedioic acid)

INCHI for CFc000148021 (2-{5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-2-ethenyl-7-hydroxy-4-oxo-4H-chromen-3-yl}propanedioic acid)

Structure for CFc000148021 (2-{5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-2-ethenyl-7-hydroxy-4-oxo-4H-chromen-3-yl}propanedioic acid)

3D Structure for CFc000148021 (2-{5-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-2-ethenyl-7-hydroxy-4-oxo-4H-chromen-3-yl}propanedioic acid)