ChemFOnt: Showing chemical card for 3,4,5-trihydroxy-6-{5-methoxy-2-[(2E)-3-phenylprop-2-enoyl]phenoxy}oxane-2-carboxylic acid (CFc000116032)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:37:55 UTC

Chemfont ID

CFc000116032

Molecule Identification

Common Name

3,4,5-trihydroxy-6-{5-methoxy-2-[(2E)-3-phenylprop-2-enoyl]phenoxy}oxane-2-carboxylic acid

Definition

3,4,5-trihydroxy-6-{5-methoxy-2-[(2e)-3-phenylprop-2-enoyl]phenoxy}oxane-2-carboxylic acid is a predicted metabolite generated by BioTransformer¹ that is produced by the metabolism of (2e)-1-(2-hydroxy-4-methoxyphenyl)-3-phenylprop-2-en-1-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
3,4,5-Trihydroxy-6-{5-methoxy-2-[(2E)-3-phenylprop-2-enoyl]phenoxy}oxane-2-carboxylate	Generator

Chemical Formula

C₂₂H₂₂O₉

Average Molecular Weight

430.409

Monoisotopic Molecular Weight

430.126382288

IUPAC Name

3,4,5-trihydroxy-6-{5-methoxy-2-[(2E)-3-phenylprop-2-enoyl]phenoxy}oxane-2-carboxylic acid

Traditional Name

3,4,5-trihydroxy-6-{5-methoxy-2-[(2E)-3-phenylprop-2-enoyl]phenoxy}oxane-2-carboxylic acid

CAS Registry Number

None

SMILES

[H]\C(=C(\[H])C1=CC=CC=C1)C(=O)C1=C(OC2OC(C(O)C(O)C2O)C(O)=O)C=C(OC)C=C1

InChI Identifier

InChI=1S/C22H22O9/c1-29-13-8-9-14(15(23)10-7-12-5-3-2-4-6-12)16(11-13)30-22-19(26)17(24)18(25)20(31-22)21(27)28/h2-11,17-20,22,24-26H,1H3,(H,27,28)/b10-7+

InChI Key

UVDMWDPJQXQRSS-JXMROGBWSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavonoid o-glycosides. Flavonoid O-glycosides are compounds containing a carbohydrate moiety which is O-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid O-glycosides

Alternative Parents

Substituents

Flavonoid o-glycoside
Linear 1,3-diarylpropanoid
Phenolic glycoside
1-o-glucuronide
O-glucuronide
Glucuronic acid or derivatives
Glycosyl compound
O-glycosyl compound
Methoxybenzene
Anisole
Aryl ketone
Phenoxy compound
Styrene
Benzoyl
Phenol ether
Alkyl aryl ether
Beta-hydroxy acid
Benzenoid
Hydroxy acid
Monocyclic benzene moiety
Monosaccharide
Pyran
Oxane
Enone
Acryloyl-group
Alpha,beta-unsaturated ketone
Secondary alcohol
Ketone
Oxacycle
Organoheterocyclic compound
Polyol
Carboxylic acid derivative
Carboxylic acid
Acetal
Ether
Monocarboxylic acid or derivatives
Organooxygen compound
Carbonyl group
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Endogenous (HMDB: HMDB0135623)

Plant

Plant (HMDB: HMDB0135623)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.35 g/L	ALOGPS
logP	1.4	ALOGPS
logP	1.48	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	2.91	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	142.75 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	107.33 m³·mol⁻¹	ChemAxon
Polarizability	43.33 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	Yes	ChemAxon

External Links

HMDB ID

HMDB0135623

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB092589

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

131839146

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

Showing chemical card for 3,4,5-trihydroxy-6-{5-methoxy-2-[(2E)-3-phenylprop-2-enoyl]phenoxy}oxane-2-carboxylic acid (CFc000116032)

MOL for CFc000116032 (3,4,5-trihydroxy-6-{5-methoxy-2-[(2E)-3-phenylprop-2-enoyl]phenoxy}oxane-2-carboxylic acid)

3D MOL for CFc000116032 (3,4,5-trihydroxy-6-{5-methoxy-2-[(2E)-3-phenylprop-2-enoyl]phenoxy}oxane-2-carboxylic acid)

3D SDF for CFc000116032 (3,4,5-trihydroxy-6-{5-methoxy-2-[(2E)-3-phenylprop-2-enoyl]phenoxy}oxane-2-carboxylic acid)

3D-SDF for CFc000116032 (3,4,5-trihydroxy-6-{5-methoxy-2-[(2E)-3-phenylprop-2-enoyl]phenoxy}oxane-2-carboxylic acid)

PDB for CFc000116032 (3,4,5-trihydroxy-6-{5-methoxy-2-[(2E)-3-phenylprop-2-enoyl]phenoxy}oxane-2-carboxylic acid)

3D PDB for CFc000116032 (3,4,5-trihydroxy-6-{5-methoxy-2-[(2E)-3-phenylprop-2-enoyl]phenoxy}oxane-2-carboxylic acid)

SMILES for CFc000116032 (3,4,5-trihydroxy-6-{5-methoxy-2-[(2E)-3-phenylprop-2-enoyl]phenoxy}oxane-2-carboxylic acid)

INCHI for CFc000116032 (3,4,5-trihydroxy-6-{5-methoxy-2-[(2E)-3-phenylprop-2-enoyl]phenoxy}oxane-2-carboxylic acid)

Structure for CFc000116032 (3,4,5-trihydroxy-6-{5-methoxy-2-[(2E)-3-phenylprop-2-enoyl]phenoxy}oxane-2-carboxylic acid)

3D Structure for CFc000116032 (3,4,5-trihydroxy-6-{5-methoxy-2-[(2E)-3-phenylprop-2-enoyl]phenoxy}oxane-2-carboxylic acid)