ChemFOnt: Showing chemical card for Luteolin 7-malonylglucoside (CFc000281197)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-14 03:32:20 UTC

Chemfont ID

CFc000281197

Molecule Identification

Common Name

Luteolin 7-malonylglucoside

Definition

Luteolin 7-malonylglucoside, also known as luteolin 7-O-B-D-(6''-O-malonyl) glucopyranoside, is a member of the class of compounds known as flavonoid-7-o-glycosides. Flavonoid-7-o-glycosides are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position. Luteolin 7-malonylglucoside is practically insoluble (in water) and a weakly acidic compound (based on its pKa). Luteolin 7-malonylglucoside can be found in celery leaves, globe artichoke, and wild celery, which makes luteolin 7-malonylglucoside a potential biomarker for the consumption of these food products.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
Luteolin 7-O-(6''-malonylglucoside)	ChEBI
Luteolin 7-O-(6-malonyl-beta-D-glucoside)	ChEBI
Luteolin 7-O-beta-D-(6''-O-malonyl) glucopyranoside	ChEBI
Luteolin 7-O-(6-malonyl-b-D-glucoside)	Generator
Luteolin 7-O-(6-malonyl-β-D-glucoside)	Generator
Luteolin 7-O-b-D-(6''-O-malonyl) glucopyranoside	Generator
Luteolin 7-O-β-D-(6''-O-malonyl) glucopyranoside	Generator
Luteolin 7-O-(6-O-malonyl-b-D-glucoside)	Generator
Luteolin 7-O-(6-O-malonyl-β-D-glucoside)	Generator

Chemical Formula

C₂₄H₂₂O₁₄

Average Molecular Weight

534.4231

Monoisotopic Molecular Weight

534.100955412

IUPAC Name

3-{[(2R,3S,4S,5R,6S)-6-{[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3-oxopropanoic acid

Traditional Name

3-{[(2R,3S,4S,5R,6S)-6-{[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3-oxopropanoic acid

CAS Registry Number

98767-38-5

SMILES

O[C@H]1[C@H](O)[C@@H](COC(=O)CC(O)=O)O[C@@H](OC2=CC(O)=C3C(=O)C=C(OC3=C2)C2=CC=C(O)C(O)=C2)[C@@H]1O

InChI Identifier

InChI=1S/C24H22O14/c25-11-2-1-9(3-12(11)26)15-6-14(28)20-13(27)4-10(5-16(20)37-15)36-24-23(34)22(33)21(32)17(38-24)8-35-19(31)7-18(29)30/h1-6,17,21-27,32-34H,7-8H2,(H,29,30)/t17-,21-,22+,23-,24-/m1/s1

InChI Key

RNDGJCZQVKFBPI-ASDZUOGYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavonoid-7-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid-7-O-glycosides

Alternative Parents

Substituents

Flavonoid-7-o-glycoside
3'-hydroxyflavonoid
4'-hydroxyflavonoid
5-hydroxyflavonoid
Flavone
Hydroxyflavonoid
Phenolic glycoside
Chromone
Glycosyl compound
O-glycosyl compound
1-benzopyran
Benzopyran
Catechol
Pyranone
Phenol
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Monocyclic benzene moiety
Monosaccharide
Pyran
1,3-dicarbonyl compound
Oxane
Dicarboxylic acid or derivatives
Benzenoid
Heteroaromatic compound
Vinylogous acid
Carboxylic acid ester
Secondary alcohol
Carboxylic acid
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Acetal
Polyol
Organic oxide
Organic oxygen compound
Carbonyl group
Alcohol
Hydrocarbon derivative
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

beta-D-glucoside (CHEBI:6579 )
glycosyloxyflavone (CHEBI:6579 )
trihydroxyflavone (CHEBI:6579 )
malonate ester (CHEBI:6579 )
flavones (C10103 )
Flavones and Flavonols (C10103 )

Functional Ontology

Not Available

Exogenous (HMDB: HMDB0301681)

Food

Vegetable

Shoot vegetable

Globe artichoke (FooDB: FOOD00071)

Herb and spice

Herb

Celery leaves (FooDB: FOOD00249)

Spice

Wild celery (FooDB: FOOD00015)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.64 g/L	ALOGPS
logP	1.26	ALOGPS
logP	0.47	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	3.37	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	229.74 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	122.53 m³·mol⁻¹	ChemAxon
Polarizability	49.8 Å³	ChemAxon
Number of Rings	4	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

HMDB0301681

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

KNApSAcK ID

Chemspider ID

KEGG Compound ID

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

6579

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

Showing chemical card for Luteolin 7-malonylglucoside (CFc000281197)

MOL for CFc000281197 (Luteolin 7-malonylglucoside)

3D MOL for CFc000281197 (Luteolin 7-malonylglucoside)

3D SDF for CFc000281197 (Luteolin 7-malonylglucoside)

3D-SDF for CFc000281197 (Luteolin 7-malonylglucoside)

PDB for CFc000281197 (Luteolin 7-malonylglucoside)

3D PDB for CFc000281197 (Luteolin 7-malonylglucoside)

SMILES for CFc000281197 (Luteolin 7-malonylglucoside)

INCHI for CFc000281197 (Luteolin 7-malonylglucoside)

Structure for CFc000281197 (Luteolin 7-malonylglucoside)

3D Structure for CFc000281197 (Luteolin 7-malonylglucoside)