ChemFOnt: Showing chemical card for 6-({9,10-dihydroxy-8-methyl-2-oxo-2H,8H,9H,10H-pyrano[2,3-h]chromen-8-yl}methoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid (CFc000118486)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:41:38 UTC

Chemfont ID

CFc000118486

Molecule Identification

Common Name

6-({9,10-dihydroxy-8-methyl-2-oxo-2H,8H,9H,10H-pyrano[2,3-h]chromen-8-yl}methoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid

Definition

6-({9,10-dihydroxy-8-methyl-2-oxo-2h,8h,9h,10h-pyrano[2,3-h]chromen-8-yl}methoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid is a predicted metabolite generated by BioTransformer¹ that is produced by the metabolism of 9,10-dihydroxy-8-(hydroxymethyl)-8-methyl-2h,8h,9h,10h-pyrano[2,3-h]chromen-2-one. It is generated by UDP-glucuronosyltransferase 1-1 (P22309) enzyme via an alkyl-OH-glucuronidation reaction. This alkyl-OH-glucuronidation occurs in humans.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
6-({9,10-dihydroxy-8-methyl-2-oxo-2H,8H,9H,10H-pyrano[2,3-H]chromen-8-yl}methoxy)-3,4,5-trihydroxyoxane-2-carboxylate	Generator

Chemical Formula

C₂₀H₂₂O₁₂

Average Molecular Weight

454.384

Monoisotopic Molecular Weight

454.111126148

IUPAC Name

6-({9,10-dihydroxy-8-methyl-2-oxo-2H,8H,9H,10H-pyrano[2,3-h]chromen-8-yl}methoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid

Traditional Name

6-({9,10-dihydroxy-8-methyl-2-oxo-9H,10H-pyrano[2,3-h]chromen-8-yl}methoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC1(COC2OC(C(O)C(O)C2O)C(O)=O)OC2=C(C(O)C1O)C1=C(C=CC(=O)O1)C=C2

InChI Identifier

InChI=1S/C20H22O12/c1-20(6-29-19-14(25)12(23)13(24)16(31-19)18(27)28)17(26)11(22)10-8(32-20)4-2-7-3-5-9(21)30-15(7)10/h2-5,11-14,16-17,19,22-26H,6H2,1H3,(H,27,28)

InChI Key

TXOBMGUHFHTLBD-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as angular pyranocoumarins. These are organic compounds containing a pyran (or a hydrogenated derivative) angularly fused to a coumarin moiety.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Coumarins and derivatives

Sub Class

Pyranocoumarins

Direct Parent

Angular pyranocoumarins

Alternative Parents

Substituents

Angular pyranocoumarin
1-o-glucuronide
O-glucuronide
Pyranochromene
Glucuronic acid or derivatives
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Chromane
Benzopyran
1-benzopyran
Pyranone
Alkyl aryl ether
Beta-hydroxy acid
Pyran
Benzenoid
Oxane
Monosaccharide
Hydroxy acid
Heteroaromatic compound
Secondary alcohol
Lactone
Polyol
Organoheterocyclic compound
Acetal
Oxacycle
Carboxylic acid derivative
Carboxylic acid
Ether
Monocarboxylic acid or derivatives
Organooxygen compound
Alcohol
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Endogenous (HMDB: HMDB0138077)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	7.58 g/L	ALOGPS
logP	-1.2	ALOGPS
logP	-1.7	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Acidic)	3.09	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	192.44 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	101.37 m³·mol⁻¹	ChemAxon
Polarizability	42.2 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	No	ChemAxon

External Links

HMDB ID

HMDB0138077

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-({9,10-dihydroxy-8-methyl-2-oxo-2H,8H,9H,10H-pyrano[2,3-h]chromen-8-yl}methoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid (CFc000118486)

MOL for CFc000118486 (6-({9,10-dihydroxy-8-methyl-2-oxo-2H,8H,9H,10H-pyrano[2,3-h]chromen-8-yl}methoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D MOL for CFc000118486 (6-({9,10-dihydroxy-8-methyl-2-oxo-2H,8H,9H,10H-pyrano[2,3-h]chromen-8-yl}methoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D SDF for CFc000118486 (6-({9,10-dihydroxy-8-methyl-2-oxo-2H,8H,9H,10H-pyrano[2,3-h]chromen-8-yl}methoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D-SDF for CFc000118486 (6-({9,10-dihydroxy-8-methyl-2-oxo-2H,8H,9H,10H-pyrano[2,3-h]chromen-8-yl}methoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

PDB for CFc000118486 (6-({9,10-dihydroxy-8-methyl-2-oxo-2H,8H,9H,10H-pyrano[2,3-h]chromen-8-yl}methoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D PDB for CFc000118486 (6-({9,10-dihydroxy-8-methyl-2-oxo-2H,8H,9H,10H-pyrano[2,3-h]chromen-8-yl}methoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

SMILES for CFc000118486 (6-({9,10-dihydroxy-8-methyl-2-oxo-2H,8H,9H,10H-pyrano[2,3-h]chromen-8-yl}methoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

INCHI for CFc000118486 (6-({9,10-dihydroxy-8-methyl-2-oxo-2H,8H,9H,10H-pyrano[2,3-h]chromen-8-yl}methoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

Structure for CFc000118486 (6-({9,10-dihydroxy-8-methyl-2-oxo-2H,8H,9H,10H-pyrano[2,3-h]chromen-8-yl}methoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D Structure for CFc000118486 (6-({9,10-dihydroxy-8-methyl-2-oxo-2H,8H,9H,10H-pyrano[2,3-h]chromen-8-yl}methoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)