ChemFOnt: Showing chemical card for {2-[(3,4-dihydroxy-5-oxo-2,5-dihydrofuran-2-yl)methoxy]-4,5-dihydroxyoxan-3-yl}oxidanesulfonic acid (CFc000145080)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 23:23:39 UTC

Chemfont ID

CFc000145080

Molecule Identification

Common Name

{2-[(3,4-dihydroxy-5-oxo-2,5-dihydrofuran-2-yl)methoxy]-4,5-dihydroxyoxan-3-yl}oxidanesulfonic acid

Definition

{2-[(3,4-dihydroxy-5-oxo-2,5-dihydrofuran-2-yl)methoxy]-4,5-dihydroxyoxan-3-yl}oxidanesulfonic acid belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. Based on a literature review very few articles have been published on {2-[(3,4-dihydroxy-5-oxo-2,5-dihydrofuran-2-yl)methoxy]-4,5-dihydroxyoxan-3-yl}oxidanesulfonic acid.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
{2-[(3,4-dihydroxy-5-oxo-2,5-dihydrofuran-2-yl)methoxy]-4,5-dihydroxyoxan-3-yl}oxidanesulfonate	Generator
{2-[(3,4-dihydroxy-5-oxo-2,5-dihydrofuran-2-yl)methoxy]-4,5-dihydroxyoxan-3-yl}oxidanesulphonate	Generator
{2-[(3,4-dihydroxy-5-oxo-2,5-dihydrofuran-2-yl)methoxy]-4,5-dihydroxyoxan-3-yl}oxidanesulphonic acid	Generator

Chemical Formula

C₁₀H₁₄O₁₂S

Average Molecular Weight

358.27

Monoisotopic Molecular Weight

358.020597065

IUPAC Name

{2-[(3,4-dihydroxy-5-oxo-2,5-dihydrofuran-2-yl)methoxy]-4,5-dihydroxyoxan-3-yl}oxidanesulfonic acid

Traditional Name

{2-[(3,4-dihydroxy-5-oxo-2H-furan-2-yl)methoxy]-4,5-dihydroxyoxan-3-yl}oxidanesulfonic acid

CAS Registry Number

Not Available

SMILES

OC1COC(OCC2OC(=O)C(O)=C2O)C(OS(O)(=O)=O)C1O

InChI Identifier

InChI=1S/C10H14O12S/c11-3-1-19-10(8(5(3)12)22-23(16,17)18)20-2-4-6(13)7(14)9(15)21-4/h3-5,8,10-14H,1-2H2,(H,16,17,18)

InChI Key

BGQUBUUFYUMCBX-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glycosyl compounds

Alternative Parents

Substituents

O-glycosyl compound
2-furanone
Monosaccharide
Oxane
Sulfuric acid monoester
Sulfate-ester
Alkyl sulfate
Sulfuric acid ester
Dihydrofuran
Organic sulfuric acid or derivatives
Vinylogous acid
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Lactone
Enediol
1,2-diol
Carboxylic acid ester
Secondary alcohol
Acetal
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organoheterocyclic compound
Hydrocarbon derivative
Carbonyl group
Alcohol
Organic oxide
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Not Available

Not Available

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	40.5 g/L	ALOGPS
logP	-2.1	ALOGPS
logP	-4.2	ChemAxon
logS	-0.95	ALOGPS
pKa (Strongest Acidic)	-2	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	189.28 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	67.51 m³·mol⁻¹	ChemAxon
Polarizability	29.98 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0164672

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-[(3,4-dihydroxy-5-oxo-2,5-dihydrofuran-2-yl)methoxy]-4,5-dihydroxyoxan-3-yl}oxidanesulfonic acid (CFc000145080)

MOL for CFc000145080 ({2-[(3,4-dihydroxy-5-oxo-2,5-dihydrofuran-2-yl)methoxy]-4,5-dihydroxyoxan-3-yl}oxidanesulfonic acid)

3D MOL for CFc000145080 ({2-[(3,4-dihydroxy-5-oxo-2,5-dihydrofuran-2-yl)methoxy]-4,5-dihydroxyoxan-3-yl}oxidanesulfonic acid)

3D SDF for CFc000145080 ({2-[(3,4-dihydroxy-5-oxo-2,5-dihydrofuran-2-yl)methoxy]-4,5-dihydroxyoxan-3-yl}oxidanesulfonic acid)

3D-SDF for CFc000145080 ({2-[(3,4-dihydroxy-5-oxo-2,5-dihydrofuran-2-yl)methoxy]-4,5-dihydroxyoxan-3-yl}oxidanesulfonic acid)

PDB for CFc000145080 ({2-[(3,4-dihydroxy-5-oxo-2,5-dihydrofuran-2-yl)methoxy]-4,5-dihydroxyoxan-3-yl}oxidanesulfonic acid)

3D PDB for CFc000145080 ({2-[(3,4-dihydroxy-5-oxo-2,5-dihydrofuran-2-yl)methoxy]-4,5-dihydroxyoxan-3-yl}oxidanesulfonic acid)

SMILES for CFc000145080 ({2-[(3,4-dihydroxy-5-oxo-2,5-dihydrofuran-2-yl)methoxy]-4,5-dihydroxyoxan-3-yl}oxidanesulfonic acid)

INCHI for CFc000145080 ({2-[(3,4-dihydroxy-5-oxo-2,5-dihydrofuran-2-yl)methoxy]-4,5-dihydroxyoxan-3-yl}oxidanesulfonic acid)

Structure for CFc000145080 ({2-[(3,4-dihydroxy-5-oxo-2,5-dihydrofuran-2-yl)methoxy]-4,5-dihydroxyoxan-3-yl}oxidanesulfonic acid)

3D Structure for CFc000145080 ({2-[(3,4-dihydroxy-5-oxo-2,5-dihydrofuran-2-yl)methoxy]-4,5-dihydroxyoxan-3-yl}oxidanesulfonic acid)