ChemFOnt: Showing chemical card for {6,7,8,11,12,13,20,22-octahydroxy-3,16-dioxo-2,17,19-trioxatetracyclo[16.3.1.0⁴,⁹.0¹⁰,¹⁵]docosa-4,6,8,10,12,14-hexaen-21-yl}oxidanesulfonic acid (CFc000122328)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:47:27 UTC

Chemfont ID

CFc000122328

Molecule Identification

Common Name

{6,7,8,11,12,13,20,22-octahydroxy-3,16-dioxo-2,17,19-trioxatetracyclo[16.3.1.0⁴,⁹.0¹⁰,¹⁵]docosa-4,6,8,10,12,14-hexaen-21-yl}oxidanesulfonic acid

Definition

{6,7,8,11,12,13,20,22-octahydroxy-3,16-dioxo-2,17,19-trioxatetracyclo[16.3.1.0⁴,⁹.0¹⁰,¹⁵]docosa-4,6,8,10,12,14-hexaen-21-yl}oxidanesulfonic acid is a predicted metabolite generated by BioTransformer¹ that is produced by the metabolism of 6,7,8,11,12,13,20,21,22-nonahydroxy-2,17,19-trioxatetracyclo[16.3.1.0⁴,⁹.0¹⁰,¹⁵]docosa-4,6,8,10,12,14-hexaene-3,16-dione. It is generated by Sulfotransferase family cytosolic 2B member 1 (O00204) and Sulfotransferase enzymes via a sulfation-of-secondary-alcohol reaction. This sulfation-of-secondary-alcohol occurs in humans.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
{6,7,8,11,12,13,20,22-octahydroxy-3,16-dioxo-2,17,19-trioxatetracyclo[16.3.1.0,.0,]docosa-4,6,8,10,12,14-hexaen-21-yl}oxidanesulfonate	Generator
{6,7,8,11,12,13,20,22-octahydroxy-3,16-dioxo-2,17,19-trioxatetracyclo[16.3.1.0,.0,]docosa-4,6,8,10,12,14-hexaen-21-yl}oxidanesulphonate	Generator
{6,7,8,11,12,13,20,22-octahydroxy-3,16-dioxo-2,17,19-trioxatetracyclo[16.3.1.0,.0,]docosa-4,6,8,10,12,14-hexaen-21-yl}oxidanesulphonic acid	Generator
{6,7,8,11,12,13,20,22-octahydroxy-3,16-dioxo-2,17,19-trioxatetracyclo[16.3.1.0⁴,⁹.0¹⁰,¹⁵]docosa-4,6,8,10,12,14-hexaen-21-yl}oxidanesulfonate	Generator
{6,7,8,11,12,13,20,22-octahydroxy-3,16-dioxo-2,17,19-trioxatetracyclo[16.3.1.0⁴,⁹.0¹⁰,¹⁵]docosa-4,6,8,10,12,14-hexaen-21-yl}oxidanesulphonate	Generator
{6,7,8,11,12,13,20,22-octahydroxy-3,16-dioxo-2,17,19-trioxatetracyclo[16.3.1.0⁴,⁹.0¹⁰,¹⁵]docosa-4,6,8,10,12,14-hexaen-21-yl}oxidanesulphonic acid	Generator

Chemical Formula

C₁₉H₁₆O₁₇S

Average Molecular Weight

548.38

Monoisotopic Molecular Weight

548.010820229

IUPAC Name

{6,7,8,11,12,13,20,22-octahydroxy-3,16-dioxo-2,17,19-trioxatetracyclo[16.3.1.0^{4,9}.0^{10,15}]docosa-4,6,8,10,12,14-hexaen-21-yl}oxidanesulfonic acid

Traditional Name

{6,7,8,11,12,13,20,22-octahydroxy-3,16-dioxo-2,17,19-trioxatetracyclo[16.3.1.0^{4,9}.0^{10,15}]docosa-4,6,8,10,12,14-hexaen-21-yl}oxidanesulfonic acid

CAS Registry Number

Not Available

SMILES

OC1OC2OC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC(C2O)C1OS(O)(=O)=O

InChI Identifier

InChI=1S/C19H16O17S/c20-5-1-3-7(11(24)9(5)22)8-4(2-6(21)10(23)12(8)25)17(28)34-19-13(26)14(33-16(3)27)15(18(29)35-19)36-37(30,31)32/h1-2,13-15,18-26,29H,(H,30,31,32)

InChI Key

KRWMYPMGPVRHBU-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Tannins

Sub Class

Hydrolyzable tannins

Direct Parent

Hydrolyzable tannins

Alternative Parents

Substituents

Hydrolyzable tannin
Gallic acid or derivatives
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Monosaccharide
Oxane
Sulfuric acid monoester
Sulfate-ester
Alkyl sulfate
Dicarboxylic acid or derivatives
Benzenoid
Sulfuric acid ester
Organic sulfuric acid or derivatives
Lactone
Carboxylic acid ester
Hemiacetal
Secondary alcohol
Acetal
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Polyol
Organic oxide
Hydrocarbon derivative
Alcohol
Organic oxygen compound
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Endogenous (HMDB: HMDB0141919)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	33 g/L	ALOGPS
logP	0.38	ALOGPS
logP	-0.17	ChemAxon
logS	-1.2	ALOGPS
pKa (Strongest Acidic)	-2.4	ChemAxon
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	287.27 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	111.59 m³·mol⁻¹	ChemAxon
Polarizability	44.79 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

HMDB0141919

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 {6,7,8,11,12,13,20,22-octahydroxy-3,16-dioxo-2,17,19-trioxatetracyclo[16.3.1.0⁴,⁹.0¹⁰,¹⁵]docosa-4,6,8,10,12,14-hexaen-21-yl}oxidanesulfonic acid (CFc000122328)

MOL for CFc000122328 ({6,7,8,11,12,13,20,22-octahydroxy-3,16-dioxo-2,17,19-trioxatetracyclo[16.3.1.0⁴,⁹.0¹⁰,¹⁵]docosa-4,6,8,10,12,14-hexaen-21-yl}oxidanesulfonic acid)

3D MOL for CFc000122328 ({6,7,8,11,12,13,20,22-octahydroxy-3,16-dioxo-2,17,19-trioxatetracyclo[16.3.1.0⁴,⁹.0¹⁰,¹⁵]docosa-4,6,8,10,12,14-hexaen-21-yl}oxidanesulfonic acid)

3D SDF for CFc000122328 ({6,7,8,11,12,13,20,22-octahydroxy-3,16-dioxo-2,17,19-trioxatetracyclo[16.3.1.0⁴,⁹.0¹⁰,¹⁵]docosa-4,6,8,10,12,14-hexaen-21-yl}oxidanesulfonic acid)

3D-SDF for CFc000122328 ({6,7,8,11,12,13,20,22-octahydroxy-3,16-dioxo-2,17,19-trioxatetracyclo[16.3.1.0⁴,⁹.0¹⁰,¹⁵]docosa-4,6,8,10,12,14-hexaen-21-yl}oxidanesulfonic acid)

PDB for CFc000122328 ({6,7,8,11,12,13,20,22-octahydroxy-3,16-dioxo-2,17,19-trioxatetracyclo[16.3.1.0⁴,⁹.0¹⁰,¹⁵]docosa-4,6,8,10,12,14-hexaen-21-yl}oxidanesulfonic acid)

3D PDB for CFc000122328 ({6,7,8,11,12,13,20,22-octahydroxy-3,16-dioxo-2,17,19-trioxatetracyclo[16.3.1.0⁴,⁹.0¹⁰,¹⁵]docosa-4,6,8,10,12,14-hexaen-21-yl}oxidanesulfonic acid)

SMILES for CFc000122328 ({6,7,8,11,12,13,20,22-octahydroxy-3,16-dioxo-2,17,19-trioxatetracyclo[16.3.1.0⁴,⁹.0¹⁰,¹⁵]docosa-4,6,8,10,12,14-hexaen-21-yl}oxidanesulfonic acid)

INCHI for CFc000122328 ({6,7,8,11,12,13,20,22-octahydroxy-3,16-dioxo-2,17,19-trioxatetracyclo[16.3.1.0⁴,⁹.0¹⁰,¹⁵]docosa-4,6,8,10,12,14-hexaen-21-yl}oxidanesulfonic acid)

Structure for CFc000122328 ({6,7,8,11,12,13,20,22-octahydroxy-3,16-dioxo-2,17,19-trioxatetracyclo[16.3.1.0⁴,⁹.0¹⁰,¹⁵]docosa-4,6,8,10,12,14-hexaen-21-yl}oxidanesulfonic acid)

3D Structure for CFc000122328 ({6,7,8,11,12,13,20,22-octahydroxy-3,16-dioxo-2,17,19-trioxatetracyclo[16.3.1.0⁴,⁹.0¹⁰,¹⁵]docosa-4,6,8,10,12,14-hexaen-21-yl}oxidanesulfonic acid)