Showing chemical card for [4-(5-hydroxy-7-phenylheptyl)phenyl]oxidanesulfonic acid (CFc000118696)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:41:57 UTC

Chemfont ID

CFc000118696

Molecule Identification

Common Name

[4-(5-hydroxy-7-phenylheptyl)phenyl]oxidanesulfonic acid

Definition

[4-(5-hydroxy-7-phenylheptyl)phenyl]oxidanesulfonic acid is a predicted metabolite generated by BioTransformer¹ that is produced by the metabolism of 4-(5-hydroxy-7-phenylheptyl)phenol. It is generated by Sulfotransferase 1A3 (P0DMM9) and Sulfotransferase enzymes via a -4-O-sulfation-of-phenolic-compound reaction. This -4-O-sulfation-of-phenolic-compound occurs in humans.

Structure

MOL SDF PDB SMILES InChI

MOL for CFc000118696 ([4-(5-hydroxy-7-phenylheptyl)phenyl]oxidanesulfonic acid)

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3D MOL for CFc000118696 ([4-(5-hydroxy-7-phenylheptyl)phenyl]oxidanesulfonic acid)

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3D SDF for CFc000118696 ([4-(5-hydroxy-7-phenylheptyl)phenyl]oxidanesulfonic acid)

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3D-SDF for CFc000118696 ([4-(5-hydroxy-7-phenylheptyl)phenyl]oxidanesulfonic acid)

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PDB for CFc000118696 ([4-(5-hydroxy-7-phenylheptyl)phenyl]oxidanesulfonic acid)

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3D PDB for CFc000118696 ([4-(5-hydroxy-7-phenylheptyl)phenyl]oxidanesulfonic acid)

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SMILES for CFc000118696 ([4-(5-hydroxy-7-phenylheptyl)phenyl]oxidanesulfonic acid)

OC(CCCCC1=CC=C(OS(O)(=O)=O)C=C1)CCC1=CC=CC=C1

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INCHI for CFc000118696 ([4-(5-hydroxy-7-phenylheptyl)phenyl]oxidanesulfonic acid)

InChI=1S/C19H24O5S/c20-18(13-10-16-6-2-1-3-7-16)9-5-4-8-17-11-14-19(15-12-17)24-25(21,22)23/h1-3,6-7,11-12,14-15,18,20H,4-5,8-10,13H2,(H,21,22,23)

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Structure for CFc000118696 ([4-(5-hydroxy-7-phenylheptyl)phenyl]oxidanesulfonic acid)

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3D Structure for CFc000118696 ([4-(5-hydroxy-7-phenylheptyl)phenyl]oxidanesulfonic acid)

Synonyms

Value	Source
[4-(5-Hydroxy-7-phenylheptyl)phenyl]oxidanesulfonate	Generator
[4-(5-Hydroxy-7-phenylheptyl)phenyl]oxidanesulphonate	Generator
[4-(5-Hydroxy-7-phenylheptyl)phenyl]oxidanesulphonic acid	Generator

Chemical Formula

C₁₉H₂₄O₅S

Average Molecular Weight

364.46

Monoisotopic Molecular Weight

364.134445047

IUPAC Name

[4-(5-hydroxy-7-phenylheptyl)phenyl]oxidanesulfonic acid

Traditional Name

[4-(5-hydroxy-7-phenylheptyl)phenyl]oxidanesulfonic acid

CAS Registry Number

Not Available

SMILES

OC(CCCCC1=CC=C(OS(O)(=O)=O)C=C1)CCC1=CC=CC=C1

InChI Identifier

InChI=1S/C19H24O5S/c20-18(13-10-16-6-2-1-3-7-16)9-5-4-8-17-11-14-19(15-12-17)24-25(21,22)23/h1-3,6-7,11-12,14-15,18,20H,4-5,8-10,13H2,(H,21,22,23)

InChI Key

OPJIKSYMRWBXMT-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as linear diarylheptanoids. These are diarylheptanoids with an open heptane chain. The two aromatic rings are linked only by the heptane chain.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Diarylheptanoids

Sub Class

Linear diarylheptanoids

Direct Parent

Linear diarylheptanoids

Alternative Parents

Phenylsulfates
Phenoxy compounds
Sulfuric acid monoesters
Secondary alcohols
Organic oxides
Hydrocarbon derivatives

Substituents

Linear 1,7-diphenylheptane skeleton
Phenylsulfate
Arylsulfate
Phenoxy compound
Monocyclic benzene moiety
Benzenoid
Sulfuric acid ester
Sulfate-ester
Sulfuric acid monoester
Organic sulfuric acid or derivatives
Secondary alcohol
Hydrocarbon derivative
Organooxygen compound
Alcohol
Organic oxide
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Endogenous (HMDB: HMDB0138287)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.0021 g/L	ALOGPS
logP	1.4	ALOGPS
logP	2.8	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	-1.9	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	97.04 m³·mol⁻¹	ChemAxon
Polarizability	39.61 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0138287

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