ChemFOnt: Showing chemical card for (4-{2-[(3-aminopropyl)(4-oxobutyl)carbamoyl]eth-1-en-1-yl}-2,6-dimethoxyphenyl)oxidanesulfonic acid (CFc000120479)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:44:39 UTC

Chemfont ID

CFc000120479

Molecule Identification

Common Name

(4-{2-[(3-aminopropyl)(4-oxobutyl)carbamoyl]eth-1-en-1-yl}-2,6-dimethoxyphenyl)oxidanesulfonic acid

Definition

(4-{2-[(3-aminopropyl)(4-oxobutyl)carbamoyl]eth-1-en-1-yl}-2,6-dimethoxyphenyl)oxidanesulfonic acid is a predicted metabolite generated by BioTransformer¹ that is produced by the metabolism of n-(3-aminopropyl)-3-(4-hydroxy-3,5-dimethoxyphenyl)-n-(4-oxobutyl)prop-2-enamide. 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

Synonyms

Value	Source
(4-{2-[(3-aminopropyl)(4-oxobutyl)carbamoyl]eth-1-en-1-yl}-2,6-dimethoxyphenyl)oxidanesulfonate	Generator
(4-{2-[(3-aminopropyl)(4-oxobutyl)carbamoyl]eth-1-en-1-yl}-2,6-dimethoxyphenyl)oxidanesulphonate	Generator
(4-{2-[(3-aminopropyl)(4-oxobutyl)carbamoyl]eth-1-en-1-yl}-2,6-dimethoxyphenyl)oxidanesulphonic acid	Generator

Chemical Formula

C₁₈H₂₆N₂O₈S

Average Molecular Weight

430.47

Monoisotopic Molecular Weight

430.140986979

IUPAC Name

(4-{2-[(3-aminopropyl)(4-oxobutyl)carbamoyl]eth-1-en-1-yl}-2,6-dimethoxyphenyl)oxidanesulfonic acid

Traditional Name

(4-{2-[(3-aminopropyl)(4-oxobutyl)carbamoyl]eth-1-en-1-yl}-2,6-dimethoxyphenyl)oxidanesulfonic acid

CAS Registry Number

Not Available

SMILES

COC1=CC(C=CC(=O)N(CCCN)CCCC=O)=CC(OC)=C1OS(O)(=O)=O

InChI Identifier

InChI=1S/C18H26N2O8S/c1-26-15-12-14(13-16(27-2)18(15)28-29(23,24)25)6-7-17(22)20(10-5-8-19)9-3-4-11-21/h6-7,11-13H,3-5,8-10,19H2,1-2H3,(H,23,24,25)

InChI Key

LDNWDJHCERWULR-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cinnamic acids and derivatives. These are organic aromatic compounds containing a benzene and a carboxylic acid group (or a derivative thereof) forming 3-phenylprop-2-enoic acid.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Not Available

Direct Parent

Cinnamic acids and derivatives

Alternative Parents

Substituents

Cinnamic acid or derivatives
Phenylsulfate
Dimethoxybenzene
M-dimethoxybenzene
Arylsulfate
Anisole
Phenol ether
Methoxybenzene
Phenoxy compound
Styrene
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Sulfuric acid monoester
Sulfate-ester
Sulfuric acid ester
Tertiary carboxylic acid amide
Alpha-hydrogen aldehyde
Organic sulfuric acid or derivatives
Amino acid or derivatives
Carboxamide group
Carboxylic acid derivative
Ether
Aldehyde
Organic nitrogen compound
Primary amine
Organooxygen compound
Carbonyl group
Organic oxygen compound
Hydrocarbon derivative
Organopnictogen compound
Organic oxide
Amine
Primary aliphatic amine
Organonitrogen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Endogenous (HMDB: HMDB0140070)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.14 g/L	ALOGPS
logP	0.12	ALOGPS
logP	-1.2	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	-2.2	ChemAxon
pKa (Strongest Basic)	9.57	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	145.46 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	107 m³·mol⁻¹	ChemAxon
Polarizability	43.94 Å³	ChemAxon
Number of Rings	1	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

HMDB0140070

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 (4-{2-[(3-aminopropyl)(4-oxobutyl)carbamoyl]eth-1-en-1-yl}-2,6-dimethoxyphenyl)oxidanesulfonic acid (CFc000120479)

MOL for CFc000120479 ((4-{2-[(3-aminopropyl)(4-oxobutyl)carbamoyl]eth-1-en-1-yl}-2,6-dimethoxyphenyl)oxidanesulfonic acid)

3D MOL for CFc000120479 ((4-{2-[(3-aminopropyl)(4-oxobutyl)carbamoyl]eth-1-en-1-yl}-2,6-dimethoxyphenyl)oxidanesulfonic acid)

3D SDF for CFc000120479 ((4-{2-[(3-aminopropyl)(4-oxobutyl)carbamoyl]eth-1-en-1-yl}-2,6-dimethoxyphenyl)oxidanesulfonic acid)

3D-SDF for CFc000120479 ((4-{2-[(3-aminopropyl)(4-oxobutyl)carbamoyl]eth-1-en-1-yl}-2,6-dimethoxyphenyl)oxidanesulfonic acid)

PDB for CFc000120479 ((4-{2-[(3-aminopropyl)(4-oxobutyl)carbamoyl]eth-1-en-1-yl}-2,6-dimethoxyphenyl)oxidanesulfonic acid)

3D PDB for CFc000120479 ((4-{2-[(3-aminopropyl)(4-oxobutyl)carbamoyl]eth-1-en-1-yl}-2,6-dimethoxyphenyl)oxidanesulfonic acid)

SMILES for CFc000120479 ((4-{2-[(3-aminopropyl)(4-oxobutyl)carbamoyl]eth-1-en-1-yl}-2,6-dimethoxyphenyl)oxidanesulfonic acid)

INCHI for CFc000120479 ((4-{2-[(3-aminopropyl)(4-oxobutyl)carbamoyl]eth-1-en-1-yl}-2,6-dimethoxyphenyl)oxidanesulfonic acid)

Structure for CFc000120479 ((4-{2-[(3-aminopropyl)(4-oxobutyl)carbamoyl]eth-1-en-1-yl}-2,6-dimethoxyphenyl)oxidanesulfonic acid)

3D Structure for CFc000120479 ((4-{2-[(3-aminopropyl)(4-oxobutyl)carbamoyl]eth-1-en-1-yl}-2,6-dimethoxyphenyl)oxidanesulfonic acid)