ChemFOnt: Showing chemical card for 8-(2-aminoethyl)-2-[4-hydroxy-3-(sulfooxy)phenyl]-1H,2H,6H-furo[3,2-e]indole-1-carboxylic acid (CFc000119865)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:43:43 UTC

Chemfont ID

CFc000119865

Molecule Identification

Common Name

8-(2-aminoethyl)-2-[4-hydroxy-3-(sulfooxy)phenyl]-1H,2H,6H-furo[3,2-e]indole-1-carboxylic acid

Definition

8-(2-aminoethyl)-2-[4-hydroxy-3-(sulfooxy)phenyl]-1h,2h,6h-furo[3,2-e]indole-1-carboxylic acid is a predicted metabolite generated by BioTransformer¹ that is produced by the metabolism of 8-(2-aminoethyl)-2-(3,4-dihydroxyphenyl)-1h,2h,6h-furo[3,2-e]indole-1-carboxylic acid. It is generated by Sulfotransferase 1A3 (P0DMM9) and Sulfotransferase enzymes via a -3-O-sulfation-of-phenolic-compound reaction. This -3-O-sulfation-of-phenolic-compound occurs in humans.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
8-(2-Aminoethyl)-2-[4-hydroxy-3-(sulfooxy)phenyl]-1H,2H,6H-furo[3,2-e]indole-1-carboxylate	Generator
8-(2-Aminoethyl)-2-[4-hydroxy-3-(sulphooxy)phenyl]-1H,2H,6H-furo[3,2-e]indole-1-carboxylate	Generator
8-(2-Aminoethyl)-2-[4-hydroxy-3-(sulphooxy)phenyl]-1H,2H,6H-furo[3,2-e]indole-1-carboxylic acid	Generator

Chemical Formula

C₁₉H₁₈N₂O₈S

Average Molecular Weight

434.42

Monoisotopic Molecular Weight

434.078386722

IUPAC Name

8-(2-aminoethyl)-2-[4-hydroxy-3-(sulfooxy)phenyl]-1H,2H,6H-furo[3,2-e]indole-1-carboxylic acid

Traditional Name

8-(2-aminoethyl)-2-[4-hydroxy-3-(sulfooxy)phenyl]-1H,2H,6H-furo[3,2-e]indole-1-carboxylic acid

CAS Registry Number

Not Available

SMILES

NCCC1=CNC2=C1C1=C(OC(C1C(O)=O)C1=CC(OS(O)(=O)=O)=C(O)C=C1)C=C2

InChI Identifier

InChI=1S/C19H18N2O8S/c20-6-5-10-8-21-11-2-4-13-16(15(10)11)17(19(23)24)18(28-13)9-1-3-12(22)14(7-9)29-30(25,26)27/h1-4,7-8,17-18,21-22H,5-6,20H2,(H,23,24)(H,25,26,27)

InChI Key

GIUVLBBDFNOIDM-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

2-arylbenzofuran flavonoids

Sub Class

Not Available

Direct Parent

2-arylbenzofuran flavonoids

Alternative Parents

Substituents

2-arylbenzofuran flavonoid
Phenylsulfate
Arylsulfate
3-alkylindole
Indole
Indole or derivatives
Coumaran
Phenoxy compound
2-arylethylamine
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Phenol
Aralkylamine
Monocyclic benzene moiety
Substituted pyrrole
Sulfuric acid monoester
Sulfate-ester
Sulfuric acid ester
Benzenoid
Heteroaromatic compound
Organic sulfuric acid or derivatives
Pyrrole
Amino acid or derivatives
Amino acid
Azacycle
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Carboxylic acid
Ether
Monocarboxylic acid or derivatives
Primary aliphatic amine
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Carbonyl group
Organonitrogen compound
Organooxygen compound
Organic oxide
Amine
Primary amine
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Endogenous (HMDB: HMDB0139456)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.24 g/L	ALOGPS
logP	-0.89	ALOGPS
logP	1.09	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	-2.2	ChemAxon
pKa (Strongest Basic)	9.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	172.17 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	104.47 m³·mol⁻¹	ChemAxon
Polarizability	40.86 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

HMDB0139456

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 8-(2-aminoethyl)-2-[4-hydroxy-3-(sulfooxy)phenyl]-1H,2H,6H-furo[3,2-e]indole-1-carboxylic acid (CFc000119865)

MOL for CFc000119865 (8-(2-aminoethyl)-2-[4-hydroxy-3-(sulfooxy)phenyl]-1H,2H,6H-furo[3,2-e]indole-1-carboxylic acid)

3D MOL for CFc000119865 (8-(2-aminoethyl)-2-[4-hydroxy-3-(sulfooxy)phenyl]-1H,2H,6H-furo[3,2-e]indole-1-carboxylic acid)

3D SDF for CFc000119865 (8-(2-aminoethyl)-2-[4-hydroxy-3-(sulfooxy)phenyl]-1H,2H,6H-furo[3,2-e]indole-1-carboxylic acid)

3D-SDF for CFc000119865 (8-(2-aminoethyl)-2-[4-hydroxy-3-(sulfooxy)phenyl]-1H,2H,6H-furo[3,2-e]indole-1-carboxylic acid)

PDB for CFc000119865 (8-(2-aminoethyl)-2-[4-hydroxy-3-(sulfooxy)phenyl]-1H,2H,6H-furo[3,2-e]indole-1-carboxylic acid)

3D PDB for CFc000119865 (8-(2-aminoethyl)-2-[4-hydroxy-3-(sulfooxy)phenyl]-1H,2H,6H-furo[3,2-e]indole-1-carboxylic acid)

SMILES for CFc000119865 (8-(2-aminoethyl)-2-[4-hydroxy-3-(sulfooxy)phenyl]-1H,2H,6H-furo[3,2-e]indole-1-carboxylic acid)

INCHI for CFc000119865 (8-(2-aminoethyl)-2-[4-hydroxy-3-(sulfooxy)phenyl]-1H,2H,6H-furo[3,2-e]indole-1-carboxylic acid)

Structure for CFc000119865 (8-(2-aminoethyl)-2-[4-hydroxy-3-(sulfooxy)phenyl]-1H,2H,6H-furo[3,2-e]indole-1-carboxylic acid)

3D Structure for CFc000119865 (8-(2-aminoethyl)-2-[4-hydroxy-3-(sulfooxy)phenyl]-1H,2H,6H-furo[3,2-e]indole-1-carboxylic acid)