ChemFOnt: Showing chemical card for 2-amino-3-[4-(4-hydroxyphenoxy)-3,5-diiodophenyl]-3-(sulfooxy)propanoic acid (CFc000140868)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 23:17:05 UTC

Chemfont ID

CFc000140868

Molecule Identification

Common Name

2-amino-3-[4-(4-hydroxyphenoxy)-3,5-diiodophenyl]-3-(sulfooxy)propanoic acid

Definition

2-amino-3-[4-(4-hydroxyphenoxy)-3,5-diiodophenyl]-3-(sulfooxy)propanoic acid belongs to the class of organic compounds known as phenylalanine and derivatives. Phenylalanine and derivatives are compounds containing phenylalanine or a derivative thereof resulting from reaction of phenylalanine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. Based on a literature review very few articles have been published on 2-amino-3-[4-(4-hydroxyphenoxy)-3,5-diiodophenyl]-3-(sulfooxy)propanoic acid.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
2-Amino-3-[4-(4-hydroxyphenoxy)-3,5-diiodophenyl]-3-(sulfooxy)propanoate	Generator
2-Amino-3-[4-(4-hydroxyphenoxy)-3,5-diiodophenyl]-3-(sulphooxy)propanoate	Generator
2-Amino-3-[4-(4-hydroxyphenoxy)-3,5-diiodophenyl]-3-(sulphooxy)propanoic acid	Generator

Chemical Formula

C₁₅H₁₃I₂NO₈S

Average Molecular Weight

621.14

Monoisotopic Molecular Weight

620.84513

IUPAC Name

2-amino-3-[4-(4-hydroxyphenoxy)-3,5-diiodophenyl]-3-(sulfooxy)propanoic acid

Traditional Name

2-amino-3-[4-(4-hydroxyphenoxy)-3,5-diiodophenyl]-3-(sulfooxy)propanoic acid

CAS Registry Number

Not Available

SMILES

NC(C(OS(O)(=O)=O)C1=CC(I)=C(OC2=CC=C(O)C=C2)C(I)=C1)C(O)=O

InChI Identifier

InChI=1S/C15H13I2NO8S/c16-10-5-7(13(12(18)15(20)21)26-27(22,23)24)6-11(17)14(10)25-9-3-1-8(19)2-4-9/h1-6,12-13,19H,18H2,(H,20,21)(H,22,23,24)

InChI Key

FARBWXQIMSSPKX-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenylalanine and derivatives. Phenylalanine and derivatives are compounds containing phenylalanine or a derivative thereof resulting from reaction of phenylalanine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Phenylalanine and derivatives

Alternative Parents

Substituents

Phenylalanine or derivatives
Diphenylether
Diaryl ether
3-phenylpropanoic-acid
Alpha-amino acid
Phenoxy compound
Phenol ether
1-hydroxy-2-unsubstituted benzenoid
Halobenzene
Iodobenzene
Phenol
Aralkylamine
Sulfuric acid ester
Alkyl sulfate
Sulfate-ester
Sulfuric acid monoester
Aryl iodide
Aryl halide
Benzenoid
Monocyclic benzene moiety
Organic sulfuric acid or derivatives
Amino acid
Carboxylic acid
Ether
Monocarboxylic acid or derivatives
Primary amine
Organohalogen compound
Primary aliphatic amine
Amine
Organoiodide
Organic nitrogen compound
Organonitrogen compound
Carbonyl group
Organooxygen compound
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Organic oxide
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Not Available

Not Available

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.1 g/L	ALOGPS
logP	0.19	ALOGPS
logP	2.03	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	-2.6	ChemAxon
pKa (Strongest Basic)	8.5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	156.38 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	111.26 m³·mol⁻¹	ChemAxon
Polarizability	44.29 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0160460

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-amino-3-[4-(4-hydroxyphenoxy)-3,5-diiodophenyl]-3-(sulfooxy)propanoic acid (CFc000140868)

MOL for CFc000140868 (2-amino-3-[4-(4-hydroxyphenoxy)-3,5-diiodophenyl]-3-(sulfooxy)propanoic acid)

3D MOL for CFc000140868 (2-amino-3-[4-(4-hydroxyphenoxy)-3,5-diiodophenyl]-3-(sulfooxy)propanoic acid)

3D SDF for CFc000140868 (2-amino-3-[4-(4-hydroxyphenoxy)-3,5-diiodophenyl]-3-(sulfooxy)propanoic acid)

3D-SDF for CFc000140868 (2-amino-3-[4-(4-hydroxyphenoxy)-3,5-diiodophenyl]-3-(sulfooxy)propanoic acid)

PDB for CFc000140868 (2-amino-3-[4-(4-hydroxyphenoxy)-3,5-diiodophenyl]-3-(sulfooxy)propanoic acid)

3D PDB for CFc000140868 (2-amino-3-[4-(4-hydroxyphenoxy)-3,5-diiodophenyl]-3-(sulfooxy)propanoic acid)

SMILES for CFc000140868 (2-amino-3-[4-(4-hydroxyphenoxy)-3,5-diiodophenyl]-3-(sulfooxy)propanoic acid)

INCHI for CFc000140868 (2-amino-3-[4-(4-hydroxyphenoxy)-3,5-diiodophenyl]-3-(sulfooxy)propanoic acid)

Structure for CFc000140868 (2-amino-3-[4-(4-hydroxyphenoxy)-3,5-diiodophenyl]-3-(sulfooxy)propanoic acid)

3D Structure for CFc000140868 (2-amino-3-[4-(4-hydroxyphenoxy)-3,5-diiodophenyl]-3-(sulfooxy)propanoic acid)