ChemFOnt: Showing chemical card for 6-[5-(2-amino-2-carboxyethyl)-2-hydroxy-3-iodophenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid (CFc000135184)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 22:07:58 UTC

Chemfont ID

CFc000135184

Molecule Identification

Common Name

6-[5-(2-amino-2-carboxyethyl)-2-hydroxy-3-iodophenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid

Definition

6-[5-(2-amino-2-carboxyethyl)-2-hydroxy-3-iodophenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid belongs to the class of organic compounds known as tyrosine and derivatives. Tyrosine and derivatives are compounds containing tyrosine or a derivative thereof resulting from reaction of tyrosine 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 6-[5-(2-amino-2-carboxyethyl)-2-hydroxy-3-iodophenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
6-[5-(2-Amino-2-carboxyethyl)-2-hydroxy-3-iodophenoxy]-3,4,5-trihydroxyoxane-2-carboxylate	Generator

Chemical Formula

C₁₅H₁₈INO₁₀

Average Molecular Weight

499.21

Monoisotopic Molecular Weight

498.99754

IUPAC Name

6-[5-(2-amino-2-carboxyethyl)-2-hydroxy-3-iodophenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid

Traditional Name

6-[5-(2-amino-2-carboxyethyl)-2-hydroxy-3-iodophenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

NC(CC1=CC(I)=C(O)C(OC2OC(C(O)C(O)C2O)C(O)=O)=C1)C(O)=O

InChI Identifier

InChI=1S/C15H18INO10/c16-5-1-4(2-6(17)13(22)23)3-7(8(5)18)26-15-11(21)9(19)10(20)12(27-15)14(24)25/h1,3,6,9-12,15,18-21H,2,17H2,(H,22,23)(H,24,25)

InChI Key

VIFVZVYMINEWFW-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tyrosine and derivatives. Tyrosine and derivatives are compounds containing tyrosine or a derivative thereof resulting from reaction of tyrosine 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

Tyrosine and derivatives

Alternative Parents

Substituents

Tyrosine or derivatives
Phenylalanine or derivatives
Phenolic glycoside
1-o-glucuronide
O-glucuronide
Glucuronic acid or derivatives
Hexose monosaccharide
O-glycosyl compound
3-phenylpropanoic-acid
Glycosyl compound
Alpha-amino acid
Amphetamine or derivatives
Phenoxy compound
Phenol ether
2-iodophenol
2-halophenol
Halobenzene
Aralkylamine
Beta-hydroxy acid
Phenol
Iodobenzene
Aryl halide
Monosaccharide
Oxane
Pyran
Benzenoid
Hydroxy acid
Dicarboxylic acid or derivatives
Monocyclic benzene moiety
Aryl iodide
Amino acid
Secondary alcohol
Acetal
Oxacycle
Carboxylic acid
Organoheterocyclic compound
Polyol
Organic oxygen compound
Primary amine
Amine
Organic nitrogen compound
Carbonyl group
Alcohol
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organooxygen compound
Organonitrogen compound
Organoiodide
Organohalogen compound
Primary aliphatic amine
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Not Available

Not Available

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	2.43 g/L	ALOGPS
logP	-2.1	ALOGPS
logP	-2.9	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	0.73	ChemAxon
pKa (Strongest Basic)	9.51	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	200 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	94.45 m³·mol⁻¹	ChemAxon
Polarizability	40.15 Å³	ChemAxon
Number of Rings	2	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

HMDB0154776

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-[5-(2-amino-2-carboxyethyl)-2-hydroxy-3-iodophenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid (CFc000135184)

MOL for CFc000135184 (6-[5-(2-amino-2-carboxyethyl)-2-hydroxy-3-iodophenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D MOL for CFc000135184 (6-[5-(2-amino-2-carboxyethyl)-2-hydroxy-3-iodophenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D SDF for CFc000135184 (6-[5-(2-amino-2-carboxyethyl)-2-hydroxy-3-iodophenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D-SDF for CFc000135184 (6-[5-(2-amino-2-carboxyethyl)-2-hydroxy-3-iodophenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid)

PDB for CFc000135184 (6-[5-(2-amino-2-carboxyethyl)-2-hydroxy-3-iodophenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D PDB for CFc000135184 (6-[5-(2-amino-2-carboxyethyl)-2-hydroxy-3-iodophenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid)

SMILES for CFc000135184 (6-[5-(2-amino-2-carboxyethyl)-2-hydroxy-3-iodophenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid)

INCHI for CFc000135184 (6-[5-(2-amino-2-carboxyethyl)-2-hydroxy-3-iodophenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid)

Structure for CFc000135184 (6-[5-(2-amino-2-carboxyethyl)-2-hydroxy-3-iodophenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D Structure for CFc000135184 (6-[5-(2-amino-2-carboxyethyl)-2-hydroxy-3-iodophenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid)