ChemFOnt: Showing chemical card for 6-{2-carboxy-2-[(1-hydroxy-2-phenylethylidene)amino]-1-phenylethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid (CFc000164197)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 23:55:40 UTC

Chemfont ID

CFc000164197

Molecule Identification

Common Name

6-{2-carboxy-2-[(1-hydroxy-2-phenylethylidene)amino]-1-phenylethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid

Definition

6-{2-carboxy-2-[(1-hydroxy-2-phenylethylidene)amino]-1-phenylethoxy}-3,4,5-trihydroxyoxane-2-carboxylic 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 6-{2-carboxy-2-[(1-hydroxy-2-phenylethylidene)amino]-1-phenylethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
6-{2-carboxy-2-[(1-hydroxy-2-phenylethylidene)amino]-1-phenylethoxy}-3,4,5-trihydroxyoxane-2-carboxylate	Generator

Chemical Formula

C₂₃H₂₅NO₁₀

Average Molecular Weight

475.45

Monoisotopic Molecular Weight

475.147846009

IUPAC Name

6-{2-carboxy-2-[(1-hydroxy-2-phenylethylidene)amino]-1-phenylethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid

Traditional Name

6-{2-carboxy-2-[(1-hydroxy-2-phenylethylidene)amino]-1-phenylethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

OC1C(O)C(OC(C(N=C(O)CC2=CC=CC=C2)C(O)=O)C2=CC=CC=C2)OC(C1O)C(O)=O

InChI Identifier

InChI=1S/C23H25NO10/c25-14(11-12-7-3-1-4-8-12)24-15(21(29)30)19(13-9-5-2-6-10-13)33-23-18(28)16(26)17(27)20(34-23)22(31)32/h1-10,15-20,23,26-28H,11H2,(H,24,25)(H,29,30)(H,31,32)

InChI Key

CUZRWLWVYUAGTJ-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
1-o-glucuronide
O-glucuronide
Glucuronic acid or derivatives
N-acyl-alpha-amino acid
N-acyl-alpha amino acid or derivatives
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
3-phenylpropanoic-acid
Beta-hydroxy acid
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Hydroxy acid
Monosaccharide
Oxane
Benzenoid
Pyran
Secondary alcohol
Propargyl-type 1,3-dipolar organic compound
Organic 1,3-dipolar compound
Organoheterocyclic compound
Oxacycle
Acetal
Carboximidic acid
Polyol
Carboximidic acid derivative
Carboxylic acid
Hydrocarbon derivative
Alcohol
Organic oxygen compound
Organopnictogen compound
Organonitrogen compound
Organooxygen compound
Organic nitrogen compound
Carbonyl group
Organic oxide
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	0.39 g/L	ALOGPS
logP	0.89	ALOGPS
logP	1.18	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	3.07	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	186.34 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	113.29 m³·mol⁻¹	ChemAxon
Polarizability	45.31 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

HMDB0183908

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-{2-carboxy-2-[(1-hydroxy-2-phenylethylidene)amino]-1-phenylethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid (CFc000164197)

MOL for CFc000164197 (6-{2-carboxy-2-[(1-hydroxy-2-phenylethylidene)amino]-1-phenylethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D MOL for CFc000164197 (6-{2-carboxy-2-[(1-hydroxy-2-phenylethylidene)amino]-1-phenylethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D SDF for CFc000164197 (6-{2-carboxy-2-[(1-hydroxy-2-phenylethylidene)amino]-1-phenylethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D-SDF for CFc000164197 (6-{2-carboxy-2-[(1-hydroxy-2-phenylethylidene)amino]-1-phenylethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

PDB for CFc000164197 (6-{2-carboxy-2-[(1-hydroxy-2-phenylethylidene)amino]-1-phenylethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D PDB for CFc000164197 (6-{2-carboxy-2-[(1-hydroxy-2-phenylethylidene)amino]-1-phenylethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

SMILES for CFc000164197 (6-{2-carboxy-2-[(1-hydroxy-2-phenylethylidene)amino]-1-phenylethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

INCHI for CFc000164197 (6-{2-carboxy-2-[(1-hydroxy-2-phenylethylidene)amino]-1-phenylethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

Structure for CFc000164197 (6-{2-carboxy-2-[(1-hydroxy-2-phenylethylidene)amino]-1-phenylethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D Structure for CFc000164197 (6-{2-carboxy-2-[(1-hydroxy-2-phenylethylidene)amino]-1-phenylethoxy}-3,4,5-trihydroxyoxane-2-carboxylic acid)