ChemFOnt: Showing chemical card for N-(4-Aminobenzoyl)-L-glutamic acid (CFc000234532)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-14 02:05:29 UTC

Chemfont ID

CFc000234532

Molecule Identification

Common Name

N-(4-Aminobenzoyl)-L-glutamic acid

Definition

N-(4-Aminobenzoyl)-L-glutamic acid belongs to the class of organic compounds known as glutamic acid and derivatives. Glutamic acid and derivatives are compounds containing glutamic acid or a derivative thereof resulting from reaction of glutamic acid 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 a significant number of articles have been published on N-(4-Aminobenzoyl)-L-glutamic acid.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
N-(4-Aminobenzoyl)-L-glutamate	Generator

Chemical Formula

C₁₂H₁₄N₂O₅

Average Molecular Weight

266.253

Monoisotopic Molecular Weight

266.090271559

IUPAC Name

2-[(4-aminophenyl)formamido]pentanedioic acid

Traditional Name

2-[(4-aminophenyl)formamido]pentanedioic acid

CAS Registry Number

Not Available

SMILES

NC1=CC=C(C=C1)C(=O)NC(CCC(O)=O)C(O)=O

InChI Identifier

InChI=1S/C12H14N2O5/c13-8-3-1-7(2-4-8)11(17)14-9(12(18)19)5-6-10(15)16/h1-4,9H,5-6,13H2,(H,14,17)(H,15,16)(H,18,19)

InChI Key

GADGMZDHLQLZRI-UHFFFAOYSA-N

Chemical Taxonomy

Description

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

Glutamic acid and derivatives

Alternative Parents

Substituents

Glutamic acid or derivatives
Hippuric acid or derivatives
Hippuric acid
N-acyl-alpha-amino acid
N-acyl-alpha amino acid or derivatives
Aminobenzamide
Aminobenzoic acid or derivatives
Benzamide
Benzoic acid or derivatives
Benzoyl
Aniline or substituted anilines
Monocyclic benzene moiety
Benzenoid
Dicarboxylic acid or derivatives
Secondary carboxylic acid amide
Carboxamide group
Amino acid
Carboxylic acid
Organooxygen compound
Hydrocarbon derivative
Organic nitrogen compound
Carbonyl group
Amine
Organic oxide
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Primary amine
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Source

Exogenous

Exogenous (PMID: 31557052)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.72 g/L	ALOGPS
logP	0.11	ALOGPS
logP	-0.86	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	2.72	ChemAxon
pKa (Strongest Basic)	4.51	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	129.72 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	66.1 m³·mol⁻¹	ChemAxon
Polarizability	25.94 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

HMDB0255007

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

58647

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

65138

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

Showing chemical card for N-(4-Aminobenzoyl)-L-glutamic acid (CFc000234532)

MOL for CFc000234532 (N-(4-Aminobenzoyl)-L-glutamic acid)

3D MOL for CFc000234532 (N-(4-Aminobenzoyl)-L-glutamic acid)

3D SDF for CFc000234532 (N-(4-Aminobenzoyl)-L-glutamic acid)

3D-SDF for CFc000234532 (N-(4-Aminobenzoyl)-L-glutamic acid)

PDB for CFc000234532 (N-(4-Aminobenzoyl)-L-glutamic acid)

3D PDB for CFc000234532 (N-(4-Aminobenzoyl)-L-glutamic acid)

SMILES for CFc000234532 (N-(4-Aminobenzoyl)-L-glutamic acid)

INCHI for CFc000234532 (N-(4-Aminobenzoyl)-L-glutamic acid)

Structure for CFc000234532 (N-(4-Aminobenzoyl)-L-glutamic acid)

3D Structure for CFc000234532 (N-(4-Aminobenzoyl)-L-glutamic acid)