METHYL ANTHRANILATE
Relevant Data
Food Additives Approved in the United States
Flavouring Substances Approved by European Union:
General Information
| Synonyms: | 2-AMINOBENZOIC ACID METHYL ESTER, METHYL 2-AMINOBENZOATE, METHYL o-AMINOBENZOATE |
| Chemical Names: | METHYL 2-AMINOBENZOATE |
| CAS number: | 134-20-3 |
| COE number: | 9715 |
| JECFA number: | 1534 |
| FEMA number: | 2682 |
| Functional Class: |
Flavouring Agent FLAVOURING_AGENT |
From apps.who.int
Evaluations
| Evaluation year: | 2005 |
| ADI: | 0-1.5 mg/kg bw (1979) |
| Meeting: | 23 |
| Specs Code: | R |
| Comments: | The ADI established at the twenty-third meeting was maintained. |
| Report: | TRS 934-JECFA 65/54 |
| Tox Monograph: | FAS 56-JECFA 65 |
| Specification: | COMPENDIUM ADDENDUM 13/FNP 52 Add. 13/61 |
From apps.who.int
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 8635 |
| IUPAC Name | methyl 2-aminobenzoate |
| InChI | InChI=1S/C8H9NO2/c1-11-8(10)6-4-2-3-5-7(6)9/h2-5H,9H2,1H3 |
| InChI Key | VAMXMNNIEUEQDV-UHFFFAOYSA-N |
| Canonical SMILES | COC(=O)C1=CC=CC=C1N |
| Molecular Formula | C8H9NO2 |
| Wikipedia | methyl anthranilate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 151.165 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 2 |
| Complexity | 147.0 |
| CACTVS Substructure Key Fingerprint | A A A D c c B y M A A A A A A A A A A A A A A A A A A A A A A A A A A w A A A A A A A A A A A B A A A A H g A Q A A A A D A i B m A I y y I B A B A C I A i T S S A C C A A A k A g A I i A E A b M g I J j q A t Z m A M Y B m 0 A E I 6 c e Y y C C O A A A A A A A C A A A A A A A A A A Q A A A A A A A A A A A = = |
| Topological Polar Surface Area | 52.3 |
| Monoisotopic Mass | 151.063 |
| Exact Mass | 151.063 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 11 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Isotope Atom Count | 0 |
| Covalently-Bonded Unit Count | 1 |
From Pubchem
ADMET Predicted Profile --- Classification
| Model | Result | Probability |
|---|---|---|
| Absorption | ||
| Blood-Brain Barrier | BBB+ | 0.9426 |
| Human Intestinal Absorption | HIA+ | 0.9856 |
| Caco-2 Permeability | Caco2+ | 0.7499 |
| P-glycoprotein Substrate | Non-substrate | 0.8735 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9147 |
| Non-inhibitor | 0.9719 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8988 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.6508 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.7972 |
| CYP450 2D6 Substrate | Non-substrate | 0.8588 |
| CYP450 3A4 Substrate | Non-substrate | 0.7209 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.5937 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8920 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9565 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9392 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9695 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8714 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9670 |
| Non-inhibitor | 0.9619 | |
| AMES Toxicity | Non AMES toxic | 0.9132 |
| Carcinogens | Non-carcinogens | 0.7031 |
| Fish Toxicity | High FHMT | 0.8527 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.5173 |
| Honey Bee Toxicity | Low HBT | 0.6482 |
| Biodegradation | Ready biodegradable | 0.7404 |
| Acute Oral Toxicity | III | 0.8093 |
| Carcinogenicity (Three-class) | Non-required | 0.6075 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.2160 | LogS |
| Caco-2 Permeability | 1.5443 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.7247 | LD50, mol/kg |
| Fish Toxicity | 1.8593 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.5052 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Benzene and substituted derivatives |
| Subclass | Benzoic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Benzoic acid esters |
| Alternative Parents | |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Aminobenzoic acid or derivatives - Benzoate ester - Benzoyl - Aniline or substituted anilines - Vinylogous amide - Methyl ester - Amino acid or derivatives - Carboxylic acid ester - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Amine - Organonitrogen compound - Organooxygen compound - Primary amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as benzoic acid esters. These are ester derivatives of benzoic acid. |
From ClassyFire