LINALYL ANTHRANILATE
Relevant Data
Food Additives Approved in the United States
Flavouring Substances Approved by European Union:
General Information
| Synonyms: | LINALYL 2-AMINOBENZOATE |
| Chemical Names: | 1,5-DIMETHYL-1-VINYLHEX-4-ENYL 2-AMINOBENZOATE |
| CAS number: | 7149-26-0 |
| COE number: | 9721 |
| JECFA number: | 1540 |
| FEMA number: | 2637 |
| Functional Class: |
Flavouring Agent FLAVOURING_AGENT |
From apps.who.int
Evaluations
| Evaluation year: | 2005 |
| ADI: | No safety concern at current levels of intake when used as a flavouring agent |
| 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 | 23535 |
| IUPAC Name | 3,7-dimethylocta-1,6-dien-3-yl 2-aminobenzoate |
| InChI | InChI=1S/C17H23NO2/c1-5-17(4,12-8-9-13(2)3)20-16(19)14-10-6-7-11-15(14)18/h5-7,9-11H,1,8,12,18H2,2-4H3 |
| InChI Key | WHIJSULEEDNKPD-UHFFFAOYSA-N |
| Canonical SMILES | CC(=CCCC(C)(C=C)OC(=O)C1=CC=CC=C1N)C |
| Molecular Formula | C17H23NO2 |
| Wikipedia | linalyl anthranilate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 273.376 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 7 |
| Complexity | 371.0 |
| CACTVS Substructure Key Fingerprint | A A A D c e B 6 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 E y B m A A 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 C 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 | 273.173 |
| Exact Mass | 273.173 |
| XLogP3 | None |
| XLogP3-AA | 4.8 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 20 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| 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+ | 0.9014 |
| Human Intestinal Absorption | HIA+ | 0.9669 |
| Caco-2 Permeability | Caco2+ | 0.6309 |
| P-glycoprotein Substrate | Non-substrate | 0.6279 |
| P-glycoprotein Inhibitor | Inhibitor | 0.6509 |
| Non-inhibitor | 0.7166 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8465 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.5916 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8682 |
| CYP450 2D6 Substrate | Non-substrate | 0.8014 |
| CYP450 3A4 Substrate | Substrate | 0.6376 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.6075 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.6582 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.7810 |
| CYP450 2C19 Inhibitor | Inhibitor | 0.5962 |
| CYP450 3A4 Inhibitor | Inhibitor | 0.5882 |
| CYP Inhibitory Promiscuity | High CYP Inhibitory Promiscuity | 0.6952 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9334 |
| Non-inhibitor | 0.8559 | |
| AMES Toxicity | Non AMES toxic | 0.9133 |
| Carcinogens | Non-carcinogens | 0.6622 |
| Fish Toxicity | High FHMT | 0.9858 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9912 |
| Honey Bee Toxicity | High HBT | 0.5541 |
| Biodegradation | Not ready biodegradable | 0.6818 |
| Acute Oral Toxicity | III | 0.7792 |
| Carcinogenicity (Three-class) | Non-required | 0.5084 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -3.8446 | LogS |
| Caco-2 Permeability | 1.4426 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.8391 | LD50, mol/kg |
| Fish Toxicity | 0.2340 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.7583 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Prenol lipids |
| Subclass | Monoterpenoids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Aromatic monoterpenoids |
| Alternative Parents |
|
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Aminobenzoic acid or derivatives - Aromatic monoterpenoid - Benzoate ester - Monocyclic monoterpenoid - Benzoic acid or derivatives - Aniline or substituted anilines - Benzoyl - Benzenoid - Monocyclic benzene moiety - Vinylogous amide - Amino acid or derivatives - Carboxylic acid ester - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organopnictogen compound - Amine - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - Primary amine - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as aromatic monoterpenoids. These are monoterpenoids containing at least one aromatic ring. |
From ClassyFire