AMYL SALICYLATE
Relevant Data
Flavouring Substances Approved by European Union:
General Information
Mainterm | AMYL SALICYLATE |
Doc Type | NIL |
CAS Reg.No.(or other ID) | 2050-08-0 |
Regnum |
From www.fda.gov
Computed Descriptors
Download SDF2D Structure | |
CID | 16299 |
IUPAC Name | pentyl 2-hydroxybenzoate |
InChI | InChI=1S/C12H16O3/c1-2-3-6-9-15-12(14)10-7-4-5-8-11(10)13/h4-5,7-8,13H,2-3,6,9H2,1H3 |
InChI Key | RANVDUNFZBMTBK-UHFFFAOYSA-N |
Canonical SMILES | CCCCCOC(=O)C1=CC=CC=C1O |
Molecular Formula | C12H16O3 |
Wikipedia | amyl salicylate |
From Pubchem
Computed Properties
Property Name | Property Value |
---|---|
Molecular Weight | 208.257 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 3 |
Rotatable Bond Count | 6 |
Complexity | 191.0 |
CACTVS Substructure Key Fingerprint | A A A D c e B w 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 G g A A C A A A D A S g m A I y D o A A B g C I A i D S C A A C A A A k I A A I i A E G C M g I J z a C N R q C c U A l 4 B E I u Y e I y C C O A A A A A A A I A A A A A A A A A B A A A A A A A A A A A A = = |
Topological Polar Surface Area | 46.5 |
Monoisotopic Mass | 208.11 |
Exact Mass | 208.11 |
Compound Is Canonicalized | True |
Formal Charge | 0 |
Heavy Atom Count | 15 |
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+ | 0.8808 |
Human Intestinal Absorption | HIA+ | 0.9954 |
Caco-2 Permeability | Caco2+ | 0.8119 |
P-glycoprotein Substrate | Substrate | 0.5164 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.8334 |
Non-inhibitor | 0.9495 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.8161 |
Distribution | ||
Subcellular localization | Mitochondria | 0.8943 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.7822 |
CYP450 2D6 Substrate | Non-substrate | 0.8472 |
CYP450 3A4 Substrate | Non-substrate | 0.5666 |
CYP450 1A2 Inhibitor | Inhibitor | 0.7528 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.7889 |
CYP450 2D6 Inhibitor | Non-inhibitor | 0.8580 |
CYP450 2C19 Inhibitor | Inhibitor | 0.7044 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.9244 |
CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.7842 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8865 |
Non-inhibitor | 0.7730 | |
AMES Toxicity | Non AMES toxic | 0.9367 |
Carcinogens | Non-carcinogens | 0.8526 |
Fish Toxicity | High FHMT | 0.9299 |
Tetrahymena Pyriformis Toxicity | High TPT | 0.9876 |
Honey Bee Toxicity | High HBT | 0.6654 |
Biodegradation | Ready biodegradable | 0.8029 |
Acute Oral Toxicity | III | 0.8472 |
Carcinogenicity (Three-class) | Non-required | 0.6050 |
From admetSAR
ADMET Predicted Profile --- Regression
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | -3.3664 | LogS |
Caco-2 Permeability | 1.1936 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 1.9119 | LD50, mol/kg |
Fish Toxicity | 0.5544 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | 1.8856 | 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 | Benzoic acid esters |
Direct Parent | o-Hydroxybenzoic acid esters |
Alternative Parents | |
Molecular Framework | Aromatic homomonocyclic compounds |
Substituents | O-hydroxybenzoic acid ester - Salicylic acid or derivatives - Benzoyl - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Vinylogous acid - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound |
Description | This compound belongs to the class of organic compounds known as o-hydroxybenzoic acid esters. These are benzoic acid esters where the benzene ring is ortho-substituted with a hydroxy group. |
From ClassyFire