P-PROPYLANISOLE
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
| Mainterm | P-PROPYLANISOLE |
| Doc Type | ASP |
| CAS Reg.No.(or other ID) | 104-45-0 |
| Regnum |
172.515 |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 7702 |
| IUPAC Name | 1-methoxy-4-propylbenzene |
| InChI | InChI=1S/C10H14O/c1-3-4-9-5-7-10(11-2)8-6-9/h5-8H,3-4H2,1-2H3 |
| InChI Key | KBHWKXNXTURZCD-UHFFFAOYSA-N |
| Canonical SMILES | CCCC1=CC=C(C=C1)OC |
| Molecular Formula | C10H14O |
| Wikipedia | 4-propylanisole |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 150.221 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 3 |
| Complexity | 93.0 |
| CACTVS Substructure Key Fingerprint | A A A D c c B w I 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 A A A A D A S A m A I y B o A A B A C A A i B C A A A C C A A g I A A I i A A G C I g M J i K E M R q A M C A k w B E I q A e A w K A O I A A A A A A A A A B A A A A A A A A A A A A A A A A A A A = = |
| Topological Polar Surface Area | 9.2 |
| Monoisotopic Mass | 150.104 |
| Exact Mass | 150.104 |
| 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+ | 0.9623 |
| Human Intestinal Absorption | HIA+ | 0.9974 |
| Caco-2 Permeability | Caco2+ | 0.8941 |
| P-glycoprotein Substrate | Non-substrate | 0.6585 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8831 |
| Non-inhibitor | 0.8464 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8188 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.7334 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8214 |
| CYP450 2D6 Substrate | Non-substrate | 0.6935 |
| CYP450 3A4 Substrate | Non-substrate | 0.5650 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.8008 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9220 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.8506 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.6909 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9704 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.6488 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.6695 |
| Non-inhibitor | 0.8849 | |
| AMES Toxicity | Non AMES toxic | 0.8548 |
| Carcinogens | Non-carcinogens | 0.7349 |
| Fish Toxicity | High FHMT | 0.8007 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.8908 |
| Honey Bee Toxicity | High HBT | 0.8498 |
| Biodegradation | Ready biodegradable | 0.5341 |
| Acute Oral Toxicity | III | 0.8923 |
| Carcinogenicity (Three-class) | Non-required | 0.5380 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.9669 | LogS |
| Caco-2 Permeability | 1.7288 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.5640 | LD50, mol/kg |
| Fish Toxicity | 1.2743 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.8149 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Benzene and substituted derivatives |
| Subclass | Phenylpropanes |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Phenylpropanes |
| Alternative Parents | |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Phenylpropane - Phenoxy compound - Methoxybenzene - Phenol ether - Anisole - Alkyl aryl ether - Ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as phenylpropanes. These are organic compounds containing a phenylpropane moiety. |
From ClassyFire