Relevant Data

Food Additives Approved by WHO:


General Information

Chemical name3-Propylpyridine
CAS number4673-31-8
COE number11419
Flavouring typesubstances
FL No.14.143
MixtureNo
Purity of the named substance at least 95% unless otherwise specified
Reference bodyEFSA

From webgate.ec.europa.eu

Computed Descriptors

Download SDF
2D Structure
CID78405
IUPAC Name3-propylpyridine
InChIInChI=1S/C8H11N/c1-2-4-8-5-3-6-9-7-8/h3,5-7H,2,4H2,1H3
InChI KeyMLAXEZHEGARMPE-UHFFFAOYSA-N
Canonical SMILESCCCC1=CN=CC=C1
Molecular FormulaC8H11N
Wikipedia3-propylpyridine

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight121.183
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count2
Complexity71.0
CACTVS Substructure Key Fingerprint A A A D c c B y 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 A s A A A A A A A A A A A B g A A A H A A A A A A A D A D B G g Q + g J I I E A C g A j B n R A C C g C A x A i A I 2 C A 4 Z J g I I O L A k Z G E I A h g g A D I y A c Q g A A O 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 A A A A = =
Topological Polar Surface Area12.9
Monoisotopic Mass121.089
Exact Mass121.089
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count9
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Isotope Atom Count0
Covalently-Bonded Unit Count1

From Pubchem


ADMET Predicted Profile --- Classification

Model Result Probability
Absorption
Blood-Brain BarrierBBB+0.9796
Human Intestinal AbsorptionHIA+0.9939
Caco-2 PermeabilityCaco2+0.8640
P-glycoprotein SubstrateNon-substrate0.7102
P-glycoprotein InhibitorNon-inhibitor0.9697
Non-inhibitor0.9805
Renal Organic Cation TransporterNon-inhibitor0.8055
Distribution
Subcellular localizationMitochondria0.4920
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8273
CYP450 2D6 SubstrateNon-substrate0.7764
CYP450 3A4 SubstrateNon-substrate0.7868
CYP450 1A2 InhibitorInhibitor0.6975
CYP450 2C9 InhibitorNon-inhibitor0.7218
CYP450 2D6 InhibitorNon-inhibitor0.7150
CYP450 2C19 InhibitorNon-inhibitor0.6977
CYP450 3A4 InhibitorNon-inhibitor0.8266
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.6177
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.8035
Non-inhibitor0.9136
AMES ToxicityNon AMES toxic0.9411
CarcinogensNon-carcinogens0.8613
Fish ToxicityLow FHMT0.6444
Tetrahymena Pyriformis ToxicityHigh TPT0.9529
Honey Bee ToxicityLow HBT0.5156
BiodegradationReady biodegradable0.7041
Acute Oral ToxicityIII0.6207
Carcinogenicity (Three-class)Warning0.5145

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-0.5977LogS
Caco-2 Permeability1.9687LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity2.1567LD50, mol/kg
Fish Toxicity1.7241pLC50, mg/L
Tetrahymena Pyriformis Toxicity0.4197pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassPyridines and derivatives
SubclassNot available
Intermediate Tree NodesNot available
Direct ParentPyridines and derivatives
Alternative Parents
Molecular FrameworkAromatic heteromonocyclic compounds
SubstituentsPyridine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as pyridines and derivatives. These are compounds containing a pyridine ring, which is a six-member aromatic heterocycle which consists of one nitrogen atom and five carbon atoms.

From ClassyFire