General Information

Chemical name3-Pentylpyridine
CAS number1802-20-6
Flavouring typesubstances
FL No.14.140
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
CID238307
IUPAC Name3-pentylpyridine
InChIInChI=1S/C10H15N/c1-2-3-4-6-10-7-5-8-11-9-10/h5,7-9H,2-4,6H2,1H3
InChI KeyWPFPTAWUHHGUDQ-UHFFFAOYSA-N
Canonical SMILESCCCCCC1=CN=CC=C1
Molecular FormulaC10H15N

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight149.237
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count4
Complexity90.9
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 M 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 Mass149.12
Exact Mass149.12
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count11
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+0.9867
Human Intestinal AbsorptionHIA+0.9930
Caco-2 PermeabilityCaco2+0.8159
P-glycoprotein SubstrateNon-substrate0.5808
P-glycoprotein InhibitorNon-inhibitor0.9627
Non-inhibitor0.9776
Renal Organic Cation TransporterNon-inhibitor0.7722
Distribution
Subcellular localizationLysosome0.4224
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8265
CYP450 2D6 SubstrateNon-substrate0.7298
CYP450 3A4 SubstrateNon-substrate0.7665
CYP450 1A2 InhibitorInhibitor0.7377
CYP450 2C9 InhibitorNon-inhibitor0.6232
CYP450 2D6 InhibitorNon-inhibitor0.6749
CYP450 2C19 InhibitorNon-inhibitor0.6171
CYP450 3A4 InhibitorNon-inhibitor0.8232
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.5707
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.8001
Non-inhibitor0.7849
AMES ToxicityNon AMES toxic0.9542
CarcinogensNon-carcinogens0.8829
Fish ToxicityHigh FHMT0.7074
Tetrahymena Pyriformis ToxicityHigh TPT0.9896
Honey Bee ToxicityLow HBT0.5507
BiodegradationReady biodegradable0.5817
Acute Oral ToxicityIII0.6641
Carcinogenicity (Three-class)Non-required0.5335

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-1.5677LogS
Caco-2 Permeability1.7437LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity2.1209LD50, mol/kg
Fish Toxicity1.1209pLC50, mg/L
Tetrahymena Pyriformis Toxicity1.0590pIGC50, 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