General Information

Chemical namePent-4-en-1-ol
CAS number821-09-0
Flavouring typesubstances
FL No.02.201
MixtureNo
Purity of the named substance at least 95% unless otherwise specified

From webgate.ec.europa.eu

Computed Descriptors

Download SDF
2D Structure
CID13181
IUPAC Namepent-4-en-1-ol
InChIInChI=1S/C5H10O/c1-2-3-4-5-6/h2,6H,1,3-5H2
InChI KeyLQAVWYMTUMSFBE-UHFFFAOYSA-N
Canonical SMILESC=CCCCO
Molecular FormulaC5H10O
Wikipedia4-pentenol

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight86.134
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count3
Complexity32.9
CACTVS Substructure Key Fingerprint A A A D c c B g 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 A A A A A A A A A A A A A A A A A G g A A C A A A C A C g g A I A A A A A A g C A A C B C A A A A A A A g A A A I A A A A A A g A E A A A A Q A A Q A A E g 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 A A A A A A A A A A A = =
Topological Polar Surface Area20.2
Monoisotopic Mass86.073
Exact Mass86.073
XLogP3None
XLogP3-AA1.0
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count6
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+0.9656
Human Intestinal AbsorptionHIA+0.9759
Caco-2 PermeabilityCaco2+0.7123
P-glycoprotein SubstrateNon-substrate0.8177
P-glycoprotein InhibitorNon-inhibitor0.8822
Non-inhibitor0.9532
Renal Organic Cation TransporterNon-inhibitor0.8746
Distribution
Subcellular localizationLysosome0.4996
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8392
CYP450 2D6 SubstrateNon-substrate0.8836
CYP450 3A4 SubstrateNon-substrate0.7702
CYP450 1A2 InhibitorNon-inhibitor0.6692
CYP450 2C9 InhibitorNon-inhibitor0.9162
CYP450 2D6 InhibitorNon-inhibitor0.9521
CYP450 2C19 InhibitorNon-inhibitor0.9037
CYP450 3A4 InhibitorNon-inhibitor0.9197
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.9099
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.8471
Non-inhibitor0.9567
AMES ToxicityNon AMES toxic0.7957
CarcinogensNon-carcinogens0.5803
Fish ToxicityHigh FHMT0.5647
Tetrahymena Pyriformis ToxicityLow TPT0.9919
Honey Bee ToxicityHigh HBT0.7906
BiodegradationReady biodegradable0.8909
Acute Oral ToxicityIII0.5533
Carcinogenicity (Three-class)Non-required0.6996

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-0.2126LogS
Caco-2 Permeability1.6012LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity2.0239LD50, mol/kg
Fish Toxicity1.0739pLC50, mg/L
Tetrahymena Pyriformis Toxicity-1.3448pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassOrganic oxygen compounds
ClassOrganooxygen compounds
SubclassAlcohols and polyols
Intermediate Tree NodesNot available
Direct ParentPrimary alcohols
Alternative Parents
Molecular FrameworkAliphatic acyclic compounds
SubstituentsHydrocarbon derivative - Primary alcohol - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as primary alcohols. These are compounds comprising the primary alcohol functional group, with the general structure RCOH (R=alkyl, aryl).

From ClassyFire