General Information

Chemical name2-Butylthiophene
CAS number1455-20-5
Flavouring typesubstances
FL No.15.045
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
CID73818
IUPAC Name2-butylthiophene
InChIInChI=1S/C8H12S/c1-2-3-5-8-6-4-7-9-8/h4,6-7H,2-3,5H2,1H3
InChI KeyMNDZHERKKXUTOE-UHFFFAOYSA-N
Canonical SMILESCCCCC1=CC=CS1
Molecular FormulaC8H12S

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight140.244
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count3
Complexity71.0
CACTVS Substructure Key Fingerprint A A A D c c B w A A B 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 A A A A A A B g A A A G A Q A A A A A C A C E U A C y A Y A A A A i E A C B C A A A D A I A g C B B I i B g A A I g I I C K g E R C A A A A g g A A o i A c A 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 = =
Topological Polar Surface Area28.2
Monoisotopic Mass140.066
Exact Mass140.066
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+0.9827
Human Intestinal AbsorptionHIA+0.9970
Caco-2 PermeabilityCaco2+0.6696
P-glycoprotein SubstrateNon-substrate0.6118
P-glycoprotein InhibitorNon-inhibitor0.9212
Non-inhibitor0.7860
Renal Organic Cation TransporterNon-inhibitor0.8395
Distribution
Subcellular localizationLysosome0.4968
Metabolism
CYP450 2C9 SubstrateNon-substrate0.6710
CYP450 2D6 SubstrateNon-substrate0.8224
CYP450 3A4 SubstrateNon-substrate0.7643
CYP450 1A2 InhibitorInhibitor0.5506
CYP450 2C9 InhibitorNon-inhibitor0.5862
CYP450 2D6 InhibitorNon-inhibitor0.7372
CYP450 2C19 InhibitorInhibitor0.5649
CYP450 3A4 InhibitorNon-inhibitor0.9434
CYP Inhibitory PromiscuityHigh CYP Inhibitory Promiscuity0.6557
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9507
Non-inhibitor0.9172
AMES ToxicityNon AMES toxic0.9413
CarcinogensNon-carcinogens0.7429
Fish ToxicityHigh FHMT0.9520
Tetrahymena Pyriformis ToxicityHigh TPT0.9957
Honey Bee ToxicityHigh HBT0.7477
BiodegradationReady biodegradable0.5112
Acute Oral ToxicityIII0.7727
Carcinogenicity (Three-class)Non-required0.4040

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-3.5438LogS
Caco-2 Permeability1.6691LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity1.7409LD50, mol/kg
Fish Toxicity0.9575pLC50, mg/L
Tetrahymena Pyriformis Toxicity0.9120pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassHeteroaromatic compounds
SubclassNot available
Intermediate Tree NodesNot available
Direct ParentHeteroaromatic compounds
Alternative Parents
Molecular FrameworkAromatic heteromonocyclic compounds
SubstituentsHeteroaromatic compound - Thiophene - Hydrocarbon derivative - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as heteroaromatic compounds. These are compounds containing an aromatic ring where a carbon atom is linked to an hetero atom.

From ClassyFire