2-Butylthiophene
General Information
Chemical name | 2-Butylthiophene |
CAS number | 1455-20-5 |
Flavouring type | substances |
FL No. | 15.045 |
Mixture | No |
Purity of the named substance at least 95% unless otherwise specified | |
Reference body | EFSA |
From webgate.ec.europa.eu
Computed Descriptors
Download SDF2D Structure | |
CID | 73818 |
IUPAC Name | 2-butylthiophene |
InChI | InChI=1S/C8H12S/c1-2-3-5-8-6-4-7-9-8/h4,6-7H,2-3,5H2,1H3 |
InChI Key | MNDZHERKKXUTOE-UHFFFAOYSA-N |
Canonical SMILES | CCCCC1=CC=CS1 |
Molecular Formula | C8H12S |
From Pubchem
Computed Properties
Property Name | Property Value |
---|---|
Molecular Weight | 140.244 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 1 |
Rotatable Bond Count | 3 |
Complexity | 71.0 |
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 Area | 28.2 |
Monoisotopic Mass | 140.066 |
Exact Mass | 140.066 |
Compound Is Canonicalized | True |
Formal Charge | 0 |
Heavy Atom Count | 9 |
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+ | 0.9827 |
Human Intestinal Absorption | HIA+ | 0.9970 |
Caco-2 Permeability | Caco2+ | 0.6696 |
P-glycoprotein Substrate | Non-substrate | 0.6118 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.9212 |
Non-inhibitor | 0.7860 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.8395 |
Distribution | ||
Subcellular localization | Lysosome | 0.4968 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.6710 |
CYP450 2D6 Substrate | Non-substrate | 0.8224 |
CYP450 3A4 Substrate | Non-substrate | 0.7643 |
CYP450 1A2 Inhibitor | Inhibitor | 0.5506 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.5862 |
CYP450 2D6 Inhibitor | Non-inhibitor | 0.7372 |
CYP450 2C19 Inhibitor | Inhibitor | 0.5649 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.9434 |
CYP Inhibitory Promiscuity | High CYP Inhibitory Promiscuity | 0.6557 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9507 |
Non-inhibitor | 0.9172 | |
AMES Toxicity | Non AMES toxic | 0.9413 |
Carcinogens | Non-carcinogens | 0.7429 |
Fish Toxicity | High FHMT | 0.9520 |
Tetrahymena Pyriformis Toxicity | High TPT | 0.9957 |
Honey Bee Toxicity | High HBT | 0.7477 |
Biodegradation | Ready biodegradable | 0.5112 |
Acute Oral Toxicity | III | 0.7727 |
Carcinogenicity (Three-class) | Non-required | 0.4040 |
From admetSAR
ADMET Predicted Profile --- Regression
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | -3.5438 | LogS |
Caco-2 Permeability | 1.6691 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 1.7409 | LD50, mol/kg |
Fish Toxicity | 0.9575 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | 0.9120 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
Kingdom | Organic compounds |
---|---|
Superclass | Organoheterocyclic compounds |
Class | Heteroaromatic compounds |
Subclass | Not available |
Intermediate Tree Nodes | Not available |
Direct Parent | Heteroaromatic compounds |
Alternative Parents | |
Molecular Framework | Aromatic heteromonocyclic compounds |
Substituents | Heteroaromatic compound - Thiophene - Hydrocarbon derivative - Aromatic heteromonocyclic compound |
Description | This 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