Pent-4-en-1-ol
General Information
Chemical name | Pent-4-en-1-ol |
CAS number | 821-09-0 |
Flavouring type | substances |
FL No. | 02.201 |
Mixture | No |
Purity of the named substance at least 95% unless otherwise specified |
From webgate.ec.europa.eu
Computed Descriptors
Download SDF2D Structure | |
CID | 13181 |
IUPAC Name | pent-4-en-1-ol |
InChI | InChI=1S/C5H10O/c1-2-3-4-5-6/h2,6H,1,3-5H2 |
InChI Key | LQAVWYMTUMSFBE-UHFFFAOYSA-N |
Canonical SMILES | C=CCCCO |
Molecular Formula | C5H10O |
Wikipedia | 4-pentenol |
From Pubchem
Computed Properties
Property Name | Property Value |
---|---|
Molecular Weight | 86.134 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 1 |
Rotatable Bond Count | 3 |
Complexity | 32.9 |
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 Area | 20.2 |
Monoisotopic Mass | 86.073 |
Exact Mass | 86.073 |
XLogP3 | None |
XLogP3-AA | 1.0 |
Compound Is Canonicalized | True |
Formal Charge | 0 |
Heavy Atom Count | 6 |
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+ | 0.9656 |
Human Intestinal Absorption | HIA+ | 0.9759 |
Caco-2 Permeability | Caco2+ | 0.7123 |
P-glycoprotein Substrate | Non-substrate | 0.8177 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.8822 |
Non-inhibitor | 0.9532 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.8746 |
Distribution | ||
Subcellular localization | Lysosome | 0.4996 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.8392 |
CYP450 2D6 Substrate | Non-substrate | 0.8836 |
CYP450 3A4 Substrate | Non-substrate | 0.7702 |
CYP450 1A2 Inhibitor | Non-inhibitor | 0.6692 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.9162 |
CYP450 2D6 Inhibitor | Non-inhibitor | 0.9521 |
CYP450 2C19 Inhibitor | Non-inhibitor | 0.9037 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.9197 |
CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9099 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8471 |
Non-inhibitor | 0.9567 | |
AMES Toxicity | Non AMES toxic | 0.7957 |
Carcinogens | Non-carcinogens | 0.5803 |
Fish Toxicity | High FHMT | 0.5647 |
Tetrahymena Pyriformis Toxicity | Low TPT | 0.9919 |
Honey Bee Toxicity | High HBT | 0.7906 |
Biodegradation | Ready biodegradable | 0.8909 |
Acute Oral Toxicity | III | 0.5533 |
Carcinogenicity (Three-class) | Non-required | 0.6996 |
From admetSAR
ADMET Predicted Profile --- Regression
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | -0.2126 | LogS |
Caco-2 Permeability | 1.6012 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 2.0239 | LD50, mol/kg |
Fish Toxicity | 1.0739 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | -1.3448 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
Kingdom | Organic compounds |
---|---|
Superclass | Organic oxygen compounds |
Class | Organooxygen compounds |
Subclass | Alcohols and polyols |
Intermediate Tree Nodes | Not available |
Direct Parent | Primary alcohols |
Alternative Parents | |
Molecular Framework | Aliphatic acyclic compounds |
Substituents | Hydrocarbon derivative - Primary alcohol - Aliphatic acyclic compound |
Description | This 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