3-METHYL-2-(n-PENTANYL)-2-CYCLOPENTEN-1-ONE
Relevant Data
Flavouring Substances Approved by European Union:
General Information
| Chemical Names: | 3-METHYL-2-PENTYLCYCLOPENT-2-EN-1-ONE |
| CAS number: | 1128-08-01 |
| JECFA number: | 1406 |
| FEMA number: | 3763 |
| Functional Class: |
Flavouring Agent FLAVOURING_AGENT |
From apps.who.int
Evaluations
| Evaluation year: | 2004 |
| ADI: | No safety concern at current levels of intake when used as a flavouring agent |
| Report: | TRS 928-JECFA 63/86 |
| Tox Monograph: | FAS 54-JECFA 63/385 |
| Specification: | COMPENDIUM ADDENDUM 12/FNP 52 Add. 12/86 |
From apps.who.int
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 11815386 |
| IUPAC Name | 3-hydroxy-5-methylhexan-2-one |
| InChI | InChI=1S/C7H14O2/c1-5(2)4-7(9)6(3)8/h5,7,9H,4H2,1-3H3 |
| InChI Key | LZDPYURTPRCDJG-UHFFFAOYSA-N |
| Canonical SMILES | CC(C)CC(C(=O)C)O |
| Molecular Formula | C7H14O2 |
| Wikipedia | 3-hydroxy-5-methyl-hexan-2-one |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 130.187 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 3 |
| Complexity | 97.1 |
| CACTVS Substructure Key Fingerprint | A A A D c c B g M 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 D R S g g A I C A A A A A g A I A I A Q A A I A A A A A A A A A A A F A A A A A E B I A A A A A Q A A E A A A A A A E I A A A M 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 | 37.3 |
| Monoisotopic Mass | 130.099 |
| Exact Mass | 130.099 |
| XLogP3 | None |
| XLogP3-AA | 1.0 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 9 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| 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+ | 0.9614 |
| Human Intestinal Absorption | HIA+ | 0.9959 |
| Caco-2 Permeability | Caco2+ | 0.6383 |
| P-glycoprotein Substrate | Non-substrate | 0.6920 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.7900 |
| Non-inhibitor | 0.8413 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.9503 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.6891 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.7996 |
| CYP450 2D6 Substrate | Non-substrate | 0.8402 |
| CYP450 3A4 Substrate | Non-substrate | 0.6178 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.8245 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9495 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9197 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9141 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9683 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9741 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9861 |
| Non-inhibitor | 0.9281 | |
| AMES Toxicity | Non AMES toxic | 0.8374 |
| Carcinogens | Carcinogens | 0.6569 |
| Fish Toxicity | High FHMT | 0.6783 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.8384 |
| Honey Bee Toxicity | High HBT | 0.7656 |
| Biodegradation | Ready biodegradable | 0.7261 |
| Acute Oral Toxicity | III | 0.9059 |
| Carcinogenicity (Three-class) | Non-required | 0.8166 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -0.7170 | LogS |
| Caco-2 Permeability | 1.2237 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.4810 | LD50, mol/kg |
| Fish Toxicity | 2.8029 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.1460 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Class | Organooxygen compounds |
| Subclass | Carbonyl compounds |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Acyloins |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Acyloin - Alpha-hydroxy ketone - Secondary alcohol - Ketone - Organic oxide - Hydrocarbon derivative - Alcohol - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as acyloins. These are organic compounds containing an alpha hydroxy ketone. Acyloins are formally derived from reductive coupling of carboxylic acyl groups. |
From ClassyFire