3-Methyl-2-pentylcyclopent-2-en-1-one
Relevant Data
Food Additives Approved in the United States:
Food Additives Approved by WHO:
General Information
| Chemical name | 3-Methyl-2-pentylcyclopent-2-en-1-one |
| CAS number | 1128-08-1 |
| JECFA number | 1406 |
| Flavouring type | substances |
| FL No. | 07.140 |
| Mixture | No |
| Purity of the named substance at least 95% unless otherwise specified | |
| Reference body | EFSA |
From webgate.ec.europa.eu
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 62378 |
| IUPAC Name | 3-methyl-2-pentylcyclopent-2-en-1-one |
| InChI | InChI=1S/C11H18O/c1-3-4-5-6-10-9(2)7-8-11(10)12/h3-8H2,1-2H3 |
| InChI Key | YCIXWYOBMVNGTB-UHFFFAOYSA-N |
| Canonical SMILES | CCCCCC1=C(CCC1=O)C |
| Molecular Formula | C11H18O |
| Wikipedia | dihydrojasmone |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 166.264 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 4 |
| Complexity | 201.0 |
| CACTVS Substructure Key Fingerprint | A A A D c e B w I A A A A A A A A A A A A A A A A A A A A Q 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 A A A A D A S A g A A C A A A A A A C I A o B Q A A A A A A A g A A A A C A E A A E g A A B I A A A A A A A A A g A A I A Q M I i I C 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 | 17.1 |
| Monoisotopic Mass | 166.136 |
| Exact Mass | 166.136 |
| XLogP3 | None |
| XLogP3-AA | 2.9 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 12 |
| 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+ | 0.9683 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.8095 |
| P-glycoprotein Substrate | Non-substrate | 0.5688 |
| P-glycoprotein Inhibitor | Inhibitor | 0.5294 |
| Non-inhibitor | 0.8831 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.7961 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.4633 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8759 |
| CYP450 2D6 Substrate | Non-substrate | 0.8564 |
| CYP450 3A4 Substrate | Substrate | 0.5340 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.6184 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9321 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9133 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.8770 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9499 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.7004 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.6129 |
| Non-inhibitor | 0.8044 | |
| AMES Toxicity | Non AMES toxic | 0.9473 |
| Carcinogens | Non-carcinogens | 0.7933 |
| Fish Toxicity | High FHMT | 0.9025 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9422 |
| Honey Bee Toxicity | High HBT | 0.8284 |
| Biodegradation | Ready biodegradable | 0.7346 |
| Acute Oral Toxicity | III | 0.8042 |
| Carcinogenicity (Three-class) | Non-required | 0.5843 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.6441 | LogS |
| Caco-2 Permeability | 1.4816 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.7855 | LD50, mol/kg |
| Fish Toxicity | 0.5295 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.5258 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Class | Organooxygen compounds |
| Subclass | Carbonyl compounds |
| Intermediate Tree Nodes | Ketones |
| Direct Parent | Cyclic ketones |
| Alternative Parents | |
| Molecular Framework | Aliphatic homomonocyclic compounds |
| Substituents | Cyclic ketone - Organic oxide - Hydrocarbon derivative - Aliphatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as cyclic ketones. These are organic compounds containing a ketone that is conjugated to a cyclic moiety. |
From ClassyFire