4-METHYLCYCLOHEXANONE
Relevant Data
Food Additives Approved by WHO:
General Information
Mainterm | 4-METHYLCYCLOHEXANONE |
Doc Type | EAF |
CAS Reg.No.(or other ID) | 589-92-4 |
Regnum |
From www.fda.gov
Computed Descriptors
Download SDF2D Structure | |
CID | 11525 |
IUPAC Name | 4-methylcyclohexan-1-one |
InChI | InChI=1S/C7H12O/c1-6-2-4-7(8)5-3-6/h6H,2-5H2,1H3 |
InChI Key | VGVHNLRUAMRIEW-UHFFFAOYSA-N |
Canonical SMILES | CC1CCC(=O)CC1 |
Molecular Formula | C7H12O |
Wikipedia | 4-methylcyclohexanone |
From Pubchem
Computed Properties
Property Name | Property Value |
---|---|
Molecular Weight | 112.172 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 1 |
Rotatable Bond Count | 0 |
Complexity | 86.6 |
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 w 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 Q S A g A A C A A A A A A A I A I A Q A A A A A A A A A A A A A A E A A A A A A B I A A A A A A A A A A A A A A A E I i A A O 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 | 112.089 |
Exact Mass | 112.089 |
Compound Is Canonicalized | True |
Formal Charge | 0 |
Heavy Atom Count | 8 |
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
Food Additives Biosynthesis/Degradation
ADMET Predicted Profile --- Classification
Model | Result | Probability |
---|---|---|
Absorption | ||
Blood-Brain Barrier | BBB+ | 0.9673 |
Human Intestinal Absorption | HIA+ | 1.0000 |
Caco-2 Permeability | Caco2+ | 0.8690 |
P-glycoprotein Substrate | Non-substrate | 0.6622 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.9093 |
Non-inhibitor | 0.9776 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.7728 |
Distribution | ||
Subcellular localization | Mitochondria | 0.6475 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.7826 |
CYP450 2D6 Substrate | Non-substrate | 0.8282 |
CYP450 3A4 Substrate | Non-substrate | 0.6293 |
CYP450 1A2 Inhibitor | Non-inhibitor | 0.7409 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.9189 |
CYP450 2D6 Inhibitor | Non-inhibitor | 0.9670 |
CYP450 2C19 Inhibitor | Non-inhibitor | 0.9553 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.9786 |
CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9698 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.7515 |
Non-inhibitor | 0.9147 | |
AMES Toxicity | Non AMES toxic | 0.8866 |
Carcinogens | Non-carcinogens | 0.8514 |
Fish Toxicity | High FHMT | 0.7587 |
Tetrahymena Pyriformis Toxicity | Low TPT | 0.7432 |
Honey Bee Toxicity | High HBT | 0.7416 |
Biodegradation | Ready biodegradable | 0.6051 |
Acute Oral Toxicity | III | 0.9095 |
Carcinogenicity (Three-class) | Non-required | 0.7226 |
From admetSAR
ADMET Predicted Profile --- Regression
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | -1.3123 | LogS |
Caco-2 Permeability | 1.8271 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 2.0673 | LD50, mol/kg |
Fish Toxicity | 1.8253 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | -0.8896 | 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