DIHYDROCARVYL ACETATE
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
| Mainterm | DIHYDROCARVYL ACETATE |
| Doc Type | ASP |
| CAS Reg.No.(or other ID) | 20777-49-5 |
| Regnum |
172.515 |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 30248 |
| IUPAC Name | (2-methyl-5-prop-1-en-2-ylcyclohexyl) acetate |
| InChI | InChI=1S/C12H20O2/c1-8(2)11-6-5-9(3)12(7-11)14-10(4)13/h9,11-12H,1,5-7H2,2-4H3 |
| InChI Key | TUSIZTVSUSBSQI-UHFFFAOYSA-N |
| Canonical SMILES | CC1CCC(CC1OC(=O)C)C(=C)C |
| Molecular Formula | C12H20O2 |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 196.29 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 3 |
| Complexity | 233.0 |
| CACTVS Substructure Key Fingerprint | A A A D c e B w 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 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 R S g g A I C C A A A B A C I A g D S C A A A A A A g A A A A A A A A A A g A A A I A A Q A C A A A E g A A A A A G A w P A O A A A A A A A A A A C A A A I A A B A A A A A A A A A A A A = = |
| Topological Polar Surface Area | 26.3 |
| Monoisotopic Mass | 196.146 |
| Exact Mass | 196.146 |
| XLogP3 | None |
| XLogP3-AA | 3.5 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 14 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 3 |
| 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+ | 0.8786 |
| Human Intestinal Absorption | HIA+ | 0.9934 |
| Caco-2 Permeability | Caco2+ | 0.7953 |
| P-glycoprotein Substrate | Non-substrate | 0.6116 |
| P-glycoprotein Inhibitor | Inhibitor | 0.6081 |
| Non-inhibitor | 0.8168 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.7934 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.7123 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8736 |
| CYP450 2D6 Substrate | Non-substrate | 0.8522 |
| CYP450 3A4 Substrate | Substrate | 0.6224 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.7554 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9516 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9377 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.6473 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.7626 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8782 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.7180 |
| Non-inhibitor | 0.8657 | |
| AMES Toxicity | Non AMES toxic | 0.9425 |
| Carcinogens | Non-carcinogens | 0.8203 |
| Fish Toxicity | High FHMT | 0.9767 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.8987 |
| Honey Bee Toxicity | High HBT | 0.8771 |
| Biodegradation | Ready biodegradable | 0.7809 |
| Acute Oral Toxicity | III | 0.8119 |
| Carcinogenicity (Three-class) | Non-required | 0.5667 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -3.7644 | LogS |
| Caco-2 Permeability | 1.5121 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.5723 | LD50, mol/kg |
| Fish Toxicity | 0.2615 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 1.1216 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Prenol lipids |
| Subclass | Monoterpenoids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Menthane monoterpenoids |
| Alternative Parents | |
| Molecular Framework | Aliphatic homomonocyclic compounds |
| Substituents | P-menthane monoterpenoid - Monocyclic monoterpenoid - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes. |
From ClassyFire