YUZUNONE
Relevant Data
Food Additives Approved in the United States
General Information
| Chemical Names: | YUZUNONE |
| CAS number: | 1009814-14-5 |
| JECFA number: | 2217 |
| FEMA number: | 4691 |
| Functional Class: |
Flavouring Agent FLAVOURING_AGENT |
From apps.who.int
Evaluations
| Evaluation year: | 2016 |
| ADI: | No safety concern at current levels of intake when used as a flavouring agent |
| Meeting: | 82 |
| Specs Code: | N |
| Report: | TRS 1000-JECFA 82/105 |
| Specification: | FAO JECFA Monographs 19/136 |
From apps.who.int
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 29025 |
| IUPAC Name | 2,6,6-trimethylbicyclo[3.1.1]hept-2-en-4-one |
| InChI | InChI=1S/C10H14O/c1-6-4-9(11)8-5-7(6)10(8,2)3/h4,7-8H,5H2,1-3H3 |
| InChI Key | DCSCXTJOXBUFGB-UHFFFAOYSA-N |
| Canonical SMILES | CC1=CC(=O)C2CC1C2(C)C |
| Molecular Formula | C10H14O |
| Wikipedia | 4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-one |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 150.221 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Complexity | 248.0 |
| CACTVS Substructure Key Fingerprint | A A A D c c B w I A A A A A A A A A A A A A A A A A B g A A A A A A A g Q A A A A A A A A A A A A A A A G g A A A A A A D w S A g A A C A A A A A A C I A q B S 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 Q A A A A A A g A A I A Q M I i E A P 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 = = |
| Topological Polar Surface Area | 17.1 |
| Monoisotopic Mass | 150.104 |
| Exact Mass | 150.104 |
| XLogP3 | None |
| XLogP3-AA | 1.6 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 11 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 2 |
| 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+ | 0.8112 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.7542 |
| P-glycoprotein Substrate | Substrate | 0.5734 |
| P-glycoprotein Inhibitor | Inhibitor | 0.6144 |
| Non-inhibitor | 0.8807 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.7773 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.5296 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.7993 |
| CYP450 2D6 Substrate | Non-substrate | 0.8622 |
| CYP450 3A4 Substrate | Substrate | 0.6200 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.7658 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.7575 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.8873 |
| CYP450 2C19 Inhibitor | Inhibitor | 0.5593 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.8309 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.5888 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9654 |
| Non-inhibitor | 0.9060 | |
| AMES Toxicity | Non AMES toxic | 0.9454 |
| Carcinogens | Non-carcinogens | 0.7742 |
| Fish Toxicity | High FHMT | 0.7933 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9611 |
| Honey Bee Toxicity | High HBT | 0.8999 |
| Biodegradation | Not ready biodegradable | 0.5870 |
| Acute Oral Toxicity | III | 0.7560 |
| Carcinogenicity (Three-class) | Non-required | 0.4705 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.8718 | LogS |
| Caco-2 Permeability | 1.9684 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 2.1323 | LD50, mol/kg |
| Fish Toxicity | 0.3418 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.8075 | 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 | Bicyclic monoterpenoids |
| Alternative Parents | |
| Molecular Framework | Aliphatic homopolycyclic compounds |
| Substituents | Pinane monoterpenoid - Bicyclic monoterpenoid - Cyclohexenone - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic homopolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other. |
From ClassyFire