d-3-CARENE
Relevant Data
Food Additives Approved in the United States
Flavouring Substances Approved by European Union:
General Information
| Chemical Names: | 3,7,7-TRIMETHYL-BICYCLO-[4.1.0] HEPT-3-ENE |
| CAS number: | 13466-78-9 |
| COE number: | 10983 |
| JECFA number: | 1342 |
| FEMA number: | 3821 |
| Functional Class: |
Flavouring Agent FLAVOURING_AGENT |
From apps.who.int
Evaluations
| Evaluation year: | 2008 |
| ADI: | No safety concern at current levels of intake when used as a flavouring agent |
| Meeting: | 69 |
| Specs Code: | S |
| Report: | RS 952-JECFA 69/150 |
| Tox Monograph: | FAS 60-JECFA 69/628 |
| Specification: | FAO JECFA Monographs 5/136 |
From apps.who.int
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 26049 |
| IUPAC Name | 4,7,7-trimethylbicyclo[4.1.0]hept-3-ene |
| InChI | InChI=1S/C10H16/c1-7-4-5-8-9(6-7)10(8,2)3/h4,8-9H,5-6H2,1-3H3 |
| InChI Key | BQOFWKZOCNGFEC-UHFFFAOYSA-N |
| Canonical SMILES | CC1=CCC2C(C1)C2(C)C |
| Molecular Formula | C10H16 |
| Wikipedia | carene |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 136.238 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 0 |
| Complexity | 186.0 |
| CACTVS Substructure Key Fingerprint | A A A D c e B w A A A A A A A A A A A A A A A A G A A A A A A A A A A g A A A A B A A A A A A A A A A A G A A A A A A A D w C A A A A C A A A A A A C A A i B C A A A A A A A g A A A A C A A A A A g A A A I A A Q A A A A A A g A A I A A M A g M 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 | 0.0 |
| Monoisotopic Mass | 136.125 |
| Exact Mass | 136.125 |
| XLogP3 | None |
| XLogP3-AA | 2.8 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 10 |
| 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+ | 0.9473 |
| Human Intestinal Absorption | HIA+ | 0.9943 |
| Caco-2 Permeability | Caco2+ | 0.6326 |
| P-glycoprotein Substrate | Substrate | 0.5441 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.7102 |
| Non-inhibitor | 0.7484 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8448 |
| Distribution | ||
| Subcellular localization | Lysosome | 0.7499 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8350 |
| CYP450 2D6 Substrate | Non-substrate | 0.8356 |
| CYP450 3A4 Substrate | Substrate | 0.5518 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.7877 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.7654 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9171 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.7419 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.8365 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.7928 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9774 |
| Non-inhibitor | 0.8544 | |
| AMES Toxicity | Non AMES toxic | 0.7511 |
| Carcinogens | Non-carcinogens | 0.6647 |
| Fish Toxicity | High FHMT | 0.9770 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9793 |
| Honey Bee Toxicity | High HBT | 0.8634 |
| Biodegradation | Not ready biodegradable | 0.7256 |
| Acute Oral Toxicity | III | 0.8186 |
| Carcinogenicity (Three-class) | Warning | 0.4828 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -4.2272 | LogS |
| Caco-2 Permeability | 1.7833 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.4843 | LD50, mol/kg |
| Fish Toxicity | -0.2751 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.9781 | 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 | Carane monoterpenoid - Bicyclic monoterpenoid - Branched unsaturated hydrocarbon - Polycyclic hydrocarbon - Cyclic olefin - Unsaturated aliphatic hydrocarbon - Unsaturated hydrocarbon - Olefin - Hydrocarbon - 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