(+/-)-TRANS- AND CIS-2-HEXENAL GLYCERYL ACETAL
Relevant Data
Food Additives Approved by WHO:
General Information
| Mainterm | (+/-)-TRANS- AND CIS-2-HEXENAL GLYCERYL ACETAL |
| FEMA Number | 4273 |
| CAS Reg.No.(or other ID) | 897672-51-4 |
| Regnum |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 71587852 |
| IUPAC Name | 2-[(Z)-pent-1-enyl]-1,3-dioxan-5-ol |
| InChI | InChI=1S/C9H16O3/c1-2-3-4-5-9-11-6-8(10)7-12-9/h4-5,8-10H,2-3,6-7H2,1H3/b5-4- |
| InChI Key | KFIARNWETLECIZ-PLNGDYQASA-N |
| Canonical SMILES | CCCC=CC1OCC(CO1)O |
| Molecular Formula | C9H16O3 |
| Wikipedia | (Z)-pentenyl-1,3-dioxan-5-ol |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 172.224 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 3 |
| Complexity | 137.0 |
| 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 k A A A A A A A A A A A A A A A A G g A A C A A A C B S w g A M C C A A A B g C A A C B C A A A A A A A g A A A I C A A A A A g R F A A A I Q A i E A A B g A A P I A 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 A A A A A A A A A = = |
| Topological Polar Surface Area | 38.7 |
| Monoisotopic Mass | 172.11 |
| Exact Mass | 172.11 |
| XLogP3 | None |
| XLogP3-AA | 1.1 |
| 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 | 1 |
| 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+ | 0.8794 |
| Human Intestinal Absorption | HIA+ | 0.9808 |
| Caco-2 Permeability | Caco2+ | 0.5975 |
| P-glycoprotein Substrate | Non-substrate | 0.5630 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.7338 |
| Non-inhibitor | 0.9534 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8596 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.6210 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8397 |
| CYP450 2D6 Substrate | Non-substrate | 0.8472 |
| CYP450 3A4 Substrate | Non-substrate | 0.6953 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.8813 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9666 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9481 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.8297 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9490 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9652 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8622 |
| Non-inhibitor | 0.9566 | |
| AMES Toxicity | Non AMES toxic | 0.7256 |
| Carcinogens | Non-carcinogens | 0.9131 |
| Fish Toxicity | Low FHMT | 0.8509 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9828 |
| Honey Bee Toxicity | High HBT | 0.6931 |
| Biodegradation | Not ready biodegradable | 0.6593 |
| Acute Oral Toxicity | III | 0.7606 |
| Carcinogenicity (Three-class) | Non-required | 0.5931 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -1.6443 | LogS |
| Caco-2 Permeability | 1.0328 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.5521 | LD50, mol/kg |
| Fish Toxicity | 2.4971 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.1767 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Dioxanes |
| Subclass | 1,3-dioxanes |
| Intermediate Tree Nodes | Not available |
| Direct Parent | 1,3-dioxanes |
| Alternative Parents | |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | Meta-dioxane - Secondary alcohol - Oxacycle - Acetal - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aliphatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as 1,3-dioxanes. These are organic compounds containing 1,3-dioxane, an aliphatic six-member ring with two oxygen atoms in ring positions 1 and 3. |
From ClassyFire