5-OXOOCTANOIC ACID
Relevant Data
Food Additives Approved by WHO:
General Information
| Mainterm | 5-OXOOCTANOIC ACID |
| Doc Type | EAF |
| CAS Reg.No.(or other ID) | 3637-14-7 |
| Regnum |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 280190 |
| IUPAC Name | 5-oxooctanoic acid |
| InChI | InChI=1S/C8H14O3/c1-2-4-7(9)5-3-6-8(10)11/h2-6H2,1H3,(H,10,11) |
| InChI Key | OHGVWVVPDOAZSH-UHFFFAOYSA-N |
| Canonical SMILES | CCCC(=O)CCCC(=O)O |
| Molecular Formula | C8H14O3 |
| Wikipedia | 5-oxooctanoic acid |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 158.197 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 6 |
| Complexity | 140.0 |
| CACTVS Substructure Key Fingerprint | A A A D c c 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 A 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 A S A g A A C C A A A A g A I A I C Q C 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 Q A A E A A A A A A G I z q C 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 A = = |
| Topological Polar Surface Area | 54.4 |
| Monoisotopic Mass | 158.094 |
| Exact Mass | 158.094 |
| XLogP3 | None |
| XLogP3-AA | 0.6 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 11 |
| 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
ADMET Predicted Profile --- Classification
| Model | Result | Probability |
|---|---|---|
| Absorption | ||
| Blood-Brain Barrier | BBB+ | 0.8993 |
| Human Intestinal Absorption | HIA+ | 0.9830 |
| Caco-2 Permeability | Caco2+ | 0.7089 |
| P-glycoprotein Substrate | Non-substrate | 0.6445 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9060 |
| Non-inhibitor | 0.7865 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.9355 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.8436 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8217 |
| CYP450 2D6 Substrate | Non-substrate | 0.8988 |
| CYP450 3A4 Substrate | Non-substrate | 0.6839 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.6708 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9162 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9542 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9545 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9433 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9765 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9108 |
| Non-inhibitor | 0.8875 | |
| AMES Toxicity | Non AMES toxic | 0.9642 |
| Carcinogens | Non-carcinogens | 0.7035 |
| Fish Toxicity | High FHMT | 0.7663 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9776 |
| Honey Bee Toxicity | High HBT | 0.6478 |
| Biodegradation | Ready biodegradable | 0.9520 |
| Acute Oral Toxicity | III | 0.6215 |
| Carcinogenicity (Three-class) | Non-required | 0.6683 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.3975 | LogS |
| Caco-2 Permeability | 0.9637 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.6790 | LD50, mol/kg |
| Fish Toxicity | 2.0183 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.4118 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Fatty Acyls |
| Subclass | Fatty acids and conjugates |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Medium-chain fatty acids |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Medium-chain fatty acid - Ketone - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as medium-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms. |
From ClassyFire