ISOOCTANOL
General Information
| Mainterm | ISOOCTANOL |
| CAS Reg.No.(or other ID) | 26952-21-6 |
| Regnum |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 15450 |
| IUPAC Name | 6-methylheptan-1-ol |
| InChI | InChI=1S/C8H18O/c1-8(2)6-4-3-5-7-9/h8-9H,3-7H2,1-2H3 |
| InChI Key | BWDBEAQIHAEVLV-UHFFFAOYSA-N |
| Canonical SMILES | CC(C)CCCCCO |
| Molecular Formula | C8H18 O |
| Wikipedia | 6-methylheptan-1-ol |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 130.231 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 5 |
| Complexity | 50.5 |
| CACTVS Substructure Key Fingerprint | A A A D c e B w 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 A A A A A A A A G g A A C A A A D Q C g g A I C A A A A A 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 E A I A A A A A Q A A E A A A A A A G A w G A 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 = = |
| Topological Polar Surface Area | 20.2 |
| Monoisotopic Mass | 130.136 |
| Exact Mass | 130.136 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 9 |
| 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+ | 0.9695 |
| Human Intestinal Absorption | HIA+ | 0.9873 |
| Caco-2 Permeability | Caco2+ | 0.7467 |
| P-glycoprotein Substrate | Non-substrate | 0.6253 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9396 |
| Non-inhibitor | 0.9147 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8626 |
| Distribution | ||
| Subcellular localization | Lysosome | 0.6482 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.7989 |
| CYP450 2D6 Substrate | Non-substrate | 0.8085 |
| CYP450 3A4 Substrate | Non-substrate | 0.6242 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.7547 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8928 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9473 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9404 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9449 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9468 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9077 |
| Non-inhibitor | 0.7973 | |
| AMES Toxicity | Non AMES toxic | 0.9769 |
| Carcinogens | Non-carcinogens | 0.5970 |
| Fish Toxicity | High FHMT | 0.8456 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9697 |
| Honey Bee Toxicity | High HBT | 0.6941 |
| Biodegradation | Ready biodegradable | 0.8270 |
| Acute Oral Toxicity | III | 0.7514 |
| Carcinogenicity (Three-class) | Non-required | 0.7709 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.7451 | LogS |
| Caco-2 Permeability | 1.3619 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.4918 | LD50, mol/kg |
| Fish Toxicity | 1.3486 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.9041 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Fatty Acyls |
| Subclass | Fatty alcohols |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Fatty alcohols |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Fatty alcohol - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms. |
From ClassyFire