19-HEPTATRIACONTANONE
General Information
| Mainterm | 19-HEPTATRIACONTANONE |
| CAS Reg.No.(or other ID) | 2123-20-8 |
| Regnum |
177.1200 |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 75035 |
| IUPAC Name | heptatriacontan-19-one |
| InChI | InChI=1S/C37H74O/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-35-37(38)36-34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-36H2,1-2H3 |
| InChI Key | KCNOEZOXGYXXQU-UHFFFAOYSA-N |
| Canonical SMILES | CCCCCCCCCCCCCCCCCCC(=O)CCCCCCCCCCCCCCCCCC |
| Molecular Formula | C37H74O |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 534.998 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 34 |
| Complexity | 390.0 |
| CACTVS Substructure Key Fingerprint | A A A D c f B 8 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 A A A A C A S A g A A C A A A A A A A I A I A Q A 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 A A A A A A A A A A E I i I C 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 | 17.1 |
| Monoisotopic Mass | 534.574 |
| Exact Mass | 534.574 |
| XLogP3 | None |
| XLogP3-AA | 17.9 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 38 |
| 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+ | 0.9882 |
| Human Intestinal Absorption | HIA+ | 0.9955 |
| Caco-2 Permeability | Caco2+ | 0.8766 |
| P-glycoprotein Substrate | Non-substrate | 0.6680 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8320 |
| Non-inhibitor | 0.7768 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8727 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.4585 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8589 |
| CYP450 2D6 Substrate | Non-substrate | 0.8439 |
| CYP450 3A4 Substrate | Non-substrate | 0.6531 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.6890 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9433 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9502 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9645 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9815 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8752 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8043 |
| Non-inhibitor | 0.7659 | |
| AMES Toxicity | Non AMES toxic | 0.9859 |
| Carcinogens | Carcinogens | 0.6310 |
| Fish Toxicity | High FHMT | 0.7423 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.8910 |
| Honey Bee Toxicity | High HBT | 0.7254 |
| Biodegradation | Ready biodegradable | 0.8731 |
| Acute Oral Toxicity | III | 0.8455 |
| Carcinogenicity (Three-class) | Non-required | 0.7622 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.2537 | LogS |
| Caco-2 Permeability | 1.3709 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.5870 | LD50, mol/kg |
| Fish Toxicity | 0.8094 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.5873 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Class | Organooxygen compounds |
| Subclass | Carbonyl compounds |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Ketones |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Ketone - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as ketones. These are organic compounds in which a carbonyl group is bonded to two carbon atoms R2C=O (neither R may be a hydrogen atom). Ketones that have one or more alpha-hydrogen atoms undergo keto-enol tautomerization, the tautomer being an enol. |
From ClassyFire