Naphthalene, octadecyl-
General Information
Mainterm | Naphthalene, octadecyl- |
CAS Reg.No.(or other ID) | 56388-48-8 |
Regnum |
From www.fda.gov
Computed Descriptors
Download SDF2D Structure | |
CID | 91832 |
IUPAC Name | 1-octadecylnaphthalene |
InChI | InChI=1S/C28H44/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-21-26-23-20-24-27-22-18-19-25-28(26)27/h18-20,22-25H,2-17,21H2,1H3 |
InChI Key | DKTSRTYLZGWAIT-UHFFFAOYSA-N |
Canonical SMILES | CCCCCCCCCCCCCCCCCCC1=CC=CC2=CC=CC=C21 |
Molecular Formula | C28H44 |
Wikipedia | 1-octadecylnaphthalene |
From Pubchem
Computed Properties
Property Name | Property Value |
---|---|
Molecular Weight | 380.66 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 0 |
Rotatable Bond Count | 17 |
Complexity | 333.0 |
CACTVS Substructure Key Fingerprint | A A A D c f B 4 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 w Y A A A A A A A A A D B U A A A G A A A A A A A D A C A G A A y A M A A A A C A A i B C A A A C A A A g A A A I i A A A A I g I I C K A E R C A I A A g g A A I i A c A g M A O g A A C A A A Q A A A A A A Q A A C A A A A A A A A A A A A = = |
Topological Polar Surface Area | 0.0 |
Monoisotopic Mass | 380.344 |
Exact Mass | 380.344 |
Compound Is Canonicalized | True |
Formal Charge | 0 |
Heavy Atom Count | 28 |
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+ | 0.9774 |
Human Intestinal Absorption | HIA+ | 1.0000 |
Caco-2 Permeability | Caco2+ | 0.7959 |
P-glycoprotein Substrate | Substrate | 0.5365 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.6417 |
Inhibitor | 0.6608 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.7287 |
Distribution | ||
Subcellular localization | Lysosome | 0.5629 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.7775 |
CYP450 2D6 Substrate | Non-substrate | 0.7300 |
CYP450 3A4 Substrate | Non-substrate | 0.6610 |
CYP450 1A2 Inhibitor | Inhibitor | 0.6389 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.8599 |
CYP450 2D6 Inhibitor | Non-inhibitor | 0.8908 |
CYP450 2C19 Inhibitor | Non-inhibitor | 0.7301 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.9182 |
CYP Inhibitory Promiscuity | High CYP Inhibitory Promiscuity | 0.6332 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.7447 |
Inhibitor | 0.5407 | |
AMES Toxicity | Non AMES toxic | 0.8652 |
Carcinogens | Non-carcinogens | 0.7850 |
Fish Toxicity | High FHMT | 0.9973 |
Tetrahymena Pyriformis Toxicity | High TPT | 1.0000 |
Honey Bee Toxicity | High HBT | 0.6813 |
Biodegradation | Not ready biodegradable | 0.8956 |
Acute Oral Toxicity | III | 0.6282 |
Carcinogenicity (Three-class) | Non-required | 0.4440 |
From admetSAR
ADMET Predicted Profile --- Regression
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | -6.8737 | LogS |
Caco-2 Permeability | 1.6019 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 1.4725 | LD50, mol/kg |
Fish Toxicity | -1.3185 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | 2.7564 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
Kingdom | Organic compounds |
---|---|
Superclass | Benzenoids |
Class | Naphthalenes |
Subclass | Not available |
Intermediate Tree Nodes | Not available |
Direct Parent | Naphthalenes |
Alternative Parents | |
Molecular Framework | Aromatic homopolycyclic compounds |
Substituents | Naphthalene - Aromatic hydrocarbon - Polycyclic hydrocarbon - Unsaturated hydrocarbon - Hydrocarbon - Aromatic homopolycyclic compound |
Description | This compound belongs to the class of organic compounds known as naphthalenes. These are compounds containing a naphthalene moiety, which consists of two fused benzene rings. |
From ClassyFire