N,N-DIMETHYLDODECYLAMINE
General Information
Mainterm | N,N-DIMETHYLDODECYLAMINE |
CAS Reg.No.(or other ID) | 112-18-5 |
Regnum |
177.1680 |
From www.fda.gov
Computed Descriptors
Download SDF2D Structure | |
CID | 8168 |
IUPAC Name | N,N-dimethyldodecan-1-amine |
InChI | InChI=1S/C14H31N/c1-4-5-6-7-8-9-10-11-12-13-14-15(2)3/h4-14H2,1-3H3 |
InChI Key | YWFWDNVOPHGWMX-UHFFFAOYSA-N |
Canonical SMILES | CCCCCCCCCCCCN(C)C |
Molecular Formula | C14H31N |
Wikipedia | dimethyl lauramine |
From Pubchem
Computed Properties
Property Name | Property Value |
---|---|
Molecular Weight | 213.409 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 1 |
Rotatable Bond Count | 11 |
Complexity | 110.0 |
CACTVS Substructure Key Fingerprint | A A A D c e B y 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 A H A A A A A A A C A D B A A Q C A 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 I A A A A A A I A g A A E A A A A A A A A A A E Q g 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 = = |
Topological Polar Surface Area | 3.2 |
Monoisotopic Mass | 213.246 |
Exact Mass | 213.246 |
Compound Is Canonicalized | True |
Formal Charge | 0 |
Heavy Atom Count | 15 |
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+ | 0.9688 |
Human Intestinal Absorption | HIA+ | 0.9838 |
Caco-2 Permeability | Caco2+ | 0.7458 |
P-glycoprotein Substrate | Non-substrate | 0.5223 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.8389 |
Non-inhibitor | 0.8170 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.5634 |
Distribution | ||
Subcellular localization | Lysosome | 0.6802 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.8581 |
CYP450 2D6 Substrate | Non-substrate | 0.5402 |
CYP450 3A4 Substrate | Non-substrate | 0.5158 |
CYP450 1A2 Inhibitor | Non-inhibitor | 0.5090 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.9480 |
CYP450 2D6 Inhibitor | Non-inhibitor | 0.9208 |
CYP450 2C19 Inhibitor | Non-inhibitor | 0.9268 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.9825 |
CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9621 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.7187 |
Non-inhibitor | 0.5703 | |
AMES Toxicity | Non AMES toxic | 0.9354 |
Carcinogens | Carcinogens | 0.6932 |
Fish Toxicity | High FHMT | 0.7905 |
Tetrahymena Pyriformis Toxicity | High TPT | 0.7764 |
Honey Bee Toxicity | High HBT | 0.5129 |
Biodegradation | Not ready biodegradable | 0.5229 |
Acute Oral Toxicity | II | 0.7356 |
Carcinogenicity (Three-class) | Non-required | 0.7378 |
From admetSAR
ADMET Predicted Profile --- Regression
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | -2.7771 | LogS |
Caco-2 Permeability | 1.2106 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 2.9560 | LD50, mol/kg |
Fish Toxicity | 1.2561 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | 0.1777 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
Kingdom | Organic compounds |
---|---|
Superclass | Organic nitrogen compounds |
Class | Organonitrogen compounds |
Subclass | Amines |
Intermediate Tree Nodes | Tertiary amines |
Direct Parent | Trialkylamines |
Alternative Parents | |
Molecular Framework | Aliphatic acyclic compounds |
Substituents | Tertiary aliphatic amine - Organopnictogen compound - Hydrocarbon derivative - Aliphatic acyclic compound |
Description | This compound belongs to the class of organic compounds known as trialkylamines. These are organic compounds containing a trialkylamine group, characterized by exactly three alkyl groups bonded to the amino nitrogen. |
From ClassyFire