3,5-DIETHYL-2-METHYLPYRAZINE
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
Mainterm | 3,5-DIETHYL-2-METHYLPYRAZINE |
Doc Type | EAF |
CAS Reg.No.(or other ID) | 18138-05-1 |
Regnum |
From www.fda.gov
Computed Descriptors
Download SDF2D Structure | |
CID | 28906 |
IUPAC Name | 3,5-diethyl-2-methylpyrazine |
InChI | InChI=1S/C9H14N2/c1-4-8-6-10-7(3)9(5-2)11-8/h6H,4-5H2,1-3H3 |
InChI Key | MRWLZECVHMHMGI-UHFFFAOYSA-N |
Canonical SMILES | CCC1=CN=C(C(=N1)CC)C |
Molecular Formula | C9H14N2 |
Wikipedia | 3,5-diethyl-2-methylpyrazine |
From Pubchem
Computed Properties
Property Name | Property Value |
---|---|
Molecular Weight | 150.225 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 2 |
Rotatable Bond Count | 2 |
Complexity | 114.0 |
CACTVS Substructure Key Fingerprint | A A A D c c B z 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 s A A A A A A A A A A A B g A A A H A A A A A A A C A j B F g Q u g B I I E A C g A R R n R A A A g C Q x E i A A W A A 4 c A g A Y E J A g Q A U A A A g A A D I S A 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 = = |
Topological Polar Surface Area | 25.8 |
Monoisotopic Mass | 150.116 |
Exact Mass | 150.116 |
XLogP3 | None |
XLogP3-AA | 1.8 |
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+ | 0.9719 |
Human Intestinal Absorption | HIA+ | 0.9863 |
Caco-2 Permeability | Caco2+ | 0.6946 |
P-glycoprotein Substrate | Non-substrate | 0.5494 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.6982 |
Non-inhibitor | 0.9955 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.7840 |
Distribution | ||
Subcellular localization | Mitochondria | 0.5932 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.8578 |
CYP450 2D6 Substrate | Non-substrate | 0.7238 |
CYP450 3A4 Substrate | Non-substrate | 0.7328 |
CYP450 1A2 Inhibitor | Inhibitor | 0.6535 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.8947 |
CYP450 2D6 Inhibitor | Non-inhibitor | 0.8555 |
CYP450 2C19 Inhibitor | Non-inhibitor | 0.8203 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.8273 |
CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.7577 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9486 |
Non-inhibitor | 0.9199 | |
AMES Toxicity | Non AMES toxic | 0.8956 |
Carcinogens | Non-carcinogens | 0.8722 |
Fish Toxicity | High FHMT | 0.7195 |
Tetrahymena Pyriformis Toxicity | High TPT | 0.9476 |
Honey Bee Toxicity | Low HBT | 0.6418 |
Biodegradation | Not ready biodegradable | 0.9874 |
Acute Oral Toxicity | II | 0.6639 |
Carcinogenicity (Three-class) | Non-required | 0.6559 |
From admetSAR
ADMET Predicted Profile --- Regression
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | -1.7647 | LogS |
Caco-2 Permeability | 1.6564 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 2.3655 | LD50, mol/kg |
Fish Toxicity | 1.6548 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | 0.7929 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
Kingdom | Organic compounds |
---|---|
Superclass | Organoheterocyclic compounds |
Class | Diazines |
Subclass | Pyrazines |
Intermediate Tree Nodes | Not available |
Direct Parent | Pyrazines |
Alternative Parents | |
Molecular Framework | Aromatic heteromonocyclic compounds |
Substituents | Pyrazine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound |
Description | This compound belongs to the class of organic compounds known as pyrazines. These are compounds containing a pyrazine ring, which is a six-member aromatic heterocycle, that consists of two nitrogen atoms (at positions 1 and 4) and four carbon atoms. |
From ClassyFire