Relevant Data

Food Additives Approved by WHO:

Flavouring Substances Approved by European Union:

  • 3,5-Diethyl-2-methylpyrazine [show]

General Information

Mainterm3,5-DIETHYL-2-METHYLPYRAZINE
Doc TypeEAF
CAS Reg.No.(or other ID)18138-05-1
Regnum

From www.fda.gov

Computed Descriptors

Download SDF
2D Structure
CID28906
IUPAC Name3,5-diethyl-2-methylpyrazine
InChIInChI=1S/C9H14N2/c1-4-8-6-10-7(3)9(5-2)11-8/h6H,4-5H2,1-3H3
InChI KeyMRWLZECVHMHMGI-UHFFFAOYSA-N
Canonical SMILESCCC1=CN=C(C(=N1)CC)C
Molecular FormulaC9H14N2
Wikipedia3,5-diethyl-2-methylpyrazine

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight150.225
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count2
Complexity114.0
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 Area25.8
Monoisotopic Mass150.116
Exact Mass150.116
XLogP3None
XLogP3-AA1.8
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count11
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Isotope Atom Count0
Covalently-Bonded Unit Count1

From Pubchem


ADMET Predicted Profile --- Classification

Model Result Probability
Absorption
Blood-Brain BarrierBBB+0.9719
Human Intestinal AbsorptionHIA+0.9863
Caco-2 PermeabilityCaco2+0.6946
P-glycoprotein SubstrateNon-substrate0.5494
P-glycoprotein InhibitorNon-inhibitor0.6982
Non-inhibitor0.9955
Renal Organic Cation TransporterNon-inhibitor0.7840
Distribution
Subcellular localizationMitochondria0.5932
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8578
CYP450 2D6 SubstrateNon-substrate0.7238
CYP450 3A4 SubstrateNon-substrate0.7328
CYP450 1A2 InhibitorInhibitor0.6535
CYP450 2C9 InhibitorNon-inhibitor0.8947
CYP450 2D6 InhibitorNon-inhibitor0.8555
CYP450 2C19 InhibitorNon-inhibitor0.8203
CYP450 3A4 InhibitorNon-inhibitor0.8273
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.7577
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9486
Non-inhibitor0.9199
AMES ToxicityNon AMES toxic0.8956
CarcinogensNon-carcinogens0.8722
Fish ToxicityHigh FHMT0.7195
Tetrahymena Pyriformis ToxicityHigh TPT0.9476
Honey Bee ToxicityLow HBT0.6418
BiodegradationNot ready biodegradable0.9874
Acute Oral ToxicityII0.6639
Carcinogenicity (Three-class)Non-required0.6559

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-1.7647LogS
Caco-2 Permeability1.6564LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity2.3655LD50, mol/kg
Fish Toxicity1.6548pLC50, mg/L
Tetrahymena Pyriformis Toxicity0.7929pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassDiazines
SubclassPyrazines
Intermediate Tree NodesNot available
Direct ParentPyrazines
Alternative Parents
Molecular FrameworkAromatic heteromonocyclic compounds
SubstituentsPyrazine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound
DescriptionThis 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