Relevant Data

Food Additives Approved by WHO:


General Information

Mainterm2,5 OR 6-METHOXY-3-METHYLPYRAZINE (MIXTURE OF ISOMERS)
FEMA Number3183
CAS Reg.No.(or other ID)2882-21-5
Regnum

From www.fda.gov

Computed Descriptors

Download SDF
2D Structure
CID520395
IUPAC Name2-methoxy-6-methylpyrazine
InChIInChI=1S/C6H8N2O/c1-5-3-7-4-6(8-5)9-2/h3-4H,1-2H3
InChI KeyMYDVJLOKNIAHPH-UHFFFAOYSA-N
Canonical SMILESCC1=CN=CC(=N1)OC
Molecular FormulaC6H8N2O
Wikipedia2-methoxy-6-methylpyrazine

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight124.143
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Complexity87.1
CACTVS Substructure Key Fingerprint A A A D c c B j 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 s A A A A A A A A A A A B g A A A H g A A A A A A C A j B l g Y u h B I I F A C g A R R n R A Q A i C Q R U i A A U A A 7 c A A G Q E B A A Q A V A A A A A A D Q 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 = =
Topological Polar Surface Area35.0
Monoisotopic Mass124.064
Exact Mass124.064
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count9
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+0.9853
Human Intestinal AbsorptionHIA+0.9753
Caco-2 PermeabilityCaco2+0.6178
P-glycoprotein SubstrateNon-substrate0.6928
P-glycoprotein InhibitorNon-inhibitor0.9638
Non-inhibitor0.9962
Renal Organic Cation TransporterNon-inhibitor0.8917
Distribution
Subcellular localizationMitochondria0.7592
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8358
CYP450 2D6 SubstrateNon-substrate0.7319
CYP450 3A4 SubstrateNon-substrate0.5855
CYP450 1A2 InhibitorNon-inhibitor0.5331
CYP450 2C9 InhibitorNon-inhibitor0.9852
CYP450 2D6 InhibitorNon-inhibitor0.9786
CYP450 2C19 InhibitorNon-inhibitor0.8871
CYP450 3A4 InhibitorNon-inhibitor0.9502
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.9223
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9829
Non-inhibitor0.9592
AMES ToxicityNon AMES toxic0.8198
CarcinogensNon-carcinogens0.9580
Fish ToxicityLow FHMT0.9414
Tetrahymena Pyriformis ToxicityLow TPT0.8481
Honey Bee ToxicityLow HBT0.5000
BiodegradationNot ready biodegradable0.9549
Acute Oral ToxicityIII0.7592
Carcinogenicity (Three-class)Non-required0.6478

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-0.4919LogS
Caco-2 Permeability1.4409LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity2.0502LD50, mol/kg
Fish Toxicity2.8066pLC50, mg/L
Tetrahymena Pyriformis Toxicity-0.1820pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassDiazines
SubclassPyrazines
Intermediate Tree NodesNot available
Direct ParentMethoxypyrazines
Alternative Parents
Molecular FrameworkAromatic heteromonocyclic compounds
SubstituentsMethoxypyrazine - Alkyl aryl ether - Heteroaromatic compound - Azacycle - Ether - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as methoxypyrazines. These are pyrazines containing a methoxyl group attached to the pyrazine ring.

From ClassyFire