Relevant Data

Food Additives Approved by WHO:


General Information

Mainterm2-METHOXY-3(5 AND 6)-ISOPROPYLPYRAZINE
FEMA Number3358
CAS Reg.No.(or other ID)68039-46-3
Regnum

From www.fda.gov

Computed Descriptors

Download SDF
2D Structure
CID106441
IUPAC Name2-methoxy-6-propan-2-ylpyrazine
InChIInChI=1S/C8H12N2O/c1-6(2)7-4-9-5-8(10-7)11-3/h4-6H,1-3H3
InChI KeyQFGMXPJWRJAIMB-UHFFFAOYSA-N
Canonical SMILESCC(C)C1=CN=CC(=N1)OC
Molecular FormulaC8H12N2O
Wikipedia2-isopropyl-6-methoxypyrazine

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight152.197
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count3
Rotatable Bond Count2
Complexity117.0
CACTVS Substructure Key Fingerprint A A A D c c B z 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 D Q 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 x U i A A U A A 7 c A g G Y E B A g Q A V A A A A A A D Q Q A A A A A 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 = =
Topological Polar Surface Area35.0
Monoisotopic Mass152.095
Exact Mass152.095
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+0.9760
Human Intestinal AbsorptionHIA+0.9798
Caco-2 PermeabilityCaco2+0.6149
P-glycoprotein SubstrateNon-substrate0.6658
P-glycoprotein InhibitorNon-inhibitor0.9305
Non-inhibitor0.9951
Renal Organic Cation TransporterNon-inhibitor0.9067
Distribution
Subcellular localizationMitochondria0.8161
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8241
CYP450 2D6 SubstrateNon-substrate0.6713
CYP450 3A4 SubstrateNon-substrate0.5000
CYP450 1A2 InhibitorNon-inhibitor0.5177
CYP450 2C9 InhibitorNon-inhibitor0.9763
CYP450 2D6 InhibitorNon-inhibitor0.9688
CYP450 2C19 InhibitorNon-inhibitor0.8472
CYP450 3A4 InhibitorNon-inhibitor0.9334
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.9140
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9872
Non-inhibitor0.9464
AMES ToxicityNon AMES toxic0.8307
CarcinogensNon-carcinogens0.9484
Fish ToxicityLow FHMT0.8620
Tetrahymena Pyriformis ToxicityLow TPT0.8543
Honey Bee ToxicityHigh HBT0.5739
BiodegradationNot ready biodegradable0.9776
Acute Oral ToxicityIII0.7029
Carcinogenicity (Three-class)Non-required0.6620

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-1.1584LogS
Caco-2 Permeability1.5447LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity2.1774LD50, mol/kg
Fish Toxicity2.2736pLC50, mg/L
Tetrahymena Pyriformis Toxicity0.1649pIGC50, 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