Relevant Data

Flavouring Substances Approved by European Union:

  • 3,5-Dimethylpyridine [show]

General Information

Mainterm3,5-DIMETHYLPYRIDINE
CAS Reg.No.(or other ID)591-22-0
Regnum 177.1520

From www.fda.gov

Computed Descriptors

Download SDF
2D Structure
CID11565
IUPAC Name3,5-dimethylpyridine
InChIInChI=1S/C7H9N/c1-6-3-7(2)5-8-4-6/h3-5H,1-2H3
InChI KeyHWWYDZCSSYKIAD-UHFFFAOYSA-N
Canonical SMILESCC1=CC(=CN=C1)C
Molecular FormulaC7H9N
Wikipedia3,5-dimethylpyridine

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight107.156
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Complexity62.8
CACTVS Substructure Key Fingerprint A A A D c c B 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 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 D A D B G g Q + g J I I E A C g A j B n R A C C g C A x A C A A 2 C A o R J g I I O L A k Z G E I A h g g A D I y A Y Q A 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 A A A A A A = =
Topological Polar Surface Area12.9
Monoisotopic Mass107.073
Exact Mass107.073
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count8
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+0.9816
Human Intestinal AbsorptionHIA+0.9881
Caco-2 PermeabilityCaco2+0.8993
P-glycoprotein SubstrateNon-substrate0.7843
P-glycoprotein InhibitorNon-inhibitor0.9878
Non-inhibitor0.9970
Renal Organic Cation TransporterNon-inhibitor0.8425
Distribution
Subcellular localizationMitochondria0.5138
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8448
CYP450 2D6 SubstrateNon-substrate0.8507
CYP450 3A4 SubstrateNon-substrate0.7675
CYP450 1A2 InhibitorNon-inhibitor0.5064
CYP450 2C9 InhibitorNon-inhibitor0.7542
CYP450 2D6 InhibitorNon-inhibitor0.7077
CYP450 2C19 InhibitorNon-inhibitor0.6212
CYP450 3A4 InhibitorNon-inhibitor0.7691
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.8558
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9367
Non-inhibitor0.9398
AMES ToxicityNon AMES toxic0.9342
CarcinogensNon-carcinogens0.8331
Fish ToxicityLow FHMT0.7914
Tetrahymena Pyriformis ToxicityHigh TPT0.5773
Honey Bee ToxicityHigh HBT0.5640
BiodegradationReady biodegradable0.6200
Acute Oral ToxicityII0.7894
Carcinogenicity (Three-class)Warning0.4907

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility0.4427LogS
Caco-2 Permeability1.9819LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity2.4346LD50, mol/kg
Fish Toxicity2.0693pLC50, mg/L
Tetrahymena Pyriformis Toxicity-0.2402pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassPyridines and derivatives
SubclassMethylpyridines
Intermediate Tree NodesNot available
Direct ParentMethylpyridines
Alternative Parents
Molecular FrameworkAromatic heteromonocyclic compounds
SubstituentsMethylpyridine - 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 methylpyridines. These are organic compounds containing a pyridine ring substituted at one or more positions by a methyl group.

From ClassyFire