3,5-DIMETHYLPYRIDINE
Relevant Data
Flavouring Substances Approved by European Union:
General Information
Mainterm | 3,5-DIMETHYLPYRIDINE |
CAS Reg.No.(or other ID) | 591-22-0 |
Regnum |
177.1520 |
From www.fda.gov
Computed Descriptors
Download SDF2D Structure | |
CID | 11565 |
IUPAC Name | 3,5-dimethylpyridine |
InChI | InChI=1S/C7H9N/c1-6-3-7(2)5-8-4-6/h3-5H,1-2H3 |
InChI Key | HWWYDZCSSYKIAD-UHFFFAOYSA-N |
Canonical SMILES | CC1=CC(=CN=C1)C |
Molecular Formula | C7H9N |
Wikipedia | 3,5-dimethylpyridine |
From Pubchem
Computed Properties
Property Name | Property Value |
---|---|
Molecular Weight | 107.156 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 1 |
Rotatable Bond Count | 0 |
Complexity | 62.8 |
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 Area | 12.9 |
Monoisotopic Mass | 107.073 |
Exact Mass | 107.073 |
Compound Is Canonicalized | True |
Formal Charge | 0 |
Heavy Atom Count | 8 |
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+ | 0.9816 |
Human Intestinal Absorption | HIA+ | 0.9881 |
Caco-2 Permeability | Caco2+ | 0.8993 |
P-glycoprotein Substrate | Non-substrate | 0.7843 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.9878 |
Non-inhibitor | 0.9970 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.8425 |
Distribution | ||
Subcellular localization | Mitochondria | 0.5138 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.8448 |
CYP450 2D6 Substrate | Non-substrate | 0.8507 |
CYP450 3A4 Substrate | Non-substrate | 0.7675 |
CYP450 1A2 Inhibitor | Non-inhibitor | 0.5064 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.7542 |
CYP450 2D6 Inhibitor | Non-inhibitor | 0.7077 |
CYP450 2C19 Inhibitor | Non-inhibitor | 0.6212 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.7691 |
CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8558 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9367 |
Non-inhibitor | 0.9398 | |
AMES Toxicity | Non AMES toxic | 0.9342 |
Carcinogens | Non-carcinogens | 0.8331 |
Fish Toxicity | Low FHMT | 0.7914 |
Tetrahymena Pyriformis Toxicity | High TPT | 0.5773 |
Honey Bee Toxicity | High HBT | 0.5640 |
Biodegradation | Ready biodegradable | 0.6200 |
Acute Oral Toxicity | II | 0.7894 |
Carcinogenicity (Three-class) | Warning | 0.4907 |
From admetSAR
ADMET Predicted Profile --- Regression
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | 0.4427 | LogS |
Caco-2 Permeability | 1.9819 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 2.4346 | LD50, mol/kg |
Fish Toxicity | 2.0693 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | -0.2402 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
Kingdom | Organic compounds |
---|---|
Superclass | Organoheterocyclic compounds |
Class | Pyridines and derivatives |
Subclass | Methylpyridines |
Intermediate Tree Nodes | Not available |
Direct Parent | Methylpyridines |
Alternative Parents | |
Molecular Framework | Aromatic heteromonocyclic compounds |
Substituents | Methylpyridine - 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 methylpyridines. These are organic compounds containing a pyridine ring substituted at one or more positions by a methyl group. |
From ClassyFire