1,3-BENZENEDIAMINE
General Information
Mainterm | 1,3-BENZENEDIAMINE |
CAS Reg.No.(or other ID) | 108-45-2 |
Regnum |
177.2800 177.2280 177.2550 |
From www.fda.gov
Computed Descriptors
Download SDF2D Structure | |
CID | 7935 |
IUPAC Name | benzene-1,3-diamine |
InChI | InChI=1S/C6H8N2/c7-5-2-1-3-6(8)4-5/h1-4H,7-8H2 |
InChI Key | WZCQRUWWHSTZEM-UHFFFAOYSA-N |
Canonical SMILES | C1=CC(=CC(=C1)N)N |
Molecular Formula | C6H8N2 |
Wikipedia | m-Phenylenediamine |
From Pubchem
Computed Properties
Property Name | Property Value |
---|---|
Molecular Weight | 108.144 |
Hydrogen Bond Donor Count | 2 |
Hydrogen Bond Acceptor Count | 2 |
Rotatable Bond Count | 0 |
Complexity | 64.9 |
CACTVS Substructure Key Fingerprint | A A A D c c B j 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 w A A A A A A A A A A A B A A A A H A A Q A A A A C A i B E A A w w I B A A A C A A C R C Q A C C A A A g A g A I i A A A Z I g I I C K A 0 d G A I A B g k A A I y A c Q A A A A A A A A A A Q A A A A A A A A A C A A A A A A A A A A A A A = = |
Topological Polar Surface Area | 52.0 |
Monoisotopic Mass | 108.069 |
Exact Mass | 108.069 |
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+ | 0.8707 |
Human Intestinal Absorption | HIA+ | 0.9202 |
Caco-2 Permeability | Caco2+ | 0.7040 |
P-glycoprotein Substrate | Non-substrate | 0.8417 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.9789 |
Non-inhibitor | 0.9634 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.8795 |
Distribution | ||
Subcellular localization | Lysosome | 0.8552 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.8497 |
CYP450 2D6 Substrate | Non-substrate | 0.8810 |
CYP450 3A4 Substrate | Non-substrate | 0.8218 |
CYP450 1A2 Inhibitor | Inhibitor | 0.7062 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.7146 |
CYP450 2D6 Inhibitor | Non-inhibitor | 0.9701 |
CYP450 2C19 Inhibitor | Non-inhibitor | 0.7789 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.8651 |
CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.6731 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9824 |
Non-inhibitor | 0.9393 | |
AMES Toxicity | AMES toxic | 0.9107 |
Carcinogens | Carcinogens | 0.5771 |
Fish Toxicity | Low FHMT | 0.5328 |
Tetrahymena Pyriformis Toxicity | Low TPT | 0.5233 |
Honey Bee Toxicity | Low HBT | 0.7283 |
Biodegradation | Not ready biodegradable | 0.8796 |
Acute Oral Toxicity | II | 0.7881 |
Carcinogenicity (Three-class) | Non-required | 0.6990 |
From admetSAR
ADMET Predicted Profile --- Regression
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | -0.7134 | LogS |
Caco-2 Permeability | 1.2582 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 2.5559 | LD50, mol/kg |
Fish Toxicity | 2.2246 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | -0.6224 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
Kingdom | Organic compounds |
---|---|
Superclass | Benzenoids |
Class | Benzene and substituted derivatives |
Subclass | Aniline and substituted anilines |
Intermediate Tree Nodes | Not available |
Direct Parent | Aniline and substituted anilines |
Alternative Parents | |
Molecular Framework | Aromatic homomonocyclic compounds |
Substituents | Aniline or substituted anilines - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Amine - Aromatic homomonocyclic compound |
Description | This compound belongs to the class of organic compounds known as aniline and substituted anilines. These are organic compounds containing an aminobenzene moiety. |
From ClassyFire