THIAZOLE
Relevant Data
Food Additives Approved by WHO:
General Information
Mainterm | THIAZOLE |
Doc Type | ASP |
CAS Reg.No.(or other ID) | 288-47-1 |
Regnum |
From www.fda.gov
Computed Descriptors
Download SDF2D Structure | |
CID | 9256 |
IUPAC Name | 1,3-thiazole |
InChI | InChI=1S/C3H3NS/c1-2-5-3-4-1/h1-3H |
InChI Key | FZWLAAWBMGSTSO-UHFFFAOYSA-N |
Canonical SMILES | C1=CSC=N1 |
Molecular Formula | C3H3NS |
Wikipedia | thiazole |
From Pubchem
Computed Properties
Property Name | Property Value |
---|---|
Molecular Weight | 85.124 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 2 |
Rotatable Bond Count | 0 |
Complexity | 30.1 |
CACTVS Substructure Key Fingerprint | A A A D c Q B C A A B 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 A A A A A A B g A A A H A Q A A A A A A A D F Q g S s g R I I E A i k A B A n R A A A 8 K B R C j h I Q A w Y 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 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 | 41.1 |
Monoisotopic Mass | 84.999 |
Exact Mass | 84.999 |
Compound Is Canonicalized | True |
Formal Charge | 0 |
Heavy Atom Count | 5 |
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+ | 0.9859 |
Human Intestinal Absorption | HIA+ | 0.9680 |
Caco-2 Permeability | Caco2+ | 0.5818 |
P-glycoprotein Substrate | Non-substrate | 0.8661 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.9635 |
Non-inhibitor | 0.9920 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.8522 |
Distribution | ||
Subcellular localization | Mitochondria | 0.4987 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.8840 |
CYP450 2D6 Substrate | Non-substrate | 0.9044 |
CYP450 3A4 Substrate | Non-substrate | 0.8202 |
CYP450 1A2 Inhibitor | Inhibitor | 0.6341 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.7567 |
CYP450 2D6 Inhibitor | Non-inhibitor | 0.5529 |
CYP450 2C19 Inhibitor | Inhibitor | 0.6720 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.9679 |
CYP Inhibitory Promiscuity | High CYP Inhibitory Promiscuity | 0.7013 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9692 |
Non-inhibitor | 0.9620 | |
AMES Toxicity | AMES toxic | 0.6944 |
Carcinogens | Non-carcinogens | 0.8526 |
Fish Toxicity | High FHMT | 0.5839 |
Tetrahymena Pyriformis Toxicity | High TPT | 0.8427 |
Honey Bee Toxicity | High HBT | 0.6632 |
Biodegradation | Not ready biodegradable | 0.6582 |
Acute Oral Toxicity | II | 0.7443 |
Carcinogenicity (Three-class) | Warning | 0.4821 |
From admetSAR
ADMET Predicted Profile --- Regression
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | -0.1147 | LogS |
Caco-2 Permeability | 1.5145 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 2.4153 | LD50, mol/kg |
Fish Toxicity | 2.0290 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | 0.6516 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
Kingdom | Organic compounds |
---|---|
Superclass | Organoheterocyclic compounds |
Class | Azoles |
Subclass | Thiazoles |
Intermediate Tree Nodes | Not available |
Direct Parent | Thiazoles |
Alternative Parents | |
Molecular Framework | Aromatic heteromonocyclic compounds |
Substituents | Heteroaromatic compound - Thiazole - 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 thiazoles. These are heterocyclic compounds containing a five-member aromatic ring made up of one sulfur atom, one nitrogen, and three carbon atoms. |
From ClassyFire