Relevant Data

Food Additives Approved by WHO:


General Information

MaintermTHIAZOLE
Doc TypeASP
CAS Reg.No.(or other ID)288-47-1
Regnum

From www.fda.gov

Computed Descriptors

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2D Structure
CID9256
IUPAC Name1,3-thiazole
InChIInChI=1S/C3H3NS/c1-2-5-3-4-1/h1-3H
InChI KeyFZWLAAWBMGSTSO-UHFFFAOYSA-N
Canonical SMILESC1=CSC=N1
Molecular FormulaC3H3NS
Wikipediathiazole

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight85.124
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Complexity30.1
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 Area41.1
Monoisotopic Mass84.999
Exact Mass84.999
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count5
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+0.9859
Human Intestinal AbsorptionHIA+0.9680
Caco-2 PermeabilityCaco2+0.5818
P-glycoprotein SubstrateNon-substrate0.8661
P-glycoprotein InhibitorNon-inhibitor0.9635
Non-inhibitor0.9920
Renal Organic Cation TransporterNon-inhibitor0.8522
Distribution
Subcellular localizationMitochondria0.4987
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8840
CYP450 2D6 SubstrateNon-substrate0.9044
CYP450 3A4 SubstrateNon-substrate0.8202
CYP450 1A2 InhibitorInhibitor0.6341
CYP450 2C9 InhibitorNon-inhibitor0.7567
CYP450 2D6 InhibitorNon-inhibitor0.5529
CYP450 2C19 InhibitorInhibitor0.6720
CYP450 3A4 InhibitorNon-inhibitor0.9679
CYP Inhibitory PromiscuityHigh CYP Inhibitory Promiscuity0.7013
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9692
Non-inhibitor0.9620
AMES ToxicityAMES toxic0.6944
CarcinogensNon-carcinogens0.8526
Fish ToxicityHigh FHMT0.5839
Tetrahymena Pyriformis ToxicityHigh TPT0.8427
Honey Bee ToxicityHigh HBT0.6632
BiodegradationNot ready biodegradable0.6582
Acute Oral ToxicityII0.7443
Carcinogenicity (Three-class)Warning0.4821

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-0.1147LogS
Caco-2 Permeability1.5145LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity2.4153LD50, mol/kg
Fish Toxicity2.0290pLC50, mg/L
Tetrahymena Pyriformis Toxicity0.6516pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassAzoles
SubclassThiazoles
Intermediate Tree NodesNot available
Direct ParentThiazoles
Alternative Parents
Molecular FrameworkAromatic heteromonocyclic compounds
SubstituentsHeteroaromatic compound - Thiazole - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound
DescriptionThis 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