General Information

Chemical name1,2,4,5-Tetrathiane
CAS number291-22-5
Flavouring typesubstances
FL No.15.103
MixtureNo
Purity of the named substance at least 95% unless otherwise specified
Reference bodyEFSA

From webgate.ec.europa.eu

Computed Descriptors

Download SDF
2D Structure
CID520409
IUPAC Name1,2,4,5-tetrathiane
InChIInChI=1S/C2H4S4/c1-3-5-2-6-4-1/h1-2H2
InChI KeyVXTWQLLUXWBOGW-UHFFFAOYSA-N
Canonical SMILESC1SSCSS1
Molecular FormulaC2H4S4
WikipediaS-tetrathiane

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight156.294
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count4
Rotatable Bond Count0
Complexity26.5
CACTVS Substructure Key Fingerprint A A A D c Y B A A A B w A A A A A A A A A A A A A A A A A A A A A A A k A A A A A A A A A A A A A A A A E A Q A A A A A A A A A A A C 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 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 Area101.0
Monoisotopic Mass155.92
Exact Mass155.92
XLogP3None
XLogP3-AA1.6
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count6
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+0.9684
Human Intestinal AbsorptionHIA+0.9401
Caco-2 PermeabilityCaco2+0.5936
P-glycoprotein SubstrateNon-substrate0.7025
P-glycoprotein InhibitorNon-inhibitor0.9495
Non-inhibitor0.9956
Renal Organic Cation TransporterNon-inhibitor0.8282
Distribution
Subcellular localizationMitochondria0.6452
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8808
CYP450 2D6 SubstrateNon-substrate0.8301
CYP450 3A4 SubstrateNon-substrate0.7994
CYP450 1A2 InhibitorNon-inhibitor0.5841
CYP450 2C9 InhibitorNon-inhibitor0.6560
CYP450 2D6 InhibitorNon-inhibitor0.7517
CYP450 2C19 InhibitorNon-inhibitor0.6142
CYP450 3A4 InhibitorNon-inhibitor0.8357
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.5798
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.8935
Non-inhibitor0.9517
AMES ToxicityAMES toxic0.6121
CarcinogensNon-carcinogens0.7183
Fish ToxicityLow FHMT0.8331
Tetrahymena Pyriformis ToxicityHigh TPT0.7693
Honey Bee ToxicityHigh HBT0.7495
BiodegradationNot ready biodegradable0.9641
Acute Oral ToxicityII0.4989
Carcinogenicity (Three-class)Non-required0.5017

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-1.5102LogS
Caco-2 Permeability1.6870LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity2.5094LD50, mol/kg
Fish Toxicity2.3110pLC50, mg/L
Tetrahymena Pyriformis Toxicity0.0851pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassTetrathianes
SubclassNot available
Intermediate Tree NodesNot available
Direct ParentTetrathianes
Alternative Parents
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents1,2,4,5-tetrathiane - Organic disulfide - Hydrocarbon derivative - Aliphatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as tetrathianes. These are organic compounds containing a tetrathiane ring, which is a six-member saturated aliphatic ring made up of four sulfur atoms and two carbon atoms.

From ClassyFire