General Information

Chemical nameLenthionine
CAS number292-46-6
COE number11619
Flavouring typesubstances
FL No.15.081
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
CID67521
IUPAC Name1,2,3,5,6-pentathiepane
InChIInChI=1S/C2H4S5/c1-3-4-2-6-7-5-1/h1-2H2
InChI KeyDZKOKXZNCDGVRY-UHFFFAOYSA-N
Canonical SMILESC1SSCSSS1
Molecular FormulaC2H4S5
Wikipedialenthionine

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight188.354
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count5
Rotatable Bond Count0
Complexity39.3
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 A A A A A B I 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 Area127.0
Monoisotopic Mass187.892
Exact Mass187.892
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count7
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+0.9711
Human Intestinal AbsorptionHIA+0.9502
Caco-2 PermeabilityCaco2+0.5270
P-glycoprotein SubstrateNon-substrate0.7198
P-glycoprotein InhibitorNon-inhibitor0.9098
Non-inhibitor0.9839
Renal Organic Cation TransporterNon-inhibitor0.8301
Distribution
Subcellular localizationMitochondria0.5332
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8674
CYP450 2D6 SubstrateNon-substrate0.8195
CYP450 3A4 SubstrateNon-substrate0.7712
CYP450 1A2 InhibitorNon-inhibitor0.7266
CYP450 2C9 InhibitorNon-inhibitor0.7321
CYP450 2D6 InhibitorNon-inhibitor0.8342
CYP450 2C19 InhibitorNon-inhibitor0.6990
CYP450 3A4 InhibitorNon-inhibitor0.9456
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.6555
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9374
Non-inhibitor0.9352
AMES ToxicityAMES toxic0.5642
CarcinogensNon-carcinogens0.6238
Fish ToxicityLow FHMT0.5780
Tetrahymena Pyriformis ToxicityHigh TPT0.8700
Honey Bee ToxicityHigh HBT0.7728
BiodegradationNot ready biodegradable0.9276
Acute Oral ToxicityII0.5240
Carcinogenicity (Three-class)Non-required0.5004

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-2.3933LogS
Caco-2 Permeability1.4959LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity2.7280LD50, mol/kg
Fish Toxicity1.9118pLC50, mg/L
Tetrahymena Pyriformis Toxicity0.4239pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassOrganosulfur compounds
ClassOrganic trisulfides
SubclassNot available
Intermediate Tree NodesNot available
Direct ParentOrganic trisulfides
Alternative Parents
Molecular FrameworkAliphatic heteromonocyclic compounds
SubstituentsOrganic trisulfide - Organic disulfide - Organoheterocyclic compound - Hydrocarbon derivative - Aliphatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as organic trisulfides. These are organosulfur compounds with the general formula RSSSR' (R,R'=alkyl, aryl).

From ClassyFire