Lenthionine
General Information
Chemical name | Lenthionine |
CAS number | 292-46-6 |
COE number | 11619 |
Flavouring type | substances |
FL No. | 15.081 |
Mixture | No |
Purity of the named substance at least 95% unless otherwise specified | |
Reference body | EFSA |
From webgate.ec.europa.eu
Computed Descriptors
Download SDF2D Structure | |
CID | 67521 |
IUPAC Name | 1,2,3,5,6-pentathiepane |
InChI | InChI=1S/C2H4S5/c1-3-4-2-6-7-5-1/h1-2H2 |
InChI Key | DZKOKXZNCDGVRY-UHFFFAOYSA-N |
Canonical SMILES | C1SSCSSS1 |
Molecular Formula | C2H4S5 |
Wikipedia | lenthionine |
From Pubchem
Computed Properties
Property Name | Property Value |
---|---|
Molecular Weight | 188.354 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 5 |
Rotatable Bond Count | 0 |
Complexity | 39.3 |
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 Area | 127.0 |
Monoisotopic Mass | 187.892 |
Exact Mass | 187.892 |
Compound Is Canonicalized | True |
Formal Charge | 0 |
Heavy Atom Count | 7 |
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+ | 0.9711 |
Human Intestinal Absorption | HIA+ | 0.9502 |
Caco-2 Permeability | Caco2+ | 0.5270 |
P-glycoprotein Substrate | Non-substrate | 0.7198 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.9098 |
Non-inhibitor | 0.9839 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.8301 |
Distribution | ||
Subcellular localization | Mitochondria | 0.5332 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.8674 |
CYP450 2D6 Substrate | Non-substrate | 0.8195 |
CYP450 3A4 Substrate | Non-substrate | 0.7712 |
CYP450 1A2 Inhibitor | Non-inhibitor | 0.7266 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.7321 |
CYP450 2D6 Inhibitor | Non-inhibitor | 0.8342 |
CYP450 2C19 Inhibitor | Non-inhibitor | 0.6990 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.9456 |
CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.6555 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9374 |
Non-inhibitor | 0.9352 | |
AMES Toxicity | AMES toxic | 0.5642 |
Carcinogens | Non-carcinogens | 0.6238 |
Fish Toxicity | Low FHMT | 0.5780 |
Tetrahymena Pyriformis Toxicity | High TPT | 0.8700 |
Honey Bee Toxicity | High HBT | 0.7728 |
Biodegradation | Not ready biodegradable | 0.9276 |
Acute Oral Toxicity | II | 0.5240 |
Carcinogenicity (Three-class) | Non-required | 0.5004 |
From admetSAR
ADMET Predicted Profile --- Regression
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | -2.3933 | LogS |
Caco-2 Permeability | 1.4959 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 2.7280 | LD50, mol/kg |
Fish Toxicity | 1.9118 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | 0.4239 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
Kingdom | Organic compounds |
---|---|
Superclass | Organosulfur compounds |
Class | Organic trisulfides |
Subclass | Not available |
Intermediate Tree Nodes | Not available |
Direct Parent | Organic trisulfides |
Alternative Parents | |
Molecular Framework | Aliphatic heteromonocyclic compounds |
Substituents | Organic trisulfide - Organic disulfide - Organoheterocyclic compound - Hydrocarbon derivative - Aliphatic heteromonocyclic compound |
Description | This 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