Relevant Data

Flavouring Substances Approved by European Union:

  • Hydrogen sulfide [show]

General Information

MaintermHYDROGEN SULFIDE
Doc TypeASP
CAS Reg.No.(or other ID)7783-06-4
Regnum

From www.fda.gov

Computed Descriptors

Download SDF
2D Structure
CID402
IUPAC Namesulfane
InChIInChI=1S/H2S/h1H2
InChI KeyRWSOTUBLDIXVET-UHFFFAOYSA-N
Canonical SMILESS
Molecular FormulaH2S
Wikipediahydrogen sulfide

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight34.076
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Complexity0.0
CACTVS Substructure Key Fingerprint A A A D c Q A A A A B A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A 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 Area1.0
Monoisotopic Mass33.988
Exact Mass33.988
XLogP3None
XLogP3-AA0.5
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count1
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


Food Additives Biosynthesis/Degradation


ADMET Predicted Profile --- Classification

Model Result Probability
Absorption
Blood-Brain BarrierBBB+0.9758
Human Intestinal AbsorptionHIA+0.9913
Caco-2 PermeabilityCaco2+0.7372
P-glycoprotein SubstrateNon-substrate0.8956
P-glycoprotein InhibitorNon-inhibitor0.9765
Non-inhibitor0.9903
Renal Organic Cation TransporterNon-inhibitor0.9215
Distribution
Subcellular localizationLysosome0.5942
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8443
CYP450 2D6 SubstrateNon-substrate0.8344
CYP450 3A4 SubstrateNon-substrate0.8266
CYP450 1A2 InhibitorNon-inhibitor0.8598
CYP450 2C9 InhibitorNon-inhibitor0.8992
CYP450 2D6 InhibitorNon-inhibitor0.9686
CYP450 2C19 InhibitorNon-inhibitor0.9331
CYP450 3A4 InhibitorNon-inhibitor0.9853
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.7956
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9638
Non-inhibitor0.9738
AMES ToxicityNon AMES toxic0.9470
CarcinogensCarcinogens 0.6471
Fish ToxicityHigh FHMT0.6004
Tetrahymena Pyriformis ToxicityLow TPT0.5333
Honey Bee ToxicityHigh HBT0.8726
BiodegradationNot ready biodegradable0.7810
Acute Oral ToxicityIII0.5765
Carcinogenicity (Three-class)Non-required0.5045

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-0.7560LogS
Caco-2 Permeability1.6822LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity2.1523LD50, mol/kg
Fish Toxicity1.5979pLC50, mg/L
Tetrahymena Pyriformis Toxicity-0.1288pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomInorganic compounds
SuperclassHomogeneous non-metal compounds
ClassOther non-metal organides
SubclassOther non-metal sulfides
Intermediate Tree NodesNot available
Direct ParentOther non-metal sulfides
Alternative Parents
Molecular FrameworkNot available
SubstituentsOther non-metal sulfide - Inorganic sulfide
DescriptionThis compound belongs to the class of inorganic compounds known as other non-metal sulfides. These are inorganic compounds containing a sulfur atom of an oxidation state of -2, in which the heaviest atom bonded to the oxygen belongs to the class of other non-metals.

From ClassyFire