Relevant Data

Food Additives Approved by WHO:

Flavouring Substances Approved by European Union:

  • Hexano-1,5-lactone [show]

General Information

MaintermDELTA-HEXALACTONE
Doc TypeASP
CAS Reg.No.(or other ID)823-22-3
Regnum

From www.fda.gov

Computed Descriptors

Download SDF
2D Structure
CID13204
IUPAC Name6-methyloxan-2-one
InChIInChI=1S/C6H10O2/c1-5-3-2-4-6(7)8-5/h5H,2-4H2,1H3
InChI KeyRZTOWFMDBDPERY-UHFFFAOYSA-N
Canonical SMILESCC1CCCC(=O)O1
Molecular FormulaC6H10O2
Wikipediaδ-hexalactone

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight114.144
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Complexity98.7
CACTVS Substructure Key Fingerprint A A A D c c B g M A A A 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 G g A A A A A A C B S g g A I C C A A A B A A I A A C Q C A A A A A A A A A A A A A E A A A A A A B I A A A A C A A A E A A A A A A G I T 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 = =
Topological Polar Surface Area26.3
Monoisotopic Mass114.068
Exact Mass114.068
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count8
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
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+0.9620
Human Intestinal AbsorptionHIA+0.9894
Caco-2 PermeabilityCaco2+0.8321
P-glycoprotein SubstrateNon-substrate0.7171
P-glycoprotein InhibitorNon-inhibitor0.9086
Non-inhibitor0.9719
Renal Organic Cation TransporterNon-inhibitor0.8057
Distribution
Subcellular localizationMitochondria0.5822
Metabolism
CYP450 2C9 SubstrateNon-substrate0.7944
CYP450 2D6 SubstrateNon-substrate0.8249
CYP450 3A4 SubstrateNon-substrate0.6084
CYP450 1A2 InhibitorNon-inhibitor0.7126
CYP450 2C9 InhibitorNon-inhibitor0.9427
CYP450 2D6 InhibitorNon-inhibitor0.9678
CYP450 2C19 InhibitorNon-inhibitor0.8354
CYP450 3A4 InhibitorNon-inhibitor0.9664
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.9843
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.8501
Non-inhibitor0.9581
AMES ToxicityNon AMES toxic0.9429
CarcinogensNon-carcinogens0.9212
Fish ToxicityLow FHMT0.8077
Tetrahymena Pyriformis ToxicityLow TPT0.7038
Honey Bee ToxicityHigh HBT0.7035
BiodegradationReady biodegradable0.9048
Acute Oral ToxicityIII0.6381
Carcinogenicity (Three-class)Non-required0.6063

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-0.9821LogS
Caco-2 Permeability1.5628LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity1.4125LD50, mol/kg
Fish Toxicity2.3600pLC50, mg/L
Tetrahymena Pyriformis Toxicity-0.9899pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassLactones
SubclassDelta valerolactones
Intermediate Tree NodesNot available
Direct ParentDelta valerolactones
Alternative Parents
Molecular FrameworkAliphatic heteromonocyclic compounds
SubstituentsDelta_valerolactone - Delta valerolactone - Oxane - Carboxylic acid ester - Oxacycle - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as delta valerolactones. These are cyclic organic compounds containing an oxan-2- one moiety.

From ClassyFire