Relevant Data

Food Additives Approved in the United States


General Information

CAS number: 80722-28-7
JECFA number: 2060
FEMA number: 4662
Functional Class: Flavouring Agent
FLAVOURING_AGENT

From apps.who.int


Evaluations

Evaluation year: 2010
ADI: No safety concern at current levels of intake when used as a flavouring agent
Specs Code: N
Report: TRS 960-JECFA 73
Tox Monograph: FAS 64-JECFA 73
Specification: Compendium of FAO food additive specifications

From apps.who.int


Computed Descriptors

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2D Structure
CID44147198
IUPAC Name2,6,6,10-tetramethyl-1-oxaspiro[4.5]deca-2,9-dien-8-one
InChIInChI=1S/C13H18O2/c1-9-7-11(14)8-12(3,4)13(9)6-5-10(2)15-13/h5,7H,6,8H2,1-4H3
InChI KeyPYBOFDINXIGETR-UHFFFAOYSA-N
Canonical SMILESCC1=CCC2(O1)C(=CC(=O)CC2(C)C)C
Molecular FormulaC13H18O2
Wikipedia2,6,10,10-tetramethyl-1-oxaspiro(4,5)deca-2,6-dien-8-one

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight206.285
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Complexity374.0
CACTVS Substructure Key Fingerprint A A A D c e B w M A A A A A A A A A A A A A A A A A A A A Q A A A A A g A A A A A A A A A A A A A A A A G g A A A A A A D k S A g A A C A A A A B A C I A q B S A A A A C A A g I A A A C A E A A E g A B B I A I Q A C E A A E w A A I I Q O K i A A P g A A A A A 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 Mass206.131
Exact Mass206.131
XLogP3None
XLogP3-AA2.0
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count15
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+0.9249
Human Intestinal AbsorptionHIA+1.0000
Caco-2 PermeabilityCaco2+0.6787
P-glycoprotein SubstrateSubstrate0.5465
P-glycoprotein InhibitorInhibitor0.7048
Non-inhibitor0.8137
Renal Organic Cation TransporterNon-inhibitor0.8530
Distribution
Subcellular localizationMitochondria0.5360
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8182
CYP450 2D6 SubstrateNon-substrate0.8692
CYP450 3A4 SubstrateSubstrate0.6459
CYP450 1A2 InhibitorNon-inhibitor0.7060
CYP450 2C9 InhibitorNon-inhibitor0.8927
CYP450 2D6 InhibitorNon-inhibitor0.9433
CYP450 2C19 InhibitorNon-inhibitor0.6159
CYP450 3A4 InhibitorNon-inhibitor0.8183
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.7764
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9442
Non-inhibitor0.8928
AMES ToxicityNon AMES toxic0.8787
CarcinogensNon-carcinogens0.8385
Fish ToxicityHigh FHMT0.6674
Tetrahymena Pyriformis ToxicityHigh TPT0.9351
Honey Bee ToxicityHigh HBT0.8908
BiodegradationNot ready biodegradable0.5096
Acute Oral ToxicityIII0.7461
Carcinogenicity (Three-class)Warning0.4596

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-2.0777LogS
Caco-2 Permeability1.6873LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity2.0356LD50, mol/kg
Fish Toxicity0.9623pLC50, mg/L
Tetrahymena Pyriformis Toxicity0.3404pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassOrganic oxygen compounds
ClassOrganooxygen compounds
SubclassCarbonyl compounds
Intermediate Tree NodesKetones - Cyclic ketones
Direct ParentCyclohexenones
Alternative Parents
Molecular FrameworkAliphatic heteropolycyclic compounds
SubstituentsCyclohexenone - Dihydrofuran - Oxacycle - Organoheterocyclic compound - Organic oxide - Hydrocarbon derivative - Aliphatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as cyclohexenones. These are compounds containing a cylohexenone moiety, which is a six-membered aliphatic ring that carries a ketone and has one endocyclic double bond.

From ClassyFire