Relevant Data

Food Additives Approved by WHO:


General Information

Mainterm8-P-MENTHENE-1,2-DIOL
Doc TypeEAF
CAS Reg.No.(or other ID)1946-00-5
Regnum

From www.fda.gov

Computed Descriptors

Download SDF
2D Structure
CID94217
IUPAC Name1-methyl-4-prop-1-en-2-ylcyclohexane-1,2-diol
InChIInChI=1S/C10H18O2/c1-7(2)8-4-5-10(3,12)9(11)6-8/h8-9,11-12H,1,4-6H2,2-3H3
InChI KeyWKZWTZTZWGWEGE-UHFFFAOYSA-N
Canonical SMILESCC(=C)C1CCC(C(C1)O)(C)O
Molecular FormulaC10H18O2
Wikipedialimonene-1,2-diol

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight170.252
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Complexity188.0
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 A A A A A A w A A A A A A A A A A A A A A A A G g A A C A A A D V S g g A I C A A A A A g C A A g B C A A A A A A A g A A A A A A A A A A g B E A I A A Q A A Q A A E g A A B A A G A w P A O A A A A A A A A A A D A A A I A A B C A A A A A A A A A A A = =
Topological Polar Surface Area40.5
Monoisotopic Mass170.131
Exact Mass170.131
XLogP3None
XLogP3-AA1.5
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count12
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count3
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+0.7788
Human Intestinal AbsorptionHIA+0.9582
Caco-2 PermeabilityCaco2+0.7602
P-glycoprotein SubstrateSubstrate0.6931
P-glycoprotein InhibitorNon-inhibitor0.7794
Non-inhibitor0.9737
Renal Organic Cation TransporterNon-inhibitor0.8627
Distribution
Subcellular localizationMitochondria0.6584
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8837
CYP450 2D6 SubstrateNon-substrate0.8597
CYP450 3A4 SubstrateSubstrate0.6380
CYP450 1A2 InhibitorNon-inhibitor0.8322
CYP450 2C9 InhibitorNon-inhibitor0.8913
CYP450 2D6 InhibitorNon-inhibitor0.9165
CYP450 2C19 InhibitorNon-inhibitor0.7863
CYP450 3A4 InhibitorNon-inhibitor0.8730
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.9394
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9093
Non-inhibitor0.7159
AMES ToxicityNon AMES toxic0.8306
CarcinogensNon-carcinogens0.9006
Fish ToxicityHigh FHMT0.9368
Tetrahymena Pyriformis ToxicityHigh TPT0.7038
Honey Bee ToxicityHigh HBT0.7557
BiodegradationNot ready biodegradable0.7174
Acute Oral ToxicityIII0.7797
Carcinogenicity (Three-class)Non-required0.5905

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-2.5068LogS
Caco-2 Permeability1.2832LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity2.2300LD50, mol/kg
Fish Toxicity1.4825pLC50, mg/L
Tetrahymena Pyriformis Toxicity0.3558pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassLipids and lipid-like molecules
ClassPrenol lipids
SubclassMonoterpenoids
Intermediate Tree NodesNot available
Direct ParentMenthane monoterpenoids
Alternative Parents
Molecular FrameworkAliphatic homomonocyclic compounds
SubstituentsP-menthane monoterpenoid - Monocyclic monoterpenoid - Cyclohexanol - Tertiary alcohol - Cyclic alcohol - Secondary alcohol - 1,2-diol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aliphatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes.

From ClassyFire