General Information

MaintermHEXYL MALEATE
CAS Reg.No.(or other ID)16064-83-8
Regnum 175.300
176.170

From www.fda.gov

Computed Descriptors

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2D Structure
CID5271573
IUPAC Namedihexyl (Z)-but-2-enedioate
InChIInChI=1S/C16H28O4/c1-3-5-7-9-13-19-15(17)11-12-16(18)20-14-10-8-6-4-2/h11-12H,3-10,13-14H2,1-2H3/b12-11-
InChI KeyQMCVOSQFZZCSLN-QXMHVHEDSA-N
Canonical SMILESCCCCCCOC(=O)C=CC(=O)OCCCCCC
Molecular FormulaC16H28O4

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight284.396
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count4
Rotatable Bond Count14
Complexity256.0
CACTVS Substructure Key Fingerprint A A A D c e B 4 O 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 G g A A A A A A C A C g g A I C C A A A B A C I A C D S C A A A A A A A A A A I C A A A A E A A B A I A I A A C E A A E A A A A I Y G A Q 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 Area52.6
Monoisotopic Mass284.199
Exact Mass284.199
XLogP3None
XLogP3-AA4.9
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count20
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
Isotope Atom Count0
Covalently-Bonded Unit Count1

From Pubchem


ADMET Predicted Profile --- Classification

Model Result Probability
Absorption
Blood-Brain BarrierBBB+0.9564
Human Intestinal AbsorptionHIA+0.9743
Caco-2 PermeabilityCaco2+0.6670
P-glycoprotein SubstrateNon-substrate0.5673
P-glycoprotein InhibitorNon-inhibitor0.7957
Non-inhibitor0.8126
Renal Organic Cation TransporterNon-inhibitor0.8818
Distribution
Subcellular localizationMitochondria0.7397
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8679
CYP450 2D6 SubstrateNon-substrate0.8928
CYP450 3A4 SubstrateNon-substrate0.6129
CYP450 1A2 InhibitorNon-inhibitor0.8020
CYP450 2C9 InhibitorNon-inhibitor0.9202
CYP450 2D6 InhibitorNon-inhibitor0.9069
CYP450 2C19 InhibitorNon-inhibitor0.9136
CYP450 3A4 InhibitorNon-inhibitor0.8873
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.8342
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9056
Non-inhibitor0.8928
AMES ToxicityNon AMES toxic0.9453
CarcinogensNon-carcinogens0.5558
Fish ToxicityHigh FHMT0.9854
Tetrahymena Pyriformis ToxicityHigh TPT0.9992
Honey Bee ToxicityHigh HBT0.7281
BiodegradationReady biodegradable0.8582
Acute Oral ToxicityIV0.6445
Carcinogenicity (Three-class)Non-required0.6977

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-3.6033LogS
Caco-2 Permeability0.6631LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity1.4785LD50, mol/kg
Fish Toxicity-0.1852pLC50, mg/L
Tetrahymena Pyriformis Toxicity1.1612pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassLipids and lipid-like molecules
ClassFatty Acyls
SubclassFatty acid esters
Intermediate Tree NodesNot available
Direct ParentFatty acid esters
Alternative Parents
Molecular FrameworkAliphatic acyclic compounds
SubstituentsFatty acid ester - Dicarboxylic acid or derivatives - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Carboxylic acid ester - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid.

From ClassyFire