General Information

MaintermDIBUTYL ITACONATE
CAS Reg.No.(or other ID)2155-60-4
Regnum 175.105
176.170
176.180

From www.fda.gov

Computed Descriptors

Download SDF
2D Structure
CID75080
IUPAC Namedibutyl 2-methylidenebutanedioate
InChIInChI=1S/C13H22O4/c1-4-6-8-16-12(14)10-11(3)13(15)17-9-7-5-2/h3-10H2,1-2H3
InChI KeyOGVXYCDTRMDYOG-UHFFFAOYSA-N
Canonical SMILESCCCCOC(=O)CC(=C)C(=O)OCCCC
Molecular FormulaC13H22O4

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight242.315
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count4
Rotatable Bond Count11
Complexity258.0
CACTVS Substructure Key Fingerprint A A A D c e B w 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 D A C g g A I C C A A A B A C I A g D S C A A A A A A g A A A A A A E A A E g A B B A A I Q A C A A A E Q A A A I I B D 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 Area52.6
Monoisotopic Mass242.152
Exact Mass242.152
XLogP3None
XLogP3-AA3.0
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count17
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


ADMET Predicted Profile --- Classification

Model Result Probability
Absorption
Blood-Brain BarrierBBB+0.8437
Human Intestinal AbsorptionHIA+0.9410
Caco-2 PermeabilityCaco2+0.6178
P-glycoprotein SubstrateSubstrate0.5148
P-glycoprotein InhibitorNon-inhibitor0.5897
Non-inhibitor0.8841
Renal Organic Cation TransporterNon-inhibitor0.8602
Distribution
Subcellular localizationMitochondria0.7623
Metabolism
CYP450 2C9 SubstrateNon-substrate0.9115
CYP450 2D6 SubstrateNon-substrate0.8800
CYP450 3A4 SubstrateNon-substrate0.5707
CYP450 1A2 InhibitorNon-inhibitor0.7758
CYP450 2C9 InhibitorNon-inhibitor0.8594
CYP450 2D6 InhibitorNon-inhibitor0.9016
CYP450 2C19 InhibitorNon-inhibitor0.8097
CYP450 3A4 InhibitorNon-inhibitor0.8002
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.7697
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.8510
Non-inhibitor0.9188
AMES ToxicityNon AMES toxic0.9403
CarcinogensNon-carcinogens0.5744
Fish ToxicityHigh FHMT0.9957
Tetrahymena Pyriformis ToxicityHigh TPT0.9959
Honey Bee ToxicityHigh HBT0.7979
BiodegradationReady biodegradable0.9590
Acute Oral ToxicityIV0.8477
Carcinogenicity (Three-class)Non-required0.6467

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-3.6348LogS
Caco-2 Permeability0.7530LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity1.2125LD50, mol/kg
Fish Toxicity-0.0534pLC50, mg/L
Tetrahymena Pyriformis Toxicity1.3675pIGC50, 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