Bis(2-methoxyethyl) phthalate

Predicted ADME Properties
TypePropertyToolInterpretationProbability/Value
AbsorptionCaco-2 permeabilityadmetSARHigh95.38 %
pkCSMLow0.598 cm/s
Human Intestinal AbsorptionadmetSARHigh95.61 %
pkCSMHigh90.292 %
SwissADMEHigh-
Human Oral BioavailabilityadmetSARHigh Bioavailability71.75 %
Log Kp (Skin permeation)pkCSMHigh-2.764 logkp (cm/h)
SwissADME--7.04 logkp (cm/s)
DistributionP-glycoprotein substrateadmetSARLow2.2 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
P-glycoprotein inhibitoradmetSARLow3.59 %
vNNNo-
P-glycoprotein inhibitor IpkCSMNo-
P-glycoprotein inhibitor IIpkCSMNo-
Blood Brain BarrieradmetSARHigh96.17 %
pkCSMModerate-0.785 logBB
SwissADMENo-
vNNNo Prediction-
CNS permeabilitypkCSMModerate-2.99 logPS
Fraction unbound in humanpkCSM-0.347
Plasma protein bindingadmetSAR39.55 %Moderate
Steady state volume of distribution (VDss)pkCSMLow-0.438 log(L/kg)
MetabolismCYP1A2 inhibitoradmetSARLow31.09 %
pkCSMNo-
SwissADMEYes-
vNNNo Prediction-
CYP2C19 inhibitoradmetSARLow49.54 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2C9 inhibitoradmetSARLow16.46 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2C9 substrateadmetSARLow6.39 %
CYP2D6 inhibitoradmetSARLow1.18 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2D6 substrateadmetSARLow1.92 %
pkCSMNo-
CYP3A4 inhibitoradmetSARLow1.22 %
pkCSMNo-
SwissADMENo-
vNNNo-
CYP3A4 substrateadmetSARLow5.38 %
pkCSMNo-
Human Liver Microsomal (HLM) stability assayvNNNo Prediction-
OATP2B1 inhibitoradmetSARLow5.5 %
OATP1B1 inhibitoradmetSARHigh99.49 %
OATP1B3 inhibitoradmetSARHigh99.71 %
MATE1 inhibitoradmetSARLow2.19 %
BSEP inhibitoradmetSARLow7.99 %
UGT catalysisadmetSARLow43.97 %
ExcretionRenal OCT2 inhibitoradmetSARLow5.98 %
Renal OCT2 substratepkCSMNo-
Total clearancepkCSM-0.955 ml/min/kg
Download
Predicted Toxicity properties
PropertyToolInterpretationProbability/Value
Acute oral toxicityadmetSAR--3.63042068481445 log(mg/kg)
ProTox-3200 mg/kg
Acute oral toxicity classadmetSARLow4.11 %
ProTox5-
BiodegradationadmetSARHigh82.06 %
ToxtreeClass 2 (persistent chemical)-
CarcinogensadmetSARLow17.45 %
ToxtreeNo-
Cramer's ruleToxtreeLow (Class I)-
CytotoxicityvNNNoPrediction-
Genotoxic carcinogenityToxtreeNo-
HepatotoxicityadmetSARHigh65.9 %
pkCSMNo-
vNNNo-
Human Ether-a-go-go-Related Gene InhibitoradmetSARLow6.16 %
vNNNo-
Human Ether-a-go-go-Related Gene Inhibitor IpkCSMNo-
Human Ether-a-go-go-Related Gene Inhibitor IIpkCSMNo-
Mitochondrial Membrane Potential (MMP)vNNNo-
Maximum Recommended Tolerated Dose (MRTD)pkCSMHigh1.408 log(mg/kg/day)
vNN-268 mg/day
Non-Genotoxic carcinogenicityToxtreeYes-
Oral rat acute toxicitypkCSM-2.312 log(mg/kg_bw/day) (LD50)
pkCSM-1.209 log(mg/kg_bw/day) (LOAEL)
MicronucleusadmetSARLow4.32 %
Skin sensitisationpkCSMNo-
Download

DISCLAIMER

We have built a comprehensive resource which compiles potential endocrine disrupting chemicals (EDCs) based on the observed adverse effects or endocrine-mediated endpoints in published experiments on humans or rodents to support basic research. We are not responsible for any errors or omissions in the published research articles or supporting literature on potential EDCs compiled in this resource. Users are advised to exercise their own judgement on the weight of evidence for potential EDCs compiled in this resource. Importantly, our sole goal to build this resource on potential EDCs is to enable future basic research towards better understanding of the systems-level perturbations upon chemical exposure rather than influencing regulatory advice on chemical use.