Bis(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,12-heneicosafluoro-1-dodecanol) hydrogen phosphate

Predicted ADME Properties
TypePropertyToolInterpretationProbability/Value
AbsorptionCaco-2 permeabilityadmetSARLow43.82 %
pkCSMHigh0.996 cm/s
Human Intestinal AbsorptionadmetSARHigh68.48 %
pkCSMHigh50.563 %
SwissADMELow-
Human Oral BioavailabilityadmetSARHigh Bioavailability51.75 %
Log Kp (Skin permeation)pkCSMHigh-2.735 logkp (cm/h)
SwissADME--3.62 logkp (cm/s)
DistributionP-glycoprotein substrateadmetSARLow9.71 %
pkCSMNo-
SwissADMEYes-
vNNNo Prediction-
P-glycoprotein inhibitoradmetSARLow36.59 %
vNNNo Prediction-
P-glycoprotein inhibitor IpkCSMYes-
P-glycoprotein inhibitor IIpkCSMYes-
Blood Brain BarrieradmetSARHigh61.51 %
pkCSMYes0.468 logBB
SwissADMENo-
vNNNo Prediction-
CNS permeabilitypkCSMNo-3.706 logPS
Fraction unbound in humanpkCSM-0.212
Plasma protein bindingadmetSAR109.26 %High
Steady state volume of distribution (VDss)pkCSMLow-0.729 log(L/kg)
MetabolismCYP1A2 inhibitoradmetSARLow20.77 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2C19 inhibitoradmetSARLow13.98 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2C9 inhibitoradmetSARLow22.25 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2C9 substrateadmetSARLow13.12 %
CYP2D6 inhibitoradmetSARLow6.19 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2D6 substrateadmetSARLow3.2 %
pkCSMNo-
CYP3A4 inhibitoradmetSARLow7.62 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP3A4 substrateadmetSARLow15.74 %
pkCSMYes-
Human Liver Microsomal (HLM) stability assayvNNNo Prediction-
OATP2B1 inhibitoradmetSARHigh55.37 %
OATP1B1 inhibitoradmetSARHigh70.7 %
OATP1B3 inhibitoradmetSARHigh76.4 %
MATE1 inhibitoradmetSARLow11.92 %
BSEP inhibitoradmetSARHigh54.95 %
UGT catalysisadmetSARHigh69.61 %
ExcretionRenal OCT2 inhibitoradmetSARLow23.15 %
Renal OCT2 substratepkCSMNo-
Total clearancepkCSM-2.113 ml/min/kg
Download
Predicted Toxicity properties
PropertyToolInterpretationProbability/Value
Acute oral toxicityadmetSAR--3.57921743392944 log(mg/kg)
ProTox-10000 mg/kg
Acute oral toxicity classadmetSARLow12.49 %
ProTox6-
BiodegradationadmetSARLow40.05 %
ToxtreeClass 2 (persistent chemical)-
CarcinogensadmetSARLow5.5 %
ToxtreeNo-
Cramer's ruleToxtreeHigh (Class III)-
CytotoxicityvNNNoPrediction-
Genotoxic carcinogenityToxtreeNo-
HepatotoxicityadmetSARLow25.8 %
pkCSMYes-
vNNNoPrediction-
Human Ether-a-go-go-Related Gene InhibitoradmetSARLow36.94 %
vNNNoPrediction-
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)pkCSMHigh0.519 log(mg/kg/day)
vNN-NoPrediction
Non-Genotoxic carcinogenicityToxtreeYes-
Oral rat acute toxicitypkCSM-1.51 log(mg/kg_bw/day) (LD50)
pkCSM-0.065 log(mg/kg_bw/day) (LOAEL)
MicronucleusadmetSARLow20.31 %
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.