Tris(1,3-dichloro-2-propyl)phosphate

Predicted ADME Properties
TypePropertyToolInterpretationProbability/Value
AbsorptionCaco-2 permeabilityadmetSARHigh83.81 %
pkCSMHigh1.164 cm/s
Human Intestinal AbsorptionadmetSARHigh97.71 %
pkCSMHigh89.06 %
SwissADMEHigh-
Human Oral BioavailabilityadmetSARLow Bioavailability13.72 %
Log Kp (Skin permeation)pkCSMLow-2.341 logkp (cm/h)
SwissADME--6.34 logkp (cm/s)
DistributionP-glycoprotein substrateadmetSARLow17.38 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
P-glycoprotein inhibitoradmetSARLow43.0 %
vNNNo Prediction-
P-glycoprotein inhibitor IpkCSMNo-
P-glycoprotein inhibitor IIpkCSMNo-
Blood Brain BarrieradmetSARHigh92.28 %
pkCSMModerate-0.568 logBB
SwissADMEYes-
vNNNo Prediction-
CNS permeabilitypkCSMModerate-2.974 logPS
Fraction unbound in humanpkCSM-0.308
Plasma protein bindingadmetSAR90.59 %High
Steady state volume of distribution (VDss)pkCSMLow-0.335 log(L/kg)
MetabolismCYP1A2 inhibitoradmetSARLow37.02 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2C19 inhibitoradmetSARLow40.84 %
pkCSMNo-
SwissADMEYes-
vNNNo Prediction-
CYP2C9 inhibitoradmetSARLow24.9 %
pkCSMNo-
SwissADMEYes-
vNNNo Prediction-
CYP2C9 substrateadmetSARLow34.58 %
CYP2D6 inhibitoradmetSARLow5.11 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2D6 substrateadmetSARLow29.58 %
pkCSMNo-
CYP3A4 inhibitoradmetSARLow5.19 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP3A4 substrateadmetSARHigh78.33 %
pkCSMNo-
Human Liver Microsomal (HLM) stability assayvNNNo Prediction-
OATP2B1 inhibitoradmetSARLow17.67 %
OATP1B1 inhibitoradmetSARHigh93.82 %
OATP1B3 inhibitoradmetSARHigh94.63 %
MATE1 inhibitoradmetSARLow11.26 %
BSEP inhibitoradmetSARHigh87.28 %
UGT catalysisadmetSARLow11.34 %
ExcretionRenal OCT2 inhibitoradmetSARLow14.65 %
Renal OCT2 substratepkCSMNo-
Total clearancepkCSM-1.689 ml/min/kg
Download
Predicted Toxicity properties
PropertyToolInterpretationProbability/Value
Acute oral toxicityadmetSAR--3.34460926055908 log(mg/kg)
ProTox-1850 mg/kg
Acute oral toxicity classadmetSARHigh67.22 %
ProTox4-
BiodegradationadmetSARLow7.94 %
ToxtreeClass 1 (easily biodegradable chemical)-
CarcinogensadmetSARHigh89.94 %
ToxtreeNo-
Cramer's ruleToxtreeHigh (Class III)-
CytotoxicityvNNNoPrediction-
Genotoxic carcinogenityToxtreeYes-
HepatotoxicityadmetSARHigh69.37 %
pkCSMNo-
vNNNoPrediction-
Human Ether-a-go-go-Related Gene InhibitoradmetSARLow29.47 %
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)pkCSMHigh0.482 log(mg/kg/day)
vNN-NoPrediction
Non-Genotoxic carcinogenicityToxtreeNo-
Oral rat acute toxicitypkCSM-3.25 log(mg/kg_bw/day) (LD50)
pkCSM--0.358 log(mg/kg_bw/day) (LOAEL)
MicronucleusadmetSARHigh65.66 %
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.