1,3,5-Tribromo-2-(prop-2-en-1-yloxy)benzene

Predicted ADME Properties
TypePropertyToolInterpretationProbability/Value
AbsorptionCaco-2 permeabilityadmetSARHigh98.65 %
pkCSMHigh1.557 cm/s
Human Intestinal AbsorptionadmetSARHigh98.83 %
pkCSMHigh91.242 %
SwissADMEHigh-
Human Oral BioavailabilityadmetSARLow Bioavailability36.41 %
Log Kp (Skin permeation)pkCSMLow-1.749 logkp (cm/h)
SwissADME--4.93 logkp (cm/s)
DistributionP-glycoprotein substrateadmetSARLow4.24 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
P-glycoprotein inhibitoradmetSARLow29.61 %
vNNNo Prediction-
P-glycoprotein inhibitor IpkCSMNo-
P-glycoprotein inhibitor IIpkCSMNo-
Blood Brain BarrieradmetSARHigh98.42 %
pkCSMYes0.445 logBB
SwissADMEYes-
vNNNo Prediction-
CNS permeabilitypkCSMYes-1.986 logPS
Fraction unbound in humanpkCSM-0.175
Plasma protein bindingadmetSAR99.55 %High
Steady state volume of distribution (VDss)pkCSMModerate0.263 log(L/kg)
MetabolismCYP1A2 inhibitoradmetSARHigh96.53 %
pkCSMYes-
SwissADMEYes-
vNNNo Prediction-
CYP2C19 inhibitoradmetSARHigh94.49 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2C9 inhibitoradmetSARHigh58.94 %
pkCSMNo-
SwissADMEYes-
vNNNo Prediction-
CYP2C9 substrateadmetSARLow49.23 %
CYP2D6 inhibitoradmetSARLow36.9 %
pkCSMNo-
SwissADMEYes-
vNNNo Prediction-
CYP2D6 substrateadmetSARLow36.99 %
pkCSMNo-
CYP3A4 inhibitoradmetSARLow6.17 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP3A4 substrateadmetSARHigh65.69 %
pkCSMNo-
Human Liver Microsomal (HLM) stability assayvNNNo Prediction-
OATP2B1 inhibitoradmetSARLow12.2 %
OATP1B1 inhibitoradmetSARHigh97.41 %
OATP1B3 inhibitoradmetSARHigh98.25 %
MATE1 inhibitoradmetSARLow6.61 %
BSEP inhibitoradmetSARHigh78.09 %
UGT catalysisadmetSARLow4.92 %
ExcretionRenal OCT2 inhibitoradmetSARLow33.99 %
Renal OCT2 substratepkCSMNo-
Total clearancepkCSM-0.011 ml/min/kg
Download
Predicted Toxicity properties
PropertyToolInterpretationProbability/Value
Acute oral toxicityadmetSAR--3.1532187461853 log(mg/kg)
ProTox-10000 mg/kg
Acute oral toxicity classadmetSARHigh59.12 %
ProTox6-
BiodegradationadmetSARLow6.31 %
ToxtreeClass 3 (unknown biodegradability)-
CarcinogensadmetSARHigh54.3 %
ToxtreeNo-
Cramer's ruleToxtreeHigh (Class III)-
CytotoxicityvNNNoPrediction-
Genotoxic carcinogenityToxtreeNo-
HepatotoxicityadmetSARHigh75.27 %
pkCSMNo-
vNNNoPrediction-
Human Ether-a-go-go-Related Gene InhibitoradmetSARLow45.19 %
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)pkCSMHigh0.922 log(mg/kg/day)
vNN-163 mg/day
Non-Genotoxic carcinogenicityToxtreeNo-
Oral rat acute toxicitypkCSM-2.805 log(mg/kg_bw/day) (LD50)
pkCSM-1.068 log(mg/kg_bw/day) (LOAEL)
MicronucleusadmetSARLow18.25 %
Skin sensitisationpkCSMYes-
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.