Hexachlorobenzene

Predicted ADME Properties
TypePropertyToolInterpretationProbability/Value
AbsorptionCaco-2 permeabilityadmetSARHigh85.7 %
pkCSMHigh1.602 cm/s
Human Intestinal AbsorptionadmetSARHigh90.25 %
pkCSMHigh85.938 %
SwissADMELow-
Human Oral BioavailabilityadmetSARLow Bioavailability42.67 %
Log Kp (Skin permeation)pkCSMLow-1.257 logkp (cm/h)
SwissADME--3.97 logkp (cm/s)
DistributionP-glycoprotein substrateadmetSARLow1.53 %
pkCSMNo-
SwissADMENo-
vNNNo-
P-glycoprotein inhibitoradmetSARLow30.87 %
vNNNo-
P-glycoprotein inhibitor IpkCSMNo-
P-glycoprotein inhibitor IIpkCSMNo-
Blood Brain BarrieradmetSARHigh92.26 %
pkCSMModerate0.156 logBB
SwissADMENo-
vNNNo Prediction-
CNS permeabilitypkCSMYes-1.831 logPS
Fraction unbound in humanpkCSM-0.182
Plasma protein bindingadmetSAR102.3 %High
Steady state volume of distribution (VDss)pkCSMModerate0.125 log(L/kg)
MetabolismCYP1A2 inhibitoradmetSARHigh88.4 %
pkCSMYes-
SwissADMENo-
vNNNo Prediction-
CYP2C19 inhibitoradmetSARHigh70.34 %
pkCSMYes-
SwissADMENo-
vNNNo Prediction-
CYP2C9 inhibitoradmetSARLow46.0 %
pkCSMNo-
SwissADMEYes-
vNNNo Prediction-
CYP2C9 substrateadmetSARHigh53.89 %
CYP2D6 inhibitoradmetSARLow16.96 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2D6 substrateadmetSARLow12.12 %
pkCSMNo-
CYP3A4 inhibitoradmetSARLow4.16 %
pkCSMNo-
SwissADMENo-
vNNNo-
CYP3A4 substrateadmetSARLow48.11 %
pkCSMNo-
Human Liver Microsomal (HLM) stability assayvNNNo Prediction-
OATP2B1 inhibitoradmetSARLow36.01 %
OATP1B1 inhibitoradmetSARHigh89.98 %
OATP1B3 inhibitoradmetSARHigh94.09 %
MATE1 inhibitoradmetSARLow9.07 %
BSEP inhibitoradmetSARHigh75.95 %
UGT catalysisadmetSARLow10.9 %
ExcretionRenal OCT2 inhibitoradmetSARLow18.08 %
Renal OCT2 substratepkCSMNo-
Total clearancepkCSM-0.676 ml/min/kg
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Predicted Toxicity properties
PropertyToolInterpretationProbability/Value
Acute oral toxicityadmetSAR--2.62930583953857 log(mg/kg)
ProTox-300 mg/kg
Acute oral toxicity classadmetSARLow34.55 %
ProTox3-
BiodegradationadmetSARLow15.1 %
ToxtreeClass 2 (persistent chemical)-
CarcinogensadmetSARLow14.94 %
ToxtreeNo-
Cramer's ruleToxtreeHigh (Class III)-
CytotoxicityvNNNoPrediction-
Genotoxic carcinogenityToxtreeNo-
HepatotoxicityadmetSARHigh56.82 %
pkCSMNo-
vNNNoPrediction-
Human Ether-a-go-go-Related Gene InhibitoradmetSARHigh53.43 %
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)pkCSMHigh0.636 log(mg/kg/day)
vNN-NoPrediction
Non-Genotoxic carcinogenicityToxtreeNo-
Oral rat acute toxicitypkCSM-3.286 log(mg/kg_bw/day) (LD50)
pkCSM-0.383 log(mg/kg_bw/day) (LOAEL)
MicronucleusadmetSARLow25.27 %
Skin sensitisationpkCSMYes-
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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.