1,2-Dichlorobenzene

Predicted ADME Properties
TypePropertyToolInterpretationProbability/Value
AbsorptionCaco-2 permeabilityadmetSARHigh96.15 %
pkCSMHigh1.563 cm/s
Human Intestinal AbsorptionadmetSARHigh96.61 %
pkCSMHigh92.582 %
SwissADMELow-
Human Oral BioavailabilityadmetSARHigh Bioavailability80.42 %
Log Kp (Skin permeation)pkCSMLow-1.071 logkp (cm/h)
SwissADME--4.76 logkp (cm/s)
DistributionP-glycoprotein substrateadmetSARLow3.54 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
P-glycoprotein inhibitoradmetSARLow1.18 %
vNNNo-
P-glycoprotein inhibitor IpkCSMNo-
P-glycoprotein inhibitor IIpkCSMNo-
Blood Brain BarrieradmetSARHigh98.55 %
pkCSMYes0.325 logBB
SwissADMEYes-
vNNNo Prediction-
CNS permeabilitypkCSMYes-1.648 logPS
Fraction unbound in humanpkCSM-0.354
Plasma protein bindingadmetSAR80.0 %Moderate
Steady state volume of distribution (VDss)pkCSMModerate0.164 log(L/kg)
MetabolismCYP1A2 inhibitoradmetSARHigh75.86 %
pkCSMNo-
SwissADMEYes-
vNNNo Prediction-
CYP2C19 inhibitoradmetSARHigh66.85 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2C9 inhibitoradmetSARLow16.17 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2C9 substrateadmetSARLow39.16 %
CYP2D6 inhibitoradmetSARLow19.02 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2D6 substrateadmetSARLow29.02 %
pkCSMNo-
CYP3A4 inhibitoradmetSARLow1.16 %
pkCSMNo-
SwissADMENo-
vNNNo-
CYP3A4 substrateadmetSARLow45.01 %
pkCSMNo-
Human Liver Microsomal (HLM) stability assayvNNNo Prediction-
OATP2B1 inhibitoradmetSARLow8.79 %
OATP1B1 inhibitoradmetSARHigh99.04 %
OATP1B3 inhibitoradmetSARHigh99.39 %
MATE1 inhibitoradmetSARLow3.44 %
BSEP inhibitoradmetSARLow22.36 %
UGT catalysisadmetSARLow3.72 %
ExcretionRenal OCT2 inhibitoradmetSARLow17.63 %
Renal OCT2 substratepkCSMNo-
Total clearancepkCSM-0.36 ml/min/kg
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Predicted Toxicity properties
PropertyToolInterpretationProbability/Value
Acute oral toxicityadmetSAR--3.35336780548096 log(mg/kg)
ProTox-500 mg/kg
Acute oral toxicity classadmetSARHigh57.65 %
ProTox4-
BiodegradationadmetSARLow23.34 %
ToxtreeClass 2 (persistent chemical)-
CarcinogensadmetSARHigh51.67 %
ToxtreeNo-
Cramer's ruleToxtreeHigh (Class III)-
CytotoxicityvNNNoPrediction-
Genotoxic carcinogenityToxtreeNo-
HepatotoxicityadmetSARHigh78.73 %
pkCSMNo-
vNNYes-
Human Ether-a-go-go-Related Gene InhibitoradmetSARLow20.23 %
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)pkCSMHigh0.925 log(mg/kg/day)
vNN-NoPrediction
Non-Genotoxic carcinogenicityToxtreeNo-
Oral rat acute toxicitypkCSM-2.4 log(mg/kg_bw/day) (LD50)
pkCSM-2.117 log(mg/kg_bw/day) (LOAEL)
MicronucleusadmetSARLow6.94 %
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.