Benzyl chloride

Predicted ADME Properties
TypePropertyToolInterpretationProbability/Value
AbsorptionCaco-2 permeabilityadmetSARHigh96.98 %
pkCSMHigh1.539 cm/s
Human Intestinal AbsorptionadmetSARHigh96.05 %
pkCSMHigh93.538 %
SwissADMELow-
Human Oral BioavailabilityadmetSARHigh Bioavailability76.29 %
Log Kp (Skin permeation)pkCSMLow-1.883 logkp (cm/h)
SwissADME--5.44 logkp (cm/s)
DistributionP-glycoprotein substrateadmetSARLow8.32 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
P-glycoprotein inhibitoradmetSARLow1.33 %
vNNNo-
P-glycoprotein inhibitor IpkCSMNo-
P-glycoprotein inhibitor IIpkCSMNo-
Blood Brain BarrieradmetSARHigh98.48 %
pkCSMYes0.439 logBB
SwissADMEYes-
vNNNo Prediction-
CNS permeabilitypkCSMYes-1.537 logPS
Fraction unbound in humanpkCSM-0.33
Plasma protein bindingadmetSAR68.18 %Moderate
Steady state volume of distribution (VDss)pkCSMModerate0.302 log(L/kg)
MetabolismCYP1A2 inhibitoradmetSARHigh70.3 %
pkCSMYes-
SwissADMEYes-
vNNNo Prediction-
CYP2C19 inhibitoradmetSARLow47.42 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2C9 inhibitoradmetSARLow7.43 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2C9 substrateadmetSARLow34.53 %
CYP2D6 inhibitoradmetSARLow15.68 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2D6 substrateadmetSARLow38.47 %
pkCSMNo-
CYP3A4 inhibitoradmetSARLow0.63 %
pkCSMNo-
SwissADMENo-
vNNNo-
CYP3A4 substrateadmetSARLow48.8 %
pkCSMNo-
Human Liver Microsomal (HLM) stability assayvNNNo Prediction-
OATP2B1 inhibitoradmetSARLow7.89 %
OATP1B1 inhibitoradmetSARHigh99.06 %
OATP1B3 inhibitoradmetSARHigh99.34 %
MATE1 inhibitoradmetSARLow4.49 %
BSEP inhibitoradmetSARLow15.85 %
UGT catalysisadmetSARLow2.4 %
ExcretionRenal OCT2 inhibitoradmetSARLow19.98 %
Renal OCT2 substratepkCSMNo-
Total clearancepkCSM-0.301 ml/min/kg
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Predicted Toxicity properties
PropertyToolInterpretationProbability/Value
Acute oral toxicityadmetSAR--3.21519231796265 log(mg/kg)
ProTox-1231 mg/kg
Acute oral toxicity classadmetSARHigh60.8 %
ProTox4-
BiodegradationadmetSARLow37.68 %
ToxtreeClass 3 (unknown biodegradability)-
CarcinogensadmetSARHigh80.38 %
ToxtreeNo-
Cramer's ruleToxtreeHigh (Class III)-
CytotoxicityvNNNoPrediction-
Genotoxic carcinogenityToxtreeYes-
HepatotoxicityadmetSARHigh85.78 %
pkCSMNo-
vNNYes-
Human Ether-a-go-go-Related Gene InhibitoradmetSARLow26.76 %
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)pkCSMHigh0.901 log(mg/kg/day)
vNN-NoPrediction
Non-Genotoxic carcinogenicityToxtreeNo-
Oral rat acute toxicitypkCSM-1.914 log(mg/kg_bw/day) (LD50)
pkCSM-2.074 log(mg/kg_bw/day) (LOAEL)
MicronucleusadmetSARLow7.13 %
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.