2-(2H-Benzotriazol-2-yl)-4,6-di-tert-pentylphenol

Predicted ADME Properties
TypePropertyToolInterpretationProbability/Value
AbsorptionCaco-2 permeabilityadmetSARHigh89.95 %
pkCSMHigh1.463 cm/s
Human Intestinal AbsorptionadmetSARHigh94.93 %
pkCSMHigh94.081 %
SwissADMEHigh-
Human Oral BioavailabilityadmetSARLow Bioavailability28.37 %
Log Kp (Skin permeation)pkCSMHigh-2.748 logkp (cm/h)
SwissADME--3.19 logkp (cm/s)
DistributionP-glycoprotein substrateadmetSARLow12.09 %
pkCSMYes-
SwissADMENo-
vNNNo Prediction-
P-glycoprotein inhibitoradmetSARHigh69.33 %
vNNNo Prediction-
P-glycoprotein inhibitor IpkCSMYes-
P-glycoprotein inhibitor IIpkCSMYes-
Blood Brain BarrieradmetSARHigh89.91 %
pkCSMYes0.553 logBB
SwissADMEYes-
vNNNo Prediction-
CNS permeabilitypkCSMYes-1.633 logPS
Fraction unbound in humanpkCSM-0
Plasma protein bindingadmetSAR97.31 %High
Steady state volume of distribution (VDss)pkCSMModerate0.144 log(L/kg)
MetabolismCYP1A2 inhibitoradmetSARLow44.41 %
pkCSMYes-
SwissADMENo-
vNNNo Prediction-
CYP2C19 inhibitoradmetSARHigh61.42 %
pkCSMYes-
SwissADMEYes-
vNNNo Prediction-
CYP2C9 inhibitoradmetSARLow47.74 %
pkCSMYes-
SwissADMEYes-
vNNNo Prediction-
CYP2C9 substrateadmetSARLow20.34 %
CYP2D6 inhibitoradmetSARLow10.11 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2D6 substrateadmetSARLow8.57 %
pkCSMNo-
CYP3A4 inhibitoradmetSARLow3.89 %
pkCSMYes-
SwissADMENo-
vNNNo Prediction-
CYP3A4 substrateadmetSARHigh50.47 %
pkCSMYes-
Human Liver Microsomal (HLM) stability assayvNNNo Prediction-
OATP2B1 inhibitoradmetSARLow36.54 %
OATP1B1 inhibitoradmetSARHigh88.15 %
OATP1B3 inhibitoradmetSARHigh86.41 %
MATE1 inhibitoradmetSARLow11.84 %
BSEP inhibitoradmetSARHigh86.66 %
UGT catalysisadmetSARLow15.71 %
ExcretionRenal OCT2 inhibitoradmetSARLow24.17 %
Renal OCT2 substratepkCSMNo-
Total clearancepkCSM-0.777 ml/min/kg
Download
Predicted Toxicity properties
PropertyToolInterpretationProbability/Value
Acute oral toxicityadmetSAR--3.73861742019653 log(mg/kg)
ProTox-2325 mg/kg
Acute oral toxicity classadmetSARLow4.3 %
ProTox5-
BiodegradationadmetSARLow12.81 %
ToxtreeClass 2 (persistent chemical)-
CarcinogensadmetSARLow42.08 %
ToxtreeNo-
Cramer's ruleToxtreeHigh (Class III)-
CytotoxicityvNNNoPrediction-
Genotoxic carcinogenityToxtreeNo-
HepatotoxicityadmetSARHigh58.51 %
pkCSMNo-
vNNNoPrediction-
Human Ether-a-go-go-Related Gene InhibitoradmetSARHigh75.93 %
vNNNoPrediction-
Human Ether-a-go-go-Related Gene Inhibitor IpkCSMNo-
Human Ether-a-go-go-Related Gene Inhibitor IIpkCSMYes-
Mitochondrial Membrane Potential (MMP)vNNNo-
Maximum Recommended Tolerated Dose (MRTD)pkCSMLow0.102 log(mg/kg/day)
vNN-NoPrediction
Non-Genotoxic carcinogenicityToxtreeNo-
Oral rat acute toxicitypkCSM-1.783 log(mg/kg_bw/day) (LD50)
pkCSM-1.615 log(mg/kg_bw/day) (LOAEL)
MicronucleusadmetSARLow11.16 %
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.