Cadmium

Predicted ADME Properties
TypePropertyToolInterpretationProbability/Value
AbsorptionCaco-2 permeabilityadmetSARHigh73.99 %
pkCSMHigh1.379 cm/s
Human Intestinal AbsorptionadmetSARHigh76.72 %
pkCSMHigh100 %
SwissADME-
Human Oral BioavailabilityadmetSARHigh Bioavailability74.21 %
Log Kp (Skin permeation)pkCSMHigh-2.574 logkp (cm/h)
SwissADME- logkp (cm/s)
DistributionP-glycoprotein substrateadmetSARLow21.18 %
pkCSMYes-
SwissADME-
vNNNo Prediction-
P-glycoprotein inhibitoradmetSARLow2.23 %
vNNNo Prediction-
P-glycoprotein inhibitor IpkCSMNo-
P-glycoprotein inhibitor IIpkCSMNo-
Blood Brain BarrieradmetSARHigh93.17 %
pkCSMModerate0.012 logBB
SwissADME-
vNNNo Prediction-
CNS permeabilitypkCSMModerate-2.298 logPS
Fraction unbound in humanpkCSM-0.781
Plasma protein bindingadmetSAR9.6 %Weak
Steady state volume of distribution (VDss)pkCSMModerate-0.035 log(L/kg)
MetabolismCYP1A2 inhibitoradmetSARLow10.3 %
pkCSMNo-
SwissADME-
vNNNo Prediction-
CYP2C19 inhibitoradmetSARLow6.34 %
pkCSMNo-
SwissADME-
vNNNo Prediction-
CYP2C9 inhibitoradmetSARLow4.36 %
pkCSMNo-
SwissADME-
vNNNo Prediction-
CYP2C9 substrateadmetSARLow21.65 %
CYP2D6 inhibitoradmetSARLow7.94 %
pkCSMNo-
SwissADME-
vNNNo Prediction-
CYP2D6 substrateadmetSARLow34.31 %
pkCSMNo-
CYP3A4 inhibitoradmetSARLow0.8 %
pkCSMNo-
SwissADME-
vNNNo Prediction-
CYP3A4 substrateadmetSARLow10.52 %
pkCSMNo-
Human Liver Microsomal (HLM) stability assayvNNNo Prediction-
OATP2B1 inhibitoradmetSARLow13.94 %
OATP1B1 inhibitoradmetSARHigh98.41 %
OATP1B3 inhibitoradmetSARHigh98.27 %
MATE1 inhibitoradmetSARLow12.9 %
BSEP inhibitoradmetSARLow12.9 %
UGT catalysisadmetSARLow13.78 %
ExcretionRenal OCT2 inhibitoradmetSARLow11.97 %
Renal OCT2 substratepkCSMNo-
Total clearancepkCSM-0.576 ml/min/kg
Download
Predicted Toxicity properties
PropertyToolInterpretationProbability/Value
Acute oral toxicityadmetSAR--2.6052041053772 log(mg/kg)
ProTox-890 mg/kg
Acute oral toxicity classadmetSARHigh81.87 %
ProTox4-
BiodegradationadmetSARHigh74.66 %
ToxtreeClass 3 (unknown biodegradability)-
CarcinogensadmetSARHigh71.88 %
ToxtreeNo-
Cramer's ruleToxtreeHigh (Class III)-
CytotoxicityvNNNoPrediction-
Genotoxic carcinogenityToxtreeNo-
HepatotoxicityadmetSARHigh76.57 %
pkCSMNo-
vNNNoPrediction-
Human Ether-a-go-go-Related Gene InhibitoradmetSARHigh53.44 %
vNNNoPrediction-
Human Ether-a-go-go-Related Gene Inhibitor IpkCSMNo-
Human Ether-a-go-go-Related Gene Inhibitor IIpkCSMNo-
Mitochondrial Membrane Potential (MMP)vNNNoPrediction-
Maximum Recommended Tolerated Dose (MRTD)pkCSMHigh1.164 log(mg/kg/day)
vNN-NoPrediction
Non-Genotoxic carcinogenicityToxtreeNo-
Oral rat acute toxicitypkCSM-2.217 log(mg/kg_bw/day) (LD50)
pkCSM-0.741 log(mg/kg_bw/day) (LOAEL)
MicronucleusadmetSARLow12.77 %
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.