Testolactone

Predicted ADME Properties
TypePropertyToolInterpretationProbability/Value
AbsorptionCaco-2 permeabilityadmetSARHigh93.1 %
pkCSMHigh1.355 cm/s
Human Intestinal AbsorptionadmetSARHigh94.88 %
pkCSMHigh98.861 %
SwissADMEHigh-
Human Oral BioavailabilityadmetSARHigh Bioavailability53.47 %
Log Kp (Skin permeation)pkCSMHigh-3.24 logkp (cm/h)
SwissADME--5.98 logkp (cm/s)
DistributionP-glycoprotein substrateadmetSARLow24.07 %
pkCSMNo-
SwissADMENo-
vNNNo-
P-glycoprotein inhibitoradmetSARHigh59.98 %
vNNNo Prediction-
P-glycoprotein inhibitor IpkCSMYes-
P-glycoprotein inhibitor IIpkCSMNo-
Blood Brain BarrieradmetSARHigh97.75 %
pkCSMYes0.351 logBB
SwissADMEYes-
vNNNo Prediction-
CNS permeabilitypkCSMModerate-2.727 logPS
Fraction unbound in humanpkCSM-0.223
Plasma protein bindingadmetSAR74.33 %Moderate
Steady state volume of distribution (VDss)pkCSMModerate0.337 log(L/kg)
MetabolismCYP1A2 inhibitoradmetSARLow6.17 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2C19 inhibitoradmetSARLow22.94 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2C9 inhibitoradmetSARLow7.65 %
pkCSMNo-
SwissADMEYes-
vNNNo Prediction-
CYP2C9 substrateadmetSARLow2.97 %
CYP2D6 inhibitoradmetSARLow3.55 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2D6 substrateadmetSARLow1.25 %
pkCSMNo-
CYP3A4 inhibitoradmetSARLow21.45 %
pkCSMNo-
SwissADMENo-
vNNNo-
CYP3A4 substrateadmetSARLow28.01 %
pkCSMYes-
Human Liver Microsomal (HLM) stability assayvNNNo Prediction-
OATP2B1 inhibitoradmetSARLow9.54 %
OATP1B1 inhibitoradmetSARHigh86.64 %
OATP1B3 inhibitoradmetSARHigh93.01 %
MATE1 inhibitoradmetSARLow8.18 %
BSEP inhibitoradmetSARHigh80.69 %
UGT catalysisadmetSARHigh51.41 %
ExcretionRenal OCT2 inhibitoradmetSARLow46.71 %
Renal OCT2 substratepkCSMYes-
Total clearancepkCSM-0.947 ml/min/kg
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Predicted Toxicity properties
PropertyToolInterpretationProbability/Value
Acute oral toxicityadmetSAR--3.82070064544678 log(mg/kg)
ProTox-6000 mg/kg
Acute oral toxicity classadmetSARLow1.45 %
ProTox6-
BiodegradationadmetSARLow40.02 %
ToxtreeClass 2 (persistent chemical)-
CarcinogensadmetSARHigh57.67 %
ToxtreeNo-
Cramer's ruleToxtreeHigh (Class III)-
CytotoxicityvNNNoPrediction-
Genotoxic carcinogenityToxtreeYes-
HepatotoxicityadmetSARHigh51.97 %
pkCSMNo-
vNNNo-
Human Ether-a-go-go-Related Gene InhibitoradmetSARHigh61.21 %
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)pkCSMLow-0.221 log(mg/kg/day)
vNN-73 mg/day
Non-Genotoxic carcinogenicityToxtreeNo-
Oral rat acute toxicitypkCSM-1.94 log(mg/kg_bw/day) (LD50)
pkCSM-1.514 log(mg/kg_bw/day) (LOAEL)
MicronucleusadmetSARLow20.13 %
Skin sensitisationpkCSMNo-
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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.