Flutamide

Predicted ADME Properties
TypePropertyToolInterpretationProbability/Value
AbsorptionCaco-2 permeabilityadmetSARHigh96.21 %
pkCSMLow0.826 cm/s
Human Intestinal AbsorptionadmetSARHigh99.22 %
pkCSMHigh87.749 %
SwissADMEHigh-
Human Oral BioavailabilityadmetSARHigh Bioavailability86.31 %
Log Kp (Skin permeation)pkCSMHigh-2.677 logkp (cm/h)
SwissADME--5.61 logkp (cm/s)
DistributionP-glycoprotein substrateadmetSARLow4.36 %
pkCSMYes-
SwissADMENo-
vNNNo Prediction-
P-glycoprotein inhibitoradmetSARLow29.99 %
vNNNo Prediction-
P-glycoprotein inhibitor IpkCSMNo-
P-glycoprotein inhibitor IIpkCSMNo-
Blood Brain BarrieradmetSARHigh95.11 %
pkCSMModerate-0.539 logBB
SwissADMEYes-
vNNNo Prediction-
CNS permeabilitypkCSMModerate-2.081 logPS
Fraction unbound in humanpkCSM-0.015
Plasma protein bindingadmetSAR90.01 %High
Steady state volume of distribution (VDss)pkCSMModerate-0.125 log(L/kg)
MetabolismCYP1A2 inhibitoradmetSARHigh93.44 %
pkCSMYes-
SwissADMEYes-
vNNYes-
CYP2C19 inhibitoradmetSARHigh91.05 %
pkCSMYes-
SwissADMEYes-
vNNNo-
CYP2C9 inhibitoradmetSARHigh69.75 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2C9 substrateadmetSARHigh75.79 %
CYP2D6 inhibitoradmetSARLow12.01 %
pkCSMNo-
SwissADMENo-
vNNNo-
CYP2D6 substrateadmetSARLow31.13 %
pkCSMNo-
CYP3A4 inhibitoradmetSARLow30.14 %
pkCSMYes-
SwissADMENo-
vNNNo Prediction-
CYP3A4 substrateadmetSARHigh53.61 %
pkCSMYes-
Human Liver Microsomal (HLM) stability assayvNNNo Prediction-
OATP2B1 inhibitoradmetSARLow14.58 %
OATP1B1 inhibitoradmetSARHigh97.27 %
OATP1B3 inhibitoradmetSARHigh98.03 %
MATE1 inhibitoradmetSARLow10.39 %
BSEP inhibitoradmetSARHigh79.27 %
UGT catalysisadmetSARLow34.44 %
ExcretionRenal OCT2 inhibitoradmetSARLow18.02 %
Renal OCT2 substratepkCSMNo-
Total clearancepkCSM-0.059 ml/min/kg
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Predicted Toxicity properties
PropertyToolInterpretationProbability/Value
Acute oral toxicityadmetSAR--3.07059621810913 log(mg/kg)
ProTox-787 mg/kg
Acute oral toxicity classadmetSARHigh71.34 %
ProTox4-
BiodegradationadmetSARLow3.85 %
ToxtreeClass 2 (persistent chemical)-
CarcinogensadmetSARLow45.47 %
ToxtreeNo-
Cramer's ruleToxtreeHigh (Class III)-
CytotoxicityvNNNoPrediction-
Genotoxic carcinogenityToxtreeYes-
HepatotoxicityadmetSARHigh80.45 %
pkCSMNo-
vNNYes-
Human Ether-a-go-go-Related Gene InhibitoradmetSARLow8.68 %
vNNNo-
Human Ether-a-go-go-Related Gene Inhibitor IpkCSMNo-
Human Ether-a-go-go-Related Gene Inhibitor IIpkCSMNo-
Mitochondrial Membrane Potential (MMP)vNNYes-
Maximum Recommended Tolerated Dose (MRTD)pkCSMLow0.083 log(mg/kg/day)
vNN-12 mg/day
Non-Genotoxic carcinogenicityToxtreeNo-
Oral rat acute toxicitypkCSM-2.64 log(mg/kg_bw/day) (LD50)
pkCSM-1.5 log(mg/kg_bw/day) (LOAEL)
MicronucleusadmetSARHigh76.24 %
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.