Hydroxyflutamide

Predicted ADME Properties
TypePropertyToolInterpretationProbability/Value
AbsorptionCaco-2 permeabilityadmetSARHigh94.28 %
pkCSMHigh1.079 cm/s
Human Intestinal AbsorptionadmetSARHigh98.79 %
pkCSMHigh83.834 %
SwissADMEHigh-
Human Oral BioavailabilityadmetSARHigh Bioavailability93.45 %
Log Kp (Skin permeation)pkCSMHigh-2.844 logkp (cm/h)
SwissADME--6.17 logkp (cm/s)
DistributionP-glycoprotein substrateadmetSARLow6.12 %
pkCSMYes-
SwissADMENo-
vNNNo Prediction-
P-glycoprotein inhibitoradmetSARLow35.5 %
vNNNo Prediction-
P-glycoprotein inhibitor IpkCSMNo-
P-glycoprotein inhibitor IIpkCSMNo-
Blood Brain BarrieradmetSARHigh91.8 %
pkCSMModerate-0.669 logBB
SwissADMENo-
vNNNo Prediction-
CNS permeabilitypkCSMModerate-2.397 logPS
Fraction unbound in humanpkCSM-0.153
Plasma protein bindingadmetSAR92.6 %High
Steady state volume of distribution (VDss)pkCSMLow-0.372 log(L/kg)
MetabolismCYP1A2 inhibitoradmetSARHigh60.09 %
pkCSMYes-
SwissADMEYes-
vNNYes-
CYP2C19 inhibitoradmetSARHigh64.09 %
pkCSMYes-
SwissADMENo-
vNNNo-
CYP2C9 inhibitoradmetSARLow41.96 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2C9 substrateadmetSARHigh69.98 %
CYP2D6 inhibitoradmetSARLow3.03 %
pkCSMNo-
SwissADMENo-
vNNNo-
CYP2D6 substrateadmetSARLow16.84 %
pkCSMNo-
CYP3A4 inhibitoradmetSARLow18.69 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP3A4 substrateadmetSARHigh56.86 %
pkCSMYes-
Human Liver Microsomal (HLM) stability assayvNNNo Prediction-
OATP2B1 inhibitoradmetSARLow12.81 %
OATP1B1 inhibitoradmetSARHigh94.81 %
OATP1B3 inhibitoradmetSARHigh97.32 %
MATE1 inhibitoradmetSARLow9.15 %
BSEP inhibitoradmetSARHigh73.65 %
UGT catalysisadmetSARLow49.27 %
ExcretionRenal OCT2 inhibitoradmetSARLow16.24 %
Renal OCT2 substratepkCSMNo-
Total clearancepkCSM-0.362 ml/min/kg
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Predicted Toxicity properties
PropertyToolInterpretationProbability/Value
Acute oral toxicityadmetSAR--3.01630020141602 log(mg/kg)
ProTox-550 mg/kg
Acute oral toxicity classadmetSARHigh63.99 %
ProTox4-
BiodegradationadmetSARLow5.72 %
ToxtreeClass 2 (persistent chemical)-
CarcinogensadmetSARHigh57.49 %
ToxtreeNo-
Cramer's ruleToxtreeHigh (Class III)-
CytotoxicityvNNNoPrediction-
Genotoxic carcinogenityToxtreeYes-
HepatotoxicityadmetSARHigh85.77 %
pkCSMNo-
vNNYes-
Human Ether-a-go-go-Related Gene InhibitoradmetSARLow11.57 %
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)pkCSMLow0.208 log(mg/kg/day)
vNN-58 mg/day
Non-Genotoxic carcinogenicityToxtreeNo-
Oral rat acute toxicitypkCSM-2.529 log(mg/kg_bw/day) (LD50)
pkCSM-1.901 log(mg/kg_bw/day) (LOAEL)
MicronucleusadmetSARHigh82.35 %
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.