2,2-bis(4-hydroxyphenyl)-propanol

Predicted ADME Properties
TypePropertyToolInterpretationProbability/Value
AbsorptionCaco-2 permeabilityadmetSARHigh88.19 %
pkCSMHigh1.198 cm/s
Human Intestinal AbsorptionadmetSARHigh94.39 %
pkCSMHigh95.863 %
SwissADMEHigh-
Human Oral BioavailabilityadmetSARLow Bioavailability6.93 %
Log Kp (Skin permeation)pkCSMHigh-2.761 logkp (cm/h)
SwissADME--6.3 logkp (cm/s)
DistributionP-glycoprotein substrateadmetSARLow17.16 %
pkCSMYes-
SwissADMENo-
vNNNo Prediction-
P-glycoprotein inhibitoradmetSARLow37.33 %
vNNNo Prediction-
P-glycoprotein inhibitor IpkCSMNo-
P-glycoprotein inhibitor IIpkCSMNo-
Blood Brain BarrieradmetSARHigh78.1 %
pkCSMModerate0.123 logBB
SwissADMEYes-
vNNNo Prediction-
CNS permeabilitypkCSMModerate-2.247 logPS
Fraction unbound in humanpkCSM-0.144
Plasma protein bindingadmetSAR95.83 %High
Steady state volume of distribution (VDss)pkCSMModerate-0.012 log(L/kg)
MetabolismCYP1A2 inhibitoradmetSARHigh80.67 %
pkCSMYes-
SwissADMENo-
vNNNo-
CYP2C19 inhibitoradmetSARHigh67.4 %
pkCSMYes-
SwissADMENo-
vNNNo-
CYP2C9 inhibitoradmetSARLow44.63 %
pkCSMNo-
SwissADMENo-
vNNNo-
CYP2C9 substrateadmetSARLow9.27 %
CYP2D6 inhibitoradmetSARLow44.18 %
pkCSMNo-
SwissADMEYes-
vNNNo-
CYP2D6 substrateadmetSARLow7.17 %
pkCSMNo-
CYP3A4 inhibitoradmetSARLow27.2 %
pkCSMNo-
SwissADMENo-
vNNNo-
CYP3A4 substrateadmetSARLow23.88 %
pkCSMNo-
Human Liver Microsomal (HLM) stability assayvNNNo Prediction-
OATP2B1 inhibitoradmetSARLow22.8 %
OATP1B1 inhibitoradmetSARHigh85.85 %
OATP1B3 inhibitoradmetSARHigh89.42 %
MATE1 inhibitoradmetSARLow23.73 %
BSEP inhibitoradmetSARHigh79.68 %
UGT catalysisadmetSARHigh90.62 %
ExcretionRenal OCT2 inhibitoradmetSARLow37.35 %
Renal OCT2 substratepkCSMNo-
Total clearancepkCSM-0.202 ml/min/kg
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Predicted Toxicity properties
PropertyToolInterpretationProbability/Value
Acute oral toxicityadmetSAR--3.46801424026489 log(mg/kg)
ProTox-1770 mg/kg
Acute oral toxicity classadmetSARLow37.7 %
ProTox4-
BiodegradationadmetSARLow25.07 %
ToxtreeClass 2 (persistent chemical)-
CarcinogensadmetSARHigh55.89 %
ToxtreeNo-
Cramer's ruleToxtreeHigh (Class III)-
CytotoxicityvNNNoPrediction-
Genotoxic carcinogenityToxtreeNo-
HepatotoxicityadmetSARLow33.94 %
pkCSMNo-
vNNNoPrediction-
Human Ether-a-go-go-Related Gene InhibitoradmetSARLow25.81 %
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)pkCSMLow-0.014 log(mg/kg/day)
vNN-146 mg/day
Non-Genotoxic carcinogenicityToxtreeNo-
Oral rat acute toxicitypkCSM-2.199 log(mg/kg_bw/day) (LD50)
pkCSM-2.227 log(mg/kg_bw/day) (LOAEL)
MicronucleusadmetSARLow36.07 %
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.