FD&C Red 3

Predicted ADME Properties
TypePropertyToolInterpretationProbability/Value
AbsorptionCaco-2 permeabilityadmetSARLow28.66 %
pkCSMLow-0.55 cm/s
Human Intestinal AbsorptionadmetSARHigh90.52 %
pkCSMHigh70.282 %
SwissADMELow-
Human Oral BioavailabilityadmetSARLow Bioavailability30.13 %
Log Kp (Skin permeation)pkCSMHigh-2.735 logkp (cm/h)
SwissADME--7.39 logkp (cm/s)
DistributionP-glycoprotein substrateadmetSARLow2.65 %
pkCSMNo-
SwissADMEYes-
vNNNo-
P-glycoprotein inhibitoradmetSARHigh51.26 %
vNNNo Prediction-
P-glycoprotein inhibitor IpkCSMYes-
P-glycoprotein inhibitor IIpkCSMYes-
Blood Brain BarrieradmetSARLow48.89 %
pkCSMNo-1.287 logBB
SwissADMENo-
vNNNo Prediction-
CNS permeabilitypkCSMModerate-2.973 logPS
Fraction unbound in humanpkCSM-0.217
Plasma protein bindingadmetSAR101.85 %High
Steady state volume of distribution (VDss)pkCSMLow-0.567 log(L/kg)
MetabolismCYP1A2 inhibitoradmetSARHigh77.23 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2C19 inhibitoradmetSARLow39.81 %
pkCSMYes-
SwissADMENo-
vNNNo Prediction-
CYP2C9 inhibitoradmetSARHigh69.16 %
pkCSMYes-
SwissADMENo-
vNNNo Prediction-
CYP2C9 substrateadmetSARLow41.04 %
CYP2D6 inhibitoradmetSARLow10.36 %
pkCSMNo-
SwissADMENo-
vNNNo Prediction-
CYP2D6 substrateadmetSARLow8.81 %
pkCSMNo-
CYP3A4 inhibitoradmetSARLow10.98 %
pkCSMNo-
SwissADMENo-
vNNNo-
CYP3A4 substrateadmetSARLow37.45 %
pkCSMYes-
Human Liver Microsomal (HLM) stability assayvNNNo Prediction-
OATP2B1 inhibitoradmetSARHigh53.1 %
OATP1B1 inhibitoradmetSARHigh67.31 %
OATP1B3 inhibitoradmetSARHigh77.76 %
MATE1 inhibitoradmetSARLow19.89 %
BSEP inhibitoradmetSARHigh72.25 %
UGT catalysisadmetSARHigh65.88 %
ExcretionRenal OCT2 inhibitoradmetSARLow15.06 %
Renal OCT2 substratepkCSMNo-
Total clearancepkCSM--3.07 ml/min/kg
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Predicted Toxicity properties
PropertyToolInterpretationProbability/Value
Acute oral toxicityadmetSAR--2.48055553436279 log(mg/kg)
ProTox-1264 mg/kg
Acute oral toxicity classadmetSARLow34.34 %
ProTox4-
BiodegradationadmetSARLow10.87 %
ToxtreeClass 2 (persistent chemical)-
CarcinogensadmetSARLow47.28 %
ToxtreeNo-
Cramer's ruleToxtreeHigh (Class III)-
CytotoxicityvNNNoPrediction-
Genotoxic carcinogenityToxtreeYes-
HepatotoxicityadmetSARHigh69.86 %
pkCSMNo-
vNNNo-
Human Ether-a-go-go-Related Gene InhibitoradmetSARLow28.54 %
vNNNo-
Human Ether-a-go-go-Related Gene Inhibitor IpkCSMNo-
Human Ether-a-go-go-Related Gene Inhibitor IIpkCSMYes-
Mitochondrial Membrane Potential (MMP)vNNYes-
Maximum Recommended Tolerated Dose (MRTD)pkCSMLow-0.068 log(mg/kg/day)
vNN-127 mg/day
Non-Genotoxic carcinogenicityToxtreeNo-
Oral rat acute toxicitypkCSM-3.306 log(mg/kg_bw/day) (LD50)
pkCSM--0.448 log(mg/kg_bw/day) (LOAEL)
MicronucleusadmetSARHigh63.48 %
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.