2-Ethyl-5-carboxypentyl phthalate
| Predicted ADME Properties | |||||
|---|---|---|---|---|---|
| Type | Property | Tool | Interpretation | Probability/Value | |
| Absorption | Caco-2 permeability | admetSAR | Low | 49.61 % | |
| pkCSM | High | 1.005 cm/s | |||
| Human Intestinal Absorption | admetSAR | High | 92.29 % | ||
| pkCSM | High | 43.807 % | |||
| SwissADME | High | - | |||
| Human Oral Bioavailability | admetSAR | High Bioavailability | 83.44 % | ||
| Log Kp (Skin permeation) | pkCSM | High | -2.735 logkp (cm/h) | ||
| SwissADME | - | -6.29 logkp (cm/s) | |||
| Distribution | P-glycoprotein substrate | admetSAR | Low | 2.77 % | |
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | No Prediction | - | |||
| P-glycoprotein inhibitor | admetSAR | Low | 4.67 % | ||
| vNN | No Prediction | - | |||
| P-glycoprotein inhibitor I | pkCSM | No | - | ||
| P-glycoprotein inhibitor II | pkCSM | No | - | ||
| Blood Brain Barrier | admetSAR | High | 81.87 % | ||
| pkCSM | Moderate | -0.69 logBB | |||
| SwissADME | No | - | |||
| vNN | No Prediction | - | |||
| CNS permeability | pkCSM | No | -3.313 logPS | ||
| Fraction unbound in human | pkCSM | - | 0.29 | ||
| Plasma protein binding | admetSAR | 76.11 % | Moderate | ||
| Steady state volume of distribution (VDss) | pkCSM | Low | -1.777 log(L/kg) | ||
| Metabolism | CYP1A2 inhibitor | admetSAR | Low | 11.09 % | |
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | No Prediction | - | |||
| CYP2C19 inhibitor | admetSAR | Low | 5.68 % | ||
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | No Prediction | - | |||
| CYP2C9 inhibitor | admetSAR | Low | 7.14 % | ||
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | No Prediction | - | |||
| CYP2C9 substrate | admetSAR | Low | 7.39 % | ||
| CYP2D6 inhibitor | admetSAR | Low | 2.97 % | ||
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | No Prediction | - | |||
| CYP2D6 substrate | admetSAR | Low | 0.91 % | ||
| pkCSM | No | - | |||
| CYP3A4 inhibitor | admetSAR | Low | 1.07 % | ||
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | No | - | |||
| CYP3A4 substrate | admetSAR | Low | 2.86 % | ||
| pkCSM | No | - | |||
| Human Liver Microsomal (HLM) stability assay | vNN | No Prediction | - | ||
| OATP2B1 inhibitor | admetSAR | Low | 20.53 % | ||
| OATP1B1 inhibitor | admetSAR | High | 92.1 % | ||
| OATP1B3 inhibitor | admetSAR | High | 97.27 % | ||
| MATE1 inhibitor | admetSAR | Low | 1.84 % | ||
| BSEP inhibitor | admetSAR | Low | 15.38 % | ||
| UGT catalysis | admetSAR | High | 87.14 % | ||
| Excretion | Renal OCT2 inhibitor | admetSAR | Low | 4.52 % | |
| Renal OCT2 substrate | pkCSM | No | - | ||
| Total clearance | pkCSM | - | 0.827 ml/min/kg | ||
| Predicted Toxicity properties | ||||
|---|---|---|---|---|
| Property | Tool | Interpretation | Probability/Value | |
| Acute oral toxicity | admetSAR | - | -3.275719165802 log(mg/kg) | |
| ProTox | - | 1500 mg/kg | ||
| Acute oral toxicity class | admetSAR | High | 56.24 % | |
| ProTox | 4 | - | ||
| Biodegradation | admetSAR | High | 74.19 % | |
| Toxtree | Class 1 (easily biodegradable chemical) | - | ||
| Carcinogens | admetSAR | Low | 11.15 % | |
| Toxtree | No | - | ||
| Cramer's rule | Toxtree | Low (Class I) | - | |
| Cytotoxicity | vNN | NoPrediction | - | |
| Genotoxic carcinogenity | Toxtree | No | - | |
| Hepatotoxicity | admetSAR | Low | 36.6 % | |
| pkCSM | No | - | ||
| vNN | NoPrediction | - | ||
| Human Ether-a-go-go-Related Gene Inhibitor | admetSAR | Low | 15.15 % | |
| vNN | No | - | ||
| Human Ether-a-go-go-Related Gene Inhibitor I | pkCSM | No | - | |
| Human Ether-a-go-go-Related Gene Inhibitor II | pkCSM | No | - | |
| Mitochondrial Membrane Potential (MMP) | vNN | No | - | |
| Maximum Recommended Tolerated Dose (MRTD) | pkCSM | High | 0.694 log(mg/kg/day) | |
| vNN | - | NoPrediction | ||
| Non-Genotoxic carcinogenicity | Toxtree | Yes | - | |
| Oral rat acute toxicity | pkCSM | - | 1.907 log(mg/kg_bw/day) (LD50) | |
| pkCSM | - | 1.829 log(mg/kg_bw/day) (LOAEL) | ||
| Micronucleus | admetSAR | Low | 9.72 % | |
| Skin sensitisation | pkCSM | No | - | |
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