di-N-Octyl Phthalate
| Predicted ADME Properties | |||||
|---|---|---|---|---|---|
| Type | Property | Tool | Interpretation | Probability/Value | |
| Absorption | Caco-2 permeability | admetSAR | High | 87.04 % | |
| pkCSM | High | 1.381 cm/s | |||
| Human Intestinal Absorption | admetSAR | High | 88.68 % | ||
| pkCSM | High | 90.874 % | |||
| SwissADME | High | - | |||
| Human Oral Bioavailability | admetSAR | Low Bioavailability | 23.62 % | ||
| Log Kp (Skin permeation) | pkCSM | High | -2.672 logkp (cm/h) | ||
| SwissADME | - | -2.93 logkp (cm/s) | |||
| Distribution | P-glycoprotein substrate | admetSAR | Low | 3.41 % | |
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | No | - | |||
| P-glycoprotein inhibitor | admetSAR | High | 52.03 % | ||
| vNN | No | - | |||
| P-glycoprotein inhibitor I | pkCSM | Yes | - | ||
| P-glycoprotein inhibitor II | pkCSM | Yes | - | ||
| Blood Brain Barrier | admetSAR | High | 91.72 % | ||
| pkCSM | Moderate | -0.23 logBB | |||
| SwissADME | No | - | |||
| vNN | Yes | - | |||
| CNS permeability | pkCSM | Moderate | -2.329 logPS | ||
| Fraction unbound in human | pkCSM | - | 0 | ||
| Plasma protein binding | admetSAR | 94.0 % | High | ||
| Steady state volume of distribution (VDss) | pkCSM | Moderate | 0.35 log(L/kg) | ||
| Metabolism | CYP1A2 inhibitor | admetSAR | Low | 19.54 % | |
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | Yes | - | |||
| CYP2C19 inhibitor | admetSAR | Low | 41.07 % | ||
| pkCSM | Yes | - | |||
| SwissADME | No | - | |||
| vNN | Yes | - | |||
| CYP2C9 inhibitor | admetSAR | Low | 23.05 % | ||
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | No | - | |||
| CYP2C9 substrate | admetSAR | Low | 8.85 % | ||
| CYP2D6 inhibitor | admetSAR | Low | 4.58 % | ||
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | No | - | |||
| CYP2D6 substrate | admetSAR | Low | 2.68 % | ||
| pkCSM | No | - | |||
| CYP3A4 inhibitor | admetSAR | Low | 0.84 % | ||
| pkCSM | No | - | |||
| SwissADME | Yes | - | |||
| vNN | No | - | |||
| CYP3A4 substrate | admetSAR | Low | 16.13 % | ||
| pkCSM | Yes | - | |||
| Human Liver Microsomal (HLM) stability assay | vNN | Yes | - | ||
| OATP2B1 inhibitor | admetSAR | Low | 35.42 % | ||
| OATP1B1 inhibitor | admetSAR | High | 92.34 % | ||
| OATP1B3 inhibitor | admetSAR | High | 90.12 % | ||
| MATE1 inhibitor | admetSAR | Low | 7.21 % | ||
| BSEP inhibitor | admetSAR | High | 74.17 % | ||
| UGT catalysis | admetSAR | Low | 9.25 % | ||
| Excretion | Renal OCT2 inhibitor | admetSAR | Low | 20.75 % | |
| Renal OCT2 substrate | pkCSM | No | - | ||
| Total clearance | pkCSM | - | Not predicted - | ||
| Predicted Toxicity properties | ||||
|---|---|---|---|---|
| Property | Tool | Interpretation | Probability/Value | |
| Acute oral toxicity | admetSAR | - | -4.23641490936279 log(mg/kg) | |
| ProTox | - | Not predicted - | ||
| Acute oral toxicity class | admetSAR | Low | 0.78 % | |
| ProTox | Not predicted | - | ||
| Biodegradation | admetSAR | High | 80.43 % | |
| Toxtree | Not predicted | - | ||
| Carcinogens | admetSAR | Low | 14.63 % | |
| Toxtree | Not predicted | - | ||
| Cramer's rule | Toxtree | Not predicted | - | |
| Cytotoxicity | vNN | No | - | |
| Genotoxic carcinogenity | Toxtree | Not predicted | - | |
| Hepatotoxicity | admetSAR | Low | 38.82 % | |
| pkCSM | No | - | ||
| vNN | No | - | ||
| Human Ether-a-go-go-Related Gene Inhibitor | admetSAR | Low | 41.02 % | |
| vNN | No | - | ||
| Human Ether-a-go-go-Related Gene Inhibitor I | pkCSM | No | - | |
| Human Ether-a-go-go-Related Gene Inhibitor II | pkCSM | Yes | - | |
| Mitochondrial Membrane Potential (MMP) | vNN | No | - | |
| Maximum Recommended Tolerated Dose (MRTD) | pkCSM | High | 1.246 log(mg/kg/day) | |
| vNN | - | 1299 mg/day | ||
| Non-Genotoxic carcinogenicity | Toxtree | Not predicted | - | |
| Oral rat acute toxicity | pkCSM | - | 1.305 log(mg/kg_bw/day) (LD50) | |
| pkCSM | - | 2.731 log(mg/kg_bw/day) (LOAEL) | ||
| Micronucleus | admetSAR | Low | 1.72 % | |
| Skin sensitisation | pkCSM | No | - | |
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