Diheptyl phthalate
| Predicted ADME Properties | |||||
|---|---|---|---|---|---|
| Type | Property | Tool | Interpretation | Probability/Value | |
| Absorption | Caco-2 permeability | admetSAR | High | 89.95 % | |
| pkCSM | High | 1.39 cm/s | |||
| Human Intestinal Absorption | admetSAR | High | 90.03 % | ||
| pkCSM | High | 91.574 % | |||
| SwissADME | High | - | |||
| Human Oral Bioavailability | admetSAR | Low Bioavailability | 21.35 % | ||
| Log Kp (Skin permeation) | pkCSM | High | -2.655 logkp (cm/h) | ||
| SwissADME | - | -4.39 logkp (cm/s) | |||
| Distribution | P-glycoprotein substrate | admetSAR | Low | 3.29 % | |
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | No | - | |||
| P-glycoprotein inhibitor | admetSAR | Low | 45.43 % | ||
| vNN | No | - | |||
| P-glycoprotein inhibitor I | pkCSM | Yes | - | ||
| P-glycoprotein inhibitor II | pkCSM | No | - | ||
| Blood Brain Barrier | admetSAR | High | 93.27 % | ||
| pkCSM | Moderate | -0.148 logBB | |||
| SwissADME | No | - | |||
| vNN | Yes | - | |||
| CNS permeability | pkCSM | Moderate | -2.333 logPS | ||
| Fraction unbound in human | pkCSM | - | 0 | ||
| Plasma protein binding | admetSAR | 94.34 % | High | ||
| Steady state volume of distribution (VDss) | pkCSM | Moderate | 0.299 log(L/kg) | ||
| Metabolism | CYP1A2 inhibitor | admetSAR | Low | 24.38 % | |
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | Yes | - | |||
| CYP2C19 inhibitor | admetSAR | Low | 46.23 % | ||
| pkCSM | Yes | - | |||
| SwissADME | No | - | |||
| vNN | Yes | - | |||
| CYP2C9 inhibitor | admetSAR | Low | 23.68 % | ||
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | No | - | |||
| CYP2C9 substrate | admetSAR | Low | 8.34 % | ||
| CYP2D6 inhibitor | admetSAR | Low | 4.77 % | ||
| pkCSM | No | - | |||
| SwissADME | Yes | - | |||
| vNN | No | - | |||
| CYP2D6 substrate | admetSAR | Low | 2.64 % | ||
| pkCSM | No | - | |||
| CYP3A4 inhibitor | admetSAR | Low | 0.84 % | ||
| pkCSM | No | - | |||
| SwissADME | Yes | - | |||
| vNN | No | - | |||
| CYP3A4 substrate | admetSAR | Low | 15.65 % | ||
| pkCSM | Yes | - | |||
| Human Liver Microsomal (HLM) stability assay | vNN | Yes | - | ||
| OATP2B1 inhibitor | admetSAR | Low | 30.85 % | ||
| OATP1B1 inhibitor | admetSAR | High | 93.32 % | ||
| OATP1B3 inhibitor | admetSAR | High | 91.76 % | ||
| MATE1 inhibitor | admetSAR | Low | 6.5 % | ||
| BSEP inhibitor | admetSAR | High | 73.16 % | ||
| UGT catalysis | admetSAR | Low | 8.69 % | ||
| Excretion | Renal OCT2 inhibitor | admetSAR | Low | 20.45 % | |
| Renal OCT2 substrate | pkCSM | No | - | ||
| Total clearance | pkCSM | - | Not predicted - | ||
| Predicted Toxicity properties | ||||
|---|---|---|---|---|
| Property | Tool | Interpretation | Probability/Value | |
| Acute oral toxicity | admetSAR | - | -4.26524066925049 log(mg/kg) | |
| ProTox | - | Not predicted - | ||
| Acute oral toxicity class | admetSAR | Low | 0.69 % | |
| ProTox | Not predicted | - | ||
| Biodegradation | admetSAR | High | 81.35 % | |
| Toxtree | Not predicted | - | ||
| Carcinogens | admetSAR | Low | 14.43 % | |
| Toxtree | Not predicted | - | ||
| Cramer's rule | Toxtree | Not predicted | - | |
| Cytotoxicity | vNN | No | - | |
| Genotoxic carcinogenity | Toxtree | Not predicted | - | |
| Hepatotoxicity | admetSAR | Low | 42.99 % | |
| pkCSM | No | - | ||
| vNN | No | - | ||
| Human Ether-a-go-go-Related Gene Inhibitor | admetSAR | Low | 39.21 % | |
| 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 | 1.379 log(mg/kg/day) | |
| vNN | - | 1206 mg/day | ||
| Non-Genotoxic carcinogenicity | Toxtree | Not predicted | - | |
| Oral rat acute toxicity | pkCSM | - | 1.398 log(mg/kg_bw/day) (LD50) | |
| pkCSM | - | 2.586 log(mg/kg_bw/day) (LOAEL) | ||
| Micronucleus | admetSAR | Low | 1.52 % | |
| Skin sensitisation | pkCSM | No | - | |
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