Flumethrin
| Predicted ADME Properties | |||||
|---|---|---|---|---|---|
| Type | Property | Tool | Interpretation | Probability/Value | |
| Absorption | Caco-2 permeability | admetSAR | High | 75.48 % | |
| pkCSM | High | 1.103 cm/s | |||
| Human Intestinal Absorption | admetSAR | High | 97.25 % | ||
| pkCSM | High | 91.747 % | |||
| SwissADME | Low | - | |||
| Human Oral Bioavailability | admetSAR | High Bioavailability | 0.8466878533363342 % | ||
| Log Kp (Skin permeation) | pkCSM | High | -2.728 cm/h | ||
| SwissADME | - | -4.17 cm/s | |||
| Distribution | P-glycoprotein substrate | admetSAR | Low | 17.19 % | |
| pkCSM | No | - | |||
| SwissADME | Yes | - | |||
| vNN | No | - | |||
| P-glycoprotein inhibitor | admetSAR | High | 75.25 % | ||
| vNN | Yes | - | |||
| P-glycoprotein inhibitor I | pkCSM | Yes | - | ||
| P-glycoprotein inhibitor II | pkCSM | Yes | - | ||
| Blood Brain Barrier | admetSAR | High | 92.87 % | ||
| pkCSM | Moderate | -0.564 logBB | |||
| SwissADME | No | - | |||
| vNN | Yes | - | |||
| CNS permeability | pkCSM | Yes | -1.276 logPS | ||
| Fraction unbound in human | pkCSM | - | 0.011 | ||
| Plasma protein binding | admetSAR | 102.62 % | High | ||
| Steady state volume of distribution (VDss) | pkCSM | Moderate | -0.104 L/kg | ||
| Metabolism | CYP1A2 inhibitor | admetSAR | Low | 39.17 % | |
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | No | - | |||
| CYP2C19 inhibitor | admetSAR | High | 58.69 % | ||
| pkCSM | Yes | - | |||
| SwissADME | No | - | |||
| vNN | No | - | |||
| CYP2C9 inhibitor | admetSAR | Low | 47.36 % | ||
| pkCSM | Yes | - | |||
| SwissADME | Yes | - | |||
| vNN | No | - | |||
| CYP2C9 substrate | admetSAR | High | 83.07 % | ||
| CYP2D6 inhibitor | admetSAR | Low | 21.06 % | ||
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | No | - | |||
| CYP2D6 substrate | admetSAR | High | 53.81 % | ||
| pkCSM | No | - | |||
| CYP3A4 inhibitor | admetSAR | Low | 10.18 % | ||
| pkCSM | Yes | - | |||
| SwissADME | No | - | |||
| vNN | No | - | |||
| CYP3A4 substrate | admetSAR | High | 90.58 % | ||
| pkCSM | Yes | - | |||
| Human Liver Microsomal (HLM) stability assay | vNN | Yes | - | ||
| OATP2B1 inhibitor | admetSAR | Low | 45.96 % | ||
| OATP1B1 inhibitor | admetSAR | High | 81.53 % | ||
| OATP1B3 inhibitor | admetSAR | High | 83.84 % | ||
| MATE1 inhibitor | admetSAR | Low | 11.45 % | ||
| BSEP inhibitor | admetSAR | ||||
| UGT catalysis | admetSAR | Low | 10.96 % | ||
| Excretion | Renal OCT2 inhibitor | admetSAR | Low | 17.06 % | |
| Renal OCT2 substrate | pkCSM | No | - | ||
| Total clearance | pkCSM | - | Not predicted - | ||
| Predicted Toxicity properties | ||||
|---|---|---|---|---|
| Property | Tool | Interpretation | Probability/Value | |
| Acute oral toxicity | admetSAR | - | -1.68441092967987 log(mg/kg) | |
| ProTox | - | Not predicted - | ||
| Acute oral toxicity class | admetSAR | High | 92.64 % | |
| ProTox | Not predicted | - | ||
| Biodegradation | admetSAR | Low | 4.83 % | |
| Toxtree | Not predicted | - | ||
| Carcinogens | admetSAR | Low | 0.261739045381546 | |
| Toxtree | Not predicted | - | ||
| Cramer's rule | Toxtree | Not predicted | - | |
| Cytotoxicity | vNN | No | - | |
| Genotoxic carcinogenity | Toxtree | Not predicted | - | |
| Hepatotoxicity | admetSAR | High | 0.61084645986557 | |
| pkCSM | No | - | ||
| vNN | No | - | ||
| Human Ether-a-go-go-Related Gene Inhibitor | admetSAR | High | 87.79 % | |
| vNN | Yes | - | ||
| 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 | Yes | - | |
| Maximum Recommended Tolerated Dose (MRTD) | pkCSM | Low | 0.356 log(mg/kg/day) | |
| vNN | - | 209 mg/day | ||
| Non-Genotoxic carcinogenicity | Toxtree | Not predicted | - | |
| Oral rat acute toxicity | pkCSM | - | 2.854 log(mg/kg_bw/day) (LD50) | |
| pkCSM | - | 0.922 log(mg/kg_bw/day) (LOAEL) | ||
| Micronucleus | admetSAR | High | 53.95 % | |
| Skin sensitisation | pkCSM | No | - | |
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