2-Benzyl-2-(dimethylamino)-1-(4-(morpholin-4-yl)phenyl)butan-1-one
| Predicted ADME Properties | |||||
|---|---|---|---|---|---|
| Type | Property | Tool | Interpretation | Probability/Value | |
| Absorption | Caco-2 permeability | admetSAR | High | 89.68 % | |
| pkCSM | High | 1.087 cm/s | |||
| Human Intestinal Absorption | admetSAR | High | 98.48 % | ||
| pkCSM | High | 96.693 % | |||
| SwissADME | High | - | |||
| Human Oral Bioavailability | admetSAR | Low Bioavailability | 37.54 % | ||
| Log Kp (Skin permeation) | pkCSM | Low | -2.486 logkp (cm/h) | ||
| SwissADME | - | -5.6 logkp (cm/s) | |||
| Distribution | P-glycoprotein substrate | admetSAR | High | 76.76 % | |
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | Yes | - | |||
| P-glycoprotein inhibitor | admetSAR | High | 90.34 % | ||
| vNN | Yes | - | |||
| P-glycoprotein inhibitor I | pkCSM | Yes | - | ||
| P-glycoprotein inhibitor II | pkCSM | Yes | - | ||
| Blood Brain Barrier | admetSAR | High | 94.9 % | ||
| pkCSM | Moderate | -0.019 logBB | |||
| SwissADME | Yes | - | |||
| vNN | Yes | - | |||
| CNS permeability | pkCSM | Yes | -1.845 logPS | ||
| Fraction unbound in human | pkCSM | - | 0.135 | ||
| Plasma protein binding | admetSAR | 84.22 % | Moderate | ||
| Steady state volume of distribution (VDss) | pkCSM | High | 1.245 log(L/kg) | ||
| Metabolism | CYP1A2 inhibitor | admetSAR | Low | 19.57 % | |
| pkCSM | Yes | - | |||
| SwissADME | No | - | |||
| vNN | No | - | |||
| CYP2C19 inhibitor | admetSAR | Low | 23.84 % | ||
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | No | - | |||
| CYP2C9 inhibitor | admetSAR | Low | 18.46 % | ||
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | No | - | |||
| CYP2C9 substrate | admetSAR | High | 55.97 % | ||
| CYP2D6 inhibitor | admetSAR | High | 72.78 % | ||
| pkCSM | Yes | - | |||
| SwissADME | Yes | - | |||
| vNN | No | - | |||
| CYP2D6 substrate | admetSAR | High | 88.33 % | ||
| pkCSM | No | - | |||
| CYP3A4 inhibitor | admetSAR | Low | 42.27 % | ||
| pkCSM | Yes | - | |||
| SwissADME | Yes | - | |||
| vNN | No | - | |||
| CYP3A4 substrate | admetSAR | High | 89.2 % | ||
| pkCSM | Yes | - | |||
| Human Liver Microsomal (HLM) stability assay | vNN | Yes | - | ||
| OATP2B1 inhibitor | admetSAR | Low | 11.84 % | ||
| OATP1B1 inhibitor | admetSAR | High | 92.73 % | ||
| OATP1B3 inhibitor | admetSAR | High | 94.91 % | ||
| MATE1 inhibitor | admetSAR | Low | 18.61 % | ||
| BSEP inhibitor | admetSAR | High | 92.6 % | ||
| UGT catalysis | admetSAR | Low | 27.15 % | ||
| Excretion | Renal OCT2 inhibitor | admetSAR | High | 61.46 % | |
| Renal OCT2 substrate | pkCSM | No | - | ||
| Total clearance | pkCSM | - | Not predicted - | ||
| Predicted Toxicity properties | ||||
|---|---|---|---|---|
| Property | Tool | Interpretation | Probability/Value | |
| Acute oral toxicity | admetSAR | - | -2.49283885955811 log(mg/kg) | |
| ProTox | - | Not predicted - | ||
| Acute oral toxicity class | admetSAR | High | 99.25 % | |
| ProTox | Not predicted | - | ||
| Biodegradation | admetSAR | Low | 3.07 % | |
| Toxtree | Not predicted | - | ||
| Carcinogens | admetSAR | Low | 38.25 % | |
| Toxtree | Not predicted | - | ||
| Cramer's rule | Toxtree | Not predicted | - | |
| Cytotoxicity | vNN | No | - | |
| Genotoxic carcinogenity | Toxtree | Not predicted | - | |
| Hepatotoxicity | admetSAR | Low | 47.42 % | |
| pkCSM | Yes | - | ||
| vNN | Yes | - | ||
| Human Ether-a-go-go-Related Gene Inhibitor | admetSAR | High | 85.89 % | |
| 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 | No | - | |
| Maximum Recommended Tolerated Dose (MRTD) | pkCSM | High | 0.65 log(mg/kg/day) | |
| vNN | - | 182 mg/day | ||
| Non-Genotoxic carcinogenicity | Toxtree | Not predicted | - | |
| Oral rat acute toxicity | pkCSM | - | 2.921 log(mg/kg_bw/day) (LD50) | |
| pkCSM | - | 1.056 log(mg/kg_bw/day) (LOAEL) | ||
| Micronucleus | admetSAR | High | 78.2 % | |
| Skin sensitisation | pkCSM | No | - | |
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