Aluminum sulfate
| Predicted ADME Properties | |||||
|---|---|---|---|---|---|
| Type | Property | Tool | Interpretation | Probability/Value | |
| Absorption | Caco-2 permeability | admetSAR | High | 58.6 % | |
| pkCSM | Low | -0.927 cm/s | |||
| Human Intestinal Absorption | admetSAR | High | 65.38 % | ||
| pkCSM | Low | 0.0 % | |||
| SwissADME | Low | - | |||
| Human Oral Bioavailability | admetSAR | High Bioavailability | 0.8094379901885986 % | ||
| Log Kp (Skin permeation) | pkCSM | High | -2.735 cm/h | ||
| SwissADME | - | -3.23 cm/s | |||
| Distribution | P-glycoprotein substrate | admetSAR | Low | 3.73 % | |
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | No | - | |||
| P-glycoprotein inhibitor | admetSAR | Low | 8.67 % | ||
| vNN | No | - | |||
| P-glycoprotein inhibitor I | pkCSM | No | - | ||
| P-glycoprotein inhibitor II | pkCSM | No | - | ||
| Blood Brain Barrier | admetSAR | Low | 30.57 % | ||
| pkCSM | No | -2.496 logBB | |||
| SwissADME | No | - | |||
| vNN | No | - | |||
| CNS permeability | pkCSM | No | -3.58 logPS | ||
| Fraction unbound in human | pkCSM | - | 0.453 | ||
| Plasma protein binding | admetSAR | 51.44 % | Moderate | ||
| Steady state volume of distribution (VDss) | pkCSM | Low | -0.333 L/kg | ||
| Metabolism | CYP1A2 inhibitor | admetSAR | Low | 18.54 % | |
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | No | - | |||
| CYP2C19 inhibitor | admetSAR | Low | 7.39 % | ||
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | No | - | |||
| CYP2C9 inhibitor | admetSAR | Low | 5.99 % | ||
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | No | - | |||
| CYP2C9 substrate | admetSAR | Low | 20.18 % | ||
| CYP2D6 inhibitor | admetSAR | Low | 12.94 % | ||
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | No | - | |||
| CYP2D6 substrate | admetSAR | Low | 9.02 % | ||
| pkCSM | No | - | |||
| CYP3A4 inhibitor | admetSAR | Low | 0.72 % | ||
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | No | - | |||
| CYP3A4 substrate | admetSAR | Low | 21.27 % | ||
| pkCSM | No | - | |||
| Human Liver Microsomal (HLM) stability assay | vNN | Yes | - | ||
| OATP2B1 inhibitor | admetSAR | Low | 26.74 % | ||
| OATP1B1 inhibitor | admetSAR | High | 78.92 % | ||
| OATP1B3 inhibitor | admetSAR | High | 92.17 % | ||
| MATE1 inhibitor | admetSAR | Low | 13.35 % | ||
| BSEP inhibitor | admetSAR | ||||
| UGT catalysis | admetSAR | High | 71.38 % | ||
| Excretion | Renal OCT2 inhibitor | admetSAR | Low | 8.22 % | |
| Renal OCT2 substrate | pkCSM | No | - | ||
| Total clearance | pkCSM | - | Not predicted - | ||
| Predicted Toxicity properties | ||||
|---|---|---|---|---|
| Property | Tool | Interpretation | Probability/Value | |
| Acute oral toxicity | admetSAR | - | -2.49091148376465 log(mg/kg) | |
| ProTox | - | Not predicted - | ||
| Acute oral toxicity class | admetSAR | High | 87.75 % | |
| ProTox | Not predicted | - | ||
| Biodegradation | admetSAR | Low | 39.73 % | |
| Toxtree | Not predicted | - | ||
| Carcinogens | admetSAR | High | 0.531386971473694 | |
| Toxtree | Not predicted | - | ||
| Cramer's rule | Toxtree | Not predicted | - | |
| Cytotoxicity | vNN | No | - | |
| Genotoxic carcinogenity | Toxtree | Not predicted | - | |
| Hepatotoxicity | admetSAR | High | 0.746848583221436 | |
| pkCSM | No | - | ||
| vNN | No | - | ||
| Human Ether-a-go-go-Related Gene Inhibitor | admetSAR | Low | 11.89 % | |
| 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 | 0.64 log(mg/kg/day) | |
| vNN | - | 97 mg/day | ||
| Non-Genotoxic carcinogenicity | Toxtree | Not predicted | - | |
| Oral rat acute toxicity | pkCSM | - | 2.413 log(mg/kg_bw/day) (LD50) | |
| pkCSM | - | 0.287 log(mg/kg_bw/day) (LOAEL) | ||
| Micronucleus | admetSAR | High | 58.79 % | |
| Skin sensitisation | pkCSM | No | - | |
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