3,6-Dichlorocarbazole
| Predicted ADME Properties | |||||
|---|---|---|---|---|---|
| Type | Property | Tool | Interpretation | Probability/Value | |
| Absorption | Caco-2 permeability | admetSAR | High | 88.21 % | |
| pkCSM | High | 1.363 cm/s | |||
| Human Intestinal Absorption | admetSAR | High | 98.7 % | ||
| pkCSM | High | 90.806 % | |||
| SwissADME | High | - | |||
| Human Oral Bioavailability | admetSAR | High Bioavailability | 51.48 % | ||
| Log Kp (Skin permeation) | pkCSM | High | -2.611 logkp (cm/h) | ||
| SwissADME | - | -3.93 logkp (cm/s) | |||
| Distribution | P-glycoprotein substrate | admetSAR | Low | 9.8 % | |
| pkCSM | Yes | - | |||
| SwissADME | No | - | |||
| vNN | No | - | |||
| P-glycoprotein inhibitor | admetSAR | High | 52.06 % | ||
| vNN | No | - | |||
| P-glycoprotein inhibitor I | pkCSM | No | - | ||
| P-glycoprotein inhibitor II | pkCSM | No | - | ||
| Blood Brain Barrier | admetSAR | High | 96.3 % | ||
| pkCSM | Yes | 0.671 logBB | |||
| SwissADME | Yes | - | |||
| vNN | No | - | |||
| CNS permeability | pkCSM | Yes | -1.599 logPS | ||
| Fraction unbound in human | pkCSM | - | 0.051 | ||
| Plasma protein binding | admetSAR | 106.15 % | High | ||
| Steady state volume of distribution (VDss) | pkCSM | High | 0.488 log(L/kg) | ||
| Metabolism | CYP1A2 inhibitor | admetSAR | High | 97.66 % | |
| pkCSM | Yes | - | |||
| SwissADME | Yes | - | |||
| vNN | No | - | |||
| CYP2C19 inhibitor | admetSAR | High | 85.42 % | ||
| pkCSM | Yes | - | |||
| SwissADME | Yes | - | |||
| vNN | No | - | |||
| CYP2C9 inhibitor | admetSAR | Low | 47.87 % | ||
| pkCSM | Yes | - | |||
| SwissADME | No | - | |||
| vNN | No | - | |||
| CYP2C9 substrate | admetSAR | High | 85.43 % | ||
| CYP2D6 inhibitor | admetSAR | Low | 49.05 % | ||
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | No | - | |||
| CYP2D6 substrate | admetSAR | High | 69.31 % | ||
| pkCSM | No | - | |||
| CYP3A4 inhibitor | admetSAR | Low | 15.81 % | ||
| pkCSM | No | - | |||
| SwissADME | No | - | |||
| vNN | No | - | |||
| CYP3A4 substrate | admetSAR | High | 88.81 % | ||
| pkCSM | Yes | - | |||
| Human Liver Microsomal (HLM) stability assay | vNN | Yes | - | ||
| OATP2B1 inhibitor | admetSAR | Low | 29.94 % | ||
| OATP1B1 inhibitor | admetSAR | High | 94.06 % | ||
| OATP1B3 inhibitor | admetSAR | High | 95.11 % | ||
| MATE1 inhibitor | admetSAR | Low | 14.95 % | ||
| BSEP inhibitor | admetSAR | High | 92.32 % | ||
| UGT catalysis | admetSAR | Low | 12.06 % | ||
| Excretion | Renal OCT2 inhibitor | admetSAR | Low | 24.87 % | |
| Renal OCT2 substrate | pkCSM | No | - | ||
| Total clearance | pkCSM | - | Not predicted - | ||
| Predicted Toxicity properties | ||||
|---|---|---|---|---|
| Property | Tool | Interpretation | Probability/Value | |
| Acute oral toxicity | admetSAR | - | -2.97458744049072 log(mg/kg) | |
| ProTox | - | Not predicted - | ||
| Acute oral toxicity class | admetSAR | High | 86.48 % | |
| ProTox | Not predicted | - | ||
| Biodegradation | admetSAR | Low | 4.19 % | |
| Toxtree | Not predicted | - | ||
| Carcinogens | admetSAR | High | 70.71 % | |
| Toxtree | Not predicted | - | ||
| Cramer's rule | Toxtree | Not predicted | - | |
| Cytotoxicity | vNN | No | - | |
| Genotoxic carcinogenity | Toxtree | Not predicted | - | |
| Hepatotoxicity | admetSAR | High | 72.67 % | |
| pkCSM | No | - | ||
| vNN | Yes | - | ||
| Human Ether-a-go-go-Related Gene Inhibitor | admetSAR | High | 92.56 % | |
| 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 | Low | 0.303 log(mg/kg/day) | |
| vNN | - | 169 mg/day | ||
| Non-Genotoxic carcinogenicity | Toxtree | Not predicted | - | |
| Oral rat acute toxicity | pkCSM | - | 3.094 log(mg/kg_bw/day) (LD50) | |
| pkCSM | - | 1.054 log(mg/kg_bw/day) (LOAEL) | ||
| Micronucleus | admetSAR | High | 72.61 % | |
| Skin sensitisation | pkCSM | No | - | |
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