| Literature identifier | Study type | Test dosage | Effective dosage | Endocrine-mediated endpoints | Systems-level perturbations |
|---|---|---|---|---|---|
| PMID:1658985 | IVR | 25 mg/kg | 25 mg/kg | Increase in corticosterone levels | Neurological endocrine-mediated perturbations |
| IVR | 25 mg/kg | 25 mg/kg | Decreased prolactin levels | Reproductive endocrine-mediated perturbations | |
| IVR | 25 mg/kg | 25 mg/kg | Increased levels of adrenocortical hormones (ACTH) | Metabolic endocrine-mediated perturbations | |
| IVR | 20 mg/kg | - | No significant effects observed | - | |
| IVR | 50 mg/kg | 50 mg/kg | Increase in corticosterone levels | Neurological endocrine-mediated perturbations | |
| IVR | 50 mg/kg | 50 mg/kg | Decreased prolactin levels | Reproductive endocrine-mediated perturbations | |
| IVR | 50 mg/kg | 50 mg/kg | Increased levels of adrenocortical hormones (ACTH) | Metabolic endocrine-mediated perturbations | |
| PMID:2113720 | IVR | 50 mg/kg | 50 mg/kg | Decreased FSH levels | Reproductive endocrine-mediated perturbations |
| IVR | 50 mg/kg | 50 mg/kg | Decreased testosterone levels | Reproductive endocrine-mediated perturbations | |
| IVR | 50 mg/kg | 50 mg/kg | Decrease in T3 levels | Metabolic endocrine-mediated perturbations | |
| IVR | 50 mg/kg | 50 mg/kg | Decrease in T4 levels | Metabolic endocrine-mediated perturbations | |
| IVR | 50 mg/kg | 50 mg/kg | Decreased LH levels | Reproductive endocrine-mediated perturbations | |
| IVR | 20 mg/kg | 20 mg/kg | Decrease in T3 levels | Metabolic endocrine-mediated perturbations | |
| PMID:708932 | IVR | 148 mg/kg | 148 mg/kg | Alterations in immune responses | Immunological endocrine-mediated perturbations |
| IVR | 14.8 mg/kg | - | No significant effects observed | - | |
| PMID:8050642 | IVR | 50 mg/kg | 50 mg/kg | Affects implantation | Reproductive endocrine-mediated perturbations |
| IVR | 50 mg/kg | 50 mg/kg | Affects litter size | Reproductive endocrine-mediated perturbations | |
| IVR | 50 mg/kg | 50 mg/kg | Affects ovulation | Reproductive endocrine-mediated perturbations |
We have built a comprehensive resource which compiles potential endocrine disrupting chemicals (EDCs) based on the observed adverse effects or endocrine-mediated endpoints in published experiments on humans or rodents to support basic research. We are not responsible for any errors or omissions in the published research articles or supporting literature on potential EDCs compiled in this resource. Users are advised to exercise their own judgement on the weight of evidence for potential EDCs compiled in this resource. Importantly, our sole goal to build this resource on potential EDCs is to enable future basic research towards better understanding of the systems-level perturbations upon chemical exposure rather than influencing regulatory advice on chemical use.