Literature identifier | Study type | Test dosage | Effective dosage | Endocrine-mediated endpoints | Systems-level perturbations |
---|---|---|---|---|---|
PMID:12750745 | IVR | 300 mg/L | 300 mg/L | Changes in morphology of thyroid gland | Metabolic endocrine-mediated perturbations |
IVR | 300 mg/L | 300 mg/L | Granulosa cell carcinoma | Endocrine-mediated cancer;Reproductive endocrine-mediated perturbations | |
IVR | 300 mg/L | 300 mg/L | Changes in adrenal gland morphology | Metabolic endocrine-mediated perturbations | |
IVR | 300 mg/L | 300 mg/L | Hyperplasia in thyroid gland | Metabolic endocrine-mediated perturbations | |
IVR | 150 mg/L | 150 mg/L | Changes in adrenal gland morphology | Metabolic endocrine-mediated perturbations | |
IVR | 150 mg/L | 150 mg/L | Hyperplasia in thyroid gland | Metabolic endocrine-mediated perturbations | |
IVR | 150 mg/L | 150 mg/L | Changes in morphology of thyroid gland | Metabolic endocrine-mediated perturbations | |
IVR | 150 mg/L | 150 mg/L | Granulosa cell carcinoma | Endocrine-mediated cancer;Reproductive endocrine-mediated perturbations | |
IVR | 800 mg/L | 800 mg/L | Hyperplasia in pituitary gland | Neurological endocrine-mediated perturbations | |
IVR | 1600 mg/L | - | No significant effects observed | - | |
IVR | 100 mg/L | - | No significant effects observed | - | |
IVR | 3200 mg/L | - | No significant effects observed | - | |
IVR | 50 mg/L | - | No significant effects observed | - | |
IVR | 200 mg/L | - | No significant effects observed | - | |
IVR | 400 mg/L | 400 mg/L | Hyperplasia in thyroid gland | Metabolic endocrine-mediated perturbations | |
IVR | 400 mg/L | 400 mg/L | Changes in morphology of thyroid gland | Metabolic endocrine-mediated perturbations | |
PMID:3712494 | IVR | 300 mg/L | 300 mg/L | Changes in morphology of thyroid gland | Metabolic endocrine-mediated perturbations |
IVR | 300 mg/L | 300 mg/L | Thyroid gland carcinoma | Endocrine-mediated cancer;Metabolic endocrine-mediated perturbations | |
IVR | 300 mg/L | 300 mg/L | Hematopietic carcinoma | Endocrine-mediated cancer;Immunological endocrine-mediated perturbations | |
IVR | 300 mg/L | 300 mg/L | Changes in liver morphology | Hepatic endocrine-mediated perturbations | |
IVR | 300 mg/L | 300 mg/L | Hepatocellular carcinoma | Endocrine-mediated cancer;Hepatic endocrine-mediated perturbations | |
IVR | 300 mg/L | 300 mg/L | Changes in adrenal gland morphology | Metabolic endocrine-mediated perturbations | |
IVR | 150 mg/L | 150 mg/L | Changes in liver morphology | Hepatic endocrine-mediated perturbations | |
IVR | 150 mg/L | 150 mg/L | Hepatocellular carcinoma | Endocrine-mediated cancer;Hepatic endocrine-mediated perturbations | |
IVR | 150 mg/L | 150 mg/L | Changes in adrenal gland morphology | Metabolic endocrine-mediated perturbations | |
IVR | 150 mg/L | 150 mg/L | Hematopietic carcinoma | Endocrine-mediated cancer;Immunological endocrine-mediated perturbations | |
PMID:4293143 | IVR | 100 mg/kg | 100 mg/kg | Decrease in corticosterone levels | Neurological 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.