Literature identifier | Study type | Test dosage | Effective dosage | Endocrine-mediated endpoints | Systems-level perturbations |
---|---|---|---|---|---|
PMID:12748709 | IVR | 5 mg/kg | 5 mg/kg | Hyperplasia in adrenal gland | Metabolic endocrine-mediated perturbations |
IVR | 10 mg/kg | 10 mg/kg | Affects hematopoiesis of spleen | Immunological endocrine-mediated perturbations | |
IVR | 10 mg/kg | 10 mg/kg | Hyperplasia in adrenal gland | Metabolic endocrine-mediated perturbations | |
IVR | 10 mg/kg | 10 mg/kg | Affects morphology of hepatocytes | Hepatic endocrine-mediated perturbations | |
IVR | 10 mg/kg | 10 mg/kg | Hyperplasia of bone marrow | Immunological endocrine-mediated perturbations | |
IVR | 10 mg/kg | 10 mg/kg | Affects hematopoiesis of liver | Hepatic endocrine-mediated perturbations;Immunological endocrine-mediated perturbations | |
IVR | 20 mg/kg | 20 mg/kg | Affects morphology of hepatocytes | Hepatic endocrine-mediated perturbations | |
IVR | 1200 mg/kg | - | No significant effects observed | - | |
IVR | 7.5 mg/kg | - | No significant effects observed | - | |
IVR | 600 mg/kg | - | No significant effects observed | - | |
IVR | 50 mg/kg | - | No significant effects observed | - | |
IVR | 30 mg/kg | - | No significant effects observed | - | |
IVR | 150 mg/kg | - | No significant effects observed | - | |
IVR | 12.5 mg/kg | - | No significant effects observed | - | |
IVR | 75 mg/kg | - | No significant effects observed | - | |
IVR | 25 mg/kg | - | No significant effects observed | - | |
IVR | 15 mg/kg | - | No significant effects observed | - | |
IVR | 3.75 mg/kg | - | No significant effects observed | - | |
IVR | 300 mg/kg | - | No significant effects observed | - | |
IVR | 40 mg/kg | 40 mg/kg | Affects morphology of hepatocytes | Hepatic endocrine-mediated perturbations | |
IVR | 60 mg/kg | 60 mg/kg | Affects morphology of hepatocytes | Hepatic 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.