Literature identifier | Study type | Test dosage | Effective dosage | Endocrine-mediated endpoints | Systems-level perturbations |
---|---|---|---|---|---|
DOI:10.1016/0045-6535(92)90467-6 | IVR | 0.000001 - 0.0005 mmol/kg | 0.000001 - 0.0001 mmol/kg | Affects xenobiotic metabolism | Metabolic endocrine-mediated perturbations |
PMID:17447562 | IVTH | 0.000000004 - 0.000004 M | 0.000000004 - 0.000004 M | Affects corticosterone metabolism | Metabolic endocrine-mediated perturbations;Neurological endocrine-mediated perturbations |
IVTH | 0.000000004 - 0.000004 M | 0.000000004 - 0.000004 M | Affects steroidogenesis | Reproductive endocrine-mediated perturbations | |
PMID:8248944 | IVR | 0.0001 mg/kg | 0.0001 mg/kg | Increase in T3 levels | Metabolic endocrine-mediated perturbations |
IVR | 0.0001 mg/kg | 0.0001 mg/kg | Decrease in T4 levels | Metabolic endocrine-mediated perturbations | |
IVR | 0.01 mg/kg | 0.01 mg/kg | Increased Aspartate aminotransferase (AST) levels | Hepatic endocrine-mediated perturbations | |
IVR | 0.01 mg/kg | 0.01 mg/kg | Decreased thymus gland weights | Immunological endocrine-mediated perturbations | |
IVR | 0.01 mg/kg | 0.01 mg/kg | Decreased triglycerides level | Metabolic endocrine-mediated perturbations | |
IVR | 0.01 mg/kg | 0.01 mg/kg | Increased Alanine aminotransferase (ALT) levels | Hepatic endocrine-mediated perturbations | |
IVR | 0.01 mg/kg | 0.01 mg/kg | Changes in haemocrit values | Immunological endocrine-mediated perturbations | |
IVR | 0.00001 mg/kg | - | No significant effects observed | - | |
IVR | 0.001 mg/kg | 0.001 mg/kg | Decreased triglycerides level | Metabolic endocrine-mediated perturbations | |
IVR | 0.001 mg/kg | 0.001 mg/kg | Increased Aspartate aminotransferase (AST) levels | Hepatic endocrine-mediated perturbations | |
IVR | 0.001 mg/kg | 0.001 mg/kg | Changes in haemocrit values | Immunological endocrine-mediated perturbations | |
IVR | 0.001 mg/kg | 0.001 mg/kg | Decreased thymus gland weights | Immunological endocrine-mediated perturbations | |
IVR | 0.001 mg/kg | 0.001 mg/kg | Increased Alanine aminotransferase (ALT) levels | Hepatic endocrine-mediated perturbations | |
IVR | 0.003 mg/kg | 0.003 mg/kg | Decreased triglycerides level | Metabolic endocrine-mediated perturbations | |
IVR | 0.003 mg/kg | 0.003 mg/kg | Increased Aspartate aminotransferase (AST) levels | Hepatic endocrine-mediated perturbations | |
IVR | 0.003 mg/kg | 0.003 mg/kg | Decreased thymus gland weights | Immunological endocrine-mediated perturbations | |
IVR | 0.003 mg/kg | 0.003 mg/kg | Changes in haemocrit values | Immunological endocrine-mediated perturbations | |
IVR | 0.003 mg/kg | 0.003 mg/kg | Increased Alanine aminotransferase (ALT) levels | 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.