Literature identifier | Study type | Test dosage | Effective dosage | Endocrine-mediated endpoints | Systems-level perturbations |
---|---|---|---|---|---|
PMID:18779953 | IVR | 300 mg/kg | - | No significant effects observed | - |
IVR | 40 mg/kg | - | No significant effects observed | - | |
IVR | 25 mg/kg | 25 mg/kg | Increased weights of thyroid gland | Metabolic endocrine-mediated perturbations | |
IVR | 100 mg/kg | - | No significant effects observed | - | |
IVR | 25 mg/kg | 25 mg/kg | Increased liver weights | Hepatic endocrine-mediated perturbations | |
IVR | 1000 mg/kg | - | No significant effects observed | - | |
IVR | 25 mg/kg | 25 mg/kg | Hypertrophy in thyroid gland | Metabolic endocrine-mediated perturbations | |
IVR | 5 mg/kg | - | No significant effects observed | - | |
IVR | 200 mg/kg | - | No significant effects observed | - | |
IVR | 125 mg/kg | 125 mg/kg | Increased weights of thyroid gland | Metabolic endocrine-mediated perturbations | |
IVR | 125 mg/kg | 125 mg/kg | Decrease in T3 levels | Metabolic endocrine-mediated perturbations | |
IVR | 125 mg/kg | 125 mg/kg | Increased weights of seminal vesicles | Reproductive endocrine-mediated perturbations | |
IVR | 125 mg/kg | 125 mg/kg | Decreased spleen weights | Immunological endocrine-mediated perturbations | |
IVR | 125 mg/kg | 125 mg/kg | Changes in morphology of pituitary gland | Neurological endocrine-mediated perturbations | |
IVR | 125 mg/kg | 125 mg/kg | Increase in TSH levels | Metabolic endocrine-mediated perturbations | |
IVR | 125 mg/kg | 125 mg/kg | Hypertrophy in thyroid gland | Metabolic endocrine-mediated perturbations | |
IVR | 125 mg/kg | 125 mg/kg | Increased weights of adrenal gland | Metabolic endocrine-mediated perturbations | |
IVR | 125 mg/kg | 125 mg/kg | Decreased liver weights | Hepatic endocrine-mediated perturbations | |
IVR | 125 mg/kg | 125 mg/kg | Increased weights of pituitary gland | Neurological endocrine-mediated perturbations | |
IVR | 125 mg/kg | 125 mg/kg | Decrease in T4 levels | Metabolic endocrine-mediated perturbations | |
IVR | 125 mg/kg | 125 mg/kg | Affects liver function | Hepatic endocrine-mediated perturbations | |
PMID:4177895 | IVR | 0.5 mg/L | 0.5 mg/L | Affects thyroid function | Metabolic endocrine-mediated perturbations |
IVR | 0.5 mg/L | 0.5 mg/L | Affects iodine uptake into thyroid | Metabolic endocrine-mediated perturbations | |
IVR | 0.25 mg/L | - | No significant effects observed | - | |
IVR | 10 mg/L | 10 mg/L | Affects thyroid function | Metabolic endocrine-mediated perturbations | |
IVR | 50 mg/L | 50 mg/L | Affects thyroid function | Metabolic endocrine-mediated perturbations | |
IVR | 2 mg/L | 2 mg/L | Affects iodine uptake into thyroid | Metabolic endocrine-mediated perturbations | |
IVR | 2 mg/L | 2 mg/L | Affects thyroid function | Metabolic endocrine-mediated perturbations | |
PMID:6868082 | IVR | 100 mg/L | 100 mg/L | Affects survival of live fetus | Reproductive endocrine-mediated perturbations |
IVR | 100 mg/L | 100 mg/L | Affects thyroid function | Metabolic endocrine-mediated perturbations | |
IVR | 100 mg/L | 100 mg/L | Changes in morphology of pituitary gland | Neurological endocrine-mediated perturbations | |
IVR | 100 mg/L | 100 mg/L | Thyroid gland carcinoma | Endocrine-mediated cancer;Metabolic endocrine-mediated perturbations | |
IVR | 100 mg/L | 100 mg/L | Pituitary gland carcinoma | Endocrine-mediated cancer;Neurological endocrine-mediated perturbations | |
IVR | 10 mg/L | - | No significant effects observed | - | |
IVR | 1 mg/L | - | No significant effects observed | - |
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.