Literature identifier | Study type | Test dosage | Effective dosage | Endocrine-mediated endpoints | Systems-level perturbations |
---|---|---|---|---|---|
PMID:15458793 | IVR | 250 mg/kg | 250 mg/kg | Decrease in T4 levels | Metabolic endocrine-mediated perturbations |
IVR | 250 mg/kg | 250 mg/kg | Decrease in T3 levels | Metabolic endocrine-mediated perturbations | |
IVR | 250 mg/kg | 250 mg/kg | Affects developmental process | Developmental endocrine-mediated perturbations | |
IVR | 1000 mg/kg | 1000 mg/kg | Affects developmental process | Developmental endocrine-mediated perturbations | |
IVR | 1000 mg/kg | 1000 mg/kg | Decrease in T3 levels | Metabolic endocrine-mediated perturbations | |
IVR | 1000 mg/kg | 1000 mg/kg | Decrease in T4 levels | Metabolic endocrine-mediated perturbations | |
PMID:15458797 | IVR | 250 mg/kg | 250 mg/kg | Affects the normal functioning of reproductive system | Reproductive endocrine-mediated perturbations |
IVR | 1000 mg/kg | 1000 mg/kg | Affects the normal functioning of reproductive system | Reproductive endocrine-mediated perturbations | |
IVR | 1000 mg/kg | 1000 mg/kg | Affects xenobiotic metabolism | Metabolic endocrine-mediated perturbations | |
IVR | 1000 mg/kg | 1000 mg/kg | Affects expression of estrogen receptor-beta (ER-beta) | Reproductive endocrine-mediated perturbations | |
IVR | 1000 mg/kg | 1000 mg/kg | Affects expression of estrogen receptor-alpha (ER-alpha) | Reproductive endocrine-mediated perturbations | |
PMID:15721882 | IVR | 625 mg/kg/day | - | No significant effects observed | - |
IVR | 250 mg/kg/day | - | No significant effects observed | - | |
IVR | 100 mg/kg/day | 100 mg/kg/day | Increased uterine weights | Reproductive endocrine-mediated perturbations | |
PMID:15951094 | IVR | 153 mg/kg | 153 mg/kg | Increased triglycerides level | Metabolic endocrine-mediated perturbations |
IVR | 153 mg/kg | 153 mg/kg | Decrease in T4 levels | Metabolic endocrine-mediated perturbations | |
IVR | 677 mg/kg | 677 mg/kg | Increased LH levels | Reproductive endocrine-mediated perturbations | |
PMID:17379648 | IVR | 0.01 mg/kg | - | No significant effects observed | - |
IVR | 0.1 mg/kg | - | No significant effects observed | - | |
IVR | 0.033 mg/kg | - | No significant effects observed | - | |
IVR | 1 mg/kg | 1 mg/kg | Increase in TSH levels | Metabolic endocrine-mediated perturbations | |
IVR | 1 mg/kg | 1 mg/kg | Decrease in T4 levels | Metabolic endocrine-mediated perturbations | |
IVR | 0.333 mg/kg | 0.333 mg/kg | Increase in TSH levels | Metabolic endocrine-mediated perturbations | |
IVR | 0.333 mg/kg | 0.333 mg/kg | Decrease in T4 levels | Metabolic endocrine-mediated perturbations | |
PMID:21726595 | IVR | 50 mg/kg | 50 mg/kg | Affects steroidogenesis | Reproductive endocrine-mediated perturbations |
IVR | 50 mg/kg | 50 mg/kg | Affects leydig cells function | Reproductive endocrine-mediated perturbations | |
IVR | 50 mg/kg | 50 mg/kg | Decreased testosterone levels | Reproductive endocrine-mediated perturbations | |
PMID:28990245 | IVTH | 0.00001 M | - | No significant effects observed | - |
IVTH | 0.0000001 M | 0.0000001 M | Induced migration capability of tumor cells | Endocrine-mediated cancer | |
PMID:30817981 | IVTH | 0.000005 M | 0.000005 M | Increased estradiol levels | Reproductive endocrine-mediated perturbations |
IVTH | 0.000005 M | 0.000005 M | Affects steroidogenesis | 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.