| Literature identifier | Study type | Test dosage | Effective dosage | Endocrine-mediated endpoints | Systems-level perturbations |
|---|---|---|---|---|---|
| PMID:32239163 | IVR | 0.0005 mg/kg/day | 0.0005 mg/kg/day | Abnormal estrous cycles | Reproductive endocrine-mediated perturbations |
| IVR | 0.0005 mg/kg/day | 0.0005 mg/kg/day | Increased testosterone levels | Reproductive endocrine-mediated perturbations | |
| IVR | 0.0005 mg/kg/day | 0.0005 mg/kg/day | Abnormal oocyte morphology | Reproductive endocrine-mediated perturbations | |
| IVR | 0.0005 mg/kg/day | 0.0005 mg/kg/day | Oxidative stress in ovaries | Reproductive endocrine-mediated perturbations | |
| IVR | 0.0005 mg/kg/day | 0.0005 mg/kg/day | Oxidative stress in uterus | Reproductive endocrine-mediated perturbations | |
| IVR | 0.0005 mg/kg/day | 0.0005 mg/kg/day | Affects uterine morphology | Reproductive endocrine-mediated perturbations | |
| IVR | 0.0005 mg/kg/day | 0.0005 mg/kg/day | Affects expression of estrogen receptor-alpha (ER-alpha) | Reproductive endocrine-mediated perturbations | |
| IVR | 0.0005 mg/kg/day | 0.0005 mg/kg/day | Causes inflammation | Immunological endocrine-mediated perturbations | |
| IVR | 0.0005 mg/kg/day | 0.0005 mg/kg/day | Affects ovarian follicles population | Reproductive endocrine-mediated perturbations | |
| PMID:34902535 | IVR | 0.0005 mg/kg/day | 0.0005 mg/kg/day | Increased body weights | Metabolic endocrine-mediated perturbations |
| IVR | 0.001 mg/kg/day | 0.001 mg/kg/day | Increased adiposity | Metabolic endocrine-mediated perturbations | |
| IVR | 0.0005 - 0.001 mg/kg/day | 0.0005 - 0.001 mg/kg/day | Decreased testosterone levels | Reproductive endocrine-mediated perturbations | |
| PMID:36073672 | IVR | 0.00025 mg/kg/day | 0.00025 mg/kg/day | Lead to obesity | Metabolic endocrine-mediated perturbations |
| IVR | 0.00025 - 0.0025 mg/kg/day | 0.00025 - 0.0025 mg/kg/day | Induce behavioral changes | Neurological endocrine-mediated perturbations | |
| IVR | 0.00025 - 0.025 mg/kg/day | 0.00025 - 0.025 mg/kg/day | Changes in brain morphology | Neurological endocrine-mediated perturbations | |
| PMID:38936095 | IVTH | 0.0000001 - 0.001 M | 0.0000001 - 0.001 M | Affects expression of progesterone receptor (PR) | Reproductive endocrine-mediated perturbations |
| IVTH | 0.00000005 - 0.0000001 M | 0.00000005 - 0.0000001 M | Altered adipogenesis | Metabolic endocrine-mediated perturbations | |
| IVTH | 0.0000001 M | 0.0000001 M | Cancer phenotype | Endocrine-mediated cancer | |
| IVR | 0.0001 - 0.001 mg/kg/day | 0.0001 - 0.001 mg/kg/day | Affects steroidogenesis | Reproductive endocrine-mediated perturbations | |
| IVR | 0.0001 - 0.001 mg/kg/day | 0.0001 - 0.001 mg/kg/day | Hyperplasia in mammary glands | Reproductive endocrine-mediated perturbations | |
| IVR | 0.0001 - 0.001 mg/kg/day | 0.0001 - 0.001 mg/kg/day | Affects expression of estrogen receptor-alpha (ER-alpha) | Reproductive endocrine-mediated perturbations | |
| IVR | 0.0001 - 0.001 mg/kg/day | 0.0001 - 0.001 mg/kg/day | Oxidative stress in mammary gland | Reproductive endocrine-mediated perturbations | |
| IVR | 0.0001 - 0.001 mg/kg/day | 0.0001 - 0.001 mg/kg/day | Changes in mammary gland morphology | Reproductive endocrine-mediated perturbations | |
| IVR | 0.001 mg/kg/day | 0.001 mg/kg/day | Increased progesterone levels | Reproductive endocrine-mediated perturbations | |
| IVR | 0.0001 - 0.001 mg/kg/day | 0.0001 - 0.001 mg/kg/day | Changes in ovarian morphology | Reproductive endocrine-mediated perturbations | |
| IVR | 0.0001 - 0.001 mg/kg/day | 0.0001 - 0.001 mg/kg/day | Abnormal estrous cycles | Reproductive endocrine-mediated perturbations | |
| IVR | 0.0001 mg/kg/day | 0.0001 mg/kg/day | Increased ovarian weights | Reproductive endocrine-mediated perturbations | |
| IVR | 0.0000001 - 0.001 mg/kg/day | 0.0000001 - 0.001 mg/kg/day | Affects expression of progesterone receptor (PR) | Reproductive endocrine-mediated perturbations | |
| PMID:39044430 | IVTH | 0.00000001 - 0.000000025 M | 0.00000001 - 0.000000025 M | Altered adipogenesis | Metabolic 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.