| Literature identifier | Study type | Test dosage | Effective dosage | Endocrine-mediated endpoints | Systems-level perturbations |
|---|---|---|---|---|---|
| PMID:21641976 | IVTH | 0.000000006 - 0.0006 M | 0.00006 M | Decreased testosterone levels | Reproductive endocrine-mediated perturbations |
| IVTH | 0.000000006 - 0.0006 M | 0.0006 M | Cancer phenotype | Endocrine-mediated cancer | |
| IVTH | 0.000000006 - 0.0006 M | 0.00006 M | Affects cholesterol biosynthesis | Metabolic endocrine-mediated perturbations | |
| PMID:23764977 | IVTH | 0.000000001 - 0.0001 M | 0.000029 - 0.000065 M | Affects expression of estrogen receptor-alpha (ER-alpha) | Reproductive endocrine-mediated perturbations |
| PMID:30576894 | IVR | 5 mg/kg/day | 5 mg/kg/day | Induce apoptosis in testis | Reproductive endocrine-mediated perturbations |
| IVR | 5 mg/kg/day | 5 mg/kg/day | Oxidative stress in testis | Reproductive endocrine-mediated perturbations | |
| IVR | 5 mg/kg/day | 5 mg/kg/day | Decreased testosterone levels | Reproductive endocrine-mediated perturbations | |
| IVR | 5 mg/kg/day | 5 mg/kg/day | Affects steroidogenesis | Reproductive endocrine-mediated perturbations | |
| IVR | 5 mg/kg/day | 5 mg/kg/day | Changes in morphology of seminiferous tubules | Reproductive endocrine-mediated perturbations | |
| IVR | 2 mg/kg/day | 2 mg/kg/day | Changes in morphology of seminiferous tubules | Reproductive endocrine-mediated perturbations | |
| IVR | 2 mg/kg/day | 2 mg/kg/day | Induce apoptosis in testis | Reproductive endocrine-mediated perturbations | |
| IVR | 2 mg/kg/day | 2 mg/kg/day | Affects steroidogenesis | Reproductive endocrine-mediated perturbations | |
| IVR | 2 mg/kg/day | 2 mg/kg/day | Decreased testosterone levels | Reproductive endocrine-mediated perturbations | |
| IVR | 2 mg/kg/day | 2 mg/kg/day | Oxidative stress in testis | Reproductive endocrine-mediated perturbations | |
| PMID:31389053 | IVR | 5 mg/kg/day | 5 mg/kg/day | Affects testis development | Developmental endocrine-mediated perturbations;Reproductive endocrine-mediated perturbations |
| IVR | 5 mg/kg/day | 5 mg/kg/day | Decreased testosterone levels | Reproductive endocrine-mediated perturbations | |
| IVR | 5 mg/kg/day | 5 mg/kg/day | Affects steroidogenesis | Reproductive endocrine-mediated perturbations | |
| IVR | 2 mg/kg/day | 2 mg/kg/day | Affects steroidogenesis | Reproductive endocrine-mediated perturbations | |
| IVR | 2 mg/kg/day | 2 mg/kg/day | Affects testis development | Developmental endocrine-mediated perturbations;Reproductive endocrine-mediated perturbations | |
| PMID:36122607 | IVTH | 0.0000001 - 0.0002 M | 0.00036356 M | Affects steroidogenesis | Reproductive endocrine-mediated perturbations |
| PMID:36878351 | IVTH | 0.0001 M | 0.0001 M | Affects steroidogenesis | Reproductive endocrine-mediated perturbations |
| PMID:38535903 | IVR | 5 mg/kg | 5 mg/kg | Affects intracellular signaling pathway | Metabolic endocrine-mediated perturbations |
| PMID:39136868 | IVTH | 0.00001 M | 0.00001 M | Increased estradiol levels | Reproductive endocrine-mediated perturbations |
| PMID:39205352 | IVTH | 0.00000025 - 0.000002 M | 0.00000025 - 0.000002 M | Cancer phenotype | Endocrine-mediated cancer |
| IVTH | 0.0000005 - 0.000002 M | 0.0000005 - 0.000002 M | Affects intracellular signaling pathway | Metabolic endocrine-mediated perturbations | |
| IVTH | 0.00000025 - 0.000002 M | 0.00000025 - 0.000002 M | Induce cancer metastasis | Endocrine-mediated cancer | |
| IVR | 5 mg/kg | 5 mg/kg | Induce tumor progression | Endocrine-mediated cancer | |
| IVTH | 0.00000025 - 0.000002 M | 0.00000025 - 0.000002 M | Induced migration capability of tumor cells | Endocrine-mediated cancer |
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.