Literature identifier | Study type | Test dosage | Effective dosage | Endocrine-mediated endpoints | Systems-level perturbations |
---|---|---|---|---|---|
PMID:11849735 | IVR | 0.5 mg | 0.5 mg | Decreased liver weights | Hepatic endocrine-mediated perturbations |
IVR | 0.5 mg | 0.5 mg | Increased uterine weights | Reproductive endocrine-mediated perturbations | |
IVR | 0.5 mg | 0.5 mg | Changes in morphology of pituitary gland | Neurological endocrine-mediated perturbations | |
IVR | 0.5 mg | 0.5 mg | Increase in T3 levels | Metabolic endocrine-mediated perturbations | |
IVR | 0.5 mg | 0.5 mg | Decrease in T4 levels | Metabolic endocrine-mediated perturbations | |
PMID:15501383 | IVR | 0.0125 - 0.5 mg | 0.125 - 0.5 mg | Abnormal sperm morphology | Reproductive endocrine-mediated perturbations |
IVR | 0.00625 - 0.125 mg | 0.0313 - 0.125 mg | Abnormal sperm morphology | Reproductive endocrine-mediated perturbations | |
PMID:17443786 | IVR | 0.01 mg | 0.01 mg | Affects sexual behavior | Neurological endocrine-mediated perturbations;Reproductive endocrine-mediated perturbations |
IVR | 0.01 mg | 0.01 mg | Affects neural development | Developmental endocrine-mediated perturbations;Neurological endocrine-mediated perturbations | |
PMID:18025854 | IVR | 0.025 mg | 0.025 mg | Alteration in prostate morphology | Reproductive endocrine-mediated perturbations |
IVR | 0.025 mg | 0.025 mg | Cancer phenotype | Endocrine-mediated cancer | |
IVR | 0.025 mg | 0.025 mg | Decreased prostate weights | Reproductive endocrine-mediated perturbations | |
IVR | 0.025 mg | 0.025 mg | Affects expression of estrogen receptor-beta (ER-beta) | Reproductive endocrine-mediated perturbations | |
IVR | 0.025 mg | 0.025 mg | Affects expression of androgen receptor (AR) | Reproductive endocrine-mediated perturbations | |
IVR | 0.025 mg | 0.025 mg | Increased testosterone levels | Reproductive endocrine-mediated perturbations | |
PMID:18656497 | IVR | 0.05 mg | 0.05 mg | Affects neuronal density | Neurological endocrine-mediated perturbations |
IVR | 0.05 mg | 0.05 mg | Alterations in vaginal opening | Reproductive endocrine-mediated perturbations | |
IVR | 0.05 mg | 0.05 mg | Affects sexual behavior | Neurological endocrine-mediated perturbations;Reproductive endocrine-mediated perturbations | |
IVR | 0.05 mg | 0.05 mg | Abnormal estrous cycles | Reproductive endocrine-mediated perturbations | |
PMID:19442818 | IVR | 0.025 mg | 0.025 mg | Abnormal neuronal distribution | Neurological endocrine-mediated perturbations |
PMID:19903717 | IVR | 0.2 mg/kg/day | 0.2 mg/kg/day | Affects steroidogenesis | Reproductive endocrine-mediated perturbations |
IVR | 0.2 mg/kg/day | 0.2 mg/kg/day | Induce apoptosis of spermatogenic cells | Reproductive endocrine-mediated perturbations | |
IVR | 0.2 mg/kg/day | 0.2 mg/kg/day | Decreased FSH levels | Reproductive endocrine-mediated perturbations | |
PMID:22016562 | IVR | 1 mg/kg | 1 mg/kg | Affects the normal functioning of reproductive system | Reproductive endocrine-mediated perturbations |
IVR | 1 mg/kg | 1 mg/kg | Abnormal estrous cycles | Reproductive endocrine-mediated perturbations | |
IVR | 1 mg/kg | 1 mg/kg | Decreased estradiol levels | Reproductive endocrine-mediated perturbations | |
PMID:22334722 | IVR | 0.00125 mg/day | 0.00125 mg/day | Affects testicular function | Reproductive endocrine-mediated perturbations |
IVR | 0.00125 mg/day | 0.00125 mg/day | Induce apoptosis in testis | Reproductive endocrine-mediated perturbations | |
IVR | 0.00075 mg/day | 0.00075 mg/day | Affects testicular function | Reproductive endocrine-mediated perturbations | |
IVR | 0.0025 mg/day | 0.0025 mg/day | Affects testicular function | Reproductive endocrine-mediated perturbations | |
IVR | 0.0025 mg/day | 0.0025 mg/day | Induce apoptosis in testis | Reproductive endocrine-mediated perturbations | |
IVR | 0.0025 mg/day | 0.0025 mg/day | Changes in morphology of seminiferous tubules | Reproductive endocrine-mediated perturbations | |
IVR | 0.025 mg/day | 0.025 mg/day | Testicular atrophy | Reproductive endocrine-mediated perturbations | |
PMID:24284824 | IVR | 0.05 mg/kg | 0.05 mg/kg | Delayed puberty | Reproductive endocrine-mediated perturbations |
IVR | 0.05 mg/kg | 0.05 mg/kg | Abnormal estrous cycles | Reproductive endocrine-mediated perturbations | |
IVR | 0.05 mg/kg | 0.05 mg/kg | Causes masculinized behavior | Metabolic endocrine-mediated perturbations;Reproductive endocrine-mediated perturbations | |
IVR | 0.05 mg/kg | 0.05 mg/kg | Affects neural development | Developmental endocrine-mediated perturbations;Neurological endocrine-mediated perturbations | |
PMID:26190835 | IVR | 0.05 mg/kg | 0.05 mg/kg | Affects sexual behavior | Neurological endocrine-mediated perturbations;Reproductive endocrine-mediated perturbations |
IVR | 0.05 mg/kg | 0.05 mg/kg | Affects neural development | Developmental endocrine-mediated perturbations;Neurological endocrine-mediated perturbations | |
PMID:27762633 | IVR | 0.00075 - 0.025 mg/day | 0.00075 - 0.025 mg/day | Affects testis development | Developmental endocrine-mediated perturbations;Reproductive endocrine-mediated perturbations |
IVR | 0.00075 - 0.025 mg/day | 0.00075 - 0.025 mg/day | Induce apoptosis of spermatogenic cells | Reproductive endocrine-mediated perturbations | |
PMID:29458364 | IVR | 0.05 mg/kg | 0.05 mg/kg | Affects anogenital distance in offspring | Developmental endocrine-mediated perturbations;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.