Tris(2-chloroethyl) phosphate


Literature identifierStudy typeTest dosageEffective dosageEndocrine-mediated endpointsSystems-level perturbations
PMID:22446829IVTH0.01 - 10 mg/L 0.1 - 10 mg/LIncreased estradiol levelsReproductive endocrine-mediated perturbations
IVTH0.01 - 10 mg/L 0.1 - 10 mg/LIncreased testosterone levelsReproductive endocrine-mediated perturbations
IVTH0.01 - 10 mg/L 10 mg/LAffects steroidogenesisReproductive endocrine-mediated perturbations
PMID:26183808IVR300 mg/kg 300 mg/kgDecreased testis weightsReproductive endocrine-mediated perturbations
IVR300 mg/kg 300 mg/kgAffects steroidogenesisReproductive endocrine-mediated perturbations
IVR300 mg/kg 300 mg/kgAffects the biochemical composition of liverHepatic endocrine-mediated perturbations
IVR100 mg/kg 100 mg/kgAffects the biochemical composition of liverHepatic endocrine-mediated perturbations
PMID:35780845IVR2 - 6 mg/kg 2 - 6 mg/kgIncreased LDL levelsMetabolic endocrine-mediated perturbations
IVR6 mg/kg 6 mg/kgIncreased Non esterified Fatty acid (NEFA) levelsMetabolic endocrine-mediated perturbations
IVR6 mg/kg 6 mg/kgLead to obesityMetabolic endocrine-mediated perturbations
IVR6 mg/kg 6 mg/kgIncreased triglycerides levelMetabolic endocrine-mediated perturbations
IVR2 - 6 mg/kg 2 - 6 mg/kgInduce behavioral changesNeurological endocrine-mediated perturbations
IVR6 mg/kg 6 mg/kgIncreased adiposityMetabolic endocrine-mediated perturbations
IVR2 - 6 mg/kg 2 - 6 mg/kgIncreased liver weightsHepatic endocrine-mediated perturbations
IVR6 mg/kg 6 mg/kgIncreased body weightsMetabolic endocrine-mediated perturbations
IVR mg/kg -Changes in morphology of adipose tissueMetabolic endocrine-mediated perturbations
PMID:8314462IVR44 mg/kg 44 mg/kgHematopietic carcinomaEndocrine-mediated cancer;Immunological endocrine-mediated perturbations
IVR88 mg/kg 88 mg/kgChanges in brain morphologyNeurological endocrine-mediated perturbations
IVR88 mg/kg 88 mg/kgHematopietic carcinomaEndocrine-mediated cancer;Immunological endocrine-mediated perturbations

DISCLAIMER

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.