Dichlone
No ToxCast endpoints for intended target type: RNA
ToxCast endpoints for intended target type: Protein
| Assay Name | Tissue | Organism | Target Gene ID | Target HGNC Symbol | Response | AC50 Value |
|---|
| CCTE_GLTED_hIYD | | Human | 389434 | IYD | Loss | 54.97 μM |
| CCTE_GLTED_hTBG | | Human | 6906 | SERPINA7 | Loss | 43.67 μM |
| ATG_Ahr_CIS | Liver | Human | 196 | AHR | Inhibitory | 1.86 μM |
| ATG_NRF2_ARE_CIS | Liver | Human | 4780 | NFE2L2 | Activatory | 1.91 μM |
| TOX21_Aromatase_LUC_Antagonist | Breast | Human | 1588 | CYP19A1 | Loss | 2.23 μM |
| TOX21_ERa_BLA_Antagonist_ratio | Kidney | Human | 2099 | ESR1 | Loss | 38.42 μM |
| TOX21_ERa_LUC_VM7_Antagonist_0.5nM_E2 | Breast | Human | 2099 | ESR1 | Loss | 42.53 μM |
| TOX21_GR_BLA_Agonist_ratio | Cervix | Human | 2908 | NR3C1 | Gain | 61.87 μM |
| TOX21_TR_LUC_GH3_Antagonist | Pituitary gland | Rat | 7067|7068 | THRA|THRB | Loss | 2.82 μM |
| TOX21_AP1_BLA_Agonist_ratio | Cervix | Human | 2353|3725 | FOS|JUN | Gain | 1.17 μM |
| TOX21_CAR_LUC_Antagonist | Liver | Human | 9970 | NR1I3 | Loss | 82.15 μM |
| TOX21_ERR_LUC_Antagonist | Kidney | Human | 2101 | ESRRA | Loss | 37.48 μM |
| TOX21_PR_BLA_Antagonist_ratio | Kidney | Human | 5241 | PGR | Loss | 38.83 μM |
| TOX21_AChE_Colorimetric_Antagonist | Bone | Human | 43 | ACHE | Loss | 88.08 μM |
| TOX21_AChE_ms_Antagonist | | Human | 43 | ACHE | Loss | 55.79 μM |
| TOX21_ERa_BLA_Antagonist_ratio | Kidney | Human | 2099 | ESR1 | Loss | 38.32 μM |
| TOX21_ERa_LUC_VM7_Antagonist_0.5nM_E2 | Breast | Human | 2099 | ESR1 | Loss | 45.82 μM |
| TOX21_GR_BLA_Agonist_ratio | Cervix | Human | 2908 | NR3C1 | Gain | 55.18 μM |
| TOX21_AhR_LUC_Agonist | Liver | Human | 196 | AHR | Gain | 1.54 μM |
| TOX21_VDR_BLA_Antagonist_ratio | Kidney | Human | 1591|7421 | CYP24A1|VDR | Loss | 3.21 μM |
| TOX21_RAR_LUC_Antagonist | Embryo | Mouse | 5914 | RARA | Loss | 46.08 μM |
| TOX21_AP1_BLA_Agonist_ratio | Cervix | Human | 2353|3725 | FOS|JUN | Gain | 0.99 μM |
| TOX21_CAR_LUC_Antagonist | Liver | Human | 9970 | NR1I3 | Loss | 82.65 μM |
| TOX21_ERR_LUC_Antagonist | Kidney | Human | 2101 | ESRRA | Loss | 46.08 μM |
No ToxCast endpoints for intended target type: Molecular messenger
ToxCast endpoints for intended target type: Pathway
| Assay Name | Tissue | Organism | Target Gene ID | Target HGNC Symbol | Response | AC50 Value |
|---|
| UPITT_HCI_U2OS_AR_TIF2_Nucleoli_Antagonist | Bone | Human | 367 | AR | Loss | 0.0 μM |
| UPITT_HCI_U2OS_AR_TIF2_Nucleoli_Cytoplasm_Ratio_Antagonist | Bone | Human | 367 | AR | Loss | 0.0 μM |
| TOX21_p53_BLA_p3_ratio | Intestinal | Human | 7157 | TP53 | Gain | 67.3 μM |
| TOX21_ESRE_BLA_Agonist_ratio | Cervix | Human | 22926 | ATF6 | Gain | 59.24 μM |
| TOX21_HDAC_LUC_Antagonist | Colon | Human | 3065 | HDAC1 | Loss | 46.21 μM |
| TOX21_SHH_3T3_GLI3_LUC_Antagonist | Embryo | Mouse | 6469 | SHH | Loss | 1.99 μM |
| TOX21_HSE_BLA_Agonist_ratio | Cervix | Human | 3297 | HSF1 | Gain | 46.69 μM |
| TOX21_p53_BLA_p1_ratio | Intestinal | Human | 7157 | TP53 | Gain | 55.28 μM |
| TOX21_PPARd_BLA_Antagonist_ratio | Kidney | Human | 5467 | PPARD | Loss | 2.88 μM |
| TOX21_PPARg_BLA_Antagonist_ratio | Kidney | Human | 5468 | PPARG | Loss | 1.83 μM |
| TOX21_p53_BLA_p3_ratio | Intestinal | Human | 7157 | TP53 | Gain | 54.09 μM |
| TOX21_p53_BLA_p5_ratio | Intestinal | Human | 7157 | TP53 | Gain | 63.43 μM |
| TOX21_ESRE_BLA_Agonist_ratio | Cervix | Human | 22926 | ATF6 | Gain | 68.52 μM |
| TOX21_H2AX_HTRF_CHO_Agonist_ratio | Ovary | Chinese hamster | 3014 | H2AX | Gain | 3.2 μM |
| TOX21_SHH_3T3_GLI3_LUC_Antagonist | Embryo | Mouse | 6469 | SHH | Loss | 3.03 μM |
No ToxCast endpoints for intended target type: Cellular
No ToxCast endpoints for intended target type: Hormone
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.