Trenbolone


ToxCast endpoints for intended target type: RNA
Assay NameTissueOrganismTarget Gene IDTarget HGNC SymbolResponseAC50 Value
LTEA_HepaRG_CYP2B6LiverHuman1555CYP2B6Inhibitory1.14 μM
LTEA_HepaRG_CYP2E1LiverHuman1571CYP2E1Inhibitory84.5 μM
LTEA_HepaRG_CYP3A4LiverHuman1576CYP3A4Inhibitory0.46 μM
LTEA_HepaRG_CYP4A11LiverHuman1579CYP4A11Inhibitory88.22 μM
LTEA_HepaRG_CYP4A22LiverHuman284541CYP4A22Inhibitory88.19 μM
LTEA_HepaRG_GCLMLiverHuman2730GCLMInhibitory78.95 μM
LTEA_HepaRG_PEG10LiverHuman23089PEG10Inhibitory0.8 μM
LTEA_HepaRG_SULT2A1LiverHuman6822SULT2A1Activatory81.78 μM
LTEA_HepaRG_UGT1A1LiverHuman54658UGT1A1Activatory1.0 μM

ToxCast endpoints for intended target type: Protein
Assay NameTissueOrganismTarget Gene IDTarget HGNC SymbolResponseAC50 Value
ATG_AR_TRANSLiverHuman367ARGain0.22 μM
ATG_ERE_CISLiverHuman2099ESR1Inhibitory0.76 μM
ATG_AR_TRANSLiverHuman367ARGain0.06 μM
ATG_ERa_TRANSLiverHuman2099ESR1Gain0.46 μM
ATG_ERE_CISLiverHuman2099ESR1Activatory1.64 μM
ATG_MRE_CISLiverHuman4520MTF1Inhibitory100.0 μM
ATG_ERa_TRANSLiverHuman2099ESR1Gain0.33 μM
ATG_ERE_CISLiverHuman2099ESR1Inhibitory0.62 μM
ATG_p53_CISLiverHuman7157TP53Inhibitory100.0 μM
ATG_SREBP_CISLiverHuman6720SREBF1Activatory3.8 μM
ATG_AR_TRANSLiverHuman367ARGain0.01 μM
ATG_ERa_TRANSLiverHuman2099ESR1Gain0.6 μM
NVS_NR_hERHuman2099ESR1Loss0.66 μM
NVS_NR_hGRHuman2908NR3C1Loss0.18 μM
NVS_NR_rARProstateRat24208ArLoss0.02 μM
NVS_NR_hGRHuman2908NR3C1Loss0.33 μM
NVS_NR_mERaMouse13982Esr1Loss2.67 μM
NVS_NR_rARProstateRat24208ArLoss0.01 μM
NVS_NR_hERHuman2099ESR1Loss0.05 μM
NVS_NR_hGRHuman2908NR3C1Loss0.05 μM
NVS_NR_rARProstateRat24208ArLoss0.0 μM
NVS_NR_rMRBrainRat25672Nr3c2Loss0.24 μM
ATG_ERE_CISLiverHuman2099ESR1Activatory0.94 μM
ATG_IR1_CISLiverHuman9971NR1H4Inhibitory0.76 μM
ATG_Xbp1_CISLiverHuman7494XBP1Activatory134.49 μM
ATG_ERa_TRANSLiverHuman2099ESR1Gain1.57 μM
BSK_BE3C_tPALungHuman5327PLATInhibitory3.97 μM
BSK_CASM3C_IL8VascularHuman3576CXCL8Inhibitory4.42 μM
BSK_hDFCGF_PAI1SkinHuman5054SERPINE1Inhibitory0.16 μM
BSK_LPS_EselectinVascularHuman6401SELEInhibitory4.36 μM
BSK_LPS_TNFaVascularHuman7124TNFInhibitory5.85 μM
BSK_SAg_CD38VascularHuman952CD38Inhibitory4.62 μM
NVS_ADME_hCYP2C19Human1557CYP2C19Loss5.75 μM
NVS_GPCR_gLTB4SpleenGuinea pig100379538Ltb4rLoss2.88 μM
NVS_NR_hARHuman367ARLoss0.01 μM
NVS_NR_hGRHuman2908NR3C1Loss0.6 μM
NVS_NR_hPRHuman5241PGRLoss0.0 μM
NVS_NR_mERaMouse13982Esr1Loss2.38 μM
NVS_NR_rMRBrainRat25672Nr3c2Loss0.07 μM
NVS_NR_hARHuman367ARLoss0.0 μM
NVS_NR_hERHuman2099ESR1Loss0.44 μM
NVS_TR_rSERTBrainRat25553Slc6a4Loss5.66 μM
CCTE_Simmons_AUR_rTPOThyroid glandRat54314TpoLoss6.65 μM
ATG_hAR_XSP1LiverHuman367ARGain0.0 μM
CCTE_GLTED_hDIO2Human1734DIO2Loss100.0 μM
ATG_hAR_XSP2LiverHuman367ARGain0.0 μM
ATG_hTRb_XSP2LiverHuman7068THRBGain0.03 μM
TOX21_AR_BLA_Agonist_ratioKidneyHuman367ARGain0.0 μM
TOX21_AR_LUC_MDAKB2_AgonistBreastHuman367ARGain0.0 μM
TOX21_ERa_BLA_Agonist_ratioKidneyHuman2099ESR1Gain1.22 μM
TOX21_ERa_LUC_VM7_AgonistBreastHuman2099ESR1Gain0.02 μM
TOX21_GR_BLA_Antagonist_ratioCervixHuman2908NR3C1Loss1.73 μM
TOX21_AR_LUC_MDAKB2_Agonist_3uM_NilutamideBreastHuman367ARGain0.01 μM
TOX21_ERb_BLA_Agonist_ratioKidneyHuman2100ESR2Gain0.7 μM
TOX21_PR_BLA_Agonist_ratioKidneyHuman5241PGRGain0.14 μM
TOX21_PR_BLA_Antagonist_ratioKidneyHuman5241PGRLoss0.01 μM
TOX21_ERa_LUC_VM7_Agonist_10nM_ICI182780BreastHuman2099ESR1Gain0.94 μM
TOX21_ERa_BLA_Agonist_ratioKidneyHuman2099ESR1Gain1.27 μM
TOX21_ERa_LUC_VM7_AgonistBreastHuman2099ESR1Gain0.11 μM
TOX21_GR_BLA_Antagonist_ratioCervixHuman2908NR3C1Loss3.38 μM
TOX21_ERb_BLA_Agonist_ratioKidneyHuman2100ESR2Gain1.67 μM
TOX21_ERa_LUC_VM7_Agonist_10nM_ICI182780BreastHuman2099ESR1Gain3.04 μM
TOX21_PR_BLA_Followup_Agonist_ratioKidneyHuman5241PGRGain0.29 μM
TOX21_PR_LUC_Followup_AgonistKidneyHuman5241PGRGain0.0 μM

ToxCast endpoints for intended target type: Molecular messenger
Assay NameTissueOrganismTarget Gene IDTarget HGNC SymbolResponseAC50 Value
CEETOX_H295R_ANDRAdrenal glandHuman367ARInhibitory90.14 μM
CEETOX_H295R_CORTICAdrenal glandHuman2908|4306NR3C1|NR3C2Inhibitory3.19 μM
CEETOX_H295R_ESTRONEAdrenal glandHuman2099|2100ESR1|ESR2Activatory83.15 μM
CEETOX_H295R_PROGAdrenal glandHuman5241PGRActivatory0.1 μM
CEETOX_H295R_TESTOAdrenal glandHuman367ARActivatory83.49 μM

ToxCast endpoints for intended target type: Pathway
Assay NameTissueOrganismTarget Gene IDTarget HGNC SymbolResponseAC50 Value
UPITT_HCI_U2OS_AR_TIF2_Nucleoli_AgonistBoneHuman367ARGain0.0 μM
UPITT_HCI_U2OS_AR_TIF2_Nucleoli_Cytoplasm_Ratio_AgonistBoneHuman367ARGain0.0 μM
ACEA_ER_80hrBreastHuman2099ESR1Gain0.01 μM
ACEA_ER_80hrBreastHuman2099ESR1Gain0.02 μM
ACEA_ER_80hrBreastHuman2099ESR1Gain0.0 μM
OT_AR_ARELUC_AG_1440OvaryChinese hamster367ARGain0.0 μM
OT_AR_ARSRC1_0480KidneyHuman367|6714AR|SRCGain0.18 μM
OT_AR_ARSRC1_0960KidneyHuman367|6714AR|SRCGain0.03 μM
OT_AR_ARELUC_AG_1440OvaryChinese hamster367ARGain0.21 μM
OT_AR_ARSRC1_0480KidneyHuman367|6714AR|SRCGain0.03 μM
OT_AR_ARSRC1_0480KidneyHuman367|6714AR|SRCGain0.0 μM
OT_AR_ARSRC1_0960KidneyHuman367|6714AR|SRCGain0.0 μM
OT_ER_ERaERb_1440KidneyHuman2099|2100ESR1|ESR2Gain0.16 μM
OT_ER_ERbERb_0480KidneyHuman2100ESR2Gain0.37 μM
OT_ER_ERbERb_1440KidneyHuman2100ESR2Gain0.2 μM
OT_ERa_GFPERaERE_0480CervixHuman2099ESR1Gain0.22 μM
ACEA_AR_agonist_80hrProstateHuman367ARGain0.0 μM
TOX21_ARE_BLA_Agonist_ratioLiverHuman4780NFE2L2Gain6.78 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.