Perfluorooctanoic acid


ToxCast endpoints for intended target type: RNA
Assay NameTissueOrganismTarget Gene IDTarget HGNC SymbolResponseAC50 Value
CLD_CYP3A4_24hrLiverHuman1576CYP3A4Gain20.0 μM
CLD_HMGCS2_48hrLiverHuman3158HMGCS2Gain33.7 μM
LTEA_HepaRG_ACOX1LiverHuman51ACOX1Activatory3.48 μM
LTEA_HepaRG_ALPPLiverHuman250ALPPInhibitory9.92 μM
LTEA_HepaRG_CATLiverHuman847CATActivatory23.34 μM
LTEA_HepaRG_CYP2B6LiverHuman1555CYP2B6Activatory17.85 μM
LTEA_HepaRG_CYP2C19LiverHuman1557CYP2C19Activatory9.92 μM
LTEA_HepaRG_CYP2C8LiverHuman1558CYP2C8Inhibitory17.17 μM
LTEA_HepaRG_CYP3A7LiverHuman1551CYP3A7Inhibitory22.07 μM
LTEA_HepaRG_CYP4A11LiverHuman1579CYP4A11Activatory12.76 μM
LTEA_HepaRG_CYP4A22LiverHuman284541CYP4A22Activatory6.42 μM
LTEA_HepaRG_FABP1LiverHuman2168FABP1Activatory11.03 μM
LTEA_HepaRG_HMGCS2LiverHuman3158HMGCS2Inhibitory14.95 μM
LTEA_HepaRG_PDK4LiverHuman5166PDK4Activatory26.91 μM
LTEA_HepaRG_UGT1A1LiverHuman54658UGT1A1Inhibitory3.11 μM
LTEA_HepaRG_XBP1LiverHuman7494XBP1Inhibitory50.0 μM

ToxCast endpoints for intended target type: Protein
Assay NameTissueOrganismTarget Gene IDTarget HGNC SymbolResponseAC50 Value
ATG_AP_1_CISLiverHuman2353|3725FOS|JUNInhibitory150.0 μM
ATG_ERE_CISLiverHuman2099ESR1Inhibitory7.97 μM
ATG_NRF2_ARE_CISLiverHuman4780NFE2L2Inhibitory84.61 μM
ATG_PPRE_CISLiverHuman5465|5467|5468PPARA|PPARD|PPARGActivatory85.85 μM
ATG_PXRE_CISLiverHuman8856NR1I2Activatory54.02 μM
ATG_TCF_b_cat_CISLiverHuman6932|6934|51176|83439TCF7|TCF7L2|LEF1|TCF7L1Inhibitory220.99 μM
ATG_ERa_TRANSLiverHuman2099ESR1Gain7.92 μM
ATG_PPARa_TRANSLiverHuman5465PPARAGain24.36 μM
ATG_PPARg_TRANSLiverHuman5468PPARGGain94.52 μM
ATG_RXRb_TRANSLiverHuman6257RXRBGain54.86 μM
ATG_hPPARa_EcoTox2LiverHuman5465PPARAGain10.88 μM
ATG_hPPARg_EcoTox2LiverHuman5468PPARGGain49.45 μM
ATG_hRXRb_EcoTox2LiverHuman6257RXRBGain27.58 μM
ATG_hERa_EcoTox2LiverHuman2099ESR1Gain47.36 μM
CCTE_GLTED_hTTR_0.5uMHuman7276TTRLoss0.39 μM
BSK_3C_IL8VascularHuman3576CXCL8Inhibitory16.02 μM
BSK_3C_VCAM1VascularHuman7412VCAM1Inhibitory1.92 μM
BSK_4H_Eotaxin3VascularHuman10344CCL26Inhibitory1.25 μM
BSK_4H_uPARVascularHuman5329PLAURInhibitory1.48 μM
BSK_BE3C_IP10LungHuman3627CXCL10Inhibitory15.42 μM
BSK_BE3C_MMP1LungHuman4312MMP1Inhibitory39.91 μM
BSK_CASM3C_MIGVascularHuman4283CXCL9Inhibitory36.57 μM
BSK_LPS_IL8VascularHuman3576CXCL8Inhibitory30.0 μM
BSK_LPS_MCSFVascularHuman1435CSF1Inhibitory5.95 μM
BSK_BT_xTNFaVascularHuman7124TNFInhibitory5.95 μM
BSK_MyoF_CollagenIVVascularHuman1282COL4A1Inhibitory31.61 μM
BSK_BF4T_MCP1VascularHuman6347CCL2Inhibitory50.07 μM
BSK_BF4T_tPAVascularHuman5327PLATInhibitory1.85 μM
BSK_BE3C_MMP9LungHuman4318MMP9Inhibitory42.17 μM
BSK_IMphg_IL8VascularHuman3576CXCL8Inhibitory20.52 μM
BSK_IMphg_IL10VascularHuman3586IL10Inhibitory51.96 μM
BSK_LPS_ThrombomodulinVascularHuman7056THBDInhibitory0.61 μM
BSK_LPS_CD69VascularHuman969CD69Inhibitory0.22 μM
BSK_3C_IL8VascularHuman3576CXCL8Inhibitory30.0 μM
BSK_4H_Eotaxin3VascularHuman10344CCL26Inhibitory10.79 μM
BSK_BE3C_IP10LungHuman3627CXCL10Inhibitory43.45 μM
BSK_BE3C_MMP1LungHuman4312MMP1Inhibitory30.0 μM
BSK_hDFCGF_EGFRSkinHuman1956EGFRInhibitory3.12 μM
BSK_LPS_PGE2VascularHuman5732PTGER2Inhibitory35.55 μM
BSK_BT_xTNFaVascularHuman7124TNFInhibitory0.22 μM
BSK_MyoF_CollagenIVVascularHuman1282COL4A1Inhibitory40.45 μM
BSK_BF4T_tPAVascularHuman5327PLATInhibitory30.0 μM
BSK_KF3CT_PAI1SkinHuman5054SERPINE1Inhibitory46.84 μM
BSK_IMphg_IL8VascularHuman3576CXCL8Inhibitory30.0 μM
BSK_IMphg_IL10VascularHuman3586IL10Inhibitory30.0 μM
CCTE_GLTED_hTTR_0.125uMHuman7276TTRLoss0.16 μM
ERF_TW_NR_COA_hPPARAHuman5465PPARAGain11.46 μM
NVS_ADME_rCYP2A2Rat24895Cyp2a2Loss3.36 μM
NVS_ENZ_hBACEHuman23621BACE1Loss3.32 μM
NVS_ENZ_hPI3KaHuman5290PIK3CALoss10.12 μM
NVS_ENZ_hPPP1CAHuman5499PPP1CALoss0.49 μM
NVS_ENZ_hPPP2CAHuman5515PPP2CALoss25.0 μM
NVS_ENZ_hTie2Human7010TEKLoss13.69 μM
NVS_GPCR_gLTB4SpleenGuinea pig100379538Ltb4rLoss12.09 μM
NVS_GPCR_hAdoRA2aHuman135ADORA2ALoss11.81 μM
NVS_GPCR_hLTB4_BLT1Human1241LTB4RLoss35.16 μM
NVS_NR_hCAR_AntagonistHuman9970NR1I3Loss13.66 μM
NVS_NR_hPPARgHuman5468PPARGLoss18.33 μM
ATG_DR4_LXR_CISLiverHuman7376|10062NR1H2|NR1H3Inhibitory11.5 μM
ATG_ERE_CISLiverHuman2099ESR1Inhibitory37.23 μM
ATG_NRF2_ARE_CISLiverHuman4780NFE2L2Inhibitory53.91 μM
ATG_PPRE_CISLiverHuman5465|5467|5468PPARA|PPARD|PPARGInhibitory32.49 μM
ATG_PXRE_CISLiverHuman8856NR1I2Inhibitory33.42 μM
ATG_ERa_TRANSLiverHuman2099ESR1Gain50.0 μM
ATG_PPARa_TRANSLiverHuman5465PPARAGain24.12 μM
ATG_PPARg_TRANSLiverHuman5468PPARGGain50.0 μM
BSK_3C_uPARVascularHuman5329PLAURInhibitory1.42 μM
BSK_BE3C_MMP1LungHuman4312MMP1Inhibitory20.0 μM
BSK_KF3CT_ICAM1SkinHuman3383ICAM1Inhibitory13.59 μM
BSK_LPS_EselectinVascularHuman6401SELEInhibitory12.27 μM
BSK_LPS_TNFaVascularHuman7124TNFInhibitory9.76 μM
ATG_hERb_XSP2LiverHuman2100ESR2Gain38.24 μM
ATG_hERa_XSP2LiverHuman2099ESR1Gain20.71 μM
ATG_mPPARg_XSP2LiverHuman19016PpargGain44.82 μM
ATG_hPPARg_XSP2LiverHuman5468PPARGGain42.05 μM
TOX21_ERa_BLA_Antagonist_ratioKidneyHuman2099ESR1Loss29.52 μM
TOX21_ERb_BLA_Antagonist_ratioKidneyHuman2100ESR2Loss40.6 μM
TOX21_p450_CYP2C9_AntagonistHuman1559CYP2C9Loss2.64 μM

No ToxCast endpoints for intended target type: Molecular messenger

ToxCast endpoints for intended target type: Pathway
Assay NameTissueOrganismTarget Gene IDTarget HGNC SymbolResponseAC50 Value
TOX21_ARE_BLA_Agonist_ratioLiverHuman4780NFE2L2Gain26.33 μM
TOX21_RXR_BLA_Agonist_ratioKidneyHuman6256RXRAGain22.2 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.