| 1 | [SID17388845] | Unspecified | | | qHTS assay for identifying genotoxic compounds that show differential cytotoxicity against a panel of isogenic chicken DT40 cell lines with known DNA damage response pathways [AID651838, Type: other] | |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Unspecified | | BioAssay | qHTS assay for identifying genotoxic compounds that show differential cytotoxicity against a panel of isogenic chicken DT40 cell lines with known DNA damage response pathways | | AID | 651838 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 2 | [SID103179369] | Unspecified | | | Solubility in water was determined; values expressed as -log [AID13316, Type: Literature] | |   View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 103179369 | | CID | 8003 | | Outcome | Unspecified | | BioAssay | Solubility in water was determined; values expressed as -log | | AID | 13316 | | BioAssay type | Literature | | Target | | | PubMed | 12565942 | | Data Table |  |
|
| 3 | [SID103179369] | Unspecified | | | Aqueous solubility [AID19262, Type: Literature] | |   View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 103179369 | | CID | 8003 | | Outcome | Unspecified | | BioAssay | Aqueous solubility | | AID | 19262 | | BioAssay type | Literature | | Target | | | PubMed | 10866370 | | Data Table |  |
|
| 4 | [SID103179369] | Unspecified | | | Partition coefficient in water-hexadecane (P16) was determined [AID23718, Type: Literature] | |   View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 103179369 | | CID | 8003 | | Outcome | Unspecified | | BioAssay | Partition coefficient in water-hexadecane (P16) was determined | | AID | 23718 | | BioAssay type | Literature | | Target | | | PubMed | 12565942 | | Data Table |  |
|
| 5 | [SID103179369] | Unspecified | | | Partition coefficient in alkanes was determined [AID23726, Type: Literature] | |   View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 103179369 | | CID | 8003 | | Outcome | Unspecified | | BioAssay | Partition coefficient in alkanes was determined | | AID | 23726 | | BioAssay type | Literature | | Target | | | PubMed | 12565942 | | Data Table |  |
|
| 6 | [SID103179369] | Unspecified | | | Partition coefficient in water-cyclohexane was determined [AID23729, Type: Literature] | |   View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 103179369 | | CID | 8003 | | Outcome | Unspecified | | BioAssay | Partition coefficient in water-cyclohexane was determined | | AID | 23729 | | BioAssay type | Literature | | Target | | | PubMed | 12565942 | | Data Table |  |
|
| 7 | [SID103179369] | Unspecified | | | Partition coefficient (logP) [AID23737, Type: Literature] | |   View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 103179369 | | CID | 8003 | | Outcome | Unspecified | | BioAssay | Partition coefficient (logP) | | AID | 23737 | | BioAssay type | Literature | | Target | | | PubMed | 12565942 | | Data Table |  |
|
| 8 | [SID103179369] | Unspecified | | | logBB, log(C brain / C blood) [AID26047, Type: Literature] | |   View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 103179369 | | CID | 8003 | | Outcome | Unspecified | | BioAssay | logBB, log(C brain / C blood) | | AID | 26047 | | BioAssay type | Literature | | Target | | | PubMed | 8941388 | | Data Table |  |
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| 9 | [SID103179369] | Unspecified | | | Toxicity determined using Tadpole Narcosis Test [AID212400, Type: Literature] | |   View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 103179369 | | CID | 8003 | | Outcome | Unspecified | | BioAssay | Toxicity determined using Tadpole Narcosis Test | | AID | 212400 | | BioAssay type | Literature | | Target | | | PubMed | 2033592 | | Data Table |  |
|
| 10 | [SID103179369] | Unspecified | | | Lipophilicity determined as logarithm of the partition coefficient in the alkane/water system [AID237685, Type: Literature] | |   View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 103179369 | | CID | 8003 | | Outcome | Unspecified | | BioAssay | Lipophilicity determined as logarithm of the partition coefficient in the alkane/water system | | AID | 237685 | | BioAssay type | Literature | | Target | | | PubMed | 15857133 | | Data Table |  |
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| 11 | [SID103179369] | Unspecified | | | Convulsant activity in Sprague-Dawley rat assessed as partial pressure in atmosphere at which convulsion takes place [AID416913, Type: Literature] | |   View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 103179369 | | CID | 8003 | | Outcome | Unspecified | | BioAssay | Convulsant activity in Sprague-Dawley rat assessed as partial pressure in atmosphere at which convulsion takes place | | AID | 416913 | | BioAssay type | Literature | | Target | | | PubMed | 18603335 | | Data Table |  |
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| 12 | [SID17388845] | Unspecified | | | qHTS profiling for inhibitors of Plasmodium falciparum proliferation [AID504749, Type: Literature] | |   View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Unspecified | | BioAssay | qHTS profiling for inhibitors of Plasmodium falciparum proliferation | | AID | 504749 | | BioAssay type | Literature | | Target | | | PubMed | 21817045 | | Data Table |  |
|
| 13 | [SID103179369] | Unspecified | | | In-vitro air to lung partition coefficients of the compound, logK(lung) (human/rat) [AID603950, Type: Literature] | |   View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 103179369 | | CID | 8003 | | Outcome | Unspecified | | BioAssay | In-vitro air to lung partition coefficients of the compound, logK(lung) (human/rat) | | AID | 603950 | | BioAssay type | Literature | | Target | | | PubMed | 17544548 | | Data Table |  |
|
| 14 | [SID103179369] | Unspecified | | | In-vitro air to blood partition coefficients of the compound, logK(blood) (human/rat) [AID603951, Type: Literature] | |   View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 103179369 | | CID | 8003 | | Outcome | Unspecified | | BioAssay | In-vitro air to blood partition coefficients of the compound, logK(blood) (human/rat) | | AID | 603951 | | BioAssay type | Literature | | Target | | | PubMed | 17544548 | | Data Table |  |
|
| 15 | [SID103179369] | Unspecified | | | In-vitro blood to lung partition coefficients of the compound, logP(lung) (human/rat) [AID603952, Type: Literature] | |   View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 103179369 | | CID | 8003 | | Outcome | Unspecified | | BioAssay | In-vitro blood to lung partition coefficients of the compound, logP(lung) (human/rat) | | AID | 603952 | | BioAssay type | Literature | | Target | | | PubMed | 17544548 | | Data Table |  |
|
| 16 | [SID103179369] | Unspecified | | | Octanol-water partition coefficient, log P of the compound [AID603957, Type: Literature] | |   View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 103179369 | | CID | 8003 | | Outcome | Unspecified | | BioAssay | Octanol-water partition coefficient, log P of the compound | | AID | 603957 | | BioAssay type | Literature | | Target | | | PubMed | 17629592 | | Data Table |  |
|
| 17 | [SID17388845] | Inactive | Potency | 0.1 | qHTS Assay for Agonists of the Thyroid Stimulating Hormone Receptor: Activators of Intracellular cAMP Concentrations in Parental HEK 293 [AID938, Type: confirmatory] | thyroid stimulating hormone receptor [Homo sapiens] [gi:38016895] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | 0.1 [uM] | | BioAssay | qHTS Assay for Agonists of the Thyroid Stimulating Hormone Receptor: Activators of Intracellular cAMP Concentrations in Parental HEK 293 | | AID | 938 | | BioAssay type | confirmatory | | Target | thyroid stimulating hormone receptor [Homo sapiens] [gi:38016895] | | PubMed | | | Data Table |  |
|
| 18 | [SID17388845] | Inactive | Potency | 0.1 | qHTS Assay for Agonists of the Thyroid Stimulating Hormone Receptor: Activators of Intracellular cAMP Concentrations in Parental HEK 293 [AID938, Type: confirmatory] | thyroid stimulating hormone receptor [Homo sapiens] [gi:38016895] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | 0.1 [uM] | | BioAssay | qHTS Assay for Agonists of the Thyroid Stimulating Hormone Receptor: Activators of Intracellular cAMP Concentrations in Parental HEK 293 | | AID | 938 | | BioAssay type | confirmatory | | Target | thyroid stimulating hormone receptor [Homo sapiens] [gi:38016895] | | PubMed | | | Data Table |  |
|
| 19 | [SID17388845] | Inactive | Potency | 0.1 | qHTS Assay for Agonists of the Thyroid Stimulating Hormone Receptor: Activators of Intracellular cAMP Concentrations in Parental HEK 293 [AID938, Type: confirmatory] | thyroid stimulating hormone receptor [Homo sapiens] [gi:38016895] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | 0.1 [uM] | | BioAssay | qHTS Assay for Agonists of the Thyroid Stimulating Hormone Receptor: Activators of Intracellular cAMP Concentrations in Parental HEK 293 | | AID | 938 | | BioAssay type | confirmatory | | Target | thyroid stimulating hormone receptor [Homo sapiens] [gi:38016895] | | PubMed | | | Data Table |  |
|
| 20 | [SID17388845] | Inactive | Potency | | Inhibitors of USP1/UAF1: Pilot qHTS [AID504865, Type: confirmatory] | USP1 protein [Homo sapiens] [gi:118600387] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Inhibitors of USP1/UAF1: Pilot qHTS | | AID | 504865 | | BioAssay type | confirmatory | | Target | USP1 protein [Homo sapiens] [gi:118600387] | | PubMed | | | Data Table |  |
|
| 21 | [SID17388845] | Inactive | Potency | | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 22 | [SID17388845] | Inactive | Potency | | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 23 | [SID17388845] | Inactive | Potency | | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 24 | [SID17388845] | Inactive | Potency | | Inhibitors of the vitamin D receptor (VDR): qHTS [AID504847, Type: confirmatory] | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | Inhibitors of the vitamin D receptor (VDR): qHTS | | AID | 504847 | | BioAssay type | confirmatory | | Target | vitamin D3 receptor isoform VDRA [Homo sapiens] [gi:63054845] | | PubMed | | | Data Table |  |
|
| 25 | [SID17388845] | Inactive | Potency | | qHTS assay for small molecule antagonists of vitamin D receptor signaling [AID588541, Type: confirmatory] | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule antagonists of vitamin D receptor signaling | | AID | 588541 | | BioAssay type | confirmatory | | Target | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] | | PubMed | | | Data Table |  |
|
| 26 | [SID17388845] | Inactive | Potency | | qHTS assay for small molecule antagonists of vitamin D receptor signaling [AID588541, Type: confirmatory] | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule antagonists of vitamin D receptor signaling | | AID | 588541 | | BioAssay type | confirmatory | | Target | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] | | PubMed | | | Data Table |  |
|
| 27 | [SID17388845] | Inactive | Potency | | qHTS assay for small molecule antagonists of vitamin D receptor signaling [AID588541, Type: confirmatory] | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule antagonists of vitamin D receptor signaling | | AID | 588541 | | BioAssay type | confirmatory | | Target | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] | | PubMed | | | Data Table |  |
|
| 28 | [SID17388845] | Inactive | Potency | | qHTS assay for small molecule antagonists of vitamin D receptor signaling [AID588541, Type: confirmatory] | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule antagonists of vitamin D receptor signaling | | AID | 588541 | | BioAssay type | confirmatory | | Target | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] | | PubMed | | | Data Table |  |
|
| 29 | [SID17388845] | Inactive | Potency | | qHTS assay for small molecule agonists of vitamin D receptor signaling [AID588543, Type: confirmatory] | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule agonists of vitamin D receptor signaling | | AID | 588543 | | BioAssay type | confirmatory | | Target | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] | | PubMed | | | Data Table |  |
|
| 30 | [SID17388845] | Inactive | Potency | | qHTS assay for small molecule agonists of vitamin D receptor signaling [AID588543, Type: confirmatory] | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule agonists of vitamin D receptor signaling | | AID | 588543 | | BioAssay type | confirmatory | | Target | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] | | PubMed | | | Data Table |  |
|
| 31 | [SID17388845] | Inactive | Potency | | qHTS assay for small molecule agonists of vitamin D receptor signaling [AID588543, Type: confirmatory] | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule agonists of vitamin D receptor signaling | | AID | 588543 | | BioAssay type | confirmatory | | Target | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] | | PubMed | | | Data Table |  |
|
| 32 | [SID17388845] | Inactive | Potency | | qHTS assay for small molecule agonists of vitamin D receptor signaling [AID588543, Type: confirmatory] | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule agonists of vitamin D receptor signaling | | AID | 588543 | | BioAssay type | confirmatory | | Target | vitamin D (1,25- dihydroxyvitamin D3) receptor [Homo sapiens] [gi:216409708] | | PubMed | | | Data Table |  |
|
| 33 | [SID17388845] | Inactive | Potency | | qHTS assay for small molecule antagonists of farnesoid X receptor signaling [AID588526, Type: confirmatory] | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule antagonists of farnesoid X receptor signaling | | AID | 588526 | | BioAssay type | confirmatory | | Target | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] | | PubMed | | | Data Table |  |
|
| 34 | [SID17388845] | Inactive | Potency | | qHTS assay for small molecule antagonists of farnesoid X receptor signaling [AID588526, Type: confirmatory] | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule antagonists of farnesoid X receptor signaling | | AID | 588526 | | BioAssay type | confirmatory | | Target | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] | | PubMed | | | Data Table |  |
|
| 35 | [SID17388845] | Inactive | Potency | | qHTS assay for small molecule antagonists of farnesoid X receptor signaling [AID588526, Type: confirmatory] | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule antagonists of farnesoid X receptor signaling | | AID | 588526 | | BioAssay type | confirmatory | | Target | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] | | PubMed | | | Data Table |  |
|
| 36 | [SID17388845] | Inactive | Potency | | qHTS assay for small molecule antagonists of farnesoid X receptor signaling [AID588526, Type: confirmatory] | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule antagonists of farnesoid X receptor signaling | | AID | 588526 | | BioAssay type | confirmatory | | Target | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] | | PubMed | | | Data Table |  |
|
| 37 | [SID17388845] | Inactive | Potency | | qHTS assay for small molecule agonists of farnesoid X receptor signaling [AID588527, Type: confirmatory] | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule agonists of farnesoid X receptor signaling | | AID | 588527 | | BioAssay type | confirmatory | | Target | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] | | PubMed | | | Data Table |  |
|
| 38 | [SID17388845] | Inactive | Potency | | qHTS assay for small molecule agonists of farnesoid X receptor signaling [AID588527, Type: confirmatory] | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule agonists of farnesoid X receptor signaling | | AID | 588527 | | BioAssay type | confirmatory | | Target | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] | | PubMed | | | Data Table |  |
|
| 39 | [SID17388845] | Inactive | Potency | | qHTS assay for small molecule agonists of farnesoid X receptor signaling [AID588527, Type: confirmatory] | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule agonists of farnesoid X receptor signaling | | AID | 588527 | | BioAssay type | confirmatory | | Target | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] | | PubMed | | | Data Table |  |
|
| 40 | [SID17388845] | Inactive | Potency | | qHTS assay for small molecule agonists of farnesoid X receptor signaling [AID588527, Type: confirmatory] | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay for small molecule agonists of farnesoid X receptor signaling | | AID | 588527 | | BioAssay type | confirmatory | | Target | farnesoid X nuclear receptor [Homo sapiens] [gi:325495553] | | PubMed | | | Data Table |  |
|
| 41 | [SID17388845] | Inactive | Potency | | qHTS for inhibitors of ROR gamma transcriptional activity [AID2551, Type: confirmatory] | nuclear receptor ROR-gamma [Mus musculus] [gi:188536040] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for inhibitors of ROR gamma transcriptional activity | | AID | 2551 | | BioAssay type | confirmatory | | Target | nuclear receptor ROR-gamma [Mus musculus] [gi:188536040] | | PubMed | | | Data Table |  |
|
| 42 | [SID17388845] | Inactive | Potency | | VP16 counterscreen qHTS for inhibitors of ROR gamma transcriptional activity [AID2546, Type: confirmatory] | nuclear receptor ROR-gamma [Mus musculus] [gi:188536040] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | VP16 counterscreen qHTS for inhibitors of ROR gamma transcriptional activity | | AID | 2546 | | BioAssay type | confirmatory | | Target | nuclear receptor ROR-gamma [Mus musculus] [gi:188536040] | | PubMed | | | Data Table |  |
|
| 43 | [SID17388845] | Inactive | Potency | | qHTS assay to identify small molecules that stimulate Tumor Necrosis Factor-alpha (TNF-alpha) secretion [AID651757, Type: confirmatory] | TNF gene product [Homo sapiens] [gi:25952111] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay to identify small molecules that stimulate Tumor Necrosis Factor-alpha (TNF-alpha) secretion | | AID | 651757 | | BioAssay type | confirmatory | | Target | TNF gene product [Homo sapiens] [gi:25952111] | | PubMed | | | Data Table |  |
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| 44 | [SID17388845] | Inactive | Potency | | qHTS assay to identify small molecules that stimulate Tumor Necrosis Factor-alpha (TNF-alpha) secretion [AID651757, Type: confirmatory] | TNF gene product [Homo sapiens] [gi:25952111] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS assay to identify small molecules that stimulate Tumor Necrosis Factor-alpha (TNF-alpha) secretion | | AID | 651757 | | BioAssay type | confirmatory | | Target | TNF gene product [Homo sapiens] [gi:25952111] | | PubMed | | | Data Table |  |
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| 45 | [SID17388845] | Inactive | Potency | | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature [AID924, Type: confirmatory] | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature | | AID | 924 | | BioAssay type | confirmatory | | Target | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] | | PubMed | | | Data Table |  |
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| 46 | [SID17388845] | Inactive | Potency | | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature [AID924, Type: confirmatory] | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature | | AID | 924 | | BioAssay type | confirmatory | | Target | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] | | PubMed | | | Data Table |  |
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| 47 | [SID17388845] | Inactive | Potency | | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature [AID924, Type: confirmatory] | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature | | AID | 924 | | BioAssay type | confirmatory | | Target | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] | | PubMed | | | Data Table |  |
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| 48 | [SID17388845] | Inactive | Potency | | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature [AID924, Type: confirmatory] | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Permissive Temperature | | AID | 924 | | BioAssay type | confirmatory | | Target | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] | | PubMed | | | Data Table |  |
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| 49 | [SID17388845] | Inactive | Potency | | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature [AID902, Type: confirmatory] | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature | | AID | 902 | | BioAssay type | confirmatory | | Target | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] | | PubMed | | | Data Table |  |
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| 50 | [SID17388845] | Inactive | Potency | | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature [AID902, Type: confirmatory] | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 17388845 | | CID | 8003 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature | | AID | 902 | | BioAssay type | confirmatory | | Target | cellular tumor antigen p53 isoform a [Homo sapiens] [gi:120407068] | | PubMed | | | Data Table |  |
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