| 1 | [SID103596001] | Active | IC50 | 0.00474 | Inhibition of Smoothened transfected in HEK293 cells by transient transfection cell-based assay [AID494009, Type: Literature] | |   View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 103596001 | | CID | 6878030 | | Outcome | Active | | IC50 | 0.00474 [uM] | | BioAssay | Inhibition of Smoothened transfected in HEK293 cells by transient transfection cell-based assay | | AID | 494009 | | BioAssay type | Literature | | Target | | | PubMed | 20620058 | | Data Table |  |
|
| 2 | [SID103596001] | Active | IC50 | 0.02 | Inhibition of SHH-mediated mouse C3H10T1/2 cells differentiation into osteoblasts by alkaline phosphatase assay [AID351761, Type: Literature] | Sonic hedgehog protein [gi:6094284] |   View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 103596001 | | CID | 6878030 | | Outcome | Active | | IC50 | 0.02 [uM] | | BioAssay | Inhibition of SHH-mediated mouse C3H10T1/2 cells differentiation into osteoblasts by alkaline phosphatase assay | | AID | 351761 | | BioAssay type | Literature | | Target | Sonic hedgehog protein [gi:6094284] | | PubMed | 19309080 | | Data Table |  |
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| 3 | [SID103596001] | Active | IC50 | 0.025 | Inhibition of Smoothened transfected in HEK293 cells by binding assay [AID494010, Type: Literature] | |   View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 103596001 | | CID | 6878030 | | Outcome | Active | | IC50 | 0.025 [uM] | | BioAssay | Inhibition of Smoothened transfected in HEK293 cells by binding assay | | AID | 494010 | | BioAssay type | Literature | | Target | | | PubMed | 20620058 | | Data Table |  |
|
| 4 | [SID26753181] | Active | Potency | 10 | qHTS Assay for Activators of Cytochrome P450 3A4 [AID885, Type: confirmatory] | cytochrome P450, family 3, subfamily A, polypeptide 4 [Homo sapiens] [gi:13435386] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 26753181 | | CID | 6878030 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | qHTS Assay for Activators of Cytochrome P450 3A4 | | AID | 885 | | BioAssay type | confirmatory | | Target | cytochrome P450, family 3, subfamily A, polypeptide 4 [Homo sapiens] [gi:13435386] | | PubMed | | | Data Table |  |
|
| 5 | [SID26753181] | Active | Potency | 10 | qHTS Assay for Activators of Cytochrome P450 3A4 [AID885, Type: confirmatory] | cytochrome P450, family 3, subfamily A, polypeptide 4 [Homo sapiens] [gi:13435386] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 26753181 | | CID | 6878030 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | qHTS Assay for Activators of Cytochrome P450 3A4 | | AID | 885 | | BioAssay type | confirmatory | | Target | cytochrome P450, family 3, subfamily A, polypeptide 4 [Homo sapiens] [gi:13435386] | | PubMed | | | Data Table |  |
|
| 6 | [SID26753181] | Active | Potency | 10 | qHTS Assay for Activators of Cytochrome P450 3A4 [AID885, Type: confirmatory] | cytochrome P450, family 3, subfamily A, polypeptide 4 [Homo sapiens] [gi:13435386] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 26753181 | | CID | 6878030 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | qHTS Assay for Activators of Cytochrome P450 3A4 | | AID | 885 | | BioAssay type | confirmatory | | Target | cytochrome P450, family 3, subfamily A, polypeptide 4 [Homo sapiens] [gi:13435386] | | PubMed | | | Data Table |  |
|
| 7 | [SID90341472] | Active | Potency | 16.8336 | qHTS Assay for Inhibitors of Histone Lysine Methyltransferase G9a [AID504332, Type: confirmatory] | euchromatic histone-lysine N-methyltransferase 2 [Homo sapiens] [gi:168985070] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | Outcome | Active | | Potency | 16.8336 [uM] | | BioAssay | qHTS Assay for Inhibitors of Histone Lysine Methyltransferase G9a | | AID | 504332 | | BioAssay type | confirmatory | | Target | euchromatic histone-lysine N-methyltransferase 2 [Homo sapiens] [gi:168985070] | | PubMed | | | Data Table |  |
|
| 8 | [SID90341472] | Active | Potency | 39.8107 | qHTS Validation Assay for Inhibitors of HP1-beta Chromodomain Interactions with Methylated Histone Tails [AID488953, Type: confirmatory] | chromobox protein homolog 1 [Homo sapiens] [gi:187960037] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | Outcome | Active | | Potency | 39.8107 [uM] | | BioAssay | qHTS Validation Assay for Inhibitors of HP1-beta Chromodomain Interactions with Methylated Histone Tails | | AID | 488953 | | BioAssay type | confirmatory | | Target | chromobox protein homolog 1 [Homo sapiens] [gi:187960037] | | PubMed | | | Data Table |  |
|
| 9 | [SID103596001] | Unspecified | | | Inhibition of hair growth in C3H/HeN mouse model assessed as inhibition of hair growth after 14 days [AID494011, Type: Literature] | |   View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 103596001 | | CID | 6878030 | | Outcome | Unspecified | | BioAssay | Inhibition of hair growth in C3H/HeN mouse model assessed as inhibition of hair growth after 14 days | | AID | 494011 | | BioAssay type | Literature | | Target | | | PubMed | 20620058 | | Data Table |  |
|
| 10 | [SID103596001] | Unspecified | | | Lipophilicity, log D of the compound [AID453203, Type: Literature] | |   View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 103596001 | | CID | 6878030 | | Outcome | Unspecified | | BioAssay | Lipophilicity, log D of the compound | | AID | 453203 | | BioAssay type | Literature | | Target | | | PubMed | 19963379 | | Data Table |  |
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| 11 | [SID103596001] | Unspecified | | | Permeability in human skin after 48 hrs by Franz cell permeability assay [AID453204, Type: Literature] | |   View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 103596001 | | CID | 6878030 | | Outcome | Unspecified | | BioAssay | Permeability in human skin after 48 hrs by Franz cell permeability assay | | AID | 453204 | | BioAssay type | Literature | | Target | | | PubMed | 19963379 | | Data Table |  |
|
| 12 | [SID90341472] | Inactive | Potency | 3.6624 | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Potentiators [AID488982, Type: confirmatory] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | Outcome | Inactive | | Potency | 3.6624 [uM] | | BioAssay | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Potentiators | | AID | 488982 | | BioAssay type | confirmatory | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
|
| 13 | [SID90341472] | Inactive | Potency | 3.6624 | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Potentiators [AID488982, Type: confirmatory] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | Outcome | Inactive | | Potency | 3.6624 [uM] | | BioAssay | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Potentiators | | AID | 488982 | | BioAssay type | confirmatory | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
|
| 14 | [SID90341472] | Inactive | Potency | 3.6624 | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Potentiators [AID488982, Type: confirmatory] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | Outcome | Inactive | | Potency | 3.6624 [uM] | | BioAssay | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Potentiators | | AID | 488982 | | BioAssay type | confirmatory | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
|
| 15 | [SID90341472] | Inactive | Potency | 3.6624 | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Potentiators [AID488982, Type: confirmatory] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | Outcome | Inactive | | Potency | 3.6624 [uM] | | BioAssay | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Potentiators | | AID | 488982 | | BioAssay type | confirmatory | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
|
| 16 | [SID26753181] | Inactive | Potency | 10 | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 3A4 [AID884, Type: confirmatory] | cytochrome P450, family 3, subfamily A, polypeptide 4 [Homo sapiens] [gi:13435386] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 26753181 | | CID | 6878030 | | Outcome | Inactive | | Potency | 10 [uM] | | BioAssay | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 3A4 | | AID | 884 | | BioAssay type | confirmatory | | Target | cytochrome P450, family 3, subfamily A, polypeptide 4 [Homo sapiens] [gi:13435386] | | PubMed | | | Data Table |  |
|
| 17 | [SID26753181] | Inactive | Potency | 10 | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 3A4 [AID884, Type: confirmatory] | cytochrome P450, family 3, subfamily A, polypeptide 4 [Homo sapiens] [gi:13435386] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 26753181 | | CID | 6878030 | | Outcome | Inactive | | Potency | 10 [uM] | | BioAssay | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 3A4 | | AID | 884 | | BioAssay type | confirmatory | | Target | cytochrome P450, family 3, subfamily A, polypeptide 4 [Homo sapiens] [gi:13435386] | | PubMed | | | Data Table |  |
|
| 18 | [SID26753181] | Inactive | Potency | 10 | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 3A4 [AID884, Type: confirmatory] | cytochrome P450, family 3, subfamily A, polypeptide 4 [Homo sapiens] [gi:13435386] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 26753181 | | CID | 6878030 | | Outcome | Inactive | | Potency | 10 [uM] | | BioAssay | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 3A4 | | AID | 884 | | BioAssay type | confirmatory | | Target | cytochrome P450, family 3, subfamily A, polypeptide 4 [Homo sapiens] [gi:13435386] | | PubMed | | | Data Table |  |
|
| 19 | [SID26753181] | Inactive | Potency | 17.7828 | qHTS Assay for Inhibitors of Tyrosyl-DNA Phosphodiesterase (TDP1) [AID485290, Type: confirmatory] | Chain A, Crystal Structure Of Human Tyrosyl-Dna Phosphodiesterase (Tdp1) [gi:20150581] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 26753181 | | CID | 6878030 | | Outcome | Inactive | | Potency | 17.7828 [uM] | | BioAssay | qHTS Assay for Inhibitors of Tyrosyl-DNA Phosphodiesterase (TDP1) | | AID | 485290 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of Human Tyrosyl-Dna Phosphodiesterase (Tdp1) [gi:20150581] | | PubMed | | | Data Table |  |
|
| 20 | [SID26753181] | Inactive | Potency | 19.9526 | qHTS Assay for Inhibitors of 15-hLO-2 (15-human lipoxygenase 2) [AID881, Type: confirmatory] | Arachidonate 15-lipoxygenase B [gi:317373425] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 26753181 | | CID | 6878030 | | Outcome | Inactive | | Potency | 19.9526 [uM] | | BioAssay | qHTS Assay for Inhibitors of 15-hLO-2 (15-human lipoxygenase 2) | | AID | 881 | | BioAssay type | confirmatory | | Target | Arachidonate 15-lipoxygenase B [gi:317373425] | | PubMed | | | Data Table |  |
|
| 21 | [SID26753181] | Inactive | Potency | | qHTS Assay for Inhibitors of Bloom's syndrome helicase (BLM) [AID2528, Type: confirmatory] | Bloom syndrome protein [Homo sapiens] [gi:4557365] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 26753181 | | CID | 6878030 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Bloom's syndrome helicase (BLM) | | AID | 2528 | | BioAssay type | confirmatory | | Target | Bloom syndrome protein [Homo sapiens] [gi:4557365] | | PubMed | | | Data Table |  |
|
| 22 | [SID26753181] | Inactive | Potency | | qHTS Assay for Allosteric/Competitive Inhibitors of Caspase-1 [AID900, Type: confirmatory] | caspase-1 isoform alpha precursor [Homo sapiens] [gi:15431328] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 26753181 | | CID | 6878030 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Allosteric/Competitive Inhibitors of Caspase-1 | | AID | 900 | | BioAssay type | confirmatory | | Target | caspase-1 isoform alpha precursor [Homo sapiens] [gi:15431328] | | PubMed | | | Data Table |  |
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| 23 | [SID26753181] | Inactive | Potency | | qHTS Assay for Allosteric/Competitive Inhibitors of Caspase-1 [AID900, Type: confirmatory] | caspase-1 isoform alpha precursor [Homo sapiens] [gi:15431328] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 26753181 | | CID | 6878030 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Allosteric/Competitive Inhibitors of Caspase-1 | | AID | 900 | | BioAssay type | confirmatory | | Target | caspase-1 isoform alpha precursor [Homo sapiens] [gi:15431328] | | PubMed | | | Data Table |  |
|
| 24 | [SID26753181] | Inactive | Potency | | qHTS Assay for Allosteric/Competitive Inhibitors of Caspase-7 [AID889, Type: confirmatory] | Caspase-7 [gi:1730092] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 26753181 | | CID | 6878030 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Allosteric/Competitive Inhibitors of Caspase-7 | | AID | 889 | | BioAssay type | confirmatory | | Target | Caspase-7 [gi:1730092] | | PubMed | | | Data Table |  |
|
| 25 | [SID26753181] | Inactive | Potency | | qHTS Assay for Allosteric/Competitive Inhibitors of Caspase-7 [AID889, Type: confirmatory] | Caspase-7 [gi:1730092] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 26753181 | | CID | 6878030 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Allosteric/Competitive Inhibitors of Caspase-7 | | AID | 889 | | BioAssay type | confirmatory | | Target | Caspase-7 [gi:1730092] | | PubMed | | | Data Table |  |
|
| 26 | [SID26753181] | Inactive | Potency | | qHTS Assay for Inhibitors of Human Jumonji Domain Containing 2E (JMJD2E) [AID2147, Type: confirmatory] | Chain A, Crystal Structure Of The Human 2-Oxoglutarate Oxygenase Loc390245 [gi:221046486] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 26753181 | | CID | 6878030 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Human Jumonji Domain Containing 2E (JMJD2E) | | AID | 2147 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of The Human 2-Oxoglutarate Oxygenase Loc390245 [gi:221046486] | | PubMed | | | Data Table |  |
|
| 27 | [SID90341472] | 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. | 27 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | 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 |  |
|
| 28 | [SID90341472] | 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. | 28 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | 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 |  |
|
| 29 | [SID90341472] | 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. | 29 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | 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 |  |
|
| 30 | [SID90341472] | 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. | 30 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | 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 |  |
|
| 31 | [SID85787638] | Inactive | | | NSD2 Inhibitors Measured in Biochemical System Using Plate Reader - 2115-01_Inhibitor_SinglePoint_HTS_Activity [AID624260, Type: screening] | WHSC1 gene product [Homo sapiens] [gi:109633019] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 85787638 | | CID | 6878030 | | Outcome | Inactive | | BioAssay | NSD2 Inhibitors Measured in Biochemical System Using Plate Reader - 2115-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 624260 | | BioAssay type | screening | | Target | WHSC1 gene product [Homo sapiens] [gi:109633019] | | PubMed | | | Data Table |  |
|
| 32 | [SID90341472] | Inactive | Potency | | qHTS Validation Assay for Inhibitors of Ubiquitin-specific Protease USP2a Using CHOP2 as the Reporter [AID463106, Type: confirmatory] | ubiquitin carboxyl-terminal hydrolase 2 isoform a [Homo sapiens] [gi:188528692] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Validation Assay for Inhibitors of Ubiquitin-specific Protease USP2a Using CHOP2 as the Reporter | | AID | 463106 | | BioAssay type | confirmatory | | Target | ubiquitin carboxyl-terminal hydrolase 2 isoform a [Homo sapiens] [gi:188528692] | | PubMed | | | Data Table |  |
|
| 33 | [SID90341472] | Inactive | Potency | | qHTS Validation Assay for Inhibitors of Ubiquitin-specific Protease USP2a Using CHOP2 as the Reporter [AID463106, Type: confirmatory] | ubiquitin carboxyl-terminal hydrolase 2 isoform a [Homo sapiens] [gi:188528692] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Validation Assay for Inhibitors of Ubiquitin-specific Protease USP2a Using CHOP2 as the Reporter | | AID | 463106 | | BioAssay type | confirmatory | | Target | ubiquitin carboxyl-terminal hydrolase 2 isoform a [Homo sapiens] [gi:188528692] | | PubMed | | | Data Table |  |
|
| 34 | [SID90341472] | Inactive | Potency | | qHTS Assay for Rab9 Promoter Activators [AID485297, Type: confirmatory] | RAB9A gene product [Homo sapiens] [gi:4759012] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Rab9 Promoter Activators | | AID | 485297 | | BioAssay type | confirmatory | | Target | RAB9A gene product [Homo sapiens] [gi:4759012] | | PubMed | | | Data Table |  |
|
| 35 | [SID90341472] | Inactive | Potency | | qHTS for Inhibitors of Cell Surface uPA Generation: Validation Assay [AID493164, Type: confirmatory] | urokinase-type plasminogen activator [Mus musculus] [gi:6679377] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Cell Surface uPA Generation: Validation Assay | | AID | 493164 | | BioAssay type | confirmatory | | Target | urokinase-type plasminogen activator [Mus musculus] [gi:6679377] | | PubMed | | | Data Table |  |
|
| 36 | [SID90341472] | Inactive | Potency | | qHTS for Inhibitors of Cell Surface uPA Generation: Validation Assay [AID493164, Type: confirmatory] | urokinase-type plasminogen activator [Mus musculus] [gi:6679377] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Cell Surface uPA Generation: Validation Assay | | AID | 493164 | | BioAssay type | confirmatory | | Target | urokinase-type plasminogen activator [Mus musculus] [gi:6679377] | | PubMed | | | Data Table |  |
|
| 37 | [SID26753181] | 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. | 37 | | Structure |
| | Substance | | | SID | 26753181 | | CID | 6878030 | | 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 |  |
|
| 38 | [SID26753181] | 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. | 38 | | Structure |
| | Substance | | | SID | 26753181 | | CID | 6878030 | | 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 |  |
|
| 39 | [SID90341472] | Inactive | Potency | | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Agonists [AID488981, Type: confirmatory] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Agonists | | AID | 488981 | | BioAssay type | confirmatory | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
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| 40 | [SID90341472] | Inactive | Potency | | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Agonists [AID488981, Type: confirmatory] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Agonists | | AID | 488981 | | BioAssay type | confirmatory | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
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| 41 | [SID90341472] | Inactive | Potency | | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Agonists [AID488981, Type: confirmatory] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Agonists | | AID | 488981 | | BioAssay type | confirmatory | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
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| 42 | [SID90341472] | Inactive | Potency | | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Agonists [AID488981, Type: confirmatory] | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | HTS Assay for Allosteric Agonists of the Human D1 Dopamine Receptor: Primary Screen for Agonists | | AID | 488981 | | BioAssay type | confirmatory | | Target | D(1A) dopamine receptor [Homo sapiens] [gi:4503383] | | PubMed | | | Data Table |  |
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| 43 | [SID90341472] | Inactive | Potency | | qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1) [AID488772, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1) | | AID | 488772 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
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| 44 | [SID90341472] | Inactive | Potency | | qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1) [AID488772, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1) | | AID | 488772 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
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| 45 | [SID90341472] | Inactive | Potency | | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1) [AID488773, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1) | | AID | 488773 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
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| 46 | [SID90341472] | Inactive | Potency | | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1) [AID488773, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1) | | AID | 488773 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
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| 47 | [SID90341472] | Inactive | Potency | | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS [AID588453, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS | | AID | 588453 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
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| 48 | [SID90341472] | Inactive | Potency | | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS [AID588453, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS | | AID | 588453 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
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| 49 | [SID90341472] | Inactive | Potency | | qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS [AID588456, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS | | AID | 588456 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
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| 50 | [SID90341472] | Inactive | Potency | | qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS [AID588456, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 90341472 | | CID | 6878030 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS | | AID | 588456 | | BioAssay type | confirmatory | | Target | thioredoxin reductase [Rattus norvegicus] [gi:8659577] | | PubMed | | | Data Table |  |
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