| 1 | [SID103166710] | Active | Ki | 0.3 | Inhibition of binding of 17 beta-estradiol to human Estrogen receptor beta [AID70660, Type: Literature] | |   View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 103166710 | | CID | 5281708 | | Outcome | Active | | Ki | 0.3 [uM] | | BioAssay | Inhibition of binding of 17 beta-estradiol to human Estrogen receptor beta | | AID | 70660 | | BioAssay type | Literature | | Target | | | PubMed | 11459643 | | Data Table |  |
|
| 2 | [SID103166710] | Active | IC50 | 0.303 | Binding affinity against human estrogen receptor beta (ER beta) in competitive binding assay [AID70514, Type: Literature] | |   View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 103166710 | | CID | 5281708 | | Outcome | Active | | IC50 | 0.303 [uM] | | BioAssay | Binding affinity against human estrogen receptor beta (ER beta) in competitive binding assay | | AID | 70514 | | BioAssay type | Literature | | Target | | | PubMed | 15006374 | | Data Table |  |
|
| 3 | [SID103166710] | Active | IC50 | 0.45 | Displacement of fluorescent labeled ES2 from recombinant ERalpha [AID499822, Type: Literature] | |   View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 103166710 | | CID | 5281708 | | Outcome | Active | | IC50 | 0.45 [uM] | | BioAssay | Displacement of fluorescent labeled ES2 from recombinant ERalpha | | AID | 499822 | | BioAssay type | Literature | | Target | | | PubMed | 20669983 | | Data Table |  |
|
| 4 | [SID17389519] | Active | Potency | 0.7943 | qHTS assay for small molecule agonists of estrogen receptor alpha signaling [AID588514, Type: confirmatory] | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 17389519 | | CID | 5281708 | | Outcome | Active | | Potency | 0.7943 [uM] | | BioAssay | qHTS assay for small molecule agonists of estrogen receptor alpha signaling | | AID | 588514 | | BioAssay type | confirmatory | | Target | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] | | PubMed | | | Data Table |  |
|
| 5 | [SID17389519] | Active | Potency | 0.7943 | qHTS assay for small molecule agonists of estrogen receptor alpha signaling [AID588514, Type: confirmatory] | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 17389519 | | CID | 5281708 | | Outcome | Active | | Potency | 0.7943 [uM] | | BioAssay | qHTS assay for small molecule agonists of estrogen receptor alpha signaling | | AID | 588514 | | BioAssay type | confirmatory | | Target | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] | | PubMed | | | Data Table |  |
|
| 6 | [SID17389519] | Active | Potency | 0.7943 | qHTS assay for small molecule agonists of estrogen receptor alpha signaling [AID588514, Type: confirmatory] | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 17389519 | | CID | 5281708 | | Outcome | Active | | Potency | 0.7943 [uM] | | BioAssay | qHTS assay for small molecule agonists of estrogen receptor alpha signaling | | AID | 588514 | | BioAssay type | confirmatory | | Target | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] | | PubMed | | | Data Table |  |
|
| 7 | [SID17389519] | Active | Potency | 0.7943 | qHTS assay for small molecule agonists of estrogen receptor alpha signaling [AID588514, Type: confirmatory] | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 17389519 | | CID | 5281708 | | Outcome | Active | | Potency | 0.7943 [uM] | | BioAssay | qHTS assay for small molecule agonists of estrogen receptor alpha signaling | | AID | 588514 | | BioAssay type | confirmatory | | Target | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] | | PubMed | | | Data Table |  |
|
| 8 | [SID50126369] | Active | Potency | 0.8913 | qHTS assay for small molecule agonists of estrogen receptor alpha signaling [AID588514, Type: confirmatory] | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 50126369 | | CID | 5281708 | | Outcome | Active | | Potency | 0.8913 [uM] | | BioAssay | qHTS assay for small molecule agonists of estrogen receptor alpha signaling | | AID | 588514 | | BioAssay type | confirmatory | | Target | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] | | PubMed | | | Data Table |  |
|
| 9 | [SID50126369] | Active | Potency | 0.8913 | qHTS assay for small molecule agonists of estrogen receptor alpha signaling [AID588514, Type: confirmatory] | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 50126369 | | CID | 5281708 | | Outcome | Active | | Potency | 0.8913 [uM] | | BioAssay | qHTS assay for small molecule agonists of estrogen receptor alpha signaling | | AID | 588514 | | BioAssay type | confirmatory | | Target | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] | | PubMed | | | Data Table |  |
|
| 10 | [SID50126369] | Active | Potency | 0.8913 | qHTS assay for small molecule agonists of estrogen receptor alpha signaling [AID588514, Type: confirmatory] | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 50126369 | | CID | 5281708 | | Outcome | Active | | Potency | 0.8913 [uM] | | BioAssay | qHTS assay for small molecule agonists of estrogen receptor alpha signaling | | AID | 588514 | | BioAssay type | confirmatory | | Target | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] | | PubMed | | | Data Table |  |
|
| 11 | [SID50126369] | Active | Potency | 0.8913 | qHTS assay for small molecule agonists of estrogen receptor alpha signaling [AID588514, Type: confirmatory] | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 50126369 | | CID | 5281708 | | Outcome | Active | | Potency | 0.8913 [uM] | | BioAssay | qHTS assay for small molecule agonists of estrogen receptor alpha signaling | | AID | 588514 | | BioAssay type | confirmatory | | Target | estrogen nuclear receptor alpha [Homo sapiens] [gi:348019627] | | PubMed | | | Data Table |  |
|
| 12 | [SID103166710] | Active | IC50 | 1.1 | Inhibition of binding of 17 beta-estradiol to human Estrogen receptor beta [AID70654, Type: Literature] | |   View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 103166710 | | CID | 5281708 | | Outcome | Active | | IC50 | 1.1 [uM] | | BioAssay | Inhibition of binding of 17 beta-estradiol to human Estrogen receptor beta | | AID | 70654 | | BioAssay type | Literature | | Target | | | PubMed | 11459643 | | Data Table |  |
|
| 13 | [SID103166710] | Active | IC50 | 1.2 | Estrogenic activity in human Ishikawa cells assessed as induction of alkaline phosphatase activity after 4 days by para-nitrophenol release assay [AID361464, Type: Literature] | |   View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 103166710 | | CID | 5281708 | | Outcome | Active | | IC50 | 1.2 [uM] | | BioAssay | Estrogenic activity in human Ishikawa cells assessed as induction of alkaline phosphatase activity after 4 days by para-nitrophenol release assay | | AID | 361464 | | BioAssay type | Literature | | Target | | | PubMed | 12502307 | | Data Table |  |
|
| 14 | [SID103166710] | Active | IC50 | 1.2 | Displacement of [3H]estradiol from human recombinant ERbeta [AID361463, Type: Literature] | Estrogen receptor beta [gi:6166154] |   View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 103166710 | | CID | 5281708 | | Outcome | Active | | IC50 | 1.2 [uM] | | BioAssay | Displacement of [3H]estradiol from human recombinant ERbeta | | AID | 361463 | | BioAssay type | Literature | | Target | Estrogen receptor beta [gi:6166154] | | PubMed | 12502307 | | Data Table |  |
|
| 15 | [SID103166710] | Active | IC50 | 1.2 | Displacement of [3H]estradiol from human recombinant ERbeta [AID361463, Type: Literature] | Estrogen receptor beta [gi:6166154] |   View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 103166710 | | CID | 5281708 | | Outcome | Active | | IC50 | 1.2 [uM] | | BioAssay | Displacement of [3H]estradiol from human recombinant ERbeta | | AID | 361463 | | BioAssay type | Literature | | Target | Estrogen receptor beta [gi:6166154] | | PubMed | 12502307 | | Data Table |  |
|
| 16 | [SID103166710] | Active | IC50 | 1.2 | Displacement of [3H]estradiol from human recombinant ERbeta [AID361463, Type: Literature] | Estrogen receptor beta [gi:6166154] |   View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 103166710 | | CID | 5281708 | | Outcome | Active | | IC50 | 1.2 [uM] | | BioAssay | Displacement of [3H]estradiol from human recombinant ERbeta | | AID | 361463 | | BioAssay type | Literature | | Target | Estrogen receptor beta [gi:6166154] | | PubMed | 12502307 | | Data Table |  |
|
| 17 | [SID103166710] | Active | Ki | 1.8 | Inhibition of binding of 17 beta-estradiol to human Estrogen receptor alpha [AID70353, Type: Literature] | |   View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 103166710 | | CID | 5281708 | | Outcome | Active | | Ki | 1.8 [uM] | | BioAssay | Inhibition of binding of 17 beta-estradiol to human Estrogen receptor alpha | | AID | 70353 | | BioAssay type | Literature | | Target | | | PubMed | 11459643 | | Data Table |  |
|
| 18 | [SID103166710] | Active | IC50 | 2.16 | Binding affinity against human estrogen receptor alpha in competitive binding assay [AID70199, Type: Literature] | |   View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 103166710 | | CID | 5281708 | | Outcome | Active | | IC50 | 2.16 [uM] | | BioAssay | Binding affinity against human estrogen receptor alpha in competitive binding assay | | AID | 70199 | | BioAssay type | Literature | | Target | | | PubMed | 15006374 | | Data Table |  |
|
| 19 | [SID103166710] | Active | IC50 | 2.8 | Binding affinity for human Estrogen receptor beta [AID240680, Type: Literature] | Estrogen receptor beta [gi:6166154] |   View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 103166710 | | CID | 5281708 | | Outcome | Active | | IC50 | 2.8 [uM] | | BioAssay | Binding affinity for human Estrogen receptor beta | | AID | 240680 | | BioAssay type | Literature | | Target | Estrogen receptor beta [gi:6166154] | | PubMed | 15887952 | | Data Table |  |
|
| 20 | [SID103166710] | Active | IC50 | 2.8 | Binding affinity for human Estrogen receptor beta [AID240680, Type: Literature] | Estrogen receptor beta [gi:6166154] |   View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 103166710 | | CID | 5281708 | | Outcome | Active | | IC50 | 2.8 [uM] | | BioAssay | Binding affinity for human Estrogen receptor beta | | AID | 240680 | | BioAssay type | Literature | | Target | Estrogen receptor beta [gi:6166154] | | PubMed | 15887952 | | Data Table |  |
|
| 21 | [SID103166710] | Active | IC50 | 2.8 | Binding affinity for human Estrogen receptor beta [AID240680, Type: Literature] | Estrogen receptor beta [gi:6166154] |   View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 103166710 | | CID | 5281708 | | Outcome | Active | | IC50 | 2.8 [uM] | | BioAssay | Binding affinity for human Estrogen receptor beta | | AID | 240680 | | BioAssay type | Literature | | Target | Estrogen receptor beta [gi:6166154] | | PubMed | 15887952 | | Data Table |  |
|
| 22 | [SID103166710] | Active | Kd | 5.9 | Displacement of [3H]-estradiol (E2) frrom sheep uterine estrogen receptor [AID69702, Type: Literature] | |   View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 103166710 | | CID | 5281708 | | Outcome | Active | | Kd | 5.9 [uM] | | BioAssay | Displacement of [3H]-estradiol (E2) frrom sheep uterine estrogen receptor | | AID | 69702 | | BioAssay type | Literature | | Target | | | PubMed | 14761204 | | Data Table |  |
|
| 23 | [SID103166710] | Active | IC50 | 6.3 | Inhibition of binding of 17 beta-estradiol to human Estrogen receptor alpha [AID70335, Type: Literature] | |   View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 103166710 | | CID | 5281708 | | Outcome | Active | | IC50 | 6.3 [uM] | | BioAssay | Inhibition of binding of 17 beta-estradiol to human Estrogen receptor alpha | | AID | 70335 | | BioAssay type | Literature | | Target | | | PubMed | 11459643 | | Data Table |  |
|
| 24 | [SID11114077] | Active | Potency | 6.3096 | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C9 [AID883, Type: confirmatory] | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 11114077 | | CID | 5281708 | | Outcome | Active | | Potency | 6.3096 [uM] | | BioAssay | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C9 | | AID | 883 | | BioAssay type | confirmatory | | Target | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] | | PubMed | | | Data Table |  |
|
| 25 | [SID11114077] | Active | Potency | 6.3096 | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C9 [AID883, Type: confirmatory] | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 11114077 | | CID | 5281708 | | Outcome | Active | | Potency | 6.3096 [uM] | | BioAssay | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C9 | | AID | 883 | | BioAssay type | confirmatory | | Target | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] | | PubMed | | | Data Table |  |
|
| 26 | [SID11114077] | Active | Potency | 6.3096 | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C9 [AID883, Type: confirmatory] | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 11114077 | | CID | 5281708 | | Outcome | Active | | Potency | 6.3096 [uM] | | BioAssay | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C9 | | AID | 883 | | BioAssay type | confirmatory | | Target | cytochrome P450, family 2, subfamily C, polypeptide 9 [Homo sapiens] [gi:13699818] | | PubMed | | | Data Table |  |
|
| 27 | [SID90341229] | Active | Potency | 8.4368 | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1) [AID488773, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 90341229 | | CID | 5281708 | | Outcome | Active | | Potency | 8.4368 [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 |  |
|
| 28 | [SID90341229] | Active | Potency | 8.4368 | qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1) [AID488773, Type: confirmatory] | thioredoxin reductase [Rattus norvegicus] [gi:8659577] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 90341229 | | CID | 5281708 | | Outcome | Active | | Potency | 8.4368 [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 |  |
|
| 29 | [SID103166710] | Active | IC50 | 9 | Inhibition of Hamster Liver mitochondrial ALDH-2 [AID31427, Type: Literature] | |   View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 103166710 | | CID | 5281708 | | Outcome | Active | | IC50 | 9 [uM] | | BioAssay | Inhibition of Hamster Liver mitochondrial ALDH-2 | | AID | 31427 | | BioAssay type | Literature | | Target | | | PubMed | 11063613 | | Data Table |  |
|
| 30 | [SID103166710] | Active | IC50 | 9 | Inhibition of hamster liver aldehyde dehydrogenase ALDH-2 [AID34047, Type: Literature] | |   View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 103166710 | | CID | 5281708 | | Outcome | Active | | IC50 | 9 [uM] | | BioAssay | Inhibition of hamster liver aldehyde dehydrogenase ALDH-2 | | AID | 34047 | | BioAssay type | Literature | | Target | | | PubMed | 11563931 | | Data Table |  |
|
| 31 | [SID103166710] | Active | IC50 | 9 | Inhibition of hamster liver ALDH2 [AID341733, Type: Literature] | |   View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 103166710 | | CID | 5281708 | | Outcome | Active | | IC50 | 9 [uM] | | BioAssay | Inhibition of hamster liver ALDH2 | | AID | 341733 | | BioAssay type | Literature | | Target | | | PubMed | 18613661 | | Data Table |  |
|
| 32 | [SID90341229] | Active | Potency | 9.2 | qHTS Assay for NPC1 Promoter Activators [AID485313, Type: confirmatory] | NPC1 gene product [Homo sapiens] [gi:255652944] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 90341229 | | CID | 5281708 | | Outcome | Active | | Potency | 9.2 [uM] | | BioAssay | qHTS Assay for NPC1 Promoter Activators | | AID | 485313 | | BioAssay type | confirmatory | | Target | NPC1 gene product [Homo sapiens] [gi:255652944] | | PubMed | | | Data Table |  |
|
| 33 | [SID11114077] | Active | Potency | 10 | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C19 [AID899, Type: confirmatory] | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 11114077 | | CID | 5281708 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C19 | | AID | 899 | | BioAssay type | confirmatory | | Target | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] | | PubMed | | | Data Table |  |
|
| 34 | [SID11114077] | Active | Potency | 10 | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C19 [AID899, Type: confirmatory] | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 11114077 | | CID | 5281708 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2C19 | | AID | 899 | | BioAssay type | confirmatory | | Target | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] | | PubMed | | | Data Table |  |
|
| 35 | [SID11114077] | Active | Potency | 10 | qHTS Assay for Inhibitors of Firefly Luciferase [AID411, Type: confirmatory] | Luciferase [Photinus pyralis] [gi:160794] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 11114077 | | CID | 5281708 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | qHTS Assay for Inhibitors of Firefly Luciferase | | AID | 411 | | BioAssay type | confirmatory | | Target | Luciferase [Photinus pyralis] [gi:160794] | | PubMed | | | Data Table |  |
|
| 36 | [SID11114077] | Active | Potency | 10 | 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. | 36 | | Structure |
| | Substance | | | SID | 11114077 | | CID | 5281708 | | Outcome | Active | | Potency | 10 [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 |  |
|
| 37 | [SID11114077] | Active | Potency | 10 | 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. | 37 | | Structure |
| | Substance | | | SID | 11114077 | | CID | 5281708 | | Outcome | Active | | Potency | 10 [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 |  |
|
| 38 | [SID11114077] | Active | Potency | 10 | 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. | 38 | | Structure |
| | Substance | | | SID | 11114077 | | CID | 5281708 | | Outcome | Active | | Potency | 10 [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 |  |
|
| 39 | [SID11114077] | Active | Potency | 10 | 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. | 39 | | Structure |
| | Substance | | | SID | 11114077 | | CID | 5281708 | | Outcome | Active | | Potency | 10 [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 |  |
|
| 40 | [SID90341229] | Active | Potency | 10 | qHTS Assay for Rab9 Promoter Activators [AID485297, Type: confirmatory] | RAB9A gene product [Homo sapiens] [gi:4759012] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 90341229 | | CID | 5281708 | | Outcome | Active | | Potency | 10 [uM] | | BioAssay | qHTS Assay for Rab9 Promoter Activators | | AID | 485297 | | BioAssay type | confirmatory | | Target | RAB9A gene product [Homo sapiens] [gi:4759012] | | PubMed | | | Data Table |  |
|
| 41 | [SID50104845] | Active | Potency | 12.5893 | qHTS Assay for Enhancers of SMN2 Splice Variant Expression [AID1458, Type: confirmatory] | survival motor neuron protein isoform d [Homo sapiens] [gi:10937869] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 50104845 | | CID | 5281708 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS Assay for Enhancers of SMN2 Splice Variant Expression | | AID | 1458 | | BioAssay type | confirmatory | | Target | survival motor neuron protein isoform d [Homo sapiens] [gi:10937869] | | PubMed | | | Data Table |  |
|
| 42 | [SID50104845] | Active | Potency | 12.5893 | qHTS Assay for Enhancers of SMN2 Splice Variant Expression [AID1458, Type: confirmatory] | survival motor neuron protein isoform d [Homo sapiens] [gi:10937869] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 50104845 | | CID | 5281708 | | Outcome | Active | | Potency | 12.5893 [uM] | | BioAssay | qHTS Assay for Enhancers of SMN2 Splice Variant Expression | | AID | 1458 | | BioAssay type | confirmatory | | Target | survival motor neuron protein isoform d [Homo sapiens] [gi:10937869] | | PubMed | | | Data Table |  |
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| 43 | [SID103166710] | Active | IC50 | 13.63 | Inhibition of ALR2 (aldose reductase) of bovine lens [AID34338, Type: Literature] | Aldose reductase [gi:113594] |   View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 103166710 | | CID | 5281708 | | Outcome | Active | | IC50 | 13.63 [uM] | | BioAssay | Inhibition of ALR2 (aldose reductase) of bovine lens | | AID | 34338 | | BioAssay type | Literature | | Target | Aldose reductase [gi:113594] | | PubMed | 10354396 | | Data Table |  |
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| 44 | [SID103166710] | Active | IC50 | 14 | Inhibition of Hamster Liver mitochondrial Monoamine oxidase. [AID125222, Type: Literature] | |   View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 103166710 | | CID | 5281708 | | Outcome | Active | | IC50 | 14 [uM] | | BioAssay | Inhibition of Hamster Liver mitochondrial Monoamine oxidase. | | AID | 125222 | | BioAssay type | Literature | | Target | | | PubMed | 11063613 | | Data Table |  |
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| 45 | [SID103166710] | Active | IC50 | 14 | Inhibition of hamster liver mitochondrial monoamine oxidase MAO [AID125224, Type: Literature] | |   View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 103166710 | | CID | 5281708 | | Outcome | Active | | IC50 | 14 [uM] | | BioAssay | Inhibition of hamster liver mitochondrial monoamine oxidase MAO | | AID | 125224 | | BioAssay type | Literature | | Target | | | PubMed | 11563931 | | Data Table |  |
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| 46 | [SID11114077] | Active | Potency | 15.8489 | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2D6 [AID891, Type: confirmatory] | cytochrome P450 2D6 isoform 1 [Homo sapiens] [gi:40805836] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 11114077 | | CID | 5281708 | | Outcome | Active | | Potency | 15.8489 [uM] | | BioAssay | qHTS Assay for Inhibitors and Substrates of Cytochrome P450 2D6 | | AID | 891 | | BioAssay type | confirmatory | | Target | cytochrome P450 2D6 isoform 1 [Homo sapiens] [gi:40805836] | | PubMed | | | Data Table |  |
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| 47 | [SID26747166] | Active | Potency | 15.8489 | qHTS Assay for Enhancers of SMN2 Splice Variant Expression [AID1458, Type: confirmatory] | survival motor neuron protein isoform d [Homo sapiens] [gi:10937869] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 26747166 | | CID | 5281708 | | Outcome | Active | | Potency | 15.8489 [uM] | | BioAssay | qHTS Assay for Enhancers of SMN2 Splice Variant Expression | | AID | 1458 | | BioAssay type | confirmatory | | Target | survival motor neuron protein isoform d [Homo sapiens] [gi:10937869] | | PubMed | | | Data Table |  |
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| 48 | [SID26747166] | Active | Potency | 15.8489 | qHTS Assay for Enhancers of SMN2 Splice Variant Expression [AID1458, Type: confirmatory] | survival motor neuron protein isoform d [Homo sapiens] [gi:10937869] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 26747166 | | CID | 5281708 | | Outcome | Active | | Potency | 15.8489 [uM] | | BioAssay | qHTS Assay for Enhancers of SMN2 Splice Variant Expression | | AID | 1458 | | BioAssay type | confirmatory | | Target | survival motor neuron protein isoform d [Homo sapiens] [gi:10937869] | | PubMed | | | Data Table |  |
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| 49 | [SID103166710] | Active | IC50 | 17 | Displacement of [3H]estradiol from human recombinant ERalpha [AID356892, Type: Literature] | Estrogen receptor [gi:544257] |   View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 103166710 | | CID | 5281708 | | Outcome | Active | | IC50 | 17 [uM] | | BioAssay | Displacement of [3H]estradiol from human recombinant ERalpha | | AID | 356892 | | BioAssay type | Literature | | Target | Estrogen receptor [gi:544257] | | PubMed | 12502307 | | Data Table |  |
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| 50 | [SID103166710] | Active | IC50 | 17 | Displacement of [3H]estradiol from human recombinant ERalpha [AID356892, Type: Literature] | Estrogen receptor [gi:544257] |   View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 103166710 | | CID | 5281708 | | Outcome | Active | | IC50 | 17 [uM] | | BioAssay | Displacement of [3H]estradiol from human recombinant ERalpha | | AID | 356892 | | BioAssay type | Literature | | Target | Estrogen receptor [gi:544257] | | PubMed | 12502307 | | Data Table |  |
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