| 1 | [SID26751495] | Active | Potency | 0.2239 | qHTS assay for small molecule agonists of androgen receptor signaling [AID588515, Type: confirmatory] | AR protein [Homo sapiens] [gi:124375976] |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 26751495 | | CID | 5753 | | Outcome | Active | | Potency | 0.2239 [uM] | | BioAssay | qHTS assay for small molecule agonists of androgen receptor signaling | | AID | 588515 | | BioAssay type | confirmatory | | Target | AR protein [Homo sapiens] [gi:124375976] | | PubMed | | | Data Table |  |
|
| 2 | [SID26751495] | Active | Potency | 0.2239 | qHTS assay for small molecule agonists of androgen receptor signaling [AID588515, Type: confirmatory] | AR protein [Homo sapiens] [gi:124375976] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 26751495 | | CID | 5753 | | Outcome | Active | | Potency | 0.2239 [uM] | | BioAssay | qHTS assay for small molecule agonists of androgen receptor signaling | | AID | 588515 | | BioAssay type | confirmatory | | Target | AR protein [Homo sapiens] [gi:124375976] | | PubMed | | | Data Table |  |
|
| 3 | [SID17389502] | Active | Potency | 0.3162 | qHTS assay for small molecule agonists of androgen receptor signaling [AID588515, Type: confirmatory] | AR protein [Homo sapiens] [gi:124375976] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 17389502 | | CID | 5753 | | Outcome | Active | | Potency | 0.3162 [uM] | | BioAssay | qHTS assay for small molecule agonists of androgen receptor signaling | | AID | 588515 | | BioAssay type | confirmatory | | Target | AR protein [Homo sapiens] [gi:124375976] | | PubMed | | | Data Table |  |
|
| 4 | [SID17389502] | Active | Potency | 0.3162 | qHTS assay for small molecule agonists of androgen receptor signaling [AID588515, Type: confirmatory] | AR protein [Homo sapiens] [gi:124375976] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 17389502 | | CID | 5753 | | Outcome | Active | | Potency | 0.3162 [uM] | | BioAssay | qHTS assay for small molecule agonists of androgen receptor signaling | | AID | 588515 | | BioAssay type | confirmatory | | Target | AR protein [Homo sapiens] [gi:124375976] | | PubMed | | | Data Table |  |
|
| 5 | [SID56423132] | Active | Potency | 0.4109 | Nrf2 qHTS screen for inhibitors [AID504444, Type: confirmatory] | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 56423132 | | CID | 5753 | | Outcome | Active | | Potency | 0.4109 [uM] | | BioAssay | Nrf2 qHTS screen for inhibitors | | AID | 504444 | | BioAssay type | confirmatory | | Target | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] | | PubMed | | | Data Table |  |
|
| 6 | [SID56423132] | Active | Potency | 0.4109 | Nrf2 qHTS screen for inhibitors [AID504444, Type: confirmatory] | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 56423132 | | CID | 5753 | | Outcome | Active | | Potency | 0.4109 [uM] | | BioAssay | Nrf2 qHTS screen for inhibitors | | AID | 504444 | | BioAssay type | confirmatory | | Target | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] | | PubMed | | | Data Table |  |
|
| 7 | [SID56423132] | Active | Potency | 0.4109 | Nrf2 qHTS screen for inhibitors [AID504444, Type: confirmatory] | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 56423132 | | CID | 5753 | | Outcome | Active | | Potency | 0.4109 [uM] | | BioAssay | Nrf2 qHTS screen for inhibitors | | AID | 504444 | | BioAssay type | confirmatory | | Target | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] | | PubMed | | | Data Table |  |
|
| 8 | [SID56423132] | Active | Potency | 0.4109 | Nrf2 qHTS screen for inhibitors [AID504444, Type: confirmatory] | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 56423132 | | CID | 5753 | | Outcome | Active | | Potency | 0.4109 [uM] | | BioAssay | Nrf2 qHTS screen for inhibitors | | AID | 504444 | | BioAssay type | confirmatory | | Target | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] | | PubMed | | | Data Table |  |
|
| 9 | [SID90341091] | Active | Potency | 6.5131 | Nrf2 qHTS screen for inhibitors: Validation [AID493153, Type: confirmatory] | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 90341091 | | CID | 5753 | | Outcome | Active | | Potency | 6.5131 [uM] | | BioAssay | Nrf2 qHTS screen for inhibitors: Validation | | AID | 493153 | | BioAssay type | confirmatory | | Target | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] | | PubMed | | | Data Table |  |
|
| 10 | [SID90341091] | Active | Potency | 6.5131 | Nrf2 qHTS screen for inhibitors: Validation [AID493153, Type: confirmatory] | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 90341091 | | CID | 5753 | | Outcome | Active | | Potency | 6.5131 [uM] | | BioAssay | Nrf2 qHTS screen for inhibitors: Validation | | AID | 493153 | | BioAssay type | confirmatory | | Target | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] | | PubMed | | | Data Table |  |
|
| 11 | [SID90341091] | Active | Potency | 6.5131 | Nrf2 qHTS screen for inhibitors: Validation [AID493153, Type: confirmatory] | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 90341091 | | CID | 5753 | | Outcome | Active | | Potency | 6.5131 [uM] | | BioAssay | Nrf2 qHTS screen for inhibitors: Validation | | AID | 493153 | | BioAssay type | confirmatory | | Target | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] | | PubMed | | | Data Table |  |
|
| 12 | [SID90341091] | Active | Potency | 6.5131 | Nrf2 qHTS screen for inhibitors: Validation [AID493153, Type: confirmatory] | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 90341091 | | CID | 5753 | | Outcome | Active | | Potency | 6.5131 [uM] | | BioAssay | Nrf2 qHTS screen for inhibitors: Validation | | AID | 493153 | | BioAssay type | confirmatory | | Target | nuclear factor erythroid 2-related factor 2 isoform 2 [Homo sapiens] [gi:224028257] | | PubMed | | | Data Table |  |
|
| 13 | [SID103333099] | Active | IC50 | 10 | Antiplasmodial activity against Plasmodium falciparum 7G8 after 72 hrs by SYBR green assay [AID524791, Type: Literature] | |   View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Active | | IC50 | 10 [uM] | | BioAssay | Antiplasmodial activity against Plasmodium falciparum 7G8 after 72 hrs by SYBR green assay | | AID | 524791 | | BioAssay type | Literature | | Target | | | PubMed | 19734910 | | Data Table |  |
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| 14 | [SID103333099] | Active | IC50 | 10 | Antiplasmodial activity against Plasmodium falciparum W2 after 72 hrs by SYBR green assay [AID524796, Type: Literature] | |   View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Active | | IC50 | 10 [uM] | | BioAssay | Antiplasmodial activity against Plasmodium falciparum W2 after 72 hrs by SYBR green assay | | AID | 524796 | | BioAssay type | Literature | | Target | | | PubMed | 19734910 | | Data Table |  |
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| 15 | [SID103333099] | Active | IC50 | 12.5892 | Antiplasmodial activity against Plasmodium falciparum 3D7 after 72 hrs by SYBR green assay [AID524790, Type: Literature] | |   View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Active | | IC50 | 12.5892 [uM] | | BioAssay | Antiplasmodial activity against Plasmodium falciparum 3D7 after 72 hrs by SYBR green assay | | AID | 524790 | | BioAssay type | Literature | | Target | | | PubMed | 19734910 | | Data Table |  |
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| 16 | [SID103333099] | Active | IC50 | 23.4423 | Inhibitory concentration against recombinant rat androgen receptor expressed in Escherichia coli using [3H]methyltrienolone (R 1881) [AID255211, Type: Literature] | |   View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Active | | IC50 | 23.4423 [uM] | | BioAssay | Inhibitory concentration against recombinant rat androgen receptor expressed in Escherichia coli using [3H]methyltrienolone (R 1881) | | AID | 255211 | | BioAssay type | Literature | | Target | | | PubMed | 16134935 | | Data Table |  |
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| 17 | [SID103333099] | Active | Ki | 35.6 | Affinity for sigma receptor type 1 of guinea pig using [3H]ifenprodil or (+)-[3H]pentazocine radioligand [AID239347, Type: Literature] | |   View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Active | | Ki | 35.6 [uM] | | BioAssay | Affinity for sigma receptor type 1 of guinea pig using [3H]ifenprodil or (+)-[3H]pentazocine radioligand | | AID | 239347 | | BioAssay type | Literature | | Target | | | PubMed | 16033255 | | Data Table |  |
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| 18 | [SID855741] | Active | | | GR-GFP Redistribution [AID450, Type: confirmatory] | glucocorticoid receptor isoform gamma [Homo sapiens] [gi:66528677] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 855741 | | CID | 5753 | | Outcome | Active | | BioAssay | GR-GFP Redistribution | | AID | 450 | | BioAssay type | confirmatory | | Target | glucocorticoid receptor isoform gamma [Homo sapiens] [gi:66528677] | | PubMed | | | Data Table |  |
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| 19 | [SID855741] | Active | | | GR-GFP Redistribution [AID450, Type: confirmatory] | glucocorticoid receptor isoform gamma [Homo sapiens] [gi:66528677] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 855741 | | CID | 5753 | | Outcome | Active | | BioAssay | GR-GFP Redistribution | | AID | 450 | | BioAssay type | confirmatory | | Target | glucocorticoid receptor isoform gamma [Homo sapiens] [gi:66528677] | | PubMed | | | Data Table |  |
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| 20 | [SID855741] | Active | | | GR-GFP Redistribution [AID450, Type: confirmatory] | glucocorticoid receptor isoform gamma [Homo sapiens] [gi:66528677] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 855741 | | CID | 5753 | | Outcome | Active | | BioAssay | GR-GFP Redistribution | | AID | 450 | | BioAssay type | confirmatory | | Target | glucocorticoid receptor isoform gamma [Homo sapiens] [gi:66528677] | | PubMed | | | Data Table |  |
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| 21 | [SID855741] | Active | | | GR-GFP Redistribution [AID450, Type: confirmatory] | glucocorticoid receptor isoform gamma [Homo sapiens] [gi:66528677] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 855741 | | CID | 5753 | | Outcome | Active | | BioAssay | GR-GFP Redistribution | | AID | 450 | | BioAssay type | confirmatory | | Target | glucocorticoid receptor isoform gamma [Homo sapiens] [gi:66528677] | | PubMed | | | Data Table |  |
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| 22 | [SID855741] | Active | IC50 | | uHTS fluorescence polarization assay for the identification of translation initiation inhibitors (eIF4H) [AID2012, Type: confirmatory] | Eukaryotic translation initiation factor 4H [Homo sapiens] [gi:45219878] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 855741 | | CID | 5753 | | Outcome | Active | | IC50 | [uM] | | BioAssay | uHTS fluorescence polarization assay for the identification of translation initiation inhibitors (eIF4H) | | AID | 2012 | | BioAssay type | confirmatory | | Target | Eukaryotic translation initiation factor 4H [Homo sapiens] [gi:45219878] | | PubMed | | | Data Table |  |
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| 23 | [SID56423132] | Active | | | HTS using DiI-HDL to assay lipid transfer in ldlA[SR-BI] cells Measured in Cell-Based System Using Plate Reader - 2085-01_Activator_SinglePoint_HTS_Activity [AID504775, Type: screening] | Scarb1 gene product [Mus musculus] [gi:14389423] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 56423132 | | CID | 5753 | | Outcome | Active | | BioAssay | HTS using DiI-HDL to assay lipid transfer in ldlA[SR-BI] cells Measured in Cell-Based System Using Plate Reader - 2085-01_Activator_SinglePoint_HTS_Activity | | AID | 504775 | | BioAssay type | screening | | Target | Scarb1 gene product [Mus musculus] [gi:14389423] | | PubMed | | | Data Table |  |
|
| 24 | [SID103333099] | Unspecified | IC50 | 0.29 | TP_TRANSPORTER: inhibition of MPP+ uptake (MPP+: 0.25 uM) in OCT3-expressing HEK293 cells [AID682144, Type: other] | Solute carrier family 22 member 3 [gi:24212063] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | IC50 | 0.29 [uM] | | BioAssay | TP_TRANSPORTER: inhibition of MPP+ uptake (MPP+: 0.25 uM) in OCT3-expressing HEK293 cells | | AID | 682144 | | BioAssay type | other | | Target | Solute carrier family 22 member 3 [gi:24212063] | | PubMed | | | Data Table |  |
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| 25 | [SID103333099] | Unspecified | Ki | 0.39 | TP_TRANSPORTER: inhibition of Dopamine uptake in OCT2-expressing HEK293 cells [AID679639, Type: other] | Solute carrier family 22 member 2 [gi:81872789] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | Ki | 0.39 [uM] | | BioAssay | TP_TRANSPORTER: inhibition of Dopamine uptake in OCT2-expressing HEK293 cells | | AID | 679639 | | BioAssay type | other | | Target | Solute carrier family 22 member 2 [gi:81872789] | | PubMed | | | Data Table |  |
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| 26 | [SID103333099] | Unspecified | Ki | 0.42 | TP_TRANSPORTER: inhibition of Adrenaline uptake in OCT2-expressing HEK293 cells [AID679641, Type: other] | Solute carrier family 22 member 2 [gi:81872789] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | Ki | 0.42 [uM] | | BioAssay | TP_TRANSPORTER: inhibition of Adrenaline uptake in OCT2-expressing HEK293 cells | | AID | 679641 | | BioAssay type | other | | Target | Solute carrier family 22 member 2 [gi:81872789] | | PubMed | | | Data Table |  |
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| 27 | [SID103333099] | Unspecified | Ki | 0.46 | TP_TRANSPORTER: inhibition of Noradrenaline uptake in OCT2-expressing HEK293 cells [AID679637, Type: other] | Solute carrier family 22 member 2 [gi:81872789] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | Ki | 0.46 [uM] | | BioAssay | TP_TRANSPORTER: inhibition of Noradrenaline uptake in OCT2-expressing HEK293 cells | | AID | 679637 | | BioAssay type | other | | Target | Solute carrier family 22 member 2 [gi:81872789] | | PubMed | | | Data Table |  |
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| 28 | [SID103333099] | Unspecified | Ki | 0.605 | TP_TRANSPORTER: inhibition of Serotonin uptake in OCT2-expressing HEK293 cells [AID679636, Type: other] | Solute carrier family 22 member 2 [gi:81872789] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | Ki | 0.605 [uM] | | BioAssay | TP_TRANSPORTER: inhibition of Serotonin uptake in OCT2-expressing HEK293 cells | | AID | 679636 | | BioAssay type | other | | Target | Solute carrier family 22 member 2 [gi:81872789] | | PubMed | | | Data Table |  |
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| 29 | [SID103333099] | Unspecified | IC50 | 4 | TP_TRANSPORTER: inhibition of TEA uptake (TEA: 10 uM) in Xenopus laevis oocytes [AID681158, Type: other] | Solute carrier family 22 member 2 [gi:81872789] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | IC50 | 4 [uM] | | BioAssay | TP_TRANSPORTER: inhibition of TEA uptake (TEA: 10 uM) in Xenopus laevis oocytes | | AID | 681158 | | BioAssay type | other | | Target | Solute carrier family 22 member 2 [gi:81872789] | | PubMed | | | Data Table |  |
|
| 30 | [SID103333099] | Unspecified | IC50 | 4.2 | TP_TRANSPORTER: inhibition of TEA uptake (TEA: 20 uM) in OCT2-expressing HRPE cells [AID681591, Type: other] | Solute carrier family 22 member 2 [gi:81872789] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | IC50 | 4.2 [uM] | | BioAssay | TP_TRANSPORTER: inhibition of TEA uptake (TEA: 20 uM) in OCT2-expressing HRPE cells | | AID | 681591 | | BioAssay type | other | | Target | Solute carrier family 22 member 2 [gi:81872789] | | PubMed | | | Data Table |  |
|
| 31 | [SID103333099] | Unspecified | IC50 | 4.9 | TP_TRANSPORTER: inhibition of TEA uptake (TEA: 20 uM) in OCT3-expressing HRPE cells [AID678784, Type: other] | Solute carrier family 22 member 3 [gi:24212062] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | IC50 | 4.9 [uM] | | BioAssay | TP_TRANSPORTER: inhibition of TEA uptake (TEA: 20 uM) in OCT3-expressing HRPE cells | | AID | 678784 | | BioAssay type | other | | Target | Solute carrier family 22 member 3 [gi:24212062] | | PubMed | | | Data Table |  |
|
| 32 | [SID103333099] | Unspecified | Ki | 5.3 | TP_TRANSPORTER: inhibition of E217betaG uptake in Oatp1-expressing HeLa cells [AID681147, Type: other] | Solute carrier organic anion transporter family member 1A1 [gi:1171883] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | Ki | 5.3 [uM] | | BioAssay | TP_TRANSPORTER: inhibition of E217betaG uptake in Oatp1-expressing HeLa cells | | AID | 681147 | | BioAssay type | other | | Target | Solute carrier organic anion transporter family member 1A1 [gi:1171883] | | PubMed | | | Data Table |  |
|
| 33 | [SID103333099] | Unspecified | Ki | 7.02 | TP_TRANSPORTER: inhibition of TEA uptake in OCT1-expressing HeLa cells [AID681146, Type: other] | Solute carrier family 22 member 1 [gi:313104181] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | Ki | 7.02 [uM] | | BioAssay | TP_TRANSPORTER: inhibition of TEA uptake in OCT1-expressing HeLa cells | | AID | 681146 | | BioAssay type | other | | Target | Solute carrier family 22 member 1 [gi:313104181] | | PubMed | | | Data Table |  |
|
| 34 | [SID103333099] | Unspecified | Ki | 10 | TP_TRANSPORTER: inhibition of TEA uptake in Xenopus laevis oocytes [AID681157, Type: other] | Solute carrier family 22 member 1 [gi:81872095] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | Ki | 10 [uM] | | BioAssay | TP_TRANSPORTER: inhibition of TEA uptake in Xenopus laevis oocytes | | AID | 681157 | | BioAssay type | other | | Target | Solute carrier family 22 member 1 [gi:81872095] | | PubMed | | | Data Table |  |
|
| 35 | [SID103333099] | Unspecified | IC50 | 10.7 | TP_TRANSPORTER: inhibition pramipexole uptake in rOCT2-injected oocytes [AID679293, Type: other] | Solute carrier family 22 member 2 [gi:81872789] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | IC50 | 10.7 [uM] | | BioAssay | TP_TRANSPORTER: inhibition pramipexole uptake in rOCT2-injected oocytes | | AID | 679293 | | BioAssay type | other | | Target | Solute carrier family 22 member 2 [gi:81872789] | | PubMed | | | Data Table |  |
|
| 36 | [SID103333099] | Unspecified | IC50 | 21.7 | TP_TRANSPORTER: inhibition of MPP+ uptake (MPP+: 0.25 uM) in OCT1-expressing HEK293 cells [AID681560, Type: other] | Solute carrier family 22 member 1 [gi:313104181] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | IC50 | 21.7 [uM] | | BioAssay | TP_TRANSPORTER: inhibition of MPP+ uptake (MPP+: 0.25 uM) in OCT1-expressing HEK293 cells | | AID | 681560 | | BioAssay type | other | | Target | Solute carrier family 22 member 1 [gi:313104181] | | PubMed | | | Data Table |  |
|
| 37 | [SID103333099] | Unspecified | IC50 | 34.2 | TP_TRANSPORTER: inhibition of MPP+ uptake (MPP+: 0.25 uM) in OCT2-expressing HEK293 cells [AID681561, Type: other] | Solute carrier family 22 member 2 [gi:313104182] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | IC50 | 34.2 [uM] | | BioAssay | TP_TRANSPORTER: inhibition of MPP+ uptake (MPP+: 0.25 uM) in OCT2-expressing HEK293 cells | | AID | 681561 | | BioAssay type | other | | Target | Solute carrier family 22 member 2 [gi:313104182] | | PubMed | | | Data Table |  |
|
| 38 | [SID103333099] | Unspecified | Ki | 72 | TP_TRANSPORTER: inhibition of MPP+ uptake in OCT1-expressing HEK293 cells [AID681376, Type: other] | Solute carrier family 22 member 1 [gi:81872095] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | Ki | 72 [uM] | | BioAssay | TP_TRANSPORTER: inhibition of MPP+ uptake in OCT1-expressing HEK293 cells | | AID | 681376 | | BioAssay type | other | | Target | Solute carrier family 22 member 1 [gi:81872095] | | PubMed | | | Data Table |  |
|
| 39 | [SID103333099] | Unspecified | Ki | 100 | Affinity for human EMP expressed in ERG2 deficient strain of Sacchromyces cerevisiae using [3H]ifenprodil or (+)-[3H]pentazocine as radioligand [AID239597, Type: Literature] | 3-beta-hydroxysteroid-Delta(8),Delta(7)-isomerase [gi:17374795] |   View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | Ki | 100 [uM] | | BioAssay | Affinity for human EMP expressed in ERG2 deficient strain of Sacchromyces cerevisiae using [3H]ifenprodil or (+)-[3H]pentazocine as radioligand | | AID | 239597 | | BioAssay type | Literature | | Target | 3-beta-hydroxysteroid-Delta(8),Delta(7)-isomerase [gi:17374795] | | PubMed | 16033255 | | Data Table |  |
|
| 40 | [SID103333099] | Unspecified | Ki | 100 | Affinity for ERG2 of Sacchromyces cerevisiae using [3H]ifenprodil or (+)-[3H]pentazocine radioligand [AID239296, Type: Literature] | |   View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | Ki | 100 [uM] | | BioAssay | Affinity for ERG2 of Sacchromyces cerevisiae using [3H]ifenprodil or (+)-[3H]pentazocine radioligand | | AID | 239296 | | BioAssay type | Literature | | Target | | | PubMed | 16033255 | | Data Table |  |
|
| 41 | [SID103333099] | Unspecified | IC50 | 151 | TP_TRANSPORTER: inhibition of TEA uptake (TEA: 10 uM) in Xenopus laevis oocytes [AID681159, Type: other] | Solute carrier family 22 member 1 [gi:81872095] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | IC50 | 151 [uM] | | BioAssay | TP_TRANSPORTER: inhibition of TEA uptake (TEA: 10 uM) in Xenopus laevis oocytes | | AID | 681159 | | BioAssay type | other | | Target | Solute carrier family 22 member 1 [gi:81872095] | | PubMed | | | Data Table |  |
|
| 42 | [SID103333099] | Unspecified | IC50 | 163.7 | TP_TRANSPORTER: inhibition pramipexole uptake in rOCT1-injected oocytes [AID679317, Type: other] | Solute carrier family 22 member 1 [gi:81872095] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | IC50 | 163.7 [uM] | | BioAssay | TP_TRANSPORTER: inhibition pramipexole uptake in rOCT1-injected oocytes | | AID | 679317 | | BioAssay type | other | | Target | Solute carrier family 22 member 1 [gi:81872095] | | PubMed | | | Data Table |  |
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| 43 | [SID103333099] | Unspecified | | | TP_TRANSPORTER: inhibition of TEA uptake (TEA: 20 uM, Corticosterone: 100 uM) in OCT1-expressing HRPE cells [AID679211, Type: other] | Solute carrier family 22 member 1 [gi:81872095] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | BioAssay | TP_TRANSPORTER: inhibition of TEA uptake (TEA: 20 uM, Corticosterone: 100 uM) in OCT1-expressing HRPE cells | | AID | 679211 | | BioAssay type | other | | Target | Solute carrier family 22 member 1 [gi:81872095] | | PubMed | | | Data Table |  |
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| 44 | [SID103333099] | Unspecified | | | Relative binding affinity against glucocorticoid receptor in rat liver cystosol extract [AID74246, Type: Literature] | Glucocorticoid receptor [gi:1169883] |   View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | BioAssay | Relative binding affinity against glucocorticoid receptor in rat liver cystosol extract | | AID | 74246 | | BioAssay type | Literature | | Target | Glucocorticoid receptor [gi:1169883] | | PubMed | 8164266 | | Data Table |  |
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| 45 | [SID103333099] | Unspecified | | | TP_TRANSPORTER: inhibition of Carnitine uptake (Carnitine: 0.010? uM, Corticosterone: 500 uM) in OCTN2-expressing HEK293 cells [AID681677, Type: other] | Solute carrier family 22 member 5 [gi:8928257] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | BioAssay | TP_TRANSPORTER: inhibition of Carnitine uptake (Carnitine: 0.010? uM, Corticosterone: 500 uM) in OCTN2-expressing HEK293 cells | | AID | 681677 | | BioAssay type | other | | Target | Solute carrier family 22 member 5 [gi:8928257] | | PubMed | | | Data Table |  |
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| 46 | [SID103333099] | Unspecified | | | TP_TRANSPORTER: increase in brain concentration in mdr1a/1b(-/-) mouse [AID682053, Type: other] | Multidrug resistance protein 1B [gi:126927] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | BioAssay | TP_TRANSPORTER: increase in brain concentration in mdr1a/1b(-/-) mouse | | AID | 682053 | | BioAssay type | other | | Target | Multidrug resistance protein 1B [gi:126927] | | PubMed | | | Data Table |  |
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| 47 | [SID103333099] | Unspecified | | | TP_TRANSPORTER: inhibition of E1S uptake (E1S: 0.05 uM, Corticosterone: 5 uM) in Xenopus laevis oocytes [AID681227, Type: other] | Solute carrier family 22 member 8 [gi:74730587] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | BioAssay | TP_TRANSPORTER: inhibition of E1S uptake (E1S: 0.05 uM, Corticosterone: 5 uM) in Xenopus laevis oocytes | | AID | 681227 | | BioAssay type | other | | Target | Solute carrier family 22 member 8 [gi:74730587] | | PubMed | | | Data Table |  |
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| 48 | [SID103333099] | Unspecified | | | Inhibition of 4-(4-(dimethylamino)styryl)-N-methylpyridinium uptake at human OCT1 expressed in HEK293 cells at 100 uM by confocal microscopy [AID386623, Type: Literature] | Solute carrier family 22 member 1 [gi:313104181] |   View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | BioAssay | Inhibition of 4-(4-(dimethylamino)styryl)-N-methylpyridinium uptake at human OCT1 expressed in HEK293 cells at 100 uM by confocal microscopy | | AID | 386623 | | BioAssay type | Literature | | Target | Solute carrier family 22 member 1 [gi:313104181] | | PubMed | 18788725 | | Data Table |  |
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| 49 | [SID103333099] | Unspecified | | | Displacement of [3H]5alpha dihydrotestosterone from human sex hormone binding globulin [AID318680, Type: Literature] | Sex hormone-binding globulin [gi:134907] |   View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 103333099 | | CID | 5753 | | Outcome | Unspecified | | BioAssay | Displacement of [3H]5alpha dihydrotestosterone from human sex hormone binding globulin | | AID | 318680 | | BioAssay type | Literature | | Target | Sex hormone-binding globulin [gi:134907] | | PubMed | 18330978 | | Data Table |  |
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| 50 | [SID56423132] | Unspecified | Potency | | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate [AID624178, Type: confirmatory] | acid sphingomyelinase [Homo sapiens] [gi:179095] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 56423132 | | CID | 5753 | | Outcome | Unspecified | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate | | AID | 624178 | | BioAssay type | confirmatory | | Target | acid sphingomyelinase [Homo sapiens] [gi:179095] | | PubMed | | | Data Table |  |
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