| 1 | [SID103460096] | Active | IC50 | 0.02 | Inhibition of CXCL8-induced chemotaxis in human polymorphonuclear leukocyte pretreated for 15 mins measured after 4 hrs by cell migration assay [AID426392, Type: Literature] | Interleukin-8 [gi:124359] |   View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 103460096 | | CID | 180540 | | Outcome | Active | | IC50 | 0.02 [uM] | | BioAssay | Inhibition of CXCL8-induced chemotaxis in human polymorphonuclear leukocyte pretreated for 15 mins measured after 4 hrs by cell migration assay | | AID | 426392 | | BioAssay type | Literature | | Target | Interleukin-8 [gi:124359] | | PubMed | 19560921 | | Data Table |  |
|
| 2 | [SID103460096] | Active | IC50 | 0.02 | Inhibition of CXCL8-induced chemotaxis in human polymorphonuclear leukocyte pretreated for 15 mins measured after 4 hrs by cell migration assay [AID426392, Type: Literature] | Interleukin-8 [gi:124359] |   View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 103460096 | | CID | 180540 | | Outcome | Active | | IC50 | 0.02 [uM] | | BioAssay | Inhibition of CXCL8-induced chemotaxis in human polymorphonuclear leukocyte pretreated for 15 mins measured after 4 hrs by cell migration assay | | AID | 426392 | | BioAssay type | Literature | | Target | Interleukin-8 [gi:124359] | | PubMed | 19560921 | | Data Table |  |
|
| 3 | [SID103460096] | Active | IC50 | 0.02 | Inhibition of CXCL8-induced chemotaxis in human polymorphonuclear leukocyte pretreated for 15 mins measured after 4 hrs by cell migration assay [AID426392, Type: Literature] | Interleukin-8 [gi:124359] |   View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 103460096 | | CID | 180540 | | Outcome | Active | | IC50 | 0.02 [uM] | | BioAssay | Inhibition of CXCL8-induced chemotaxis in human polymorphonuclear leukocyte pretreated for 15 mins measured after 4 hrs by cell migration assay | | AID | 426392 | | BioAssay type | Literature | | Target | Interleukin-8 [gi:124359] | | PubMed | 19560921 | | Data Table |  |
|
| 4 | [SID103460096] | Active | IC50 | 0.034 | Inhibition of CXCL8-induced chemotaxis in human polymorphonuclear cells [AID248424, Type: Literature] | C-X-C chemokine receptor type 2 [gi:1352454] |   View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 103460096 | | CID | 180540 | | Outcome | Active | | IC50 | 0.034 [uM] | | BioAssay | Inhibition of CXCL8-induced chemotaxis in human polymorphonuclear cells | | AID | 248424 | | BioAssay type | Literature | | Target | C-X-C chemokine receptor type 2 [gi:1352454] | | PubMed | 15974585 | | Data Table |  |
|
| 5 | [SID11111348] | Active | | | qHTS Assay for Spectroscopic Profiling in 4-MU Spectral Region [AID589, Type: other] | |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 11111348 | | CID | 180540 | | Outcome | Active | | BioAssay | qHTS Assay for Spectroscopic Profiling in 4-MU Spectral Region | | AID | 589 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 6 | [SID11111348] | Active | | | qHTS Assay for Spectroscopic Profiling in A350 Spectral Region [AID590, Type: other] | |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 11111348 | | CID | 180540 | | Outcome | Active | | BioAssay | qHTS Assay for Spectroscopic Profiling in A350 Spectral Region | | AID | 590 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
|
| 7 | [SID103460096] | Unspecified | | | Noncompetitive inhibition of human CXCR1 assessed as inhibition of CXCL8-induced neutrophile chemotaxis at 10 nM [AID606366, Type: Literature] | C-X-C chemokine receptor type 1 [gi:108936015] |   View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 103460096 | | CID | 180540 | | Outcome | Unspecified | | BioAssay | Noncompetitive inhibition of human CXCR1 assessed as inhibition of CXCL8-induced neutrophile chemotaxis at 10 nM | | AID | 606366 | | BioAssay type | Literature | | Target | C-X-C chemokine receptor type 1 [gi:108936015] | | PubMed | 21615150 | | Data Table |  |
|
| 8 | [SID103460096] | Unspecified | | | Inhibition of CXCL8-induced chemotaxis of human polymorphonuclear cells at 10e-8 M [AID251807, Type: Literature] | C-X-C chemokine receptor type 2 [gi:1352454] |   View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 103460096 | | CID | 180540 | | Outcome | Unspecified | | BioAssay | Inhibition of CXCL8-induced chemotaxis of human polymorphonuclear cells at 10e-8 M | | AID | 251807 | | BioAssay type | Literature | | Target | C-X-C chemokine receptor type 2 [gi:1352454] | | PubMed | 15974585 | | Data Table |  |
|
| 9 | [SID11111348] | Unspecified | | | Cytochrome panel assay with activity outcomes [AID1851, Type: other] | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 11111348 | | CID | 180540 | | Outcome | Unspecified | | BioAssay | Cytochrome panel assay with activity outcomes | | AID | 1851 | | BioAssay type | other | | Target | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] | | PubMed | | | Data Table |  |
|
| 10 | [SID11111348] | Unspecified | | | Cytochrome panel assay with activity outcomes [AID1851, Type: other] | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 11111348 | | CID | 180540 | | Outcome | Unspecified | | BioAssay | Cytochrome panel assay with activity outcomes | | AID | 1851 | | BioAssay type | other | | Target | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] | | PubMed | | | Data Table |  |
|
| 11 | [SID103460096] | Unspecified | | | Inhibition of CXCL8-induced cell migration in human PMN cells at 0.01 uM by chemotaxis assay [AID297157, Type: Literature] | |   View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 103460096 | | CID | 180540 | | Outcome | Unspecified | | BioAssay | Inhibition of CXCL8-induced cell migration in human PMN cells at 0.01 uM by chemotaxis assay | | AID | 297157 | | BioAssay type | Literature | | Target | | | PubMed | 17665889 | | Data Table |  |
|
| 12 | [SID103460096] | Unspecified | | | Inhibition of CXCL1-induced cell migration in human PMN cells at 0.01 uM by chemotaxis assay [AID297158, Type: Literature] | |   View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 103460096 | | CID | 180540 | | Outcome | Unspecified | | BioAssay | Inhibition of CXCL1-induced cell migration in human PMN cells at 0.01 uM by chemotaxis assay | | AID | 297158 | | BioAssay type | Literature | | Target | | | PubMed | 17665889 | | Data Table |  |
|
| 13 | [SID103460096] | Unspecified | | | Oral bioavailability in human [AID311524, Type: Literature] | |   View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 103460096 | | CID | 180540 | | Outcome | Unspecified | | BioAssay | Oral bioavailability in human | | AID | 311524 | | BioAssay type | Literature | | Target | | | PubMed | 17870541 | | Data Table |  |
|
| 14 | [SID103460096] | Unspecified | | | Cytotoxicity against of human polymorphonuclear leukocytes assessed as cell viability by trypan blue dye exclusion assay [AID426393, Type: Literature] | |   View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 103460096 | | CID | 180540 | | Outcome | Unspecified | | BioAssay | Cytotoxicity against of human polymorphonuclear leukocytes assessed as cell viability by trypan blue dye exclusion assay | | AID | 426393 | | BioAssay type | Literature | | Target | | | PubMed | 19560921 | | Data Table |  |
|
| 15 | [SID103460096] | Unspecified | | | Cytotoxicity against mouse L1.2 cells assessed as cell viability by trypan blue dye exclusion assay [AID426478, Type: Literature] | |   View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 103460096 | | CID | 180540 | | Outcome | Unspecified | | BioAssay | Cytotoxicity against mouse L1.2 cells assessed as cell viability by trypan blue dye exclusion assay | | AID | 426478 | | BioAssay type | Literature | | Target | | | PubMed | 19560921 | | Data Table |  |
|
| 16 | [SID11112667] | Unspecified | | | Cytochrome panel assay with activity outcomes [AID1851, Type: other] | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 11112667 | | CID | 180540 | | Outcome | Unspecified | | BioAssay | Cytochrome panel assay with activity outcomes | | AID | 1851 | | BioAssay type | other | | Target | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] | | PubMed | | | Data Table |  |
|
| 17 | [SID11112667] | Unspecified | | | Cytochrome panel assay with activity outcomes [AID1851, Type: other] | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 11112667 | | CID | 180540 | | Outcome | Unspecified | | BioAssay | Cytochrome panel assay with activity outcomes | | AID | 1851 | | BioAssay type | other | | Target | cytochrome P450, family 2, subfamily C, polypeptide 19 [Homo sapiens] [gi:4503219] | | PubMed | | | Data Table |  |
|
| 18 | [SID11112667] | Unspecified | | | qHTS profiling for inhibitors of Plasmodium falciparum proliferation [AID504749, Type: Literature] | |   View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 11112667 | | CID | 180540 | | Outcome | Unspecified | | BioAssay | qHTS profiling for inhibitors of Plasmodium falciparum proliferation | | AID | 504749 | | BioAssay type | Literature | | Target | | | PubMed | 21817045 | | Data Table |  |
|
| 19 | [SID103460096] | Unspecified | | | Inhibition of lipopolysaccharide-induced PGE-2 production at 10e-5 M [AID251770, Type: Literature] | Prostaglandin G/H synthase 1 [gi:129900] |   View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 103460096 | | CID | 180540 | | Outcome | Unspecified | | BioAssay | Inhibition of lipopolysaccharide-induced PGE-2 production at 10e-5 M | | AID | 251770 | | BioAssay type | Literature | | Target | Prostaglandin G/H synthase 1 [gi:129900] | | PubMed | 15974585 | | Data Table |  |
|
| 20 | [SID11112667] | Inactive | Potency | 39.8107 | qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) [AID1490, Type: confirmatory] | phosphopantetheinyl transferase [Bacillus subtilis] [gi:10954339] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 11112667 | | CID | 180540 | | Outcome | Inactive | | Potency | 39.8107 [uM] | | BioAssay | qHTS Assay for Inhibitors of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) | | AID | 1490 | | BioAssay type | confirmatory | | Target | phosphopantetheinyl transferase [Bacillus subtilis] [gi:10954339] | | PubMed | | | Data Table |  |
|
| 21 | [SID11112667] | Inactive | Potency | | 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. | 21 | | Structure |
| | Substance | | | SID | 11112667 | | CID | 180540 | | Outcome | Inactive | | Potency | [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 |  |
|
| 22 | [SID11112667] | Inactive | Potency | | 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. | 22 | | Structure |
| | Substance | | | SID | 11112667 | | CID | 180540 | | Outcome | Inactive | | Potency | [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 |  |
|
| 23 | [SID11111348] | Inactive | Potency | | 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. | 23 | | Structure |
| | Substance | | | SID | 11111348 | | CID | 180540 | | Outcome | Inactive | | Potency | [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 |  |
|
| 24 | [SID11112667] | Inactive | Potency | | qHTS of Trypanosoma Brucei Inhibitors [AID624173, Type: confirmatory] | hypothetical protein, conserved [Trypanosoma brucei] [gi:62359610] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 11112667 | | CID | 180540 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS of Trypanosoma Brucei Inhibitors | | AID | 624173 | | BioAssay type | confirmatory | | Target | hypothetical protein, conserved [Trypanosoma brucei] [gi:62359610] | | PubMed | | | Data Table |  |
|
| 25 | [SID11111348] | Inactive | | | qHTS Assay for Inhibitors of YjeE [AID605, Type: confirmatory] | UPF0079 ATP-binding protein yjeE [gi:84028058] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 11111348 | | CID | 180540 | | Outcome | Inactive | | BioAssay | qHTS Assay for Inhibitors of YjeE | | AID | 605 | | BioAssay type | confirmatory | | Target | UPF0079 ATP-binding protein yjeE [gi:84028058] | | PubMed | | | Data Table |  |
|
| 26 | [SID11112667] | Inactive | | | qHTS Assay for Inhibitors of YjeE [AID605, Type: confirmatory] | UPF0079 ATP-binding protein yjeE [gi:84028058] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 11112667 | | CID | 180540 | | Outcome | Inactive | | BioAssay | qHTS Assay for Inhibitors of YjeE | | AID | 605 | | BioAssay type | confirmatory | | Target | UPF0079 ATP-binding protein yjeE [gi:84028058] | | PubMed | | | Data Table |  |
|
| 27 | [SID11112667] | Inactive | | | Promiscuous and Specific Inhibitors of AmpC Beta-Lactamase (assay with detergent) [AID584, Type: confirmatory] | Chain A, Ampc Beta-Lactamase In Complex With 4-Methanesulfonylamino Benzoic Acid [gi:119389684] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 11112667 | | CID | 180540 | | Outcome | Inactive | | BioAssay | Promiscuous and Specific Inhibitors of AmpC Beta-Lactamase (assay with detergent) | | AID | 584 | | BioAssay type | confirmatory | | Target | Chain A, Ampc Beta-Lactamase In Complex With 4-Methanesulfonylamino Benzoic Acid [gi:119389684] | | PubMed | | | Data Table |  |
|
| 28 | [SID11112667] | Inactive | | | Promiscuous and Specific Inhibitors of AmpC Beta-Lactamase (assay without detergent) [AID585, Type: confirmatory] | Chain A, Ampc Beta-Lactamase In Complex With 4-Methanesulfonylamino Benzoic Acid [gi:119389684] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 11112667 | | CID | 180540 | | Outcome | Inactive | | BioAssay | Promiscuous and Specific Inhibitors of AmpC Beta-Lactamase (assay without detergent) | | AID | 585 | | BioAssay type | confirmatory | | Target | Chain A, Ampc Beta-Lactamase In Complex With 4-Methanesulfonylamino Benzoic Acid [gi:119389684] | | PubMed | | | Data Table |  |
|
| 29 | [SID11111348] | Inactive | | | Promiscuous and Specific Inhibitors of AmpC Beta-Lactamase (assay with detergent) [AID584, Type: confirmatory] | Chain A, Ampc Beta-Lactamase In Complex With 4-Methanesulfonylamino Benzoic Acid [gi:119389684] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 11111348 | | CID | 180540 | | Outcome | Inactive | | BioAssay | Promiscuous and Specific Inhibitors of AmpC Beta-Lactamase (assay with detergent) | | AID | 584 | | BioAssay type | confirmatory | | Target | Chain A, Ampc Beta-Lactamase In Complex With 4-Methanesulfonylamino Benzoic Acid [gi:119389684] | | PubMed | | | Data Table |  |
|
| 30 | [SID11111348] | Inactive | | | Promiscuous and Specific Inhibitors of AmpC Beta-Lactamase (assay without detergent) [AID585, Type: confirmatory] | Chain A, Ampc Beta-Lactamase In Complex With 4-Methanesulfonylamino Benzoic Acid [gi:119389684] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 11111348 | | CID | 180540 | | Outcome | Inactive | | BioAssay | Promiscuous and Specific Inhibitors of AmpC Beta-Lactamase (assay without detergent) | | AID | 585 | | BioAssay type | confirmatory | | Target | Chain A, Ampc Beta-Lactamase In Complex With 4-Methanesulfonylamino Benzoic Acid [gi:119389684] | | PubMed | | | Data Table |  |
|
| 31 | [SID11112667] | Inactive | Potency | | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia [AID2451, Type: confirmatory] | Chain A, Structure Of Giardia Fructose-1,6-Biphosphate Aldolase In Complex With Phosphoglycolohydrox [gi:122920737] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 11112667 | | CID | 180540 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Fructose-1,6-bisphosphate Aldolase from Giardia Lamblia | | AID | 2451 | | BioAssay type | confirmatory | | Target | Chain A, Structure Of Giardia Fructose-1,6-Biphosphate Aldolase In Complex With Phosphoglycolohydrox [gi:122920737] | | PubMed | | | Data Table |  |
|
| 32 | [SID11111348] | Inactive | Potency | | qHTS Assay for Inhibitors of HSD17B4, hydroxysteroid (17-beta) dehydrogenase 4 [AID893, Type: confirmatory] | Chain A, The Structure Of Wild-Type Human Hadh2 (17beta- Hydroxysteroid Dehydrogenase Type 10) Bound [gi:122921310] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 11111348 | | CID | 180540 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of HSD17B4, hydroxysteroid (17-beta) dehydrogenase 4 | | AID | 893 | | BioAssay type | confirmatory | | Target | Chain A, The Structure Of Wild-Type Human Hadh2 (17beta- Hydroxysteroid Dehydrogenase Type 10) Bound [gi:122921310] | | PubMed | | | Data Table |  |
|
| 33 | [SID11111348] | Inactive | Potency | | qHTS Assay for Inhibitors of HADH2 (Hydroxyacyl-Coenzyme A Dehydrogenase, Type II) [AID886, Type: confirmatory] | Chain A, The Structure Of Wild-Type Human Hadh2 (17beta- Hydroxysteroid Dehydrogenase Type 10) Bound [gi:122921310] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 11111348 | | CID | 180540 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of HADH2 (Hydroxyacyl-Coenzyme A Dehydrogenase, Type II) | | AID | 886 | | BioAssay type | confirmatory | | Target | Chain A, The Structure Of Wild-Type Human Hadh2 (17beta- Hydroxysteroid Dehydrogenase Type 10) Bound [gi:122921310] | | PubMed | | | Data Table |  |
|
| 34 | [SID11112667] | Inactive | Potency | | qHTS Assay for Inhibitors of HSD17B4, hydroxysteroid (17-beta) dehydrogenase 4 [AID893, Type: confirmatory] | Chain A, The Structure Of Wild-Type Human Hadh2 (17beta- Hydroxysteroid Dehydrogenase Type 10) Bound [gi:122921310] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 11112667 | | CID | 180540 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of HSD17B4, hydroxysteroid (17-beta) dehydrogenase 4 | | AID | 893 | | BioAssay type | confirmatory | | Target | Chain A, The Structure Of Wild-Type Human Hadh2 (17beta- Hydroxysteroid Dehydrogenase Type 10) Bound [gi:122921310] | | PubMed | | | Data Table |  |
|
| 35 | [SID11112667] | Inactive | Potency | | qHTS Assay for Inhibitors of HADH2 (Hydroxyacyl-Coenzyme A Dehydrogenase, Type II) [AID886, Type: confirmatory] | Chain A, The Structure Of Wild-Type Human Hadh2 (17beta- Hydroxysteroid Dehydrogenase Type 10) Bound [gi:122921310] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 11112667 | | CID | 180540 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of HADH2 (Hydroxyacyl-Coenzyme A Dehydrogenase, Type II) | | AID | 886 | | BioAssay type | confirmatory | | Target | Chain A, The Structure Of Wild-Type Human Hadh2 (17beta- Hydroxysteroid Dehydrogenase Type 10) Bound [gi:122921310] | | PubMed | | | Data Table |  |
|
| 36 | [SID11111348] | Inactive | Potency | | qHTS Assay for Inhibitors of BRCT-Phosphoprotein Interaction (Red Fluorophore) [AID892, Type: confirmatory] | Chain A, Solution Structure Of The Brct-C Domain From Human Brca1 [gi:159162802] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 11111348 | | CID | 180540 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of BRCT-Phosphoprotein Interaction (Red Fluorophore) | | AID | 892 | | BioAssay type | confirmatory | | Target | Chain A, Solution Structure Of The Brct-C Domain From Human Brca1 [gi:159162802] | | PubMed | | | Data Table |  |
|
| 37 | [SID11111348] | Inactive | Potency | | qHTS Assay for Inhibitors of BRCT-Phosphoprotein Interaction (Green Fluorophore) [AID875, Type: confirmatory] | Chain A, Solution Structure Of The Brct-C Domain From Human Brca1 [gi:159162802] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 11111348 | | CID | 180540 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of BRCT-Phosphoprotein Interaction (Green Fluorophore) | | AID | 875 | | BioAssay type | confirmatory | | Target | Chain A, Solution Structure Of The Brct-C Domain From Human Brca1 [gi:159162802] | | PubMed | | | Data Table |  |
|
| 38 | [SID11112667] | Inactive | Potency | | qHTS Assay for Inhibitors of BRCT-Phosphoprotein Interaction (Red Fluorophore) [AID892, Type: confirmatory] | Chain A, Solution Structure Of The Brct-C Domain From Human Brca1 [gi:159162802] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 11112667 | | CID | 180540 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of BRCT-Phosphoprotein Interaction (Red Fluorophore) | | AID | 892 | | BioAssay type | confirmatory | | Target | Chain A, Solution Structure Of The Brct-C Domain From Human Brca1 [gi:159162802] | | PubMed | | | Data Table |  |
|
| 39 | [SID11112667] | Inactive | Potency | | qHTS Assay for Inhibitors of BRCT-Phosphoprotein Interaction (Green Fluorophore) [AID875, Type: confirmatory] | Chain A, Solution Structure Of The Brct-C Domain From Human Brca1 [gi:159162802] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 11112667 | | CID | 180540 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of BRCT-Phosphoprotein Interaction (Green Fluorophore) | | AID | 875 | | BioAssay type | confirmatory | | Target | Chain A, Solution Structure Of The Brct-C Domain From Human Brca1 [gi:159162802] | | PubMed | | | Data Table |  |
|
| 40 | [SID11112667] | Inactive | Potency | | qHTS for Inducers of the Endoplasmic Reticulum Stress Response (ERSR) in Human Glioma: qHTS [AID602332, Type: confirmatory] | heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa) [Homo sapiens] [gi:168984549] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 11112667 | | CID | 180540 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inducers of the Endoplasmic Reticulum Stress Response (ERSR) in Human Glioma: qHTS | | AID | 602332 | | BioAssay type | confirmatory | | Target | heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa) [Homo sapiens] [gi:168984549] | | PubMed | | | Data Table |  |
|
| 41 | [SID11112667] | Inactive | Potency | | 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. | 41 | | Structure |
| | Substance | | | SID | 11112667 | | CID | 180540 | | Outcome | Inactive | | Potency | [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 |  |
|
| 42 | [SID11112667] | 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. | 42 | | Structure |
| | Substance | | | SID | 11112667 | | CID | 180540 | | 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 |  |
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| 43 | [SID11112667] | Inactive | Potency | | qHTS Assay for Identification of Novel General Anesthetics [AID485281, Type: confirmatory] | Chain A, Horse Spleen Apoferritin [gi:254220970] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 11112667 | | CID | 180540 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Identification of Novel General Anesthetics | | AID | 485281 | | BioAssay type | confirmatory | | Target | Chain A, Horse Spleen Apoferritin [gi:254220970] | | PubMed | | | Data Table |  |
|
| 44 | [SID11112667] | Inactive | Potency | | qHTS Assay for Promiscuous and Specific Inhibitors of Cruzain (with detergent) [AID1478, Type: confirmatory] | Chain A, Crystal Structure Of Cruzain Covalently Bound To A Purine Nitrile [gi:281307097] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 11112667 | | CID | 180540 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Promiscuous and Specific Inhibitors of Cruzain (with detergent) | | AID | 1478 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of Cruzain Covalently Bound To A Purine Nitrile [gi:281307097] | | PubMed | | | Data Table |  |
|
| 45 | [SID11112667] | Inactive | Potency | | qHTS Assay for Promiscuous and Specific Inhibitors of Cruzain (without detergent) [AID1476, Type: confirmatory] | Chain A, Crystal Structure Of Cruzain Covalently Bound To A Purine Nitrile [gi:281307097] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 11112667 | | CID | 180540 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Promiscuous and Specific Inhibitors of Cruzain (without detergent) | | AID | 1476 | | BioAssay type | confirmatory | | Target | Chain A, Crystal Structure Of Cruzain Covalently Bound To A Purine Nitrile [gi:281307097] | | PubMed | | | Data Table |  |
|
| 46 | [SID11112667] | Inactive | Potency | | qHTS Assay for Inhibitors of RecQ-Like Dna Helicase 1 (RECQ1) [AID2549, Type: confirmatory] | Chain A, Structure Of Human Recq-Like Helicase In Complex With A Dna Substrate [gi:282403581] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 11112667 | | CID | 180540 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of RecQ-Like Dna Helicase 1 (RECQ1) | | AID | 2549 | | BioAssay type | confirmatory | | Target | Chain A, Structure Of Human Recq-Like Helicase In Complex With A Dna Substrate [gi:282403581] | | PubMed | | | Data Table |  |
|
| 47 | [SID11111348] | Inactive | Potency | | qHTS Validation Assay for Activators of Leishmania Mexicana Pyruvate Kinase [AID959, Type: confirmatory] | pyruvate kinase [Leishmania mexicana mexicana] [gi:290753097] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 11111348 | | CID | 180540 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Validation Assay for Activators of Leishmania Mexicana Pyruvate Kinase | | AID | 959 | | BioAssay type | confirmatory | | Target | pyruvate kinase [Leishmania mexicana mexicana] [gi:290753097] | | PubMed | | | Data Table |  |
|
| 48 | [SID11111348] | Inactive | Potency | | qHTS Validation Assay for Inhibitors of Leishmania Mexicana Pyruvate Kinase [AID945, Type: confirmatory] | pyruvate kinase [Leishmania mexicana mexicana] [gi:290753097] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 11111348 | | CID | 180540 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Validation Assay for Inhibitors of Leishmania Mexicana Pyruvate Kinase | | AID | 945 | | BioAssay type | confirmatory | | Target | pyruvate kinase [Leishmania mexicana mexicana] [gi:290753097] | | PubMed | | | Data Table |  |
|
| 49 | [SID11112667] | Inactive | Potency | | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) [AID1030, Type: confirmatory] | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 11112667 | | CID | 180540 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) | | AID | 1030 | | BioAssay type | confirmatory | | Target | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] | | PubMed | | | Data Table |  |
|
| 50 | [SID11112667] | Inactive | Potency | | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) [AID1030, Type: confirmatory] | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 11112667 | | CID | 180540 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Inhibitors of Aldehyde Dehydrogenase 1 (ALDH1A1) | | AID | 1030 | | BioAssay type | confirmatory | | Target | aldehyde dehydrogenase 1 family, member A1 [Homo sapiens] [gi:30582681] | | PubMed | | | Data Table |  |
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