| 1 | [SID103226312] | Active | Ki | 0.008 | Inhibition of Plasmodium falciparum ENR in presence of triclosan [AID277587, Type: Literature] | Enoyl-acyl-carrier protein reductase precursor [gi:74844868] |   View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | Ki | 0.008 [uM] | | BioAssay | Inhibition of Plasmodium falciparum ENR in presence of triclosan | | AID | 277587 | | BioAssay type | Literature | | Target | Enoyl-acyl-carrier protein reductase precursor [gi:74844868] | | PubMed | 17263522 | | Data Table |  |
|
| 2 | [SID103226312] | Active | Ki | 0.028 | Competitive inhibition of Spiroplasma sp. MQ1 SssI methyltransferase using pUC18 as substrate measured for 10 mins by Dixon plot analysis [AID675175, Type: Literature] | |   View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | Ki | 0.028 [uM] | | BioAssay | Competitive inhibition of Spiroplasma sp. MQ1 SssI methyltransferase using pUC18 as substrate measured for 10 mins by Dixon plot analysis | | AID | 675175 | | BioAssay type | Literature | | Target | | | PubMed | 22854677 | | Data Table |  |
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| 3 | [SID103226312] | Active | EC50 | 0.03987 | Neuroprotection against beta-amyloid peptide 1-42-induced toxicity in human SH-SY5Y cells assessed as lactate dehydrogenase release [AID392677, Type: Literature] | |   View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | EC50 | 0.03987 [uM] | | BioAssay | Neuroprotection against beta-amyloid peptide 1-42-induced toxicity in human SH-SY5Y cells assessed as lactate dehydrogenase release | | AID | 392677 | | BioAssay type | Literature | | Target | | | PubMed | 19138859 | | Data Table |  |
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| 4 | [SID103226312] | Active | Ki | 0.079 | Inhibition of Plasmodium falciparum ENR using crotonyl-CoA substrate [AID277586, Type: Literature] | Enoyl-acyl-carrier protein reductase precursor [gi:74844868] |   View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | Ki | 0.079 [uM] | | BioAssay | Inhibition of Plasmodium falciparum ENR using crotonyl-CoA substrate | | AID | 277586 | | BioAssay type | Literature | | Target | Enoyl-acyl-carrier protein reductase precursor [gi:74844868] | | PubMed | 17263522 | | Data Table |  |
|
| 5 | [SID103226312] | Active | IC50 | 0.086 | Inhibition of chymotrypsin like activity of proteasome [AID461136, Type: Literature] | |   View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 0.086 [uM] | | BioAssay | Inhibition of chymotrypsin like activity of proteasome | | AID | 461136 | | BioAssay type | Literature | | Target | | | PubMed | 20045338 | | Data Table |  |
|
| 6 | [SID103226312] | Active | IC50 | 0.18 | Inhibition of beta amyloid (1 to 40) fibril formation [AID456194, Type: Literature] | |   View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 0.18 [uM] | | BioAssay | Inhibition of beta amyloid (1 to 40) fibril formation | | AID | 456194 | | BioAssay type | Literature | | Target | | | PubMed | 19931462 | | Data Table |  |
|
| 7 | [SID103226312] | Active | Ki | 0.186 | Inhibition of Plasmodium falciparum ENR using NADH substrate [AID277585, Type: Literature] | Enoyl-acyl-carrier protein reductase precursor [gi:74844868] |   View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | Ki | 0.186 [uM] | | BioAssay | Inhibition of Plasmodium falciparum ENR using NADH substrate | | AID | 277585 | | BioAssay type | Literature | | Target | Enoyl-acyl-carrier protein reductase precursor [gi:74844868] | | PubMed | 17263522 | | Data Table |  |
|
| 8 | [SID103226312] | Active | IC50 | 0.2 | Inhibition of FabI [AID265759, Type: Literature] | Enoyl-acyl-carrier protein reductase precursor [gi:74844868] |   View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 0.2 [uM] | | BioAssay | Inhibition of FabI | | AID | 265759 | | BioAssay type | Literature | | Target | Enoyl-acyl-carrier protein reductase precursor [gi:74844868] | | PubMed | 16722653 | | Data Table |  |
|
| 9 | [SID103226312] | Active | IC50 | 0.2 | Inhibition of chymotrypsin like activity of 20S proteasome [AID300029, Type: Literature] | |   View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 0.2 [uM] | | BioAssay | Inhibition of chymotrypsin like activity of 20S proteasome | | AID | 300029 | | BioAssay type | Literature | | Target | | | PubMed | 17544279 | | Data Table |  |
|
| 10 | [SID103226312] | Active | IC50 | 0.25 | Inhibition of Plasmodium falciparum ENR [AID277583, Type: Literature] | Enoyl-acyl-carrier protein reductase precursor [gi:74844868] |   View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 0.25 [uM] | | BioAssay | Inhibition of Plasmodium falciparum ENR | | AID | 277583 | | BioAssay type | Literature | | Target | Enoyl-acyl-carrier protein reductase precursor [gi:74844868] | | PubMed | 17263522 | | Data Table |  |
|
| 11 | [SID103226312] | Active | IC50 | 0.25 | Inhibition of yeast G6PD [AID319369, Type: Literature] | Glucose-6-phosphate 1-dehydrogenase [gi:120734] |   View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 0.25 [uM] | | BioAssay | Inhibition of yeast G6PD | | AID | 319369 | | BioAssay type | Literature | | Target | Glucose-6-phosphate 1-dehydrogenase [gi:120734] | | PubMed | 18313308 | | Data Table |  |
|
| 12 | [SID103226312] | Active | IC50 | 0.3 | Inhibition of FabG [AID265760, Type: Literature] | 3-oxoacyl-acyl-carrier protein reductase precursor [gi:75020671] |   View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 0.3 [uM] | | BioAssay | Inhibition of FabG | | AID | 265760 | | BioAssay type | Literature | | Target | 3-oxoacyl-acyl-carrier protein reductase precursor [gi:75020671] | | PubMed | 16722653 | | Data Table |  |
|
| 13 | [SID103226312] | Active | EC50 | 0.391 | Antiviral activity against Influenza (A/PR8/34(H1N1)) [AID343516, Type: Literature] | |   View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | EC50 | 0.391 [uM] | | BioAssay | Antiviral activity against Influenza (A/PR8/34(H1N1)) | | AID | 343516 | | BioAssay type | Literature | | Target | | | PubMed | 18547804 | | Data Table |  |
|
| 14 | [SID103226312] | Active | IC50 | 0.4 | Inhibition of FabZ [AID265758, Type: Literature] | Beta-hydroxyacyl-ACP dehydratase precursor (Fatty acid synthesis protein) [gi:74844869] |   View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 0.4 [uM] | | BioAssay | Inhibition of FabZ | | AID | 265758 | | BioAssay type | Literature | | Target | Beta-hydroxyacyl-ACP dehydratase precursor (Fatty acid synthesis protein) [gi:74844869] | | PubMed | 16722653 | | Data Table |  |
|
| 15 | [SID26719730] | Active | Potency | 0.4467 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 26719730 | | CID | 65064 | | Outcome | Active | | Potency | 0.4467 [uM] | | BioAssay | qHTS Assay for Inhibitors of DNA Polymerase Beta | | AID | 485314 | | BioAssay type | confirmatory | | Target | DNA polymerase beta [Homo sapiens] [gi:4505931] | | PubMed | | | Data Table |  |
|
| 16 | [SID26719730] | Active | Potency | 0.4467 | qHTS Assay for Inhibitors of DNA Polymerase Beta [AID485314, Type: confirmatory] | DNA polymerase beta [Homo sapiens] [gi:4505931] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 26719730 | | CID | 65064 | | Outcome | Active | | Potency | 0.4467 [uM] | | BioAssay | qHTS Assay for Inhibitors of DNA Polymerase Beta | | AID | 485314 | | BioAssay type | confirmatory | | Target | DNA polymerase beta [Homo sapiens] [gi:4505931] | | PubMed | | | Data Table |  |
|
| 17 | [SID103226312] | Active | IC50 | 0.69 | Compound was evaluated for its inhibitory activity against recombinant rat SE(squalene epoxidase) [AID204664, Type: Literature] | |   View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 0.69 [uM] | | BioAssay | Compound was evaluated for its inhibitory activity against recombinant rat SE(squalene epoxidase) | | AID | 204664 | | BioAssay type | Literature | | Target | | | PubMed | 11086721 | | Data Table |  |
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| 18 | [SID103226312] | Active | IC50 | 0.69 | Inhibition of rat squalene epoxidase [AID357310, Type: Literature] | Squalene monooxygenase [gi:1706689] |   View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 0.69 [uM] | | BioAssay | Inhibition of rat squalene epoxidase | | AID | 357310 | | BioAssay type | Literature | | Target | Squalene monooxygenase [gi:1706689] | | PubMed | 11520216 | | Data Table |  |
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| 19 | [SID103226312] | Active | IC50 | 0.72 | Inhibition of 6PGD [AID319370, Type: Literature] | |   View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 0.72 [uM] | | BioAssay | Inhibition of 6PGD | | AID | 319370 | | BioAssay type | Literature | | Target | | | PubMed | 18313308 | | Data Table |  |
|
| 20 | [SID49681655] | Active | EC50 | 0.727 | Fluorescent Polarization Homogeneous Dose Response HTS to Indentify Inhibitors of Mex-5 Binding to TCR-2 [AID1960, Type: confirmatory] | Zinc finger protein mex- [gi:55976631] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 49681655 | | CID | 65064 | | Outcome | Active | | EC50 | 0.727 [uM] | | BioAssay | Fluorescent Polarization Homogeneous Dose Response HTS to Indentify Inhibitors of Mex-5 Binding to TCR-2 | | AID | 1960 | | BioAssay type | confirmatory | | Target | Zinc finger protein mex- [gi:55976631] | | PubMed | | | Data Table |  |
|
| 21 | [SID49681655] | Active | EC50 | 0.727 | Fluorescent Polarization Homogeneous Dose Response HTS to Indentify Inhibitors of Mex-5 Binding to TCR-2 [AID1960, Type: confirmatory] | Zinc finger protein mex- [gi:55976631] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 49681655 | | CID | 65064 | | Outcome | Active | | EC50 | 0.727 [uM] | | BioAssay | Fluorescent Polarization Homogeneous Dose Response HTS to Indentify Inhibitors of Mex-5 Binding to TCR-2 | | AID | 1960 | | BioAssay type | confirmatory | | Target | Zinc finger protein mex- [gi:55976631] | | PubMed | | | Data Table |  |
|
| 22 | [SID103226312] | Active | IC50 | 0.73 | Inhibition of polymerization in wild type HIV-1 RT with poly rC/dG12-18 template primer and [3H]dGTP [AID83435, Type: Literature] | Reverse transcriptase/RNaseH [gi:82310930] |   View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 0.73 [uM] | | BioAssay | Inhibition of polymerization in wild type HIV-1 RT with poly rC/dG12-18 template primer and [3H]dGTP | | AID | 83435 | | BioAssay type | Literature | | Target | Reverse transcriptase/RNaseH [gi:82310930] | | PubMed | 11591519 | | Data Table |  |
|
| 23 | [SID103226312] | Active | IC50 | 0.757 | Inhibition of recombinant human BACE1 using Eu-CEVNLDAEFK-Qsy7 as substrate by HTRF assay [AID646974, Type: Literature] | Beta-secretase 1 [gi:296434407] |   View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 0.757 [uM] | | BioAssay | Inhibition of recombinant human BACE1 using Eu-CEVNLDAEFK-Qsy7 as substrate by HTRF assay | | AID | 646974 | | BioAssay type | Literature | | Target | Beta-secretase 1 [gi:296434407] | | PubMed | 22225636 | | Data Table |  |
|
| 24 | [SID26719730] | Active | Potency | 0.8913 | qHTS Assay for Inhibitors of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1) [AID2517, Type: confirmatory] | Chain A, Human Ape1 Endonuclease With Bound Abasic Dna And Mn2+ Ion [gi:6980812] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 26719730 | | CID | 65064 | | Outcome | Active | | Potency | 0.8913 [uM] | | BioAssay | qHTS Assay for Inhibitors of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1) | | AID | 2517 | | BioAssay type | confirmatory | | Target | Chain A, Human Ape1 Endonuclease With Bound Abasic Dna And Mn2+ Ion [gi:6980812] | | PubMed | | | Data Table |  |
|
| 25 | [SID103226312] | Active | IC50 | 1.6 | Inhibition of BACE1 using Rh-EVNLDAEFK-Quencher as substrate [AID647157, Type: Literature] | |   View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 1.6 [uM] | | BioAssay | Inhibition of BACE1 using Rh-EVNLDAEFK-Quencher as substrate | | AID | 647157 | | BioAssay type | Literature | | Target | | | PubMed | 22225636 | | Data Table |  |
|
| 26 | [SID26719730] | Active | Potency | 1.7783 | 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. | 26 | | Structure |
| | Substance | | | SID | 26719730 | | CID | 65064 | | Outcome | Active | | Potency | 1.7783 [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 |  |
|
| 27 | [SID103226312] | Active | IC50 | 2.21 | Inhibition of p38alpha after 1 hr by ELISA [AID566611, Type: Literature] | |   View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 2.21 [uM] | | BioAssay | Inhibition of p38alpha after 1 hr by ELISA | | AID | 566611 | | BioAssay type | Literature | | Target | | | PubMed | 21080642 | | Data Table |  |
|
| 28 | [SID103226312] | Active | IC50 | 3 | Inhibition of KDM4E [AID639775, Type: Literature] | |   View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 3 [uM] | | BioAssay | Inhibition of KDM4E | | AID | 639775 | | BioAssay type | Literature | | Target | | | PubMed | 21955276 | | Data Table |  |
|
| 29 | [SID26719730] | Active | Potency | 3.1623 | 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. | 29 | | Structure |
| | Substance | | | SID | 26719730 | | CID | 65064 | | Outcome | Active | | Potency | 3.1623 [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 |  |
|
| 30 | [SID103226312] | Active | Ki | 3.3 | Inhibition of MET kinase by Dixon plot analysis [AID437511, Type: Literature] | |   View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | Ki | 3.3 [uM] | | BioAssay | Inhibition of MET kinase by Dixon plot analysis | | AID | 437511 | | BioAssay type | Literature | | Target | | | PubMed | 19839593 | | Data Table |  |
|
| 31 | [SID103226312] | Active | IC50 | 3.7 | Inhibition of reduced carboxymethylated kappa-casein fibril formation measured every 5 mins after 1000 mins by thioflavin T staining-based binding assay [AID456187, Type: Literature] | |   View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 3.7 [uM] | | BioAssay | Inhibition of reduced carboxymethylated kappa-casein fibril formation measured every 5 mins after 1000 mins by thioflavin T staining-based binding assay | | AID | 456187 | | BioAssay type | Literature | | Target | | | PubMed | 19931462 | | Data Table |  |
|
| 32 | [SID103226312] | Active | IC50 | 6.29 | Inhibition of rat liver microsomal Steroid 5-alpha-reductase after 30 mins by scintillation counting [AID548975, Type: Literature] | |   View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 6.29 [uM] | | BioAssay | Inhibition of rat liver microsomal Steroid 5-alpha-reductase after 30 mins by scintillation counting | | AID | 548975 | | BioAssay type | Literature | | Target | | | PubMed | 21044810 | | Data Table |  |
|
| 33 | [SID103226312] | Active | IC50 | 6.44 | Inhibition of IDH [AID319371, Type: Literature] | |   View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 6.44 [uM] | | BioAssay | Inhibition of IDH | | AID | 319371 | | BioAssay type | Literature | | Target | | | PubMed | 18313308 | | Data Table |  |
|
| 34 | [SID103226312] | Active | IC50 | 6.8 | Inhibition of human recombinant MT1-MMP expressed in Escherichia coli by fluorogenic peptide cleavage assay [AID428320, Type: Literature] | Matrix metalloproteinase-14 [gi:317373419] |   View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 6.8 [uM] | | BioAssay | Inhibition of human recombinant MT1-MMP expressed in Escherichia coli by fluorogenic peptide cleavage assay | | AID | 428320 | | BioAssay type | Literature | | Target | Matrix metalloproteinase-14 [gi:317373419] | | PubMed | 19524436 | | Data Table |  |
|
| 35 | [SID103226312] | Active | IC50 | 6.8 | Inhibition of human recombinant MT1-MMP expressed in Escherichia coli by fluorogenic peptide cleavage assay [AID428320, Type: Literature] | Matrix metalloproteinase-14 [gi:317373419] |   View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 6.8 [uM] | | BioAssay | Inhibition of human recombinant MT1-MMP expressed in Escherichia coli by fluorogenic peptide cleavage assay | | AID | 428320 | | BioAssay type | Literature | | Target | Matrix metalloproteinase-14 [gi:317373419] | | PubMed | 19524436 | | Data Table |  |
|
| 36 | [SID103226312] | Active | IC50 | 6.8 | Inhibition of human recombinant MT1-MMP expressed in Escherichia coli by fluorogenic peptide cleavage assay [AID428320, Type: Literature] | Matrix metalloproteinase-14 [gi:317373419] |   View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 6.8 [uM] | | BioAssay | Inhibition of human recombinant MT1-MMP expressed in Escherichia coli by fluorogenic peptide cleavage assay | | AID | 428320 | | BioAssay type | Literature | | Target | Matrix metalloproteinase-14 [gi:317373419] | | PubMed | 19524436 | | Data Table |  |
|
| 37 | [SID103226312] | Active | ED50 | 7 | Antioxidant activity assessed as DPPH radical scavenging activity [AID365747, Type: Literature] | |   View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | ED50 | 7 [uM] | | BioAssay | Antioxidant activity assessed as DPPH radical scavenging activity | | AID | 365747 | | BioAssay type | Literature | | Target | | | PubMed | 18656366 | | Data Table |  |
|
| 38 | [SID103226312] | Active | ED50 | 7 | Antioxidant activity assessed as radical DPPH scavenging activity [AID429185, Type: Literature] | |   View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | ED50 | 7 [uM] | | BioAssay | Antioxidant activity assessed as radical DPPH scavenging activity | | AID | 429185 | | BioAssay type | Literature | | Target | | | PubMed | 19596200 | | Data Table |  |
|
| 39 | [SID103226312] | Active | ED50 | 8.3 | Antiviral activity against influenza A virus (A/swine/OH/511445/2007(H1N1)) Oh7 infected in MDCK cells assessed as inhibition of viral replication after 4 days by quantitative RT-PCR [AID638568, Type: Literature] | |   View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | ED50 | 8.3 [uM] | | BioAssay | Antiviral activity against influenza A virus (A/swine/OH/511445/2007(H1N1)) Oh7 infected in MDCK cells assessed as inhibition of viral replication after 4 days by quantitative RT-PCR | | AID | 638568 | | BioAssay type | Literature | | Target | | | PubMed | 22115591 | | Data Table |  |
|
| 40 | [SID103226312] | Active | IC50 | 8.3 | Antioxidant activity assessed as DPPH radical scavenging activity after 30 mins by spectrophotometry [AID650645, Type: Literature] | |   View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 8.3 [uM] | | BioAssay | Antioxidant activity assessed as DPPH radical scavenging activity after 30 mins by spectrophotometry | | AID | 650645 | | BioAssay type | Literature | | Target | | | PubMed | 22377672 | | Data Table |  |
|
| 41 | [SID26719730] | Active | Potency | 8.9125 | 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. | 41 | | Structure |
| | Substance | | | SID | 26719730 | | CID | 65064 | | Outcome | Active | | Potency | 8.9125 [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 |  |
|
| 42 | [SID26719730] | Active | Potency | 8.9125 | qHTS Assay for Inhibitors of BAZ2B [AID504333, Type: confirmatory] | bromodomain adjacent to zinc finger domain 2B [Homo sapiens] [gi:6683500] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 26719730 | | CID | 65064 | | Outcome | Active | | Potency | 8.9125 [uM] | | BioAssay | qHTS Assay for Inhibitors of BAZ2B | | AID | 504333 | | BioAssay type | confirmatory | | Target | bromodomain adjacent to zinc finger domain 2B [Homo sapiens] [gi:6683500] | | PubMed | | | Data Table |  |
|
| 43 | [SID103226312] | Active | IC50 | 9.4 | Antiproliferative activity against human HL60 cells after 3 days [AID363881, Type: Literature] | |   View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 9.4 [uM] | | BioAssay | Antiproliferative activity against human HL60 cells after 3 days | | AID | 363881 | | BioAssay type | Literature | | Target | | | PubMed | 18693020 | | Data Table |  |
|
| 44 | [SID103226312] | Active | IC50 | 9.4 | Inhibition of lipid peroxidation in Sprague-Dawley rat heart mitochondria assessed as inhibition of FeSO4-induced malondialdehyde formation [AID398697, Type: other] | |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 9.4 [uM] | | BioAssay | Inhibition of lipid peroxidation in Sprague-Dawley rat heart mitochondria assessed as inhibition of FeSO4-induced malondialdehyde formation | | AID | 398697 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 45 | [SID103226312] | Active | IC50 | 9.6 | Inhibition of human recombinant MMP2 expressed in Escherichia coli by fluorogenic peptide cleavage assay [AID428322, Type: Literature] | 72 kDa type IV collagenase [gi:116856] |   View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 9.6 [uM] | | BioAssay | Inhibition of human recombinant MMP2 expressed in Escherichia coli by fluorogenic peptide cleavage assay | | AID | 428322 | | BioAssay type | Literature | | Target | 72 kDa type IV collagenase [gi:116856] | | PubMed | 19524436 | | Data Table |  |
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| 46 | [SID103226312] | Active | IC50 | 9.6 | Inhibition of human recombinant MMP2 expressed in Escherichia coli by fluorogenic peptide cleavage assay [AID428322, Type: Literature] | 72 kDa type IV collagenase [gi:116856] |   View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 9.6 [uM] | | BioAssay | Inhibition of human recombinant MMP2 expressed in Escherichia coli by fluorogenic peptide cleavage assay | | AID | 428322 | | BioAssay type | Literature | | Target | 72 kDa type IV collagenase [gi:116856] | | PubMed | 19524436 | | Data Table |  |
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| 47 | [SID103226312] | Active | IC50 | 9.6 | Inhibition of human recombinant MMP2 expressed in Escherichia coli by fluorogenic peptide cleavage assay [AID428322, Type: Literature] | 72 kDa type IV collagenase [gi:116856] |   View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 9.6 [uM] | | BioAssay | Inhibition of human recombinant MMP2 expressed in Escherichia coli by fluorogenic peptide cleavage assay | | AID | 428322 | | BioAssay type | Literature | | Target | 72 kDa type IV collagenase [gi:116856] | | PubMed | 19524436 | | Data Table |  |
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| 48 | [SID103226312] | Active | IC50 | 9.9 | Antiproliferative activity against rat HSC-T6 cells after 48 hrs by MTT assay [AID312043, Type: Literature] | |   View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 9.9 [uM] | | BioAssay | Antiproliferative activity against rat HSC-T6 cells after 48 hrs by MTT assay | | AID | 312043 | | BioAssay type | Literature | | Target | | | PubMed | 18052323 | | Data Table |  |
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| 49 | [SID103226312] | Active | IC50 | 9.9 | Antiplasmodial activity against chloroquine-resistant Plasmodium falciparum K1 [AID265762, Type: Literature] | |   View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 9.9 [uM] | | BioAssay | Antiplasmodial activity against chloroquine-resistant Plasmodium falciparum K1 | | AID | 265762 | | BioAssay type | Literature | | Target | | | PubMed | 16722653 | | Data Table |  |
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| 50 | [SID103226312] | Active | IC50 | 9.9 | Antifibrotic activity against rat HSC-T6 cells assessed as inhibition of proliferation after 48 hrs by BrdU incorporation assay [AID597201, Type: Literature] | |   View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 103226312 | | CID | 65064 | | Outcome | Active | | IC50 | 9.9 [uM] | | BioAssay | Antifibrotic activity against rat HSC-T6 cells assessed as inhibition of proliferation after 48 hrs by BrdU incorporation assay | | AID | 597201 | | BioAssay type | Literature | | Target | | | PubMed | 21504848 | | Data Table |  |
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