Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | SMAD family member 2 | Starlite/ChEMBL | No references |
Homo sapiens | parathyroid hormone 1 receptor | Starlite/ChEMBL | No references |
Influenza A virus | Nonstructural protein 1 | Starlite/ChEMBL | No references |
Homo sapiens | lamin A/C | Starlite/ChEMBL | No references |
Herpes simplex virus (type 1 / strain 17) | Alpha trans-inducing protein (VP16) | Starlite/ChEMBL | No references |
Homo sapiens | huntingtin | Starlite/ChEMBL | No references |
Mus musculus | RAR-related orphan receptor gamma | Starlite/ChEMBL | No references |
Homo sapiens | nuclear factor, erythroid 2-like 2 | Starlite/ChEMBL | No references |
Homo sapiens | glucagon-like peptide 1 receptor | Starlite/ChEMBL | No references |
Homo sapiens | ATPase family, AAA domain containing 5 | Starlite/ChEMBL | No references |
Homo sapiens | neuropeptide S receptor 1 | Starlite/ChEMBL | No references |
Homo sapiens | G protein-coupled receptor 55 | Starlite/ChEMBL | No references |
Homo sapiens | vitamin D (1,25- dihydroxyvitamin D3) receptor | Starlite/ChEMBL | No references |
Schistosoma mansoni | Thioredoxin glutathione reductase | Starlite/ChEMBL | No references |
Homo sapiens | geminin, DNA replication inhibitor | Starlite/ChEMBL | No references |
Homo sapiens | sphingosine-1-phosphate receptor 1 | Starlite/ChEMBL | No references |
Homo sapiens | tumor protein p53 | Starlite/ChEMBL | No references |
Homo sapiens | nuclear receptor subfamily 2, group E, member 3 | Starlite/ChEMBL | No references |
Homo sapiens | GNAS complex locus | Starlite/ChEMBL | No references |
Homo sapiens | glycoprotein hormones, alpha polypeptide | Starlite/ChEMBL | No references |
Homo sapiens | survival of motor neuron 2, centromeric | Starlite/ChEMBL | No references |
Homo sapiens | sphingosine-1-phosphate receptor 4 | Starlite/ChEMBL | No references |
Homo sapiens | paired box 8 | Starlite/ChEMBL | No references |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Mycobacterium leprae | DIHYDROLIPOAMIDE DEHYDROGENASE LPD (LIPOAMIDE REDUCTASE (NADH)) (LIPOYL DEHYDROGENASE) (DIHYDROLIPOYL DEHYDROGENASE) (DIAPHORASE | 0.0116 | 0.1005 | 1 |
Schistosoma mansoni | hypothetical protein | 0.0038 | 0.0195 | 0.1012 |
Schistosoma mansoni | hypothetical protein | 0.0043 | 0.0251 | 0.1301 |
Schistosoma mansoni | nuclear hormone receptor nor-1/nor-2 | 0.0037 | 0.018 | 0.0932 |
Brugia malayi | Nuclear hormone receptor family member nhr-31 | 0.0037 | 0.018 | 0.0571 |
Mycobacterium tuberculosis | Putative ferredoxin reductase | 0.0104 | 0.0884 | 0.8342 |
Brugia malayi | GTP-binding regulatory protein Gs alpha-S chain, putative | 0.0055 | 0.0374 | 0.1187 |
Schistosoma mansoni | intermediate filament proteins | 0.0033 | 0.0138 | 0.0714 |
Schistosoma mansoni | Guanine nucleotide-binding protein G(s) subunit alpha (Adenylate cyclase-stimulating G alpha protein) | 0.0055 | 0.0374 | 0.1937 |
Loa Loa (eye worm) | hypothetical protein | 0.0037 | 0.018 | 0.0571 |
Loa Loa (eye worm) | latrophilin receptor protein 2 | 0.0038 | 0.0195 | 0.062 |
Loa Loa (eye worm) | nuclear hormone receptor family member nhr-14 | 0.0037 | 0.018 | 0.0571 |
Entamoeba histolytica | hypothetical protein | 0.0043 | 0.0251 | 0.5 |
Brugia malayi | Nuclear hormone receptor family member nhr-14 | 0.0037 | 0.018 | 0.0571 |
Schistosoma mansoni | Tr4/Tr2 (homologue) | 0.0037 | 0.018 | 0.0932 |
Echinococcus granulosus | COUP TF:Svp nuclear hormone receptor | 0.0037 | 0.018 | 0.0315 |
Brugia malayi | Nuclear hormone receptor family member nhr-1 | 0.0037 | 0.018 | 0.0571 |
Echinococcus multilocularis | nuclear receptor 2DBD gamma | 0.0037 | 0.018 | 0.018 |
Echinococcus granulosus | lamin | 0.0033 | 0.0138 | 0.0241 |
Schistosoma mansoni | hypothetical protein | 0.0038 | 0.0195 | 0.1012 |
Brugia malayi | Intermediate filament tail domain containing protein | 0.0033 | 0.0138 | 0.0437 |
Plasmodium falciparum | glutathione reductase | 0.0046 | 0.0274 | 0.5 |
Brugia malayi | Nuclear hormone receptor family member nhr-25 | 0.0037 | 0.018 | 0.0571 |
Echinococcus granulosus | nuclear receptor 2DBD gamma | 0.0037 | 0.018 | 0.0315 |
Schistosoma mansoni | survival motor neuron protein | 0.0058 | 0.0405 | 0.21 |
Loa Loa (eye worm) | nuclear hormone receptor family member nhr-49 | 0.0037 | 0.018 | 0.0571 |
Brugia malayi | Nuclear hormone receptor family member nhr-19 | 0.0037 | 0.018 | 0.0571 |
Loa Loa (eye worm) | hypothetical protein | 0.0037 | 0.018 | 0.0571 |
Brugia malayi | Corticotropin releasing factor receptor 2 precursor, putative | 0.012 | 0.1053 | 0.3343 |
Brugia malayi | Latrophilin receptor protein 2 | 0.0038 | 0.0195 | 0.062 |
Brugia malayi | photoreceptor-specific nuclear receptor | 0.0322 | 0.315 | 1 |
Schistosoma mansoni | FTZ-F1 nuclear receptor-like protein | 0.0037 | 0.018 | 0.0932 |
Brugia malayi | latrophilin 2 splice variant baaae | 0.0082 | 0.0656 | 0.2082 |
Loa Loa (eye worm) | thioredoxin reductase | 0.0046 | 0.0274 | 0.0871 |
Schistosoma mansoni | hypothetical protein | 0.0038 | 0.0195 | 0.1012 |
Brugia malayi | Thioredoxin reductase | 0.0046 | 0.0274 | 0.0871 |
Schistosoma mansoni | hypothetical protein | 0.0082 | 0.0656 | 0.3398 |
Brugia malayi | Nuclear hormone receptor family member nhr-40 | 0.0037 | 0.018 | 0.0571 |
Loa Loa (eye worm) | hypothetical protein | 0.0038 | 0.0195 | 0.062 |
Echinococcus granulosus | Basic leucine zipper bZIP transcription | 0.0043 | 0.0251 | 0.044 |
Echinococcus granulosus | cadherin EGF LAG seven pass G type receptor | 0.0038 | 0.0195 | 0.0342 |
Onchocerca volvulus | 0.0291 | 0.2826 | 1 | |
Echinococcus multilocularis | neuropeptide receptor A26 | 0.0567 | 0.5706 | 0.5706 |
Onchocerca volvulus | 0.006 | 0.0421 | 0.1052 | |
Loa Loa (eye worm) | nuclear hormone receptor family member nhr-31 | 0.0037 | 0.018 | 0.0571 |
Echinococcus granulosus | survival motor neuron protein 1 | 0.0286 | 0.2773 | 0.4861 |
Echinococcus granulosus | ecdysone induced protein 78C | 0.0037 | 0.018 | 0.0315 |
Brugia malayi | Ligand-binding domain of nuclear hormone receptor family protein | 0.0037 | 0.018 | 0.0571 |
Loa Loa (eye worm) | hypothetical protein | 0.0148 | 0.134 | 0.4254 |
Brugia malayi | nuclear receptor NHR-88 | 0.0037 | 0.018 | 0.0571 |
Schistosoma mansoni | transcription factor LCR-F1 | 0.0043 | 0.0251 | 0.1301 |
Plasmodium falciparum | thioredoxin reductase | 0.0046 | 0.0274 | 0.5 |
Loa Loa (eye worm) | pax transcription factor protein 2 | 0.0291 | 0.2826 | 0.8973 |
Plasmodium vivax | thioredoxin reductase, putative | 0.0046 | 0.0274 | 0.5 |
Mycobacterium tuberculosis | Probable reductase | 0.0104 | 0.0884 | 0.8342 |
Echinococcus granulosus | guanine nucleotide binding protein Gs subunit | 0.0055 | 0.0374 | 0.0655 |
Onchocerca volvulus | Huntingtin homolog | 0.0148 | 0.134 | 0.4471 |
Loa Loa (eye worm) | MH2 domain-containing protein | 0.0144 | 0.13 | 0.4129 |
Loa Loa (eye worm) | nuclear Hormone Receptor family member | 0.0037 | 0.018 | 0.0571 |
Schistosoma mansoni | cellular tumor antigen P53 | 0.006 | 0.0421 | 0.2179 |
Onchocerca volvulus | Protein ultraspiracle homolog | 0.0037 | 0.018 | 0.0157 |
Loa Loa (eye worm) | hypothetical protein | 0.0037 | 0.018 | 0.0571 |
Schistosoma mansoni | Guanine nucleotide-binding protein G(s) subunit alpha (Adenylate cyclase-stimulating G alpha protein) | 0.0055 | 0.0374 | 0.1937 |
Echinococcus granulosus | FTZ F1 nuclear receptor protein | 0.0037 | 0.018 | 0.0315 |
Brugia malayi | hypothetical protein | 0.0286 | 0.2773 | 0.8805 |
Loa Loa (eye worm) | hypothetical protein | 0.0032 | 0.0132 | 0.0418 |
Brugia malayi | Nuclear hormone receptor family member nhr-19 | 0.0037 | 0.018 | 0.0571 |
Schistosoma mansoni | RAR-like nuclear receptor | 0.0037 | 0.018 | 0.0932 |
Loa Loa (eye worm) | hypothetical protein | 0.006 | 0.0421 | 0.1336 |
Schistosoma mansoni | retinoid-x-receptor (RXR) | 0.0037 | 0.018 | 0.0932 |
Trypanosoma cruzi | trypanothione reductase, putative | 0.0046 | 0.0274 | 0.5 |
Entamoeba histolytica | hypothetical protein | 0.0043 | 0.0251 | 0.5 |
Echinococcus multilocularis | diuretic hormone 44 receptor GPRdih2 | 0.0038 | 0.0195 | 0.0195 |
Schistosoma mansoni | hypothetical protein | 0.0205 | 0.193 | 1 |
Loa Loa (eye worm) | steroid hormone receptor | 0.0037 | 0.018 | 0.0571 |
Brugia malayi | hypothetical protein | 0.0148 | 0.134 | 0.4254 |
Loa Loa (eye worm) | hypothetical protein | 0.0322 | 0.315 | 1 |
Echinococcus multilocularis | guanine nucleotide binding protein G(s) subunit | 0.0055 | 0.0374 | 0.0374 |
Loa Loa (eye worm) | hypothetical protein | 0.0037 | 0.018 | 0.0571 |
Schistosoma mansoni | hypothetical protein | 0.0058 | 0.0405 | 0.21 |
Echinococcus multilocularis | cadherin EGF LAG seven pass G type receptor | 0.0038 | 0.0195 | 0.0195 |
Schistosoma mansoni | thyroid hormone receptor | 0.0037 | 0.018 | 0.0932 |
Schistosoma mansoni | Guanine nucleotide-binding protein G(s) subunit alpha (Adenylate cyclase-stimulating G alpha protein) | 0.0055 | 0.0374 | 0.1937 |
Echinococcus multilocularis | neuropeptide s receptor | 0.0567 | 0.5706 | 0.5706 |
Echinococcus multilocularis | Nuclear hormone receptor family member nhr 41 | 0.0037 | 0.018 | 0.018 |
Schistosoma mansoni | coup transcription factor | 0.0037 | 0.018 | 0.0932 |
Brugia malayi | Nuclear hormone receptor family member nhr-3 | 0.0037 | 0.018 | 0.0571 |
Echinococcus granulosus | FTZ F1 alpha | 0.0037 | 0.018 | 0.0315 |
Brugia malayi | Iron-sulfur cluster assembly accessory protein | 0.0058 | 0.0405 | 0.1287 |
Brugia malayi | Nuclear hormone receptor-like 1 | 0.0037 | 0.018 | 0.0571 |
Mycobacterium tuberculosis | Probable membrane NADH dehydrogenase NdhA | 0.0104 | 0.0884 | 0.8342 |
Echinococcus multilocularis | geminin | 0.0205 | 0.193 | 0.193 |
Echinococcus granulosus | neuropeptide receptor A26 | 0.0567 | 0.5706 | 1 |
Onchocerca volvulus | 0.0037 | 0.018 | 0.0157 | |
Echinococcus multilocularis | FTZ F1 nuclear receptor protein | 0.0037 | 0.018 | 0.018 |
Onchocerca volvulus | Huntingtin homolog | 0.0148 | 0.134 | 0.4471 |
Brugia malayi | Ligand-binding domain of nuclear hormone receptor family protein | 0.0037 | 0.018 | 0.0571 |
Loa Loa (eye worm) | hypothetical protein | 0.012 | 0.1053 | 0.3343 |
Echinococcus granulosus | nuclear receptor 2DBD gamma | 0.0037 | 0.018 | 0.0315 |
Mycobacterium tuberculosis | Probable dehydrogenase | 0.0104 | 0.0884 | 0.8342 |
Echinococcus multilocularis | lamin | 0.0033 | 0.0138 | 0.0138 |
Echinococcus multilocularis | thyroid hormone receptor alpha | 0.0037 | 0.018 | 0.018 |
Echinococcus multilocularis | hepatocyte nuclear factor 4 alpha | 0.0037 | 0.018 | 0.018 |
Brugia malayi | ecdysteroid receptor | 0.0037 | 0.018 | 0.0571 |
Echinococcus multilocularis | lamin dm0 | 0.0033 | 0.0138 | 0.0138 |
Schistosoma mansoni | nuclear receptor 2DBD-gamma | 0.0037 | 0.018 | 0.0932 |
Echinococcus multilocularis | COUP TF:Svp nuclear hormone receptor | 0.0037 | 0.018 | 0.018 |
Loa Loa (eye worm) | glutathione reductase | 0.0046 | 0.0274 | 0.0871 |
Brugia malayi | glutathione reductase | 0.0046 | 0.0274 | 0.0871 |
Echinococcus multilocularis | thioredoxin glutathione reductase | 0.0046 | 0.0281 | 0.0281 |
Schistosoma mansoni | nuclear hormone receptor | 0.0037 | 0.018 | 0.0932 |
Echinococcus granulosus | Nuclear hormone receptor family member nhr 41 | 0.0037 | 0.018 | 0.0315 |
Schistosoma mansoni | steroid hormone receptor ad4bp | 0.0037 | 0.018 | 0.0932 |
Brugia malayi | MH2 domain containing protein | 0.0144 | 0.13 | 0.4129 |
Brugia malayi | steroid hormone receptor | 0.0037 | 0.018 | 0.0571 |
Loa Loa (eye worm) | intermediate filament tail domain-containing protein | 0.0033 | 0.0138 | 0.0437 |
Toxoplasma gondii | thioredoxin reductase | 0.0046 | 0.0274 | 0.5 |
Echinococcus granulosus | diuretic hormone 44 receptor GPRdih2 | 0.0038 | 0.0195 | 0.0342 |
Mycobacterium tuberculosis | Probable oxidoreductase | 0.0116 | 0.1005 | 1 |
Echinococcus multilocularis | musashi | 0.0033 | 0.0138 | 0.0138 |
Brugia malayi | Nuclear hormone receptor family member nhr-41 | 0.0037 | 0.018 | 0.0571 |
Echinococcus granulosus | geminin | 0.0205 | 0.193 | 0.3383 |
Loa Loa (eye worm) | hypothetical protein | 0.0033 | 0.0138 | 0.0437 |
Brugia malayi | intermediate filament protein | 0.0033 | 0.0138 | 0.0437 |
Echinococcus granulosus | intermediate filament protein | 0.0033 | 0.0138 | 0.0241 |
Brugia malayi | Steroid receptor seven-up type 2 | 0.0037 | 0.018 | 0.0571 |
Mycobacterium tuberculosis | Probable NADH dehydrogenase Ndh | 0.0104 | 0.0884 | 0.8342 |
Leishmania major | trypanothione reductase | 0.0046 | 0.0274 | 0.5 |
Echinococcus granulosus | neuropeptide s receptor | 0.0567 | 0.5706 | 1 |
Echinococcus granulosus | lamin dm0 | 0.0033 | 0.0138 | 0.0241 |
Echinococcus granulosus | hepatocyte nuclear factor 4 alpha | 0.0037 | 0.018 | 0.0315 |
Schistosoma mansoni | lamin | 0.0033 | 0.0138 | 0.0714 |
Loa Loa (eye worm) | nuclear hormone receptor family member nhr-1 | 0.0037 | 0.018 | 0.0571 |
Plasmodium vivax | glutathione reductase, putative | 0.0046 | 0.0274 | 0.5 |
Loa Loa (eye worm) | intermediate filament protein | 0.0033 | 0.0138 | 0.0437 |
Loa Loa (eye worm) | nuclear hormone receptor family member nhr-40 | 0.0037 | 0.018 | 0.0571 |
Brugia malayi | calcium-independent alpha-latrotoxin receptor 2, putative | 0.0038 | 0.0195 | 0.062 |
Loa Loa (eye worm) | GTP-binding regulatory protein Gs alpha-S chain | 0.0055 | 0.0374 | 0.1187 |
Entamoeba histolytica | hypothetical protein | 0.0043 | 0.0251 | 0.5 |
Brugia malayi | Nuclear hormone receptor family member nhr-25 | 0.0037 | 0.018 | 0.0571 |
Schistosoma mansoni | hypothetical protein | 0.0205 | 0.193 | 1 |
Mycobacterium tuberculosis | Probable nitrite reductase [NAD(P)H] large subunit [FAD flavoprotein] NirB | 0.0104 | 0.0884 | 0.8342 |
Echinococcus multilocularis | tumor protein p63 | 0.0408 | 0.4049 | 0.4049 |
Loa Loa (eye worm) | hypothetical protein | 0.0037 | 0.018 | 0.0571 |
Echinococcus multilocularis | survival motor neuron protein 1 | 0.0286 | 0.2773 | 0.2773 |
Loa Loa (eye worm) | hypothetical protein | 0.0082 | 0.0656 | 0.2082 |
Onchocerca volvulus | Steroid hormone receptor family member cnr14 homolog | 0.0037 | 0.018 | 0.0157 |
Mycobacterium tuberculosis | Dihydrolipoamide dehydrogenase LpdC (lipoamide reductase (NADH)) (lipoyl dehydrogenase) (dihydrolipoyl dehydrogenase) (diaphoras | 0.0116 | 0.1005 | 1 |
Schistosoma mansoni | thyroid hormone receptor | 0.0037 | 0.018 | 0.0932 |
Onchocerca volvulus | Bile acid receptor homolog | 0.0037 | 0.018 | 0.0157 |
Schistosoma mansoni | retinoic acid receptor RXR | 0.0037 | 0.018 | 0.0932 |
Echinococcus multilocularis | ecdysone induced protein 78C | 0.0037 | 0.018 | 0.018 |
Loa Loa (eye worm) | pigment dispersing factor receptor c | 0.012 | 0.1053 | 0.3343 |
Echinococcus granulosus | thioredoxin glutathione reductase | 0.0046 | 0.0281 | 0.0492 |
Entamoeba histolytica | hypothetical protein | 0.0043 | 0.0251 | 0.5 |
Brugia malayi | hypothetical protein | 0.0043 | 0.0251 | 0.0797 |
Echinococcus multilocularis | guanine nucleotide binding protein G(s) subunit | 0.0055 | 0.0374 | 0.0374 |
Echinococcus multilocularis | nuclear receptor 2DBD gamma | 0.0037 | 0.018 | 0.018 |
Schistosoma mansoni | lamin | 0.0033 | 0.0138 | 0.0714 |
Schistosoma mansoni | hypothetical protein | 0.0038 | 0.0195 | 0.1012 |
Echinococcus multilocularis | GPCR, family 2 | 0.0038 | 0.0195 | 0.0195 |
Echinococcus multilocularis | FTZ F1 alpha | 0.0037 | 0.018 | 0.018 |
Mycobacterium tuberculosis | NAD(P)H quinone reductase LpdA | 0.0116 | 0.1005 | 1 |
Echinococcus granulosus | retinoic acid receptor rxr beta a | 0.0037 | 0.018 | 0.0315 |
Brugia malayi | nuclear hormone receptor | 0.0037 | 0.018 | 0.0571 |
Brugia malayi | Calcitonin receptor-like protein seb-1 | 0.012 | 0.1053 | 0.3343 |
Brugia malayi | Pax transcription factor protein 2 | 0.0291 | 0.2826 | 0.8973 |
Loa Loa (eye worm) | hypothetical protein | 0.0037 | 0.018 | 0.0571 |
Brugia malayi | Nuclear hormone receptor family member nhr-49 | 0.0037 | 0.018 | 0.0571 |
Echinococcus multilocularis | Basic leucine zipper (bZIP) transcription | 0.0043 | 0.0251 | 0.0251 |
Loa Loa (eye worm) | transcription factor SMAD2 | 0.0144 | 0.13 | 0.4129 |
Loa Loa (eye worm) | nuclear hormone receptor family member nhr-41 | 0.0037 | 0.018 | 0.0571 |
Loa Loa (eye worm) | hypothetical protein | 0.0148 | 0.134 | 0.4254 |
Onchocerca volvulus | 0.0058 | 0.0405 | 0.0995 | |
Echinococcus granulosus | guanine nucleotide binding protein Gs subunit | 0.0055 | 0.0374 | 0.0655 |
Trypanosoma brucei | trypanothione reductase | 0.0046 | 0.0274 | 0.5 |
Echinococcus granulosus | GPCR family 2 | 0.0038 | 0.0195 | 0.0342 |
Echinococcus granulosus | tumor protein p63 | 0.0408 | 0.4049 | 0.7097 |
Schistosoma mansoni | photoreceptor-specific nuclear receptor related | 0.0037 | 0.018 | 0.0932 |
Loa Loa (eye worm) | hypothetical protein | 0.0286 | 0.2773 | 0.8805 |
Loa Loa (eye worm) | hypothetical protein | 0.0037 | 0.018 | 0.0571 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
AC50 (functional) | = 4.66 uM | PubChem BioAssay. HTS for PAX8 inhibitors using PAX8 luciferase reporter gene assay in RMG-I cells Measured in Cell-Based System Using Plate Reader - 7054-01_Inhibitor_Dose_CherryPick_Activity. (Class of assay: confirmatory) | ChEMBL. | No reference |
EC50 (functional) | = 1.608518 uM | PUBCHEM_BIOASSAY: Image-based HTS for Selective Agonists of GPR55. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID1965, AID2338, AID2339, AID2340, AID2341, AID2347, AID2843, AID2844, AID434922, AID434924, AID434925, AID434928, AID434929, AID463192, AID485279] | ChEMBL. | No reference |
EC50 (functional) | > 120 um | PUBCHEM_BIOASSAY: Luminescence Cell-Based Dose Response HTS to Identify Activators of 5'UTR Stem-Loop Driven Prion Protein mRNA Translation in H4 Neuroglioblastoma Cells. (Class of assay: confirmatory) [Related pubchem assays: 1829 (Project Summary), 1814 (Primary HTS)] | ChEMBL. | No reference |
IC50 (functional) | = 0.965 um | PUBCHEM_BIOASSAY: Fluorescence dose response cell-based high throughput screening assay for antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4). (Class of assay: confirmatory) [Related pubchem assays: 1524 (Confirmation in triplicates.), 1510 (Primary screen.)] | ChEMBL. | No reference |
IC50 (functional) | 4.079 uM | PubChem BioAssay. Luminescence-based cell-based high throughput dose response assay for agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3). (Class of assay: confirmatory) | ChEMBL. | No reference |
IC50 (functional) | 7.958 uM | PubChem BioAssay. Counterscreen for agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3):Luminescence-based cell-based high throughput dose response assay to identify inhibitors of the Herpes Virus Virion Protein 16 (VP16). (Class of assay: confirmatory) | ChEMBL. | No reference |
IC50 (functional) | = 8.814 um | PUBCHEM_BIOASSAY: Fluorescence-based counterscreen assay for S1P4 antagonists: Cell-based dose response high throughput screening assay to identify antagonists of the Sphingosine 1-Phosphate Receptor 1 (S1P1). (Class of assay: confirmatory) [Related pubchem assays: 1524 (Confirmation screen.), 1510 (Primary screen.)] | ChEMBL. | No reference |
IC50 (functional) | 26.682 uM | PubChem BioAssay. Counterscreen for inhibitors of the interaction of nucleotide-binding oligomerization domain containing 2 (NOD2) and receptor-interacting serine-threonine kinase 2 (RIPK2): Fluorescence-based cell-based high throughput dose response assay to identify non-selective inhibitors of the beta-lactamase enzyme (BLA). (Class of assay: confirmatory) | ChEMBL. | No reference |
IC50 (functional) | > 50 um | PUBCHEM_BIOASSAY: Late stage fluorescence dose response cell-based screening assay for antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4). (Class of assay: confirmatory) [Related pubchem assays: 1524 (Confirmation screen (S1P4 antagonists).), 1510 (Primary screen (S1P4 antagonists).), 1853 (Summary AID (S1P4 antagonists).), 1692 (Dose response screen (S1P4 antagonists).)] | ChEMBL. | No reference |
Potency (functional) | 2.2387 uM | PubChem BioAssay. qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode). (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | = 2.5119 um | PUBCHEM_BIOASSAY: qHTS Assay for Inhibitors of Influenza NS1 Protein Function. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | = 3.1623 um | PUBCHEM_BIOASSAY: qHTS Multiplex Assay to Identify Dual Action Probes in a Cell Model of Huntington: Aggregate Formation (GFP). (Class of assay: confirmatory) [Related pubchem assays: 1482, 1471 ] | ChEMBL. | No reference |
Potency (functional) | 3.1623 uM | PUBCHEM_BIOASSAY: qHTS for Inhibitors of the vitamin D receptor (VDR): Hit Validation using a Texas Red Assay. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | = 3.5481 um | PUBCHEM_BIOASSAY: qHTS Assay for Modulators of Lamin A Splicing. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 3.9811 uM | PUBCHEM_BIOASSAY: qHTS for Inhibitors of the vitamin D receptor (VDR): Hit Validation using a Fluorescein Assay. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 4.4668 uM | PUBCHEM_BIOASSAY: qHTS for Inhibitors of TGF-b. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID588856, AID588860] | ChEMBL. | No reference |
Potency (functional) | 4.4668 uM | PubChem BioAssay. qHTS for Agonist of gsp, the Etiologic Mutation Responsible for Fibrous Dysplasia/McCune-Albright Syndrome: qHTS. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | = 5.0119 um | PUBCHEM_BIOASSAY: qHTS Assay for Enhancers of SMN2 Splice Variant Expression. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 5.0119 uM | PubChem BioAssay. qHTS of Nrf2 Activators. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | = 5.6234 um | PUBCHEM_BIOASSAY: VP16 counterscreen qHTS for inhibitors of ROR gamma transcriptional activity. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 6.5131 uM | PubChem BioAssay. A quantitative high throughput screen for small molecules that induce DNA re-replication in MCF 10a normal breast cells. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 7.3078 uM | PUBCHEM_BIOASSAY: qHTS screen for small molecules that inhibit ELG1-dependent DNA repair in human embryonic kidney (HEK293T) cells expressing luciferase-tagged ELG1. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID493107, AID493125] | ChEMBL. | No reference |
Potency (functional) | = 8.9125 um | PUBCHEM_BIOASSAY: qHTS Assay for the Inhibitors of Schistosoma Mansoni Peroxiredoxins. (Class of assay: confirmatory) [Related pubchem assays: 1011 (Confirmation Concentration-Response Assay for Inhibitors of the Schistosoma mansoni Redox Cascade ), 448 (Schistosoma Mansoni Peroxiredoxins (Prx2) and thioredoxin glutathione reductase (TGR) coupled assay)] | ChEMBL. | No reference |
Potency (functional) | = 8.9125 um | PUBCHEM_BIOASSAY: qHTS for inhibitors of ROR gamma transcriptional activity. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 8.9125 uM | PubChem BioAssay. qHTS for Activators of Integrin-Mediated Alleviation for Muscular Dystrophy. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 11.2202 uM | PubChem BioAssay. qHTS of GLP-1 Receptor Agonists. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 11.5821 uM | PUBCHEM_BIOASSAY: qHTS for Inhibitors of the vitamin D receptor (VDR): Hit Validation using a Beta-Lactamase Assay. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | = 12.5893 um | PUBCHEM_BIOASSAY: qHTS Assay for Antagonists of the Neuropeptide S Receptor: cAMP Signal Transduction. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 14.1254 uM | PUBCHEM_BIOASSAY: qHTS for Inhibitors of TGF-b: Cytotox Counterscreen. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID588855, AID588860] | ChEMBL. | No reference |
Potency (functional) | 15.003 uM | PUBCHEM_BIOASSAY: qHTS for Inhibitors of the vitamin D receptor (VDR): Hit Validation in Primary Screen. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | = 15.8489 um | PUBCHEM_BIOASSAY: qHTS Screen for Compounds that Selectively Target Cancer Cells with p53 Mutations: Cytotoxicity of p53ts Cells at the Nonpermissive Temperature. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 17.7828 uM | PubChem BioAssay. qHTS of PTHR Inhibitors: Primary Screen. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 18.3564 uM | PUBCHEM_BIOASSAY: Nrf2 qHTS screen for inhibitors. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID493153, AID493163, AID504648] | ChEMBL. | No reference |
Potency (functional) | 18.526 uM | PUBCHEM_BIOASSAY: Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 96 hour incubation. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID488745, AID488752, AID488774, AID504848, AID504850] | ChEMBL. | No reference |
Potency (functional) | 18.526 uM | PUBCHEM_BIOASSAY: Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID488752, AID488774, AID504848, AID504850] | ChEMBL. | No reference |
Potency (functional) | 22.3872 uM | PUBCHEM_BIOASSAY: qHTS assay for re-activators of p53 using a Luc reporter. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID504709] | ChEMBL. | No reference |
Potency (functional) | 22.3872 uM | PubChem BioAssay. qHTS for Inhibitors of ATXN expression. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | = 28.1838 um | PUBCHEM_BIOASSAY: qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase). (Class of assay: confirmatory) [Related pubchem assays: 2429 (Confirmation qHTS Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase)), 2407 (Probe Development Summary for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase)), 2427 (Thermal Shift Assay for Inhibitors of HPGD (15-Hydroxyprostaglandin Dehydrogenase))] | ChEMBL. | No reference |
Potency (functional) | 28.1838 uM | PUBCHEM_BIOASSAY: qHTS Assay for Inhibitors of Histone Lysine Methyltransferase G9a. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID504404] | ChEMBL. | No reference |
Potency (functional) | 29.0929 uM | PubChem BioAssay. A quantitative high throughput screen for small molecules that induce DNA re-replication in SW480 colon adenocarcinoma cells. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 29.0929 uM | PubChem BioAssay. qHTS for induction of synthetic lethality in tumor cells producing 2HG: qHTS for the HT-1080-NT fibrosarcoma cell line. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 31.6228 uM | PUBCHEM_BIOASSAY: qHTS for Inhibitors of Polymerase Iota. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID588623] | ChEMBL. | No reference |
Potency (functional) | 35.4813 uM | PUBCHEM_BIOASSAY: qHTS Assay for Inhibitors of BAZ2B. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID504391] | ChEMBL. | No reference |
Potency (functional) | 35.4813 uM | PUBCHEM_BIOASSAY: qHTS for Inhibitors of binding or entry into cells for Lassa Virus. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID463114, AID540249] | ChEMBL. | No reference |
Potency (functional) | = 39.8107 um | PUBCHEM_BIOASSAY: qHTS Assay for Inhibitors Targeting the Menin-MLL Interaction in MLL Related Leukemias: Competition With Texas Red Labeled MLL-derived Mutant Peptide. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 39.8107 uM | PUBCHEM_BIOASSAY: Inhibitors of the vitamin D receptor (VDR): qHTS. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID504855] | ChEMBL. | No reference |
Potency (functional) | 50.1187 uM | PUBCHEM_BIOASSAY: Inhibitors of Regulator of G Protein Signaling (RGS) 4: qHTS. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID504856] | ChEMBL. | No reference |
Potency (functional) | 56.2341 uM | PUBCHEM_BIOASSAY: qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID488771] | ChEMBL. | No reference |
Potency (functional) | 56.2341 uM | PUBCHEM_BIOASSAY: qHTS Assay for Inhibitors of Rango (Ran-regulated importin-beta cargo) - Importin beta complex formation. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID540273] | ChEMBL. | No reference |
Potency (functional) | 58.4789 uM | PUBCHEM_BIOASSAY: qHTS for Inhibitors of mutant isocitrate dehydrogenase 1 (IDH1): qHTS. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 84.9214 uM | PubChem BioAssay. qHTS Assay to Find Inhibitors of Pin1. (Class of assay: confirmatory) | ChEMBL. | No reference |
Species name | Source | Reference | Is orphan |
---|---|---|---|
Plasmodium falciparum | ChEMBL23 | ||
Homo sapiens | ChEMBL23 |
Many chemical entities in TDR Targets come from high-throughput screenings with whole cells or tissue samples, and not all assayed compounds have been tested against a single a single target protein, probably because they get ruled out during screening process. Even if these compounds may have not been of interest in the original screening, they may come as interesting leads for other screening assays. Furthermore, we may be able to propose drug-target associations using chemical similarities and network patterns.