Detailed information for compound 1310748

Basic information

Technical information
  • TDR Targets ID: 1310748
  • Name: [3-(4-bromophenyl)-5-hydroxy-5-(trifluorometh yl)-4H-pyrazol-1-yl]-furan-2-ylmethanone
  • MW: 403.151 | Formula: C15H10BrF3N2O3
  • H donors: 1 H acceptors: 2 LogP: 3.88 Rotable bonds: 4
    Rule of 5 violations (Lipinski): 1
  • SMILES: Brc1ccc(cc1)C1=NN(C(C1)(O)C(F)(F)F)C(=O)c1ccco1
  • InChi: 1S/C15H10BrF3N2O3/c16-10-5-3-9(4-6-10)11-8-14(23,15(17,18)19)21(20-11)13(22)12-2-1-7-24-12/h1-7,23H,8H2
  • InChiKey: DOVIZSXPDSIZAH-UHFFFAOYSA-N  

Network

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Synonyms

  • [3-(4-bromophenyl)-5-hydroxy-5-(trifluoromethyl)-4H-pyrazol-1-yl]-(2-furyl)methanone
  • [3-(4-bromophenyl)-5-hydroxy-5-(trifluoromethyl)-4H-pyrazol-1-yl]-furan-2-yl-methanone
  • 3-(4-bromophenyl)-1-(2-furoyl)-5-(trifluoromethyl)-4,5-dihydro-1H-pyrazol-5-ol
  • MLS000724238
  • SMR000305832

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Homo sapiens glucagon-like peptide 1 receptor Starlite/ChEMBL No references
Homo sapiens ubiquitin specific peptidase 1 Starlite/ChEMBL No references
Homo sapiens nuclear factor, erythroid 2-like 2 Starlite/ChEMBL No references
Mus musculus RAR-related orphan receptor gamma Starlite/ChEMBL No references
Homo sapiens SMAD family member 2 Starlite/ChEMBL No references

Predicted pathogen targets for this compound

By orthology
Species Potential target Known druggable target/s Ortholog Group
Loa Loa (eye worm) transcription factor SMAD2 Get druggable targets OG5_131716 All targets in OG5_131716
Loa Loa (eye worm) MH2 domain-containing protein Get druggable targets OG5_131716 All targets in OG5_131716
Brugia malayi MH2 domain containing protein Get druggable targets OG5_131716 All targets in OG5_131716

By sequence similarity to non orthologous known druggable targets
Species Potential target Known druggable target Length Alignment span Identity
Loa Loa (eye worm) pigment dispersing factor receptor c glucagon-like peptide 1 receptor 463 aa 388 aa 25.8 %
Brugia malayi MH2 domain containing protein SMAD family member 2 467 aa 405 aa 31.6 %

Obtained from network model

Ranking Plot


Putative Targets List


Species Potential target Raw Global Species
Schistosoma mansoni hypothetical protein 0.0019 0.0687 0.2744
Schistosoma mansoni coup transcription factor 0.0012 0.0177 0.0708
Loa Loa (eye worm) hypothetical protein 0.0012 0.0177 0.0177
Schistosoma mansoni hypothetical protein 0.0019 0.0687 0.2744
Echinococcus granulosus COUP TF:Svp nuclear hormone receptor 0.0012 0.0177 0.0708
Echinococcus granulosus nuclear receptor 2DBD gamma 0.0012 0.0177 0.0708
Loa Loa (eye worm) latrophilin receptor protein 2 0.0019 0.0687 0.0687
Brugia malayi Nuclear hormone receptor family member nhr-41 0.0012 0.0177 0.0177
Loa Loa (eye worm) hypothetical protein 0.0012 0.0177 0.0177
Schistosoma mansoni retinoid-x-receptor (RXR) 0.0012 0.0177 0.0708
Entamoeba histolytica hypothetical protein 0.0043 0.2503 0.5
Brugia malayi Nuclear hormone receptor family member nhr-14 0.0012 0.0177 0.0177
Loa Loa (eye worm) nuclear hormone receptor family member nhr-41 0.0012 0.0177 0.0177
Echinococcus granulosus retinoic acid receptor rxr beta a 0.0012 0.0177 0.0708
Brugia malayi Nuclear hormone receptor family member nhr-19 0.0012 0.0177 0.0177
Schistosoma mansoni photoreceptor-specific nuclear receptor related 0.0012 0.0177 0.0708
Echinococcus granulosus Basic leucine zipper bZIP transcription 0.0043 0.2503 1
Loa Loa (eye worm) nuclear hormone receptor family member nhr-40 0.0012 0.0177 0.0177
Loa Loa (eye worm) hypothetical protein 0.0019 0.0687 0.0687
Brugia malayi Calcitonin receptor-like protein seb-1 0.006 0.375 0.375
Echinococcus multilocularis diuretic hormone 44 receptor GPRdih2 0.0019 0.0687 0.2744
Schistosoma mansoni hypothetical protein 0.0019 0.0687 0.2744
Echinococcus multilocularis Basic leucine zipper (bZIP) transcription 0.0043 0.2503 1
Echinococcus multilocularis COUP TF:Svp nuclear hormone receptor 0.0012 0.0177 0.0708
Brugia malayi ecdysteroid receptor 0.0012 0.0177 0.0177
Echinococcus multilocularis Nuclear hormone receptor family member nhr 41 0.0012 0.0177 0.0708
Schistosoma mansoni hypothetical protein 0.0041 0.2332 0.9318
Echinococcus multilocularis thyroid hormone receptor alpha 0.0012 0.0177 0.0708
Schistosoma mansoni hypothetical protein 0.0043 0.2503 1
Loa Loa (eye worm) hypothetical protein 0.0012 0.0177 0.0177
Echinococcus granulosus ecdysone induced protein 78C 0.0012 0.0177 0.0708
Onchocerca volvulus Steroid hormone receptor family member cnr14 homolog 0.0012 0.0177 0.5
Brugia malayi Nuclear hormone receptor family member nhr-25 0.0012 0.0177 0.0177
Schistosoma mansoni retinoic acid receptor RXR 0.0012 0.0177 0.0708
Brugia malayi calcium-independent alpha-latrotoxin receptor 2, putative 0.0019 0.0687 0.0687
Brugia malayi hypothetical protein 0.0043 0.2503 0.2503
Brugia malayi Steroid receptor seven-up type 2 0.0012 0.0177 0.0177
Loa Loa (eye worm) nuclear hormone receptor family member nhr-49 0.0012 0.0177 0.0177
Brugia malayi Ligand-binding domain of nuclear hormone receptor family protein 0.0012 0.0177 0.0177
Schistosoma mansoni thyroid hormone receptor 0.0012 0.0177 0.0708
Onchocerca volvulus Bile acid receptor homolog 0.0012 0.0177 0.5
Loa Loa (eye worm) steroid hormone receptor 0.0012 0.0177 0.0177
Loa Loa (eye worm) hypothetical protein 0.0012 0.0177 0.0177
Loa Loa (eye worm) transcription factor SMAD2 0.0144 1 1
Onchocerca volvulus Protein ultraspiracle homolog 0.0012 0.0177 0.5
Schistosoma mansoni Tr4/Tr2 (homologue) 0.0012 0.0177 0.0708
Echinococcus multilocularis nuclear receptor 2DBD gamma 0.0012 0.0177 0.0708
Brugia malayi Corticotropin releasing factor receptor 2 precursor, putative 0.006 0.375 0.375
Echinococcus multilocularis ecdysone induced protein 78C 0.0012 0.0177 0.0708
Schistosoma mansoni steroid hormone receptor ad4bp 0.0012 0.0177 0.0708
Schistosoma mansoni nuclear hormone receptor nor-1/nor-2 0.0012 0.0177 0.0708
Loa Loa (eye worm) nuclear Hormone Receptor family member 0.0012 0.0177 0.0177
Brugia malayi Ligand-binding domain of nuclear hormone receptor family protein 0.0012 0.0177 0.0177
Schistosoma mansoni hypothetical protein 0.0019 0.0687 0.2744
Brugia malayi nuclear hormone receptor 0.0012 0.0177 0.0177
Echinococcus multilocularis nuclear receptor 2DBD gamma 0.0012 0.0177 0.0708
Brugia malayi Nuclear hormone receptor family member nhr-49 0.0012 0.0177 0.0177
Entamoeba histolytica hypothetical protein 0.0043 0.2503 0.5
Brugia malayi steroid hormone receptor 0.0012 0.0177 0.0177
Brugia malayi photoreceptor-specific nuclear receptor 0.0012 0.0177 0.0177
Schistosoma mansoni nuclear hormone receptor 0.0012 0.0177 0.0708
Schistosoma mansoni thyroid hormone receptor 0.0012 0.0177 0.0708
Echinococcus multilocularis hepatocyte nuclear factor 4 alpha 0.0012 0.0177 0.0708
Loa Loa (eye worm) hypothetical protein 0.0041 0.2332 0.2332
Loa Loa (eye worm) nuclear hormone receptor family member nhr-1 0.0012 0.0177 0.0177
Echinococcus multilocularis FTZ F1 nuclear receptor protein 0.0012 0.0177 0.0708
Echinococcus multilocularis FTZ F1 alpha 0.0012 0.0177 0.0708
Schistosoma mansoni nuclear receptor 2DBD-gamma 0.0012 0.0177 0.0708
Brugia malayi Nuclear hormone receptor family member nhr-40 0.0012 0.0177 0.0177
Brugia malayi Latrophilin receptor protein 2 0.0019 0.0687 0.0687
Echinococcus granulosus FTZ F1 nuclear receptor protein 0.0012 0.0177 0.0708
Loa Loa (eye worm) pigment dispersing factor receptor c 0.006 0.375 0.375
Brugia malayi Nuclear hormone receptor family member nhr-25 0.0012 0.0177 0.0177
Echinococcus granulosus cadherin EGF LAG seven pass G type receptor 0.0019 0.0687 0.2744
Loa Loa (eye worm) MH2 domain-containing protein 0.0144 1 1
Schistosoma mansoni transcription factor LCR-F1 0.0043 0.2503 1
Loa Loa (eye worm) hypothetical protein 0.006 0.375 0.375
Loa Loa (eye worm) hypothetical protein 0.0012 0.0177 0.0177
Loa Loa (eye worm) hypothetical protein 0.0012 0.0177 0.0177
Echinococcus granulosus diuretic hormone 44 receptor GPRdih2 0.0019 0.0687 0.2744
Echinococcus granulosus nuclear receptor 2DBD gamma 0.0012 0.0177 0.0708
Brugia malayi Nuclear hormone receptor family member nhr-19 0.0012 0.0177 0.0177
Schistosoma mansoni FTZ-F1 nuclear receptor-like protein 0.0012 0.0177 0.0708
Echinococcus granulosus FTZ F1 alpha 0.0012 0.0177 0.0708
Onchocerca volvulus 0.0012 0.0177 0.5
Loa Loa (eye worm) nuclear hormone receptor family member nhr-14 0.0012 0.0177 0.0177
Brugia malayi Nuclear hormone receptor family member nhr-3 0.0012 0.0177 0.0177
Loa Loa (eye worm) nuclear hormone receptor family member nhr-31 0.0012 0.0177 0.0177
Loa Loa (eye worm) hypothetical protein 0.0012 0.0177 0.0177
Echinococcus granulosus GPCR family 2 0.0019 0.0687 0.2744
Entamoeba histolytica hypothetical protein 0.0043 0.2503 0.5
Echinococcus granulosus Nuclear hormone receptor family member nhr 41 0.0012 0.0177 0.0708
Brugia malayi Nuclear hormone receptor-like 1 0.0012 0.0177 0.0177
Schistosoma mansoni RAR-like nuclear receptor 0.0012 0.0177 0.0708
Brugia malayi Nuclear hormone receptor family member nhr-1 0.0012 0.0177 0.0177
Brugia malayi Nuclear hormone receptor family member nhr-31 0.0012 0.0177 0.0177
Echinococcus multilocularis GPCR, family 2 0.0019 0.0687 0.2744
Brugia malayi nuclear receptor NHR-88 0.0012 0.0177 0.0177
Brugia malayi latrophilin 2 splice variant baaae 0.0041 0.2332 0.2332
Echinococcus granulosus hepatocyte nuclear factor 4 alpha 0.0012 0.0177 0.0708
Echinococcus multilocularis cadherin EGF LAG seven pass G type receptor 0.0019 0.0687 0.2744
Loa Loa (eye worm) hypothetical protein 0.0012 0.0177 0.0177
Entamoeba histolytica hypothetical protein 0.0043 0.2503 0.5

Activities

Activity type Activity value Assay description Source Reference
AC50 (functional) = 27.11 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
Potency (functional) 0.2512 uM PubChem BioAssay. Inhibitors of USP1/UAF1: Primary Screen. (Class of assay: confirmatory) ChEMBL. No reference
Potency (functional) 2.2387 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) = 7.0795 um PUBCHEM_BIOASSAY: qHTS for inhibitors of ROR gamma transcriptional activity. (Class of assay: confirmatory) ChEMBL. No reference
Potency (functional) 7.9433 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) 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: Nrf2 qHTS screen for inhibitors. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID493153, AID493163, AID504648] ChEMBL. No reference
Potency (functional) 12.5893 uM PubChem BioAssay. qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode). (Class of assay: confirmatory) ChEMBL. No reference
Potency (functional) 12.5893 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) 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) = 25.1189 um PUBCHEM_BIOASSAY: VP16 counterscreen qHTS for inhibitors of ROR gamma transcriptional activity. (Class of assay: confirmatory) ChEMBL. No reference
Potency (functional) 29.081 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) 29.0929 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) 89.1251 uM PUBCHEM_BIOASSAY: HTS for Inhibitors of HP1-beta Chromodomain Interactions with Methylated Histone Tails. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID488962] ChEMBL. No reference
Potency (functional) 100 uM PUBCHEM_BIOASSAY: qHTS for Inhibitors of Polymerase Iota. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID588623] ChEMBL. No reference

Phenotypes

Whole-cell/tissue/organism interactions

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.

Annotated phenotypes:

We have no manually annotated phenotypes for this drug. What does this mean? / Care to help?
In TDR Targets, information about phenotypes that are caused by drugs, or by genetic manipulation of cells (e.g. gene knockouts or knockdowns) is manually curated from the literature. These descriptions help to describe the potential of the target for drug development. If no information is available for this gene or if the information is incomplete, this may mean that i) the papers containing this information either appeared after the curation effort for this organism was carried out or they were inadvertently missed by curators; or that ii) the curation effort for this organism has not yet started.
 
In any case, if you have information about papers containing relevant validation data for this target, please log in using your TDR Targets username and password and send them to us using the corresponding form in this page (only visible to registered users) or contact us.

External resources for this compound

Bibliographic References

No literature references available for this target.

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