Detailed information for compound 1844346

Basic information

Technical information
  • TDR Targets ID: 1844346
  • Name: 2-hydroxy-6-oxo-4-phenyl-1H-pyridine-3-carbon itrile
  • MW: 212.204 | Formula: C12H8N2O2
  • H donors: 2 H acceptors: 3 LogP: 1.17 Rotable bonds: 1
    Rule of 5 violations (Lipinski): 1
  • SMILES: N#Cc1c(=O)[nH]c(cc1c1ccccc1)O
  • InChi: 1S/C12H8N2O2/c13-7-10-9(6-11(15)14-12(10)16)8-4-2-1-3-5-8/h1-6H,(H2,14,15,16)
  • InChiKey: RKCOTKNKKXMGTC-UHFFFAOYSA-N  

Network

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Synonyms

  • 2-hydroxy-6-keto-4-phenyl-1H-pyridine-3-carbonitrile

Targets

Known targets for this compound

No curated genes were found associated with this compound

Predicted pathogen targets for this compound

By orthology
No druggable targets predicted by orthology data
By sequence similarity to non orthologous known druggable targets
No druggable targets predicted by sequence similarity

Obtained from network model

Ranking Plot


Putative Targets List


Species Potential target Raw Global Species
Echinococcus granulosus Nuclear hormone receptor family member nhr 41 0.0021 0.5 0.5
Echinococcus multilocularis FTZ F1 nuclear receptor protein 0.0021 0.5 0.5
Schistosoma mansoni nuclear hormone receptor 0.0021 0.5 0.5
Loa Loa (eye worm) nuclear hormone receptor family member nhr-40 0.0021 0.5 0.5
Brugia malayi Nuclear hormone receptor family member nhr-19 0.0021 0.5 0.5
Echinococcus granulosus nuclear receptor 2DBD gamma 0.0021 0.5 0.5
Brugia malayi Nuclear hormone receptor family member nhr-49 0.0021 0.5 0.5
Echinococcus multilocularis hepatocyte nuclear factor 4 alpha 0.0021 0.5 0.5
Echinococcus granulosus FTZ F1 alpha 0.0021 0.5 0.5
Brugia malayi nuclear receptor NHR-88 0.0021 0.5 0.5
Schistosoma mansoni FTZ-F1 nuclear receptor-like protein 0.0021 0.5 0.5
Brugia malayi Nuclear hormone receptor-like 1 0.0021 0.5 0.5
Loa Loa (eye worm) hypothetical protein 0.0021 0.5 0.5
Schistosoma mansoni steroid hormone receptor ad4bp 0.0021 0.5 0.5
Brugia malayi nuclear hormone receptor 0.0021 0.5 0.5
Brugia malayi Nuclear hormone receptor family member nhr-25 0.0021 0.5 0.5
Onchocerca volvulus Steroid hormone receptor family member cnr14 homolog 0.0021 0.5 0.5
Schistosoma mansoni thyroid hormone receptor 0.0021 0.5 0.5
Loa Loa (eye worm) hypothetical protein 0.0021 0.5 0.5
Brugia malayi steroid hormone receptor 0.0021 0.5 0.5
Loa Loa (eye worm) hypothetical protein 0.0021 0.5 0.5
Onchocerca volvulus Bile acid receptor homolog 0.0021 0.5 0.5
Brugia malayi Ligand-binding domain of nuclear hormone receptor family protein 0.0021 0.5 0.5
Echinococcus multilocularis Nuclear hormone receptor family member nhr 41 0.0021 0.5 0.5
Onchocerca volvulus Protein ultraspiracle homolog 0.0021 0.5 0.5
Echinococcus granulosus COUP TF:Svp nuclear hormone receptor 0.0021 0.5 0.5
Echinococcus multilocularis FTZ F1 alpha 0.0021 0.5 0.5
Brugia malayi Nuclear hormone receptor family member nhr-41 0.0021 0.5 0.5
Loa Loa (eye worm) steroid hormone receptor 0.0021 0.5 0.5
Echinococcus granulosus ecdysone induced protein 78C 0.0021 0.5 0.5
Brugia malayi Nuclear hormone receptor family member nhr-31 0.0021 0.5 0.5
Brugia malayi photoreceptor-specific nuclear receptor 0.0021 0.5 0.5
Brugia malayi Steroid receptor seven-up type 2 0.0021 0.5 0.5
Schistosoma mansoni retinoid-x-receptor (RXR) 0.0021 0.5 0.5
Echinococcus granulosus FTZ F1 nuclear receptor protein 0.0021 0.5 0.5
Loa Loa (eye worm) nuclear hormone receptor family member nhr-14 0.0021 0.5 0.5
Loa Loa (eye worm) hypothetical protein 0.0021 0.5 0.5
Schistosoma mansoni thyroid hormone receptor 0.0021 0.5 0.5
Brugia malayi Nuclear hormone receptor family member nhr-25 0.0021 0.5 0.5
Loa Loa (eye worm) hypothetical protein 0.0021 0.5 0.5
Echinococcus multilocularis nuclear receptor 2DBD gamma 0.0021 0.5 0.5
Schistosoma mansoni coup transcription factor 0.0021 0.5 0.5
Brugia malayi Nuclear hormone receptor family member nhr-3 0.0021 0.5 0.5
Loa Loa (eye worm) hypothetical protein 0.0021 0.5 0.5
Echinococcus granulosus nuclear receptor 2DBD gamma 0.0021 0.5 0.5
Schistosoma mansoni RAR-like nuclear receptor 0.0021 0.5 0.5
Echinococcus multilocularis COUP TF:Svp nuclear hormone receptor 0.0021 0.5 0.5
Echinococcus multilocularis ecdysone induced protein 78C 0.0021 0.5 0.5
Schistosoma mansoni retinoic acid receptor RXR 0.0021 0.5 0.5
Onchocerca volvulus 0.0021 0.5 0.5
Loa Loa (eye worm) nuclear hormone receptor family member nhr-31 0.0021 0.5 0.5
Loa Loa (eye worm) nuclear hormone receptor family member nhr-41 0.0021 0.5 0.5
Loa Loa (eye worm) hypothetical protein 0.0021 0.5 0.5
Loa Loa (eye worm) nuclear hormone receptor family member nhr-1 0.0021 0.5 0.5
Loa Loa (eye worm) hypothetical protein 0.0021 0.5 0.5
Schistosoma mansoni nuclear hormone receptor nor-1/nor-2 0.0021 0.5 0.5
Schistosoma mansoni Tr4/Tr2 (homologue) 0.0021 0.5 0.5
Brugia malayi Nuclear hormone receptor family member nhr-1 0.0021 0.5 0.5
Brugia malayi Nuclear hormone receptor family member nhr-19 0.0021 0.5 0.5
Echinococcus multilocularis thyroid hormone receptor alpha 0.0021 0.5 0.5
Brugia malayi Nuclear hormone receptor family member nhr-40 0.0021 0.5 0.5
Echinococcus multilocularis nuclear receptor 2DBD gamma 0.0021 0.5 0.5
Schistosoma mansoni nuclear receptor 2DBD-gamma 0.0021 0.5 0.5
Echinococcus granulosus retinoic acid receptor rxr beta a 0.0021 0.5 0.5
Brugia malayi Nuclear hormone receptor family member nhr-14 0.0021 0.5 0.5
Loa Loa (eye worm) nuclear Hormone Receptor family member 0.0021 0.5 0.5
Schistosoma mansoni photoreceptor-specific nuclear receptor related 0.0021 0.5 0.5
Echinococcus granulosus hepatocyte nuclear factor 4 alpha 0.0021 0.5 0.5
Loa Loa (eye worm) nuclear hormone receptor family member nhr-49 0.0021 0.5 0.5
Brugia malayi Ligand-binding domain of nuclear hormone receptor family protein 0.0021 0.5 0.5

Activities

Activity type Activity value Assay description Source Reference
Inhibition (binding) = 42 % Inhibition of human recombinant UP1 expressed in Escherichia coli Rosetta (DE3) using URD and inorganic phosphate as substrate at 1 uM after 60 seconds by spectrophotometric analysis relative to control ChEMBL. 24131420

Phenotypes

Whole-cell/tissue/organism interactions

We have no records of whole-cell/tissue assays done with this compound What does this mean?

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

1 literature reference was collected for this gene.

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