Detailed information for compound 329283

Basic information

Technical information
  • TDR Targets ID: 329283
  • Name: N-phenyl-4-[4-(phenylcarbamoyl)phenyl]benzami de
  • MW: 392.449 | Formula: C26H20N2O2
  • H donors: 2 H acceptors: 2 LogP: 5.22 Rotable bonds: 7
    Rule of 5 violations (Lipinski): 1
  • SMILES: O=C(c1ccc(cc1)c1ccc(cc1)C(=O)Nc1ccccc1)Nc1ccccc1
  • InChi: 1S/C26H20N2O2/c29-25(27-23-7-3-1-4-8-23)21-15-11-19(12-16-21)20-13-17-22(18-14-20)26(30)28-24-9-5-2-6-10-24/h1-18H,(H,27,29)(H,28,30)
  • InChiKey: XMTLNJDBMFSUBF-UHFFFAOYSA-N  


Substructure search Similarity search

Network

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Synonyms

  • 4-[4-[anilino(oxo)methyl]phenyl]-N-phenylbenzamide
  • 4-[4-[oxo-(phenylamino)methyl]phenyl]-N-phenylbenzamide
  • AN-652/42720559
  • ZINC00683049

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Homo sapiens protein tyrosine phosphatase, non-receptor type 1 Starlite/ChEMBL References

Predicted pathogen targets for this compound

By orthology
Species Potential target Known druggable target/s Ortholog Group
Schistosoma japonicum ko:K05696 protein tyrosine phosphatase, non-receptor type 1, putative Get druggable targets OG5_133865 All targets in OG5_133865
Schistosoma mansoni protein tyrosine phosphatase non-receptor type nt1 Get druggable targets OG5_133865 All targets in OG5_133865
Echinococcus granulosus tyrosine protein phosphatase non receptor type Get druggable targets OG5_133865 All targets in OG5_133865
Schistosoma japonicum expressed protein Get druggable targets OG5_133865 All targets in OG5_133865
Loa Loa (eye worm) protein-tyrosine phosphatase Get druggable targets OG5_133865 All targets in OG5_133865
Brugia malayi Protein-tyrosine phosphatase containing protein Get druggable targets OG5_133865 All targets in OG5_133865
Echinococcus multilocularis tyrosine protein phosphatase non receptor type Get druggable targets OG5_133865 All targets in OG5_133865
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 multilocularis glycogen phosphorylase 0.0482 1 1
Trichomonas vaginalis glycogen phosphorylase, putative 0.0482 1 0.5
Schistosoma mansoni glycogen phosphorylase 0.0482 1 1
Echinococcus granulosus Glycosyl transferase family 35 0.0482 1 1
Onchocerca volvulus Glycogen phosphorylase homolog 0.0482 1 0.5
Schistosoma mansoni glycogen phosphorylase 0.0482 1 1
Entamoeba histolytica glycogen phosphorylase, putative 0.0482 1 0.5
Chlamydia trachomatis glycogen phosphorylase 0.0482 1 0.5
Entamoeba histolytica glycogen phosphorylase, putative 0.0482 1 0.5
Echinococcus granulosus glycogen phosphorylase 0.0482 1 1
Loa Loa (eye worm) glycogen phosphorylase 0.0482 1 1
Giardia lamblia Glycogen phosphorylase 0.0482 1 0.5
Trichomonas vaginalis glycogen phosphorylase, putative 0.0482 1 0.5
Echinococcus granulosus glycogen phosphorylase 0.0482 1 1
Echinococcus multilocularis Glycosyl transferase, family 35 0.0482 1 1
Echinococcus multilocularis glycogen phosphorylase 0.0482 1 1

Activities

Activity type Activity value Assay description Source Reference
Control (functional) = 171 % Inhibition of PrPC polymerization by PrP-res at 100 uM ChEMBL. 15481988
Control (functional) = 171 % Inhibition of PrPC polymerization by PrP-res at 100 uM ChEMBL. 15481988
IC50 (binding) = 18.54 uM Inhibition of PTP1B (unknown origin) using pNPP as substrate ChEMBL. 24684845
Inhibition (functional) -ve 0 Inhibition of PrP-res formation in SMB (Scrapie mouse brain) cells at 10 uM ChEMBL. 15481988
Inhibition (binding) = 62.75 % Inhibition of PTP1B (unknown origin) using pNPP as substrate at 20 ug/ml ChEMBL. 24684845

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

2 literature references were collected for this gene.

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