Detailed information for compound 1905370

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 376.405 | Formula: C22H20N2O4
  • H donors: 3 H acceptors: 4 LogP: 3.69 Rotable bonds: 9
    Rule of 5 violations (Lipinski): 1
  • SMILES: OC(=O)CCCNC(=O)c1ccccc1NC(=O)c1cccc2c1cccc2
  • InChi: 1S/C22H20N2O4/c25-20(26)13-6-14-23-21(27)18-10-3-4-12-19(18)24-22(28)17-11-5-8-15-7-1-2-9-16(15)17/h1-5,7-12H,6,13-14H2,(H,23,27)(H,24,28)(H,25,26)
  • InChiKey: WYKOTVVGSDPHLD-UHFFFAOYSA-N  

Network

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Synonyms

No synonyms found for this compound

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

Activities

Activity type Activity value Assay description Source Reference
Activity (binding) Transactivation of human FXR expressed in human HeLa cells at 30 uM incubated for 24 hrs by luciferase reporter gene assay ChEMBL. 25583100
Activity (binding) Transactivation of Gal4-tagged PPARdelta ligand binding domain (unknown origin) expressed in COS7 cells at 30 uM measured after overnight incubation by luciferase reporter gene assay ChEMBL. 25583100
EC50 (binding) = 41 uM Transactivation of Gal4-tagged PPARgamma ligand binding domain (unknown origin) expressed in COS7 cells measured after overnight incubation by luciferase reporter gene assay ChEMBL. 25583100
max activation (binding) Agonist activity at human FXR expressed in human HeLa cells assessed as transactivation at 30 uM after 24 hrs by luciferase reporter gene assay relative to GW4064 ChEMBL. 24685112
max activation (binding) = 12 % Transactivation of Gal4-tagged PPARalpha ligand binding domain (unknown origin) expressed in COS7 cells at 10 uM measured after overnight incubation by luciferase reporter gene assay ChEMBL. 25583100
max activation (binding) = 397 % Transactivation of Gal4-tagged PPARgamma ligand binding domain (unknown origin) expressed in COS7 cells measured after overnight incubation by luciferase reporter gene assay relative to piaglitazone ChEMBL. 25583100

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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