Detailed information for compound 14373

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 364.378 | Formula: C18H12N4O3S
  • H donors: 2 H acceptors: 5 LogP: 2.66 Rotable bonds: 4
    Rule of 5 violations (Lipinski): 1
  • SMILES: O=C(c1c(O)c2cccnc2n(c1=O)c1ccccc1)Nc1nccs1
  • InChi: 1S/C18H12N4O3S/c23-14-12-7-4-8-19-15(12)22(11-5-2-1-3-6-11)17(25)13(14)16(24)21-18-20-9-10-26-18/h1-10,23H,(H,20,21,24)
  • InChiKey: SRVMZAXXKZQODG-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
Brugia malayi Nuclear hormone receptor family member nhr-31 0.005 0.5 0.5
Echinococcus multilocularis COUP TF:Svp nuclear hormone receptor 0.005 0.5 0.5
Loa Loa (eye worm) hypothetical protein 0.005 0.5 0.5
Schistosoma mansoni retinoic acid receptor RXR 0.005 0.5 0.5
Echinococcus multilocularis FTZ F1 nuclear receptor protein 0.005 0.5 0.5
Brugia malayi Nuclear hormone receptor family member nhr-25 0.005 0.5 0.5
Schistosoma mansoni thyroid hormone receptor 0.005 0.5 0.5
Onchocerca volvulus Protein ultraspiracle homolog 0.005 0.5 0.5
Loa Loa (eye worm) hypothetical protein 0.005 0.5 0.5
Loa Loa (eye worm) nuclear hormone receptor family member nhr-1 0.005 0.5 0.5
Echinococcus granulosus retinoic acid receptor rxr beta a 0.005 0.5 0.5
Brugia malayi Nuclear hormone receptor family member nhr-41 0.005 0.5 0.5
Loa Loa (eye worm) hypothetical protein 0.005 0.5 0.5
Loa Loa (eye worm) hypothetical protein 0.005 0.5 0.5
Schistosoma mansoni RAR-like nuclear receptor 0.005 0.5 0.5
Schistosoma mansoni thyroid hormone receptor 0.005 0.5 0.5
Loa Loa (eye worm) steroid hormone receptor 0.005 0.5 0.5
Brugia malayi Nuclear hormone receptor family member nhr-25 0.005 0.5 0.5
Echinococcus granulosus FTZ F1 nuclear receptor protein 0.005 0.5 0.5
Schistosoma mansoni coup transcription factor 0.005 0.5 0.5
Echinococcus granulosus COUP TF:Svp nuclear hormone receptor 0.005 0.5 0.5
Brugia malayi photoreceptor-specific nuclear receptor 0.005 0.5 0.5
Schistosoma mansoni retinoid-x-receptor (RXR) 0.005 0.5 0.5
Brugia malayi Nuclear hormone receptor family member nhr-49 0.005 0.5 0.5
Schistosoma mansoni steroid hormone receptor ad4bp 0.005 0.5 0.5
Loa Loa (eye worm) nuclear hormone receptor family member nhr-31 0.005 0.5 0.5
Onchocerca volvulus 0.005 0.5 0.5
Echinococcus granulosus hepatocyte nuclear factor 4 alpha 0.005 0.5 0.5
Brugia malayi Nuclear hormone receptor family member nhr-3 0.005 0.5 0.5
Onchocerca volvulus Bile acid receptor homolog 0.005 0.5 0.5
Echinococcus multilocularis hepatocyte nuclear factor 4 alpha 0.005 0.5 0.5
Echinococcus multilocularis Nuclear hormone receptor family member nhr 41 0.005 0.5 0.5
Brugia malayi nuclear hormone receptor 0.005 0.5 0.5
Brugia malayi steroid hormone receptor 0.005 0.5 0.5
Brugia malayi Nuclear hormone receptor family member nhr-40 0.005 0.5 0.5
Brugia malayi Nuclear hormone receptor family member nhr-1 0.005 0.5 0.5
Echinococcus multilocularis nuclear receptor 2DBD gamma 0.005 0.5 0.5
Echinococcus granulosus ecdysone induced protein 78C 0.005 0.5 0.5
Loa Loa (eye worm) nuclear Hormone Receptor family member 0.005 0.5 0.5
Schistosoma mansoni nuclear receptor 2DBD-gamma 0.005 0.5 0.5
Brugia malayi Ligand-binding domain of nuclear hormone receptor family protein 0.005 0.5 0.5
Loa Loa (eye worm) nuclear hormone receptor family member nhr-49 0.005 0.5 0.5
Loa Loa (eye worm) hypothetical protein 0.005 0.5 0.5
Schistosoma mansoni Tr4/Tr2 (homologue) 0.005 0.5 0.5
Brugia malayi Steroid receptor seven-up type 2 0.005 0.5 0.5
Brugia malayi Nuclear hormone receptor family member nhr-14 0.005 0.5 0.5
Brugia malayi Nuclear hormone receptor family member nhr-19 0.005 0.5 0.5
Schistosoma mansoni FTZ-F1 nuclear receptor-like protein 0.005 0.5 0.5
Schistosoma mansoni nuclear hormone receptor 0.005 0.5 0.5
Loa Loa (eye worm) hypothetical protein 0.005 0.5 0.5
Echinococcus granulosus nuclear receptor 2DBD gamma 0.005 0.5 0.5
Loa Loa (eye worm) hypothetical protein 0.005 0.5 0.5
Brugia malayi Nuclear hormone receptor-like 1 0.005 0.5 0.5
Schistosoma mansoni photoreceptor-specific nuclear receptor related 0.005 0.5 0.5
Echinococcus multilocularis ecdysone induced protein 78C 0.005 0.5 0.5
Onchocerca volvulus Steroid hormone receptor family member cnr14 homolog 0.005 0.5 0.5
Brugia malayi Nuclear hormone receptor family member nhr-19 0.005 0.5 0.5
Loa Loa (eye worm) nuclear hormone receptor family member nhr-40 0.005 0.5 0.5
Schistosoma mansoni nuclear hormone receptor nor-1/nor-2 0.005 0.5 0.5
Echinococcus multilocularis thyroid hormone receptor alpha 0.005 0.5 0.5
Loa Loa (eye worm) nuclear hormone receptor family member nhr-14 0.005 0.5 0.5
Echinococcus granulosus Nuclear hormone receptor family member nhr 41 0.005 0.5 0.5
Echinococcus granulosus FTZ F1 alpha 0.005 0.5 0.5
Echinococcus multilocularis nuclear receptor 2DBD gamma 0.005 0.5 0.5
Loa Loa (eye worm) hypothetical protein 0.005 0.5 0.5
Brugia malayi nuclear receptor NHR-88 0.005 0.5 0.5
Echinococcus multilocularis FTZ F1 alpha 0.005 0.5 0.5
Brugia malayi Ligand-binding domain of nuclear hormone receptor family protein 0.005 0.5 0.5
Loa Loa (eye worm) nuclear hormone receptor family member nhr-41 0.005 0.5 0.5
Echinococcus granulosus nuclear receptor 2DBD gamma 0.005 0.5 0.5

Activities

Activity type Activity value Assay description Source Reference
Inhibition (functional) = 2.5 % Inhibition of carrageenan-induced rat's paw edema (CPE) after peroral administration of 100 mg/kg dose. ChEMBL. 1552506
Inhibition (functional) = 4.6 % Inhibition of Zymosan-induced rat's paw edema(ZPE) after peroral administration of 100 mg/kg dose. ChEMBL. 1552506
Inhibition (functional) = 15.4 % Compound was tested for the inhibition of rat reversed passive Arthus pleurisy after peroral administration of 100 mg/kg dose at 3.77*10e6 no of cells with 3.86*10e6 cells of control ChEMBL. 1552506
Inhibition (functional) = 18.1 % Compound was tested for the inhibition of rat reversed passive Arthus pleurisy after peroral administration of 100 mg/kg dose at 0.64 mL of exudate volume with 0.79 mL of control (injected intrapleurally) ChEMBL. 1552506
Swelling (functional) = 66.3 % Antiinflammatory activity of the compound on Zymosan-induced rat's paw edema(ZPE) after peroral administration of 100 mg/kg dose with control swelling of 69.5% ChEMBL. 1552506
Swelling (functional) = 69.9 % Antiinflammatory activity of the compound on Carrageenan rat's paw edema(CPE) after peroral administration of 100 mg/kg dose with control swelling of 63.7% ChEMBL. 1552506

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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