Detailed information for compound 1026103

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 300.332 | Formula: C15H12N2O3S
  • H donors: 0 H acceptors: 3 LogP: 3.34 Rotable bonds: 5
    Rule of 5 violations (Lipinski): 1
  • SMILES: CCOC(=O)c1nn(c2c1cccc2)C(=O)c1cscc1
  • InChi: 1S/C15H12N2O3S/c1-2-20-15(19)13-11-5-3-4-6-12(11)17(16-13)14(18)10-7-8-21-9-10/h3-9H,2H2,1H3
  • InChiKey: OTCHEEHVDZYGKM-UHFFFAOYSA-N  


Substructure search Similarity search

Network

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Synonyms

No synonyms found for this compound

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Homo sapiens elastase, neutrophil expressed Starlite/ChEMBL References

Predicted pathogen targets for this compound

By orthology
No druggable targets predicted by orthology data
By sequence similarity to non orthologous known druggable targets
Species Potential target Known druggable target Length Alignment span Identity
Echinococcus granulosus transmembrane protease serine 3 elastase, neutrophil expressed 267 aa 236 aa 27.5 %
Obtained from network model

Ranking Plot

Putative Targets List

Species Potential target Raw Global Species
Schistosoma mansoni hypothetical protein 0.0035 1 0.5
Entamoeba histolytica hypothetical protein 0.0035 1 0.5
Plasmodium falciparum ataxin-2 like protein, putative 0.0027 0.5688 0.5
Trypanosoma cruzi PAB1-binding protein , putative 0.0027 0.5688 0.5
Plasmodium vivax ataxin-2 like protein, putative 0.0027 0.5688 0.5
Toxoplasma gondii LsmAD domain-containing protein 0.0027 0.5688 0.5
Loa Loa (eye worm) hypothetical protein 0.0027 0.5688 0.5
Trypanosoma cruzi PAB1-binding protein , putative 0.0027 0.5688 0.5
Echinococcus multilocularis Basic leucine zipper (bZIP) transcription 0.0035 1 0.5
Schistosoma mansoni transcription factor LCR-F1 0.0035 1 0.5
Entamoeba histolytica hypothetical protein 0.0035 1 0.5
Echinococcus granulosus Basic leucine zipper bZIP transcription 0.0035 1 0.5
Plasmodium falciparum ataxin-2 like protein, putative 0.0027 0.5688 0.5
Entamoeba histolytica hypothetical protein 0.0035 1 0.5
Entamoeba histolytica hypothetical protein 0.0035 1 0.5
Brugia malayi hypothetical protein 0.0027 0.5688 0.5688
Leishmania major hypothetical protein, conserved 0.0027 0.5688 0.5
Trypanosoma brucei PAB1-binding protein , putative 0.0027 0.5688 0.5

Activities

Activity type Activity value Assay description Source Reference
IC50 (binding) = 0.93 uM Inhibition of human neutrophil elastase using N-methylsuccinyl-Ala-Ala-Pro-Val-7-amino-4-methyl-coumarin as substrate measured every 30 secs for 10 mins by fluorescence microplate reader ChEMBL. 21741848

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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