Detailed information for compound 1164926

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 294.348 | Formula: C17H12NO2S+
  • H donors: 1 H acceptors: 2 LogP: 4.29 Rotable bonds: 1
    Rule of 5 violations (Lipinski): 1
  • SMILES: OC(=O)c1ccc2c(c1)cc1c([n+]2C)c2c(s1)cccc2
  • InChi: 1S/C17H11NO2S/c1-18-13-7-6-10(17(19)20)8-11(13)9-15-16(18)12-4-2-3-5-14(12)21-15/h2-9H,1H3/p+1
  • InChiKey: FEQVLPHSGNPJAP-UHFFFAOYSA-O  

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
Entamoeba histolytica hypothetical protein 0.0221 0.2585 1
Echinococcus granulosus flap endonuclease 1 0.0052 0.0479 0.1769
Brugia malayi hypothetical protein 0.0785 0.9617 1
Schistosoma mansoni transcription factor LCR-F1 0.0221 0.2585 1
Onchocerca volvulus 0.0785 0.9617 0.5
Brugia malayi Flap endonuclease-1 0.0052 0.0479 0.0498
Trypanosoma cruzi flap endonuclease-1 (FEN-1), putative 0.0052 0.0479 0.5
Brugia malayi Calcitonin receptor-like protein seb-1 0.005 0.0453 0.0472
Schistosoma mansoni flap endonuclease-1 0.0047 0.0416 0.1525
Loa Loa (eye worm) MH2 domain-containing protein 0.0366 0.4389 0.4564
Schistosoma mansoni smad 0.0025 0.0139 0.0441
Brugia malayi calcium-independent alpha-latrotoxin receptor 2, putative 0.0016 0.0026 0.0027
Loa Loa (eye worm) MH1 domain-containing protein 0.0025 0.0139 0.0144
Schistosoma mansoni TGF-beta signal transducer Smad2 0.0025 0.0139 0.0441
Entamoeba histolytica hypothetical protein 0.0221 0.2585 1
Brugia malayi MH1 domain containing protein 0.0025 0.0139 0.0144
Schistosoma mansoni Smad4 0.0025 0.0139 0.0441
Giardia lamblia Flap structure-specific endonuclease 0.0052 0.0479 0.5
Schistosoma mansoni smad1 5 8 and 0.0025 0.0139 0.0441
Schistosoma mansoni hypothetical protein 0.0034 0.0256 0.0897
Brugia malayi MH2 domain containing protein 0.0025 0.0139 0.0144
Loa Loa (eye worm) flap endonuclease-1 0.0052 0.0479 0.0498
Plasmodium falciparum flap endonuclease 1 0.0052 0.0479 0.5
Toxoplasma gondii flap structure-specific endonuclease 1, putative 0.0052 0.0479 0.5
Schistosoma mansoni smad1 5 8 and 0.0025 0.0139 0.0441
Brugia malayi Latrophilin receptor protein 2 0.0016 0.0026 0.0027
Brugia malayi latrophilin 2 splice variant baaae 0.0034 0.0256 0.0266
Schistosoma mansoni smad1 5 8 and 0.0025 0.0139 0.0441
Echinococcus granulosus Smad4 0.0025 0.0139 0.0441
Trichomonas vaginalis flap endonuclease-1, putative 0.0052 0.0479 0.5
Entamoeba histolytica hypothetical protein 0.0221 0.2585 1
Plasmodium vivax flap endonuclease 1, putative 0.0052 0.0479 0.5
Brugia malayi Smad1 0.0025 0.0139 0.0144
Echinococcus multilocularis Smad4 0.0025 0.0139 0.0113
Brugia malayi MH2 domain containing protein 0.0366 0.4389 0.4564
Loa Loa (eye worm) latrophilin receptor protein 2 0.0016 0.0026 0.0027
Echinococcus multilocularis Basic leucine zipper (bZIP) transcription 0.0221 0.2585 0.2566
Echinococcus granulosus mothers against decapentaplegic 5 0.0025 0.0139 0.0441
Loa Loa (eye worm) transcription factor SMAD2 0.0366 0.4389 0.4564
Loa Loa (eye worm) hypothetical protein 0.0785 0.9617 1
Leishmania major flap endonuclease-1 (FEN-1), putative 0.0052 0.0479 0.5
Loa Loa (eye worm) hypothetical protein 0.005 0.0453 0.0472
Echinococcus granulosus smad 0.0025 0.0139 0.0441
Echinococcus multilocularis TGF beta signal transducer SmadC 0.0025 0.0139 0.0113
Echinococcus multilocularis flap endonuclease 1 0.0052 0.0479 0.0454
Brugia malayi hypothetical protein 0.0221 0.2585 0.2688
Brugia malayi MH2 domain containing protein 0.0025 0.0139 0.0144
Schistosoma mansoni hypothetical protein 0.0221 0.2585 1
Brugia malayi MH1 domain containing protein 0.0025 0.0139 0.0144
Brugia malayi Corticotropin releasing factor receptor 2 precursor, putative 0.005 0.0453 0.0472
Echinococcus multilocularis mothers against decapentaplegic 5 0.0025 0.0139 0.0113
Loa Loa (eye worm) MH2 domain-containing protein 0.0025 0.0139 0.0144
Loa Loa (eye worm) hypothetical protein 0.0016 0.0026 0.0027
Loa Loa (eye worm) pigment dispersing factor receptor c 0.005 0.0453 0.0472
Echinococcus granulosus Basic leucine zipper bZIP transcription 0.0221 0.2585 1
Entamoeba histolytica hypothetical protein 0.0221 0.2585 1
Trypanosoma brucei flap endonuclease-1 (FEN-1), putative 0.0052 0.0479 0.5
Loa Loa (eye worm) Smad1 0.0025 0.0139 0.0144
Echinococcus granulosus TGF beta signal transducer SmadC 0.0025 0.0139 0.0441
Echinococcus multilocularis smad 0.0025 0.0139 0.0113
Loa Loa (eye worm) hypothetical protein 0.0034 0.0256 0.0266

Activities

No activities found for this compound.

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

No literature references available for this target.

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