Detailed information for compound 1836905

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 381.395 | Formula: C16H10F3N3OS2
  • H donors: 1 H acceptors: 3 LogP: 4.82 Rotable bonds: 6
    Rule of 5 violations (Lipinski): 1
  • SMILES: O=C(c1ccccc1)Nc1nnc(s1)Sc1ccc(cc1)C(F)(F)F
  • InChi: 1S/C16H10F3N3OS2/c17-16(18,19)11-6-8-12(9-7-11)24-15-22-21-14(25-15)20-13(23)10-4-2-1-3-5-10/h1-9H,(H,20,21,23)
  • InChiKey: OJVFLGZUJPYQRT-UHFFFAOYSA-N  


Substructure search Similarity search

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 Guanine nucleotide-binding protein G(s) subunit alpha (Adenylate cyclase-stimulating G alpha protein) 0.0054 0.338 0.6574
Onchocerca volvulus Eukaryotic initiation factor 4A homolog 0.0077 0.5142 0.5
Trichomonas vaginalis DEAD box ATP-dependent RNA helicase, putative 0.0077 0.5142 0.5
Brugia malayi GTP-binding regulatory protein Gs alpha-S chain, putative 0.0054 0.338 0.338
Echinococcus granulosus guanine nucleotide binding protein Gs subunit 0.0054 0.338 0.6574
Leishmania major eukaryotic initiation factor 4a, putative 0.0077 0.5142 0.5
Echinococcus multilocularis eukaryotic initiation factor 4A 0.0077 0.5142 1
Schistosoma mansoni Guanine nucleotide-binding protein G(s) subunit alpha (Adenylate cyclase-stimulating G alpha protein) 0.0054 0.338 0.6574
Loa Loa (eye worm) GTP-binding regulatory protein Gs alpha-S chain 0.0054 0.338 0.338
Trypanosoma cruzi Eukaryotic initiation factor 4A-1 0.0077 0.5142 0.5
Leishmania major eukaryotic initiation factor 4a, putative 0.0077 0.5142 0.5
Schistosoma mansoni Guanine nucleotide-binding protein G(s) subunit alpha (Adenylate cyclase-stimulating G alpha protein) 0.0054 0.338 0.6574
Loa Loa (eye worm) hypothetical protein 0.0077 0.5142 0.5142
Trypanosoma cruzi Eukaryotic initiation factor 4A-1 0.0077 0.5142 0.5
Echinococcus multilocularis eukaryotic initiation factor 4A III 0.0077 0.5142 1
Plasmodium vivax RNA helicase-1, putative 0.0077 0.5142 0.5
Entamoeba histolytica DEAD/DEAH box helicase, putative 0.0077 0.5142 0.5
Brugia malayi eukaryotic initiation factor 4A 0.0077 0.5142 0.5142
Toxoplasma gondii eukaryotic initiation factor-4A, putative 0.0077 0.5142 0.5
Echinococcus multilocularis guanine nucleotide binding protein G(s) subunit 0.0054 0.338 0.6574
Schistosoma mansoni DEAD box ATP-dependent RNA helicase 0.0077 0.5142 1
Echinococcus granulosus eukaryotic initiation factor 4A III 0.0077 0.5142 1
Plasmodium falciparum eukaryotic initiation factor 4A 0.0077 0.5142 0.5
Echinococcus granulosus guanine nucleotide binding protein Gs subunit 0.0054 0.338 0.6574
Giardia lamblia Translation initiation factor eIF-4A, putative 0.0077 0.5142 0.5
Treponema pallidum ATP-dependent RNA helicase 0.0077 0.5142 0.5
Echinococcus granulosus eukaryotic initiation factor 4A 0.0077 0.5142 1
Trichomonas vaginalis DEAD box ATP-dependent RNA helicase, putative 0.0077 0.5142 0.5
Echinococcus multilocularis guanine nucleotide binding protein G(s) subunit 0.0054 0.338 0.6574
Trypanosoma brucei Eukaryotic initiation factor 4A-1 0.0077 0.5142 0.5
Mycobacterium tuberculosis Probable cold-shock DeaD-box protein A homolog DeaD (ATP-dependent RNA helicase dead homolog) 0.0077 0.5142 0.5
Trichomonas vaginalis DEAD box ATP-dependent RNA helicase, putative 0.0077 0.5142 0.5
Schistosoma mansoni DEAD box ATP-dependent RNA helicase 0.0077 0.5142 1

Activities

Activity type Activity value Assay description Source Reference
Activity (ADMET) Toxicity in Mus musculus Swiss albino (mouse) assessed as mortality at 25 mg/kg, po ChEMBL. No reference
Activity (functional) = -29.78 % Antidepressant activity in Mus musculus Swiss albino (mouse) assessed as duration of immobility at 25 mg/kg, ip measured after 1 hr by forced swim test test relative to pretreatment ChEMBL. No reference
Activity (functional) = 0 % Anticonvulsant activity against maximal electroshock-induced seizures in Mus musculus Swiss albino (mouse) assessed as animals protected at 25 mg/kg ChEMBL. No reference
Activity (functional) = 46.93 % Antidepressant activity in Mus musculus Swiss albino (mouse) assessed as as increase in mobile phase at 25 mg/kg, ip measured after 1 hr by tail suspension test ChEMBL. No reference
TIME (functional) = 6.18 s Anticonvulsant activity against maximal electroshock-induced seizures in Mus musculus Swiss albino (mouse) assessed as time duration of tonic limb extensor at 25 mg/kg ChEMBL. No reference
TIME (functional) = 29.86 s Anxiolytic activity in Mus musculus Swiss albino (mouse) assessed as time spent in open arm by elevated plus maze test ChEMBL. No reference
TIME (functional) = 81.74 s Anticonvulsant activity against pentylenetetrazole-induced seizures in Mus musculus Swiss albino (mouse) assessed as onset of seizures at 25 mg/kg, po administered 1 hr prior challenge ChEMBL. No reference
TIME (functional) = 163 s Anxiolytic activity in Mus musculus Swiss albino (mouse) assessed as time spent in light chamber at 25 mg/kg by light-dark box test ChEMBL. No reference

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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