Detailed information for compound 1772096

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 296.152 | Formula: C13H11Cl2N3O
  • H donors: 2 H acceptors: 2 LogP: 3.26 Rotable bonds: 4
    Rule of 5 violations (Lipinski): 1
  • SMILES: CNc1nccc(c1)NC(=O)c1c(Cl)cccc1Cl
  • InChi: 1S/C13H11Cl2N3O/c1-16-11-7-8(5-6-17-11)18-13(19)12-9(14)3-2-4-10(12)15/h2-7H,1H3,(H2,16,17,18,19)
  • InChiKey: IAXCYABTSAPPTJ-UHFFFAOYSA-N  

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 Janus kinase 1 Starlite/ChEMBL References
Homo sapiens tyrosine kinase 2 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
No druggable targets predicted by sequence similarity

Obtained from network model

Ranking Plot


Putative Targets List


Species Potential target Raw Global Species
Schistosoma mansoni kinase 0.0202 0.0215 0.0215
Trypanosoma brucei protein kinase, putative 0.0035 0 0.5
Trypanosoma cruzi STE/STE11 serine/threonine-protein kinase, putative 0.0035 0 0.5
Toxoplasma gondii calcium dependent protein kinase CDPK8 0.0035 0 0.5
Trypanosoma brucei STE/STE11 serine/threonine-protein kinase, putative 0.0035 0 0.5
Onchocerca volvulus Kinase homolog 0.0202 0.0215 0.5
Echinococcus granulosus dual specificity mitogen activated protein 0.7794 1 1
Loa Loa (eye worm) STE/STE7/MEK7 protein kinase 0.7794 1 1
Echinococcus granulosus dual specificity mitogen activated protein 0.0202 0.0215 0.0215
Entamoeba histolytica protein kinase domain containing protein 0.0035 0 0.5
Echinococcus multilocularis dual specificity mitogen activated protein 0.7794 1 1
Loa Loa (eye worm) STE/STE7/MEK7 protein kinase 0.7794 1 1
Echinococcus multilocularis dual specificity mitogen activated protein 0.0202 0.0215 0.0215
Schistosoma mansoni protein kinase 0.7794 1 1
Plasmodium falciparum protein kinase, putative 0.0035 0 0.5
Leishmania major protein kinase, putative 0.0035 0 0.5
Trypanosoma cruzi STE/STE11 serine/threonine-protein kinase, putative 0.0035 0 0.5

Activities

Activity type Activity value Assay description Source Reference
Ki (binding) = 1.5 uM Inhibition of TYK2 (unknown origin) using 5-carboxyfluorescein-VALVDGYFRLTT-NH2 as substrate ChEMBL. 23867602
Ki (binding) > 3.5 uM Inhibition of JAK1 (unknown origin) ChEMBL. 23867602

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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