Detailed information for compound 948577

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 275.694 | Formula: C12H10ClN5O
  • H donors: 2 H acceptors: 3 LogP: 2.91 Rotable bonds: 3
    Rule of 5 violations (Lipinski): 1
  • SMILES: COc1ccccc1Nc1nc(Cl)nc2c1nc[nH]2
  • InChi: 1S/C12H10ClN5O/c1-19-8-5-3-2-4-7(8)16-11-9-10(15-6-14-9)17-12(13)18-11/h2-6H,1H3,(H2,14,15,16,17,18)
  • InChiKey: UDSYDQBRCXFWHS-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
Trypanosoma cruzi hypothetical protein, conserved 0.0056 0.0492 0.0607
Loa Loa (eye worm) protein-tyrosine phosphatase 0.0351 1 1
Trypanosoma cruzi mitochondrial DNA polymerase beta-PAK, putative 0.0138 0.3136 0.3871
Leishmania major mitochondrial DNA polymerase beta-PAK, putative 0.0138 0.3136 0.3475
Trypanosoma cruzi mitochondrial DNA polymerase beta-PAK, putative 0.005 0.029 0.0358
Trichomonas vaginalis low molecular weight protein-tyrosine-phosphatase, putative 0.0182 0.457 1
Echinococcus granulosus tyrosine protein phosphatase non receptor type 0.0351 1 0.5
Trypanosoma cruzi hypothetical protein, conserved 0.0056 0.0492 0.0607
Trypanosoma brucei mitochondrial DNA polymerase beta-PAK 0.0138 0.3136 0.3871
Trichomonas vaginalis low molecular weight protein tyrosine phosphatase, putative 0.0182 0.457 1
Trichomonas vaginalis low molecular weight protein-tyrosine-phosphatase, putative 0.0182 0.457 1
Onchocerca volvulus 0.0182 0.457 0.5
Trypanosoma brucei mitochondrial DNA polymerase beta 0.0292 0.8102 1
Entamoeba histolytica protein tyrosine phosphatase, putative 0.0182 0.457 0.5
Trypanosoma cruzi mitochondrial DNA polymerase beta, putative 0.0292 0.8102 1
Trypanosoma brucei low molecular weight protein tyrosine phosphatase, putative 0.0056 0.0492 0.0607
Giardia lamblia Low molecular weight protein-tyrosine-phosphatase 0.0182 0.457 0.5
Entamoeba histolytica protein tyrosine phosphatase, putative 0.0182 0.457 0.5
Trichomonas vaginalis low molecular weight protein tyrosine phosphatase, putative 0.0182 0.457 1
Mycobacterium ulcerans phosphotyrosine protein phosphatase PtpA 0.0182 0.457 1
Trichomonas vaginalis low molecular weight protein-tyrosine-phosphatase, putative 0.0182 0.457 1
Trichomonas vaginalis low molecular weight protein tyrosine phosphatase, putative 0.0182 0.457 1
Toxoplasma gondii hypothetical protein 0.0047 0.0195 0.5
Schistosoma mansoni protein tyrosine phosphatase non-receptor type nt1 0.0351 1 0.5
Mycobacterium tuberculosis Conserved hypothetical protein 0.0154 0.364 1
Trypanosoma cruzi mitochondrial DNA polymerase beta, putative 0.0292 0.8102 1
Leishmania major mitochondrial DNA polymerase beta 0.0292 0.8102 1
Echinococcus multilocularis tyrosine protein phosphatase non receptor type 0.0351 1 0.5

Activities

Activity type Activity value Assay description Source Reference
EC50 (binding) = 33 uM Activation of Arabidopsis thaliana AHK3 receptor expressed in Escherichia coli KMI001 by beta-galactosidase activity ChEMBL. 18818088
IC50 (binding) > 100 uM Inhibition of sArabidopsis thaliana CKX2 expressed in Saccharomyces cerevisiae 23344c ura- ChEMBL. 18818088

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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