Detailed information for compound 42011

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 322.2 | Formula: C14H16BrN3O
  • H donors: 1 H acceptors: 2 LogP: 3.7 Rotable bonds: 4
    Rule of 5 violations (Lipinski): 1
  • SMILES: CCCn1nc(c(c1N)C(=O)c1ccccc1Br)C
  • InChi: 1S/C14H16BrN3O/c1-3-8-18-14(16)12(9(2)17-18)13(19)10-6-4-5-7-11(10)15/h4-7H,3,8,16H2,1-2H3
  • InChiKey: VRCPYBDTSZIGPO-UHFFFAOYSA-N  

Network

Hover on a compound node to display the structore

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 protein farnesyltransferase, putative 0.0788 0.4234 0.0588
Trypanosoma cruzi glutathione-S-transferase/glutaredoxin, putative 0.1276 1 1
Trichomonas vaginalis geranylgeranyl transferase type beta subunit, putative 0.0788 0.4234 1
Trypanosoma brucei Prostaglandin E synthase 0.1276 1 1
Loa Loa (eye worm) hypothetical protein 0.1276 1 1
Trypanosoma brucei protein farnesyltransferase beta subunit 0.0788 0.4234 0.0588
Plasmodium vivax farnesyltransferase beta subunit, putative 0.0788 0.4234 1
Echinococcus multilocularis protein farnesyltransferase subunit beta 0.0788 0.4234 1
Trichomonas vaginalis geranylgeranyl transferase type I beta subunit, putative 0.0788 0.4234 1
Plasmodium vivax conserved Plasmodium protein, unknown function 0.0575 0.1703 0.4022
Trichomonas vaginalis geranylgeranyl transferase type II beta subunit, putative 0.0788 0.4234 1
Trichomonas vaginalis type I geranylgeranyltransferase beta subunit, putative 0.0788 0.4234 1
Plasmodium falciparum protein farnesyltransferase subunit beta 0.0788 0.4234 1
Trichomonas vaginalis geranylgeranyl transferase type II beta subunit, putative 0.0788 0.4234 1
Loa Loa (eye worm) prenyltransferase and squalene oxidase repeat family protein 0.0788 0.4234 0.4234
Schistosoma mansoni protein farnesyltransferase subunit beta 0.0788 0.4234 1
Leishmania major farnesyltransferase beta subunit 0.0788 0.4234 0.3339
Leishmania major glutathione-S-transferase/glutaredoxin, putative 0.1276 1 1
Giardia lamblia Prenyltransferase 0.0788 0.4234 1
Toxoplasma gondii prostaglandin-E synthase 0.1276 1 1
Entamoeba histolytica protein farnesyltransferase beta subunit, putative 0.0788 0.4234 1
Echinococcus granulosus protein farnesyltransferase subunit beta 0.0788 0.4234 1
Trypanosoma cruzi glutathione-S-transferase/glutaredoxin, putative 0.1276 1 1
Trypanosoma cruzi protein farnesyltransferase, putative 0.0788 0.4234 0.0588
Brugia malayi Prenyltransferase and squalene oxidase repeat family protein 0.0788 0.4234 0.4234
Mycobacterium tuberculosis Halimadienyl diphosphate synthase 0.0758 0.3874 0.5
Trichomonas vaginalis geranylgeranyl transferase type II beta subunit, putative 0.0788 0.4234 1
Onchocerca volvulus 0.1276 1 0.5

Activities

Activity type Activity value Assay description Source Reference
Activity (functional) = 8 mg kg-1 Central nervous system depressant activity ChEMBL. 6492070
Activity (functional) = 8 mg kg-1 Central nervous system depressant activity ChEMBL. 6492070
Activity (functional) = 32 mg kg-1 Evaluated for anticonvulsant activity to protect all rats tested, when administered subcutaneously ChEMBL. 6492070

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.

If you have references for this compound, please enter them in a user comment (below) or Contact us.