Detailed information for compound 1690862

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 322.285 | Formula: C15H13F3N4O
  • H donors: 0 H acceptors: 3 LogP: 3.06 Rotable bonds: 5
    Rule of 5 violations (Lipinski): 1
  • SMILES: CCOc1ncncc1c1cccc2c1ncn2CC(F)(F)F
  • InChi: 1S/C15H13F3N4O/c1-2-23-14-11(6-19-8-20-14)10-4-3-5-12-13(10)21-9-22(12)7-15(16,17)18/h3-6,8-9H,2,7H2,1H3
  • InChiKey: MYGRSEGEONREBO-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 cytochrome P450, family 17, subfamily A, polypeptide 1 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
Species Potential target Known druggable target Length Alignment span Identity
Brugia malayi Cytochrome P450 family protein cytochrome P450, family 17, subfamily A, polypeptide 1 508 aa 468 aa 25.2 %

Obtained from network model

Ranking Plot


Putative Targets List


Species Potential target Raw Global Species
Loa Loa (eye worm) glutamate receptor 0.0044 0.0049 0.7241
Schistosoma mansoni metabotropic glutamate receptor 0.0037 0.0036 0.5392
Brugia malayi Metabotropic glutamate receptor precursor. 0.0044 0.0049 1
Loa Loa (eye worm) hypothetical protein 0.0054 0.0068 1
Mycobacterium tuberculosis Transcriptional regulatory repressor protein (TetR-family) EthR 0.537 1 0.5
Schistosoma mansoni metabotropic glutamate receptor 2 3 (mglur group 2) 0.005 0.0061 1
Mycobacterium ulcerans AcrR family transcriptional regulator 0.537 1 0.5
Mycobacterium ulcerans TetR family transcriptional regulator 0.537 1 0.5
Echinococcus multilocularis metabotropic glutamate receptor 5 0.0054 0.0068 1
Mycobacterium ulcerans transcriptional regulator 0.537 1 0.5
Echinococcus granulosus metabotropic glutamate receptor 5 0.0054 0.0068 1
Brugia malayi metabotropic glutamate receptor subtype 5a (mGluR5a), putative 0.004 0.0042 0.8166

Activities

Activity type Activity value Assay description Source Reference
IC50 (binding) = 135 nM Inhibition of CYP17 transfected in human HEK2 cells using [3H]pregnenolone as substrate by SPA assay ChEMBL. 24900520
IC50 (binding) = 135 nM SPA Assay BINDINGDB. 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

1 literature reference was collected for this gene.

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