Detailed information for compound 931014

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 339.32 | Formula: C18H14FN3O3
  • H donors: 3 H acceptors: 3 LogP: 2.42 Rotable bonds: 5
    Rule of 5 violations (Lipinski): 1
  • SMILES: Fc1ccc(cc1)CNC(=O)c1nc([nH]c(=O)c1O)c1ccccc1
  • InChi: 1S/C18H14FN3O3/c19-13-8-6-11(7-9-13)10-20-17(24)14-15(23)18(25)22-16(21-14)12-4-2-1-3-5-12/h1-9,23H,10H2,(H,20,24)(H,21,22,25)
  • InChiKey: RBJOSAOJJYPLJG-UHFFFAOYSA-N  


Substructure search Similarity search

Network

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Synonyms

No synonyms found for this compound

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Human immunodeficiency virus 1 Integrase Starlite/ChEMBL References

Predicted pathogen targets for this compound

By orthology
Species Potential target Known druggable target/s Ortholog Group
Plasmodium yoelii integrase-related Get druggable targets OG5_139608 All targets in OG5_139608
Trypanosoma congolense RNA helicase, putative Get druggable targets OG5_139608 All targets in OG5_139608
Schistosoma mansoni hypothetical protein Get druggable targets OG5_139608 All targets in OG5_139608
Trypanosoma brucei RNA helicase, putative Get druggable targets OG5_139608 All targets in OG5_139608
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
Mycobacterium ulcerans linoleoyl-CoA desaturase, DesA3_2 0.0316 0 0.5
Toxoplasma gondii sphingolipid delta 4 desaturase/c-4 hydroxylase protein des2 family protein 0.0316 0 0.5
Trypanosoma cruzi fatty acid desaturase, putative 0.3447 0.9083 0.9083
Plasmodium falciparum stearoyl-CoA desaturase 0.3447 0.9083 0.5
Echinococcus multilocularis Peptidase M, neutral zinc metallopeptidases, zinc binding site 0.0316 0 0.5
Mycobacterium tuberculosis Possible electron transfer protein FdxB 0.0316 0 0.5
Mycobacterium tuberculosis Probable transmembrane alkane 1-monooxygenase AlkB (alkane 1-hydroxylase) (lauric acid omega-hydroxylase) (omega-hydroxylase) (f 0.0316 0 0.5
Brugia malayi acyl-CoA desaturase 0.3447 0.9083 1
Mycobacterium ulcerans hypothetical protein 0.0316 0 0.5
Onchocerca volvulus 0.3763 1 1
Leishmania major fatty-acid desaturase, putative 0.3763 1 1
Loa Loa (eye worm) acyl-CoA desaturase 0.3447 0.9083 1
Onchocerca volvulus 0.3763 1 1
Mycobacterium ulcerans linoleoyl-CoA desaturase, DesA3 0.0316 0 0.5
Trypanosoma brucei fatty acid desaturase, putative 0.3763 1 1
Echinococcus multilocularis Fatty acid desaturase, type 1 0.0316 0 0.5
Mycobacterium ulcerans transmembrane alkane 1-monooxygenase AlkB 0.0316 0 0.5
Schistosoma mansoni fatty acid desaturase 0.0316 0 0.5
Mycobacterium ulcerans electron transfer protein FdxB 0.0316 0 0.5
Mycobacterium tuberculosis Probable conserved membrane protein 0.0316 0 0.5
Trypanosoma cruzi fatty acid desaturase, putative 0.3763 1 1
Echinococcus granulosus Sphingolipid delta4 desaturase DES1 0.0316 0 0.5
Plasmodium vivax stearoyl-CoA desaturase (acyl-CoA desaturase, faty acid desaturase), putative 0.3447 0.9083 0.5
Trypanosoma cruzi fatty acid desaturase, putative 0.3447 0.9083 0.9083
Mycobacterium ulcerans linoleoyl-CoA desaturase, DesA3 0.0316 0 0.5
Echinococcus multilocularis Peptidase M, neutral zinc metallopeptidases, zinc binding site 0.0316 0 0.5
Echinococcus granulosus Fatty acid desaturase type 1 0.0316 0 0.5
Mycobacterium ulcerans hypothetical protein 0.0316 0 0.5

Activities

Activity type Activity value Assay description Source Reference
IC50 (binding) = 1 uM Inhibition of HIV1 recombinant wild type integrase strand transfer activity by gel-based assay ChEMBL. 25150089
IC50 (binding) = 17 uM Inhibition of HIV1 recombinant wild type integrase 3'-processing activity by gel-based assays ChEMBL. 25150089

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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