Detailed information for compound 1768429

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 363.388 | Formula: C20H18FN5O
  • H donors: 0 H acceptors: 3 LogP: 3.55 Rotable bonds: 4
    Rule of 5 violations (Lipinski): 1
  • SMILES: COc1cc(ccc1n1cnc(c1)C)c1nn(c(n1)c1ccc(cc1)F)C
  • InChi: 1S/C20H18FN5O/c1-13-11-26(12-22-13)17-9-6-15(10-18(17)27-3)19-23-20(25(2)24-19)14-4-7-16(21)8-5-14/h4-12H,1-3H3
  • InChiKey: KUOHWTCUNBPJRP-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 APH1B gamma secretase subunit Starlite/ChEMBL References

Predicted pathogen targets for this compound

By orthology
Species Potential target Known druggable target/s Ortholog Group
Schistosoma mansoni gamma-secretase subunit aph-1 Get druggable targets OG5_130831 All targets in OG5_130831
Echinococcus granulosus gamma secretase subunit aph 1 Get druggable targets OG5_130831 All targets in OG5_130831
Brugia malayi gamma-secretase subunit aph-1 Get druggable targets OG5_130831 All targets in OG5_130831
Loa Loa (eye worm) gamma-secretase subunit aph-1 Get druggable targets OG5_130831 All targets in OG5_130831
Schistosoma japonicum ko:K06172 anterior pharynx defective 1, putative Get druggable targets OG5_130831 All targets in OG5_130831
Echinococcus multilocularis gamma secretase subunit aph 1 Get druggable targets OG5_130831 All targets in OG5_130831

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
Entamoeba histolytica phosphoglycerate mutase family protein, putative 0.0264 0.2852 0.5
Trypanosoma brucei 6-phosphofructo-2-kinase 2 0.044 0.9706 0.9706
Leishmania major 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase, putative 0.0448 1 1
Onchocerca volvulus 0.0448 1 0.5
Loa Loa (eye worm) hypothetical protein 0.0448 1 1
Trypanosoma cruzi 6-phosphofructo-2-kinase 1 0.044 0.9706 0.9706
Trypanosoma cruzi 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase, putative 0.0448 1 1
Trypanosoma cruzi 6-phosphofructo-2-kinase 1 0.044 0.9706 0.9706
Loa Loa (eye worm) gamma-secretase subunit aph-1 0.0296 0.4085 0.2053
Schistosoma mansoni 6-phosphofructokinase 0.0448 1 1
Brugia malayi gamma-secretase subunit aph-1 0.0296 0.4085 0.5
Giardia lamblia Hypothetical protein 0.0264 0.2852 0.5
Trypanosoma cruzi 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase, putative 0.0448 1 1
Giardia lamblia Hypothetical protein 0.0264 0.2852 0.5
Mycobacterium ulcerans hypothetical protein 0.0264 0.2852 0.5
Echinococcus multilocularis 6 phosphofructo 2 kinase:fructose 2 0.0448 1 1
Trypanosoma brucei 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase, putative 0.0448 1 1
Loa Loa (eye worm) hypothetical protein 0.044 0.9706 0.9604
Mycobacterium ulcerans fructose-2,6-bisphosphatase GpmB 0.0264 0.2852 0.5
Leishmania major 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase, putative 0.044 0.9706 0.9706

Activities

Activity type Activity value Assay description Source Reference
IC50 (binding) = 0.62 uM Modulation of gamma-secretase (unknown origin) assessed as reduction of amyloid beta 42 level ChEMBL. 23890837
IC50 (binding) = 0.62 uM Inhibition of human gamma secretase assessed as reduction in Abeta42 level ChEMBL. 25454273

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

2 literature references were collected for this gene.

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