Detailed information for compound 1988240

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 381.495 | Formula: C20H23N5OS
  • H donors: 2 H acceptors: 2 LogP: 2.66 Rotable bonds: 6
    Rule of 5 violations (Lipinski): 1
  • SMILES: CSc1nn(c2c1ccc(c2)NC(=O)CN1CCNCC1)c1ccccc1
  • InChi: 1S/C20H23N5OS/c1-27-20-17-8-7-15(22-19(26)14-24-11-9-21-10-12-24)13-18(17)25(23-20)16-5-3-2-4-6-16/h2-8,13,21H,9-12,14H2,1H3,(H,22,26)
  • InChiKey: BLFZXERVWIAVIA-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
Homo sapiens ketohexokinase (fructokinase) Starlite/ChEMBL No references

Predicted pathogen targets for this compound

By orthology
Species Potential target Known druggable target/s Ortholog Group
Onchocerca volvulus Get druggable targets OG5_133459 All targets in OG5_133459
Brugia malayi hypothetical protein Get druggable targets OG5_133459 All targets in OG5_133459
Loa Loa (eye worm) hypothetical protein Get druggable targets OG5_133459 All targets in OG5_133459
By sequence similarity to non orthologous known druggable targets
Species Potential target Known druggable target Length Alignment span Identity
Trypanosoma brucei ribokinase, putative ketohexokinase (fructokinase) 298 aa 307 aa 21.5 %
Obtained from network model

Ranking Plot

Putative Targets List

Species Potential target Raw Global Species
Trypanosoma cruzi carbonic anhydrase-like protein, putative 0.0122 0.3305 0.5
Brugia malayi Putative carbonic anhydrase 5 precursor 0.0122 0.3305 0.3305
Loa Loa (eye worm) carbonic anhydrase 3 0.0122 0.3305 0.3305
Loa Loa (eye worm) hypothetical protein 0.0122 0.3299 0.3299
Toxoplasma gondii hypothetical protein 0.0028 0 0.5
Brugia malayi hypothetical protein 0.0287 0.9122 0.9122
Onchocerca volvulus 0.0312 1 0.5
Brugia malayi Eukaryotic-type carbonic anhydrase family protein 0.0122 0.3305 0.3305
Loa Loa (eye worm) eukaryotic-type carbonic anhydrase 0.0122 0.3305 0.3305
Echinococcus multilocularis carbonic anhydrase II 0.0122 0.3305 1
Loa Loa (eye worm) hypothetical protein 0.0312 1 1
Echinococcus granulosus carbonic anhydrase II 0.0122 0.3305 1
Trypanosoma brucei carbonic anhydrase-like protein 0.0122 0.3305 0.5
Plasmodium falciparum carbonic anhydrase 0.0028 0 0.5
Leishmania major carbonic anhydrase-like protein 0.0122 0.3305 0.5
Schistosoma mansoni carbonic anhydrase II (carbonate dehydratase II) 0.0122 0.3305 1
Trypanosoma cruzi carbonic anhydrase-like protein, putative 0.0122 0.3305 0.5
Schistosoma mansoni carbonic anhydrase II (carbonate dehydratase II) 0.0122 0.3305 1

Activities

Activity type Activity value Assay description Source Reference
IC50 (binding) = 680 nM BindingDB_Patents: Enzyme Assay. An enzymatic assay was developed to measure KHK-mediated conversion of D-fructose to Fructose-1-P (F-1-P) using High Throughput Mass Spectroscopy (HTMS) as a means of product detection. This assay served as a primary screen to evaluate the ability to inhibit KHK enzyme activity and it has been adapted to high throughput mass spectrometry (HTMS, BioTrove RapidFire) format for higher throughput.The compounds to be tested were dosed in 12-points concentration from 511 uM to 0.5 uM. Inhibition of the fragment, IC50, was determined in a dose-response curve under the established steady-state conditions of 200 uM fructose, 100 uM ATP and 2 nM KHK for 60 min at 25 C. The assay was carried out in 384-well plate format. ChEMBL. 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

No literature references available for this target.

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