Detailed information for compound 1055170

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 372.412 | Formula: C20H22F2N4O
  • H donors: 1 H acceptors: 3 LogP: 1.88 Rotable bonds: 6
    Rule of 5 violations (Lipinski): 1
  • SMILES: O=C(C1CC1)NC1CCN(CC1)C(c1ccc(cc1F)F)c1cnccn1
  • InChi: 1S/C20H22F2N4O/c21-14-3-4-16(17(22)11-14)19(18-12-23-7-8-24-18)26-9-5-15(6-10-26)25-20(27)13-1-2-13/h3-4,7-8,11-13,15,19H,1-2,5-6,9-10H2,(H,25,27)
  • InChiKey: QKFSMQVZXCLMLD-UHFFFAOYSA-N  

Network

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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
Leishmania major 3-oxoacyl-(acyl-carrier protein) reductase, putative 0.0055 0.0183 0.5
Echinococcus granulosus arachidonate 5 lipoxygenase 0.0053 0.0172 0.9426
Brugia malayi 3-hydroxyacyl-CoA dehydrogenase type II 0.0055 0.0183 1
Plasmodium vivax multidomain scavenger receptor, putative 0.0019 0 0.5
Onchocerca volvulus 0.0019 0 0.5
Mycobacterium tuberculosis Probable isocitrate lyase AceAa [first part] (isocitrase) (isocitratase) (Icl) 0.2008 1 1
Mycobacterium ulcerans isocitrate lyase Icl 0.2008 1 1
Onchocerca volvulus 0.0019 0 0.5
Plasmodium falciparum LCCL domain-containing protein 0.0019 0 0.5
Mycobacterium ulcerans isocitrate lyase AceAb 0.2008 1 1
Schistosoma mansoni lipoxygenase 0.0053 0.0172 0.9426
Mycobacterium tuberculosis Probable isocitrate lyase AceAb [second part] (isocitrase) (isocitratase) (Icl) 0.2008 1 1
Echinococcus granulosus 3 hydroxyacyl coenzyme A dehydrogenase type 2 0.0055 0.0183 1
Echinococcus multilocularis 3 hydroxyacyl coenzyme A dehydrogenase type 2 0.0055 0.0183 1
Schistosoma mansoni 3-hydroxyacyl-CoA dehydrogenase 0.0055 0.0183 1
Mycobacterium tuberculosis Isocitrate lyase Icl (isocitrase) (isocitratase) 0.2008 1 1
Loa Loa (eye worm) 3-hydroxyacyl-CoA dehydrogenase type II 0.0052 0.0164 1
Echinococcus multilocularis arachidonate 5 lipoxygenase 0.0053 0.0172 0.9426

Activities

Activity type Activity value Assay description Source Reference
IC50 (functional) > 1 uM DNDI: Inhibition of Chagas Disease parasite Trypanosoma cruzi (Tulahuen LacZ, Clone C4), in vitro. ChEMBL. No reference
IC90 (functional) > 1 uM DNDI: Inhibition of Chagas Disease parasite Trypanosoma cruzi (Tulahuen LacZ, Clone C4), in vitro. ChEMBL. No reference

Phenotypes

Whole-cell/tissue/organism interactions

Species name Source Reference Is orphan
Trypanosoma cruzi ChEMBL23

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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