Detailed information for compound 961224

Basic information

Technical information
  • TDR Targets ID: 961224
  • Name: 2-[4-(7-chloroquinolin-4-yl)piperazin-1-yl]et hanol
  • MW: 291.776 | Formula: C15H18ClN3O
  • H donors: 1 H acceptors: 2 LogP: 2.07 Rotable bonds: 3
    Rule of 5 violations (Lipinski): 1
  • SMILES: OCCN1CCN(CC1)c1ccnc2c1ccc(c2)Cl
  • InChi: 1S/C15H18ClN3O/c16-12-1-2-13-14(11-12)17-4-3-15(13)19-7-5-18(6-8-19)9-10-20/h1-4,11,20H,5-10H2
  • InChiKey: GEUBAJKVKVTLRU-UHFFFAOYSA-N  


Substructure search Similarity search

Network

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Synonyms

  • 2-[4-(7-chloro-4-quinolyl)piperazin-1-yl]ethanol
  • 2-[4-(7-chloro-4-quinolyl)-1-piperazinyl]ethanol

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
Schistosoma mansoni hypothetical protein 0.0190229 0.0296026 0.5
Echinococcus granulosus Basic leucine zipper bZIP transcription factor 0.0232742 0.272227 0.5
Echinococcus multilocularis jun protein 0.0232742 0.272227 0.5
Loa Loa (eye worm) hypoxia-induced factor 1 0.0332356 0.840729 0.789707
Echinococcus granulosus jun protein 0.0232742 0.272227 0.5
Loa Loa (eye worm) hypothetical protein 0.0360264 1 1
Echinococcus multilocularis Basic leucine zipper (bZIP) transcription factor 0.0232742 0.272227 0.5
Brugia malayi hypoxia-induced factor 1 0.0332356 0.840729 0.840729
Schistosoma mansoni jun-related protein 0.0190229 0.0296026 0.5
Brugia malayi bZIP transcription factor family protein 0.0232742 0.272227 0.272227
Brugia malayi hypothetical protein 0.0360264 1 1
Onchocerca volvulus 0.0185042 0 0.5

Activities

Activity type Activity value Assay description Source Reference
IC50 (functional) = 1 uM Antiplasmodial activity against chloroquine-resistant Plasmodium falciparum W2 by FACS-based assay ChEMBL. 21500839
IC50 (functional) = 3.8 uM Antiplasmodial activity against chloroquine-resistant Plasmodium falciparum Dd2 by FACS-based assay ChEMBL. 21500839
IC50 (functional) = 5.2 uM Antiplasmodial activity against chloroquine-sensitive Plasmodium falciparum D10 by FACS-based assay ChEMBL. 21500839
Inhibition (functional) Antiplasmodial activity against chloroquine-sensitive Plasmodium falciparum D10 infected in erythrocytes assessed as inhibition of sorbitol-induced hemolysis after 15 mins ChEMBL. 21500839

Phenotypes

Whole-cell/tissue/organism interactions

Species name Source Reference Is orphan
Plasmodium falciparum ChEMBL23 21500839

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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