Detailed information for compound 931237

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 282.38 | Formula: C18H22N2O
  • H donors: 0 H acceptors: 1 LogP: 2.69 Rotable bonds: 5
    Rule of 5 violations (Lipinski): 1
  • SMILES: c1ccc(cc1)CCC1OCCN(C1)Cc1cccnc1
  • InChi: 1S/C18H22N2O/c1-2-5-16(6-3-1)8-9-18-15-20(11-12-21-18)14-17-7-4-10-19-13-17/h1-7,10,13,18H,8-9,11-12,14-15H2
  • InChiKey: KHILYFXUNKRFHB-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
Echinococcus multilocularis ATP dependent DNA helicase PIF1 0.0154 0.4142 0.6976
Mycobacterium ulcerans hypothetical protein 0.0191 0.5187 0.5
Loa Loa (eye worm) CAMK/MLCK protein kinase 0.0006 0 0.5
Trypanosoma brucei mitochondrial DNA polymerase beta 0.0363 1 1
Trypanosoma cruzi DNA repair and recombination helicase protein PIF7, putative 0.0154 0.4142 0.3298
Echinococcus granulosus serine:threonine protein kinase 0.0218 0.5938 1
Trypanosoma brucei DNA repair and recombination helicase protein PIF7 0.0154 0.4142 0.3298
Mycobacterium tuberculosis Conserved hypothetical protein 0.0191 0.5187 0.5
Trypanosoma cruzi mitochondrial DNA polymerase beta-PAK, putative 0.0172 0.4643 0.3871
Leishmania major mitochondrial DNA polymerase beta-PAK, putative 0.0172 0.4643 0.0855
Trypanosoma cruzi mitochondrial DNA polymerase beta, putative 0.0363 1 1
Trichomonas vaginalis conserved hypothetical protein 0.0154 0.4142 0.5
Trypanosoma cruzi mitochondrial DNA polymerase beta-PAK, putative 0.0062 0.1572 0.0358
Toxoplasma gondii hypothetical protein 0.0058 0.147 0.5
Echinococcus granulosus ATP dependent DNA helicase PIF1 0.0154 0.4142 0.6976
Onchocerca volvulus 0.0006 0 0.5
Echinococcus granulosus myosin light chain kinase smooth muscle 0.0218 0.5938 1
Entamoeba histolytica DNA repair and recombination protein, putative 0.0154 0.4142 0.5
Echinococcus multilocularis myosin light chain kinase, smooth muscle 0.0218 0.5938 1
Brugia malayi protein unc-22 0.0006 0 0.5
Trypanosoma cruzi DNA repair and recombination helicase protein PIF6, putative 0.0154 0.4142 0.3298
Giardia lamblia Rrm3p helicase 0.0154 0.4142 0.5
Brugia malayi Immunoglobulin I-set domain containing protein 0.0006 0 0.5
Trypanosoma cruzi DNA repair and recombination helicase protein PIF7, putative 0.0154 0.4142 0.3298
Loa Loa (eye worm) CAMK protein kinase 0.0006 0 0.5
Loa Loa (eye worm) CAMK/MLCK protein kinase 0.0006 0 0.5
Trypanosoma brucei mitochondrial DNA polymerase beta-PAK 0.0172 0.4643 0.3871
Schistosoma mansoni hypothetical protein 0.0154 0.4142 1
Trypanosoma brucei DNA repair and recombination helicase protein PIF6 0.0154 0.4142 0.3298
Trypanosoma cruzi mitochondrial DNA polymerase beta, putative 0.0363 1 1
Entamoeba histolytica hypothetical protein, conserved 0.0154 0.4142 0.5
Echinococcus multilocularis serine:threonine protein kinase 0.0218 0.5938 1

Activities

Activity type Activity value Assay description Source Reference
Inhibition (binding) = 35 % Inhibition of human dopamine D4 receptor at 10 uM ChEMBL. 25221667

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

1 literature reference was collected for this gene.

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