Detailed information for compound 226608

Basic information

Technical information
  • TDR Targets ID: 226608
  • Name: N-[2-(4-chlorophenoxy)ethyl]-3-phenylsulfanyl propan-1-amine
  • MW: 321.865 | Formula: C17H20ClNOS
  • H donors: 1 H acceptors: 0 LogP: 4.66 Rotable bonds: 9
    Rule of 5 violations (Lipinski): 1
  • SMILES: Clc1ccc(cc1)OCCNCCCSc1ccccc1
  • InChi: 1S/C17H20ClNOS/c18-15-7-9-16(10-8-15)20-13-12-19-11-4-14-21-17-5-2-1-3-6-17/h1-3,5-10,19H,4,11-14H2
  • InChiKey: HGOOBSLSWOJAPR-UHFFFAOYSA-N  

Network

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Synonyms

  • N-[2-(4-chlorophenoxy)ethyl]-3-phenylsulfanyl-propan-1-amine
  • N-[2-(4-chlorophenoxy)ethyl]-3-(phenylthio)-1-propanamine
  • 2-(4-chlorophenoxy)ethyl-[3-(phenylthio)propyl]amine
  • N-[2-(4-chlorophenoxy)ethyl]-3-(phenylthio)propan-1-amine

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Homo sapiens dopamine receptor D3 Starlite/ChEMBL References
Homo sapiens dopamine receptor D2 Starlite/ChEMBL References
Homo sapiens dopamine receptor D4 Starlite/ChEMBL References

Predicted pathogen targets for this compound

By orthology
No druggable targets predicted by orthology data
By sequence similarity to non orthologous known druggable targets
Species Potential target Known druggable target Length Alignment span Identity
Brugia malayi hypothetical protein dopamine receptor D3 400 aa 392 aa 19.9 %

Obtained from network model

Ranking Plot


Putative Targets List


Species Potential target Raw Global Species
Entamoeba histolytica hypothetical protein, conserved 0.0908 1 0.5
Schistosoma mansoni lipoxygenase 0.0257 0.11 0.11
Echinococcus multilocularis ATP dependent DNA helicase PIF1 0.0908 1 1
Trypanosoma cruzi DNA repair and recombination helicase protein PIF7, putative 0.0908 1 0.5
Echinococcus multilocularis arachidonate 5 lipoxygenase 0.0257 0.11 0.11
Giardia lamblia Rrm3p helicase 0.0908 1 0.5
Trypanosoma brucei DNA repair and recombination helicase protein PIF6 0.0908 1 0.5
Trypanosoma cruzi DNA repair and recombination helicase protein PIF7, putative 0.0908 1 0.5
Trypanosoma cruzi DNA repair and recombination helicase protein PIF6, putative 0.0908 1 0.5
Entamoeba histolytica DNA repair and recombination protein, putative 0.0908 1 0.5
Leishmania major PIF1 helicase-like protein, putative,DNA repair and recombination protein, mitochondrial precursor, putative 0.0908 1 0.5
Trichomonas vaginalis conserved hypothetical protein 0.0908 1 0.5
Trypanosoma brucei DNA repair and recombination helicase protein PIF7 0.0908 1 0.5
Leishmania major PIF1 helicase-like protein, putative,DNA repair and recombination protein, mitochondrial precursor, putative 0.0908 1 0.5
Schistosoma mansoni lipoxygenase 0.0179 0.0045 0.0045
Schistosoma mansoni hypothetical protein 0.0908 1 1

Activities

Activity type Activity value Assay description Source Reference
Ki (binding) = 1.4 nM Binding affinity to recombinant human dopamine receptor D4 expressed in CHO cells by displacement of [3H]-spiperone ChEMBL. 9406594
Ki (binding) = 1.4 nM Binding affinity to recombinant human dopamine receptor D4 expressed in CHO cells by displacement of [3H]-spiperone ChEMBL. 9406594
Ki (binding) = 95 nM Binding affinity against cloned human dopamine receptor D3 expressed in Chinese hamster ovary (CHO) K-1 cells by displacement of [3H]-spiperone. ChEMBL. 9406594
Ki (binding) = 95 nM Binding affinity against cloned human dopamine receptor D3 expressed in Chinese hamster ovary (CHO) K-1 cells by displacement of [3H]-spiperone. ChEMBL. 9406594
Ki (binding) = 227 nM Binding affinity against cloned human dopamine receptor D2 expressed in Chinese hamster ovary (CHO) K-1 cells by displacement of [3H]-spiperone. ChEMBL. 9406594
Ki (binding) = 227 nM Binding affinity against cloned human dopamine receptor D2 expressed in Chinese hamster ovary (CHO) K-1 cells by displacement of [3H]-spiperone. ChEMBL. 9406594
Selectivity ratio (binding) = 162 Selectivity ratio is Ki of human dopamine D2 receptor to that of human dopamine D4 receptor. ChEMBL. 9406594

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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