Detailed information for compound 258063

Basic information

Technical information
  • TDR Targets ID: 258063
  • Name: 1-[2-(3,4-dichlorophenyl)ethyl]-3-(7-hydroxyn aphthalen-1-yl)urea
  • MW: 375.249 | Formula: C19H16Cl2N2O2
  • H donors: 3 H acceptors: 2 LogP: 5.03 Rotable bonds: 6
    Rule of 5 violations (Lipinski): 1
  • SMILES: O=C(Nc1cccc2c1cc(O)cc2)NCCc1ccc(c(c1)Cl)Cl
  • InChi: 1S/C19H16Cl2N2O2/c20-16-7-4-12(10-17(16)21)8-9-22-19(25)23-18-3-1-2-13-5-6-14(24)11-15(13)18/h1-7,10-11,24H,8-9H2,(H2,22,23,25)
  • InChiKey: FMNOTFXDWPTZQN-UHFFFAOYSA-N  


Substructure search Similarity search

Network

Hover on a compound node to display the structore

Synonyms

  • 1-[2-(3,4-dichlorophenyl)ethyl]-3-(7-hydroxy-1-naphthyl)urea

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Homo sapiens transient receptor potential cation channel, subfamily V, member 1 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
No druggable targets predicted by sequence similarity
Obtained from network model

Ranking Plot

Putative Targets List

Species Potential target Raw Global Species
Trichomonas vaginalis spcc417.12 protein, putative 0.0011 0 0.5
Onchocerca volvulus 0.0011 0 0.5
Mycobacterium tuberculosis Carboxylesterase LipT 0.0011 0 0.5
Echinococcus granulosus carboxylesterase 5A 0.0067 1 1
Trichomonas vaginalis carboxylesterase domain containing protein, putative 0.0011 0 0.5
Echinococcus multilocularis acetylcholinesterase 0.0067 1 1
Mycobacterium tuberculosis POSSIBLE PARA-NITROBENZYL ESTERASE (FRAGMENT) 0.0011 0 0.5
Onchocerca volvulus 0.0011 0 0.5
Echinococcus granulosus acetylcholinesterase 0.0067 1 1
Echinococcus granulosus acetylcholinesterase 0.0067 1 1
Echinococcus multilocularis carboxylesterase 5A 0.0067 1 1
Onchocerca volvulus 0.0011 0 0.5
Onchocerca volvulus 0.0011 0 0.5
Echinococcus multilocularis acetylcholinesterase 0.0067 1 1
Brugia malayi Carboxylesterase family protein 0.0067 1 1
Onchocerca volvulus 0.0011 0 0.5
Schistosoma mansoni family S9 non-peptidase homologue (S09 family) 0.0067 1 1
Loa Loa (eye worm) acetylcholinesterase 1 0.0067 1 1
Loa Loa (eye worm) hypothetical protein 0.0067 1 1
Mycobacterium ulcerans carboxylesterase, LipT 0.0011 0 0.5
Mycobacterium tuberculosis POSSIBLE PARA-NITROBENZYL ESTERASE (FRAGMENT) 0.0011 0 0.5
Loa Loa (eye worm) hypothetical protein 0.0067 1 1
Loa Loa (eye worm) carboxylesterase 0.0067 1 1

Activities

Activity type Activity value Assay description Source Reference
IC50 (functional) = 90 nM Functional antagonistic activity against human vanilloid receptor subtype 1 in HEK293 cell membranes was determined as inhibition of agonist-induced increases in intracellular [Ca2+] levels ChEMBL. 14698197
IC50 (functional) = 90 nM Functional antagonistic activity against human vanilloid receptor subtype 1 in HEK293 cell membranes was determined as inhibition of agonist-induced increases in intracellular [Ca2+] levels ChEMBL. 14698197
Ki (binding) = 1 nM Binding affinity towards cloned human vanilloid receptor subtype 1 in HEK293 cell membranes using [3H]-RTX as radioligand ChEMBL. 14698197
Ki (binding) = 1 nM Binding affinity towards cloned human vanilloid receptor subtype 1 in HEK293 cell membranes using [3H]-RTX as radioligand ChEMBL. 14698197

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.

If you have references for this compound, please enter them in a user comment (below) or Contact us.