Detailed information for compound 172247

Basic information

Technical information
  • TDR Targets ID: 172247
  • Name: 1-[1-[4-[1-(1-acetylpiperidin-4-yl)ethoxy]-2- methoxybenzoyl]piperidin-4-yl]-4H-3,1-benzoxa zin-2-one
  • MW: 535.631 | Formula: C30H37N3O6
  • H donors: 0 H acceptors: 3 LogP: 3.59 Rotable bonds: 8
    Rule of 5 violations (Lipinski): 2
  • SMILES: COc1cc(ccc1C(=O)N1CCC(CC1)N1C(=O)OCc2c1cccc2)OC(C1CCN(CC1)C(=O)C)C
  • InChi: 1S/C30H37N3O6/c1-20(22-10-14-31(15-11-22)21(2)34)39-25-8-9-26(28(18-25)37-3)29(35)32-16-12-24(13-17-32)33-27-7-5-4-6-23(27)19-38-30(33)36/h4-9,18,20,22,24H,10-17,19H2,1-3H3
  • InChiKey: UZDNXCMOPAZSAM-UHFFFAOYSA-N  


Substructure search Similarity search

Network

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Synonyms

  • 1-[1-[4-[1-(1-acetyl-4-piperidyl)ethoxy]-2-methoxy-benzoyl]-4-piperidyl]-4H-3,1-benzoxazin-2-one
  • 1-[1-[[4-[1-(1-acetyl-4-piperidinyl)ethoxy]-2-methoxyphenyl]-oxomethyl]-4-piperidinyl]-4H-3,1-benzoxazin-2-one
  • 1-[1-[4-[1-(1-ethanoylpiperidin-4-yl)ethoxy]-2-methoxy-phenyl]carbonylpiperidin-4-yl]-4H-3,1-benzoxazin-2-one

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Homo sapiens oxytocin receptor 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
Chlamydia trachomatis SWIB complex protein 0.1305 1 0.5
Trypanosoma brucei hypothetical protein, conserved 0.0464 0 0.5
Schistosoma mansoni inositol transporter 0.1268 0.9557 0.9557
Brugia malayi brahma associated protein 60 kDa 0.1305 1 1
Schistosoma mansoni hypothetical protein 0.1305 1 1
Schistosoma mansoni hypothetical protein 0.1305 1 1
Plasmodium falciparum SWIB/MDM2 domain-containing protein 0.1305 1 1
Plasmodium vivax SWIB/MDM2 domain-containing protein, putative 0.1305 1 0.5
Trichomonas vaginalis conserved hypothetical protein 0.1305 1 0.5
Onchocerca volvulus 0.1305 1 1
Chlamydia trachomatis DNA topoisomerase I 0.1305 1 0.5
Echinococcus granulosus solute carrier family 5 0.1268 0.9557 0.9557
Echinococcus multilocularis SWI:SNF matrix associated 0.1305 1 1
Trypanosoma cruzi hypothetical protein, conserved 0.0464 0 0.5
Echinococcus multilocularis SWI:SNF matrix associated 0.1305 1 1
Echinococcus multilocularis sodium:glucose cotransporter 2 0.1268 0.9557 0.9557
Trypanosoma cruzi Zn-finger in Ran binding protein and others/FYVE zinc finger, putative 0.0464 0 0.5
Brugia malayi SWIB/MDM2 domain containing protein 0.1305 1 1
Trypanosoma cruzi hypothetical protein, conserved 0.0464 0 0.5
Trypanosoma cruzi mitochondrial RNA binding complex 1 subunit, putative 0.0464 0 0.5
Leishmania major hypothetical protein, conserved 0.0464 0 0.5
Schistosoma mansoni brg-1 associated factor 0.1305 1 1
Plasmodium vivax hypothetical protein, conserved 0.1305 1 0.5
Loa Loa (eye worm) SWIB/MDM2 domain-containing protein 0.1305 1 1
Trypanosoma cruzi hypothetical protein, conserved 0.0464 0 0.5
Plasmodium falciparum SWIB/MDM2 domain-containing protein 0.1305 1 1
Echinococcus granulosus Upstream activation factor subunit UAF30 0.1305 1 1
Trypanosoma brucei Zn-finger in Ran binding protein and others/FYVE zinc finger, putative 0.0464 0 0.5
Echinococcus granulosus sodium:myo inositol cotransporter 0.1268 0.9557 0.9557
Echinococcus multilocularis Upstream activation factor subunit UAF30 0.1305 1 1
Schistosoma mansoni hypothetical protein 0.1305 1 1
Loa Loa (eye worm) brahma associated protein 0.1305 1 1
Trypanosoma cruzi Zn-finger in Ran binding protein and others, putative 0.0464 0 0.5
Trypanosoma cruzi WLM domain containing protein, putative 0.0464 0 0.5
Toxoplasma gondii DNA topoisomerase domain-containing protein 0.1305 1 1
Echinococcus granulosus sodium:glucose cotransporter 0.1268 0.9557 0.9557
Leishmania major hypothetical protein, conserved 0.0464 0 0.5
Trypanosoma cruzi WLM domain containing protein, putative 0.0464 0 0.5
Trypanosoma cruzi Zn-finger in Ran binding protein and others, putative 0.0464 0 0.5
Schistosoma mansoni inositol transporter 0.1268 0.9557 0.9557
Toxoplasma gondii SWIB/MDM2 domain-containing protein 0.1305 1 1
Trypanosoma brucei hypothetical protein, conserved 0.0464 0 0.5
Trypanosoma cruzi mitochondrial RNA binding complex 1 subunit, putative 0.0464 0 0.5
Leishmania major hypothetical protein, conserved 0.0464 0 0.5
Echinococcus multilocularis solute carrier family 5 0.1268 0.9557 0.9557
Leishmania major hypothetical protein, conserved 0.0464 0 0.5
Echinococcus granulosus SWI:SNF matrix associated 0.1305 1 1
Trypanosoma brucei mitochondrial RNA binding complex 1 subunit 0.0464 0 0.5
Echinococcus granulosus sodium:glucose cotransporter 2 0.1268 0.9557 0.9557
Echinococcus multilocularis sodium:myo inositol cotransporter 0.1268 0.9557 0.9557
Echinococcus multilocularis SWI:SNF matrix associated 0.1305 1 1
Leishmania major hypothetical protein, conserved 0.0464 0 0.5

Activities

Activity type Activity value Assay description Source Reference
Ki (binding) = 54 nM Binding affinity against cloned human oxytocin receptor from human embryonic kidney cells ChEMBL. 9873680
Ki (binding) = 54 nM Binding affinity against cloned human oxytocin receptor from human embryonic kidney cells ChEMBL. 9873680

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.