Detailed information for compound 111044

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 290.356 | Formula: C20H18O2
  • H donors: 2 H acceptors: 2 LogP: 3.4 Rotable bonds: 4
    Rule of 5 violations (Lipinski): 1
  • SMILES: OCc1ccc(cc1)c1cccc(c1)c1ccc(cc1)CO
  • InChi: 1S/C20H18O2/c21-13-15-4-8-17(9-5-15)19-2-1-3-20(12-19)18-10-6-16(14-22)7-11-18/h1-12,21-22H,13-14H2
  • InChiKey: WUDFKQWGZUEYDF-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
Trichomonas vaginalis low molecular weight protein-tyrosine-phosphatase, putative 0.4762 0.5877 1
Trichomonas vaginalis low molecular weight protein tyrosine phosphatase, putative 0.4762 0.5877 1
Trichomonas vaginalis low molecular weight protein tyrosine phosphatase, putative 0.4762 0.5877 1
Giardia lamblia Low molecular weight protein-tyrosine-phosphatase 0.4762 0.5877 1
Mycobacterium tuberculosis Phosphotyrosine protein phosphatase PtpA (protein-tyrosine-phosphatase) (PTPase) (LMW phosphatase) 0.3294 0.3944 0.5
Trichomonas vaginalis low molecular weight protein tyrosine phosphatase, putative 0.1468 0.154 0.262
Schistosoma mansoni protein tyrosine phosphatase non-receptor type nt1 0.7894 1 1
Echinococcus granulosus tyrosine protein phosphatase non receptor type 0.7894 1 1
Brugia malayi Low molecular weight phosphotyrosine protein phosphatase containing protein 0.4762 0.5877 0.5877
Trichomonas vaginalis low molecular weight protein-tyrosine-phosphatase, putative 0.4762 0.5877 1
Mycobacterium ulcerans phosphotyrosine protein phosphatase PtpA 0.4762 0.5877 0.5
Trypanosoma cruzi hypothetical protein, conserved 0.1468 0.154 1
Loa Loa (eye worm) protein-tyrosine phosphatase 0.7894 1 1
Onchocerca volvulus 0.4762 0.5877 1
Leishmania major hypothetical protein, conserved 0.1468 0.154 1
Trichomonas vaginalis low molecular weight protein tyrosine phosphatase, putative 0.4762 0.5877 1
Trypanosoma brucei low molecular weight protein tyrosine phosphatase, putative 0.1468 0.154 1
Trichomonas vaginalis low molecular weight protein-tyrosine-phosphatase, putative 0.4762 0.5877 1
Loa Loa (eye worm) phosphotyrosine protein phosphatase 0.4762 0.5877 0.5877
Echinococcus multilocularis tyrosine protein phosphatase non receptor type 0.7894 1 1
Trypanosoma cruzi hypothetical protein, conserved 0.1468 0.154 1
Entamoeba histolytica protein tyrosine phosphatase, putative 0.4762 0.5877 1
Entamoeba histolytica protein tyrosine phosphatase, putative 0.4762 0.5877 1
Trichomonas vaginalis low molecular weight protein tyrosine phosphatase, putative 0.1468 0.154 0.262

Activities

Activity type Activity value Assay description Source Reference
Inhibition (functional) = 62 % In vitro inhibitory activity against lipopolysaccharide (LPS)-induced IL-6 production in murine myelomonocytic microM. ChEMBL. No reference
Inhibition (functional) = 62 % In vitro inhibitory activity against lipopolysaccharide (LPS)-induced IL-6 production in murine myelomonocytic microM. ChEMBL. No reference

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

No external resources registered for this compound

Bibliographic References

No literature references available for this target.

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