Detailed information for compound 1489635

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 421.851 | Formula: C23H17ClFN3O2
  • H donors: 1 H acceptors: 2 LogP: 6.13 Rotable bonds: 7
    Rule of 5 violations (Lipinski): 1
  • SMILES: Fc1cccc(c1)COc1ccc(cc1Cl)Nc1ncnc(c1)Oc1ccccc1
  • InChi: 1S/C23H17ClFN3O2/c24-20-12-18(9-10-21(20)29-14-16-5-4-6-17(25)11-16)28-22-13-23(27-15-26-22)30-19-7-2-1-3-8-19/h1-13,15H,14H2,(H,26,27,28)
  • InChiKey: XOXCLNHQLHSKHP-UHFFFAOYSA-N  

Network

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Synonyms

No synonyms found for this compound

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Homo sapiens epidermal growth factor receptor Starlite/ChEMBL References

Predicted pathogen targets for this compound

By orthology
Species Potential target Known druggable target/s Ortholog Group
Echinococcus multilocularis epidermal growth factor receptor Get druggable targets OG5_128597 All targets in OG5_128597
Schistosoma mansoni tyrosine kinase Get druggable targets OG5_128597 All targets in OG5_128597
Echinococcus multilocularis Get druggable targets OG5_128597 All targets in OG5_128597
Schistosoma japonicum hypothetical protein Get druggable targets OG5_128597 All targets in OG5_128597
Schistosoma japonicum IPR006212,Furin-like repeat;IPR009030,Growth factor, receptor,domain-containing Get druggable targets OG5_128597 All targets in OG5_128597
Schistosoma mansoni tyrosine kinase Get druggable targets OG5_128597 All targets in OG5_128597
Schistosoma japonicum Epidermal growth factor receptor precursor, putative Get druggable targets OG5_128597 All targets in OG5_128597
Schistosoma mansoni tyrosine kinase Get druggable targets OG5_128597 All targets in OG5_128597
Schistosoma japonicum Receptor tyrosine-protein kinase erbB-4 precursor, putative Get druggable targets OG5_128597 All targets in OG5_128597
Schistosoma japonicum Tyrosine-protein kinase transforming protein erbB, putative Get druggable targets OG5_128597 All targets in OG5_128597
Brugia malayi Furin-like cysteine rich region family protein Get druggable targets OG5_128597 All targets in OG5_128597
Schistosoma japonicum Epidermal growth factor receptor precursor, putative Get druggable targets OG5_128597 All targets in OG5_128597
Schistosoma mansoni tyrosine kinase Get druggable targets OG5_128597 All targets in OG5_128597
Schistosoma mansoni tyrosine kinase Get druggable targets OG5_128597 All targets in OG5_128597
Schistosoma mansoni tyrosine kinase Get druggable targets OG5_128597 All targets in OG5_128597
Echinococcus granulosus epidermal growth factor receptor Get druggable targets OG5_128597 All targets in OG5_128597
Echinococcus multilocularis epidermal growth factor receptor Get druggable targets OG5_128597 All targets in OG5_128597
Echinococcus granulosus melanoma receptor tyrosine protein kinase Get druggable targets OG5_128597 All targets in OG5_128597
Schistosoma japonicum IPR000494,EGF receptor, L domain,domain-containing Get druggable targets OG5_128597 All targets in OG5_128597
Echinococcus granulosus epidermal growth factor receptor Get druggable targets OG5_128597 All targets in OG5_128597
Loa Loa (eye worm) TK/EGFR protein kinase Get druggable targets OG5_128597 All targets in OG5_128597
Schistosoma japonicum Epidermal growth factor receptor precursor, putative Get druggable targets OG5_128597 All targets in OG5_128597
Schistosoma japonicum Epidermal growth factor receptor precursor, putative Get druggable targets OG5_128597 All targets in OG5_128597
Schistosoma japonicum Epidermal growth factor receptor precursor, putative Get druggable targets OG5_128597 All targets in OG5_128597
Schistosoma japonicum ko:K05085 receptor tyrosine-protein kinase erbB-4, putative Get druggable targets OG5_128597 All targets in OG5_128597
Schistosoma japonicum expressed protein Get druggable targets OG5_128597 All targets in OG5_128597
Schistosoma japonicum Receptor tyrosine-protein kinase erbB-2 precursor, putative Get druggable targets OG5_128597 All targets in OG5_128597

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
Schistosoma mansoni tyrosine kinase 0.0096 0.04 0.04
Echinococcus multilocularis epidermal growth factor receptor 0.018 0.1285 0.1285
Echinococcus multilocularis epidermal growth factor receptor 0.0097 0.0411 0.0411
Loa Loa (eye worm) hypothetical protein 0.0377 0.3351 0.3351
Schistosoma mansoni calcium-activated potassium channel 0.0797 0.7757 0.7757
Schistosoma mansoni tyrosine kinase 0.0097 0.0411 0.0411
Schistosoma mansoni tyrosine kinase 0.0096 0.04 0.04
Schistosoma mansoni calcium-activated potassium channel 0.1011 1 1
Schistosoma mansoni tyrosine kinase 0.018 0.1285 0.1285
Echinococcus multilocularis small conductance calcium activated potassium 0.1011 1 1
Loa Loa (eye worm) hypothetical protein 0.042 0.3803 0.3803
Schistosoma mansoni hypothetical protein 0.1011 1 1
Loa Loa (eye worm) hypothetical protein 0.1011 1 1
Schistosoma mansoni tyrosine kinase 0.0096 0.04 0.04
Echinococcus granulosus epidermal growth factor receptor 0.018 0.1285 0.1285
Schistosoma mansoni tyrosine kinase 0.0097 0.0411 0.0411
Echinococcus granulosus melanoma receptor tyrosine protein kinase 0.0097 0.0411 0.0411
Echinococcus granulosus epidermal growth factor receptor 0.0097 0.0411 0.0411
Loa Loa (eye worm) TK/EGFR protein kinase 0.018 0.1285 0.1285
Loa Loa (eye worm) hypothetical protein 0.0173 0.1212 0.1212
Brugia malayi Furin-like cysteine rich region family protein 0.018 0.1285 1

Activities

Activity type Activity value Assay description Source Reference
IC50 (binding) = 10 uM Inhibition of EGFR by homogeneous time-resolved fluorescence assay ChEMBL. 21334203
IC50 (binding) > 100 uM Inhibition of HER2 by homogeneous time-resolved fluorescence assay ChEMBL. 21334203

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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