Detailed information for compound 1565013

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 701.175 | Formula: C36H40ClF3N4O5
  • H donors: 2 H acceptors: 3 LogP: 5.19 Rotable bonds: 19
    Rule of 5 violations (Lipinski): 2
  • SMILES: O=C(CC(F)(F)F)NCCc1ccc(c(c1)CN(C(=O)[C@H]1CNCC(=O)N1c1ccc(cc1)OCCCOCc1ccccc1)C1CC1)Cl
  • InChi: 1S/C36H40ClF3N4O5/c37-31-14-7-25(15-16-42-33(45)20-36(38,39)40)19-27(31)23-43(28-8-9-28)35(47)32-21-41-22-34(46)44(32)29-10-12-30(13-11-29)49-18-4-17-48-24-26-5-2-1-3-6-26/h1-3,5-7,10-14,19,28,32,41H,4,8-9,15-18,20-24H2,(H,42,45)/t32-/m1/s1
  • InChiKey: XZEYEXQVTZLOBT-JGCGQSQUSA-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
Schistosoma mansoni protein kinase 0.0008 0 0.5
Echinococcus granulosus mitogen activated protein kinase 15 0.0008 0 0.5
Trichomonas vaginalis low molecular weight protein tyrosine phosphatase, putative 0.0283 1 1
Leishmania major serine/threonine kinase-like protein, putative 0.0008 0 0.5
Trypanosoma brucei protein kinase, putative 0.0008 0 0.5
Echinococcus multilocularis cyclin dependent kinase 9 0.0008 0 0.5
Echinococcus granulosus cyclin dependent kinase 9 0.0008 0 0.5
Loa Loa (eye worm) phosphotyrosine protein phosphatase 0.0283 1 1
Trypanosoma cruzi serine/threonine protein kinase, putative 0.0008 0 0.5
Plasmodium vivax cyclin dependent kinase 7 (cdk7), putative 0.0119 0.4045 1
Trichomonas vaginalis low molecular weight protein-tyrosine-phosphatase, putative 0.0283 1 1
Echinococcus multilocularis Cell division cycle 2 protein kinase 0.0008 0 0.5
Schistosoma mansoni serine/threonine protein kinase 0.0008 0 0.5
Schistosoma mansoni serine/threonine kinase 0.0008 0 0.5
Echinococcus granulosus serine:threonine protein kinase NLK 0.0008 0 0.5
Onchocerca volvulus 0.0283 1 0.5
Mycobacterium ulcerans phosphotyrosine protein phosphatase PtpA 0.0283 1 0.5
Trichomonas vaginalis low molecular weight protein tyrosine phosphatase, putative 0.0283 1 1
Entamoeba histolytica protein tyrosine phosphatase, putative 0.0283 1 1
Trichomonas vaginalis low molecular weight protein-tyrosine-phosphatase, putative 0.0283 1 1
Trypanosoma brucei Mitogen-activated protein kinase 10, putative 0.0008 0 0.5
Giardia lamblia Low molecular weight protein-tyrosine-phosphatase 0.0283 1 1
Toxoplasma gondii cell-cycle-associated protein kinase, putative 0.0111 0.3759 0.5
Trichomonas vaginalis low molecular weight protein tyrosine phosphatase, putative 0.0283 1 1
Trypanosoma cruzi Mitogen-activated protein kinase 10, putative 0.0008 0 0.5
Leishmania major mitogen-activated protein kinase, putative,map kinase-like protein 0.0008 0 0.5
Trichomonas vaginalis low molecular weight protein-tyrosine-phosphatase, putative 0.0283 1 1
Trypanosoma cruzi Mitogen-activated protein kinase 10, putative 0.0008 0 0.5
Plasmodium falciparum MO15-related protein kinase 0.0119 0.4045 0.5
Mycobacterium tuberculosis Phosphotyrosine protein phosphatase PtpA (protein-tyrosine-phosphatase) (PTPase) (LMW phosphatase) 0.0283 1 0.5
Echinococcus granulosus Cell division cycle 2 protein kinase 0.0008 0 0.5
Entamoeba histolytica protein tyrosine phosphatase, putative 0.0283 1 1
Echinococcus multilocularis serine:threonine protein kinase NLK 0.0008 0 0.5

Activities

No activities found for this compound.

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

No literature references available for this target.

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