Detailed information for compound 1895994

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 248.276 | Formula: C10H20N2O5
  • H donors: 3 H acceptors: 3 LogP: -3.41 Rotable bonds: 8
    Rule of 5 violations (Lipinski): 1
  • SMILES: CO[C@@H]([C@@H](C(=O)N[C@@H]([C@H](OC)C)C(=O)O)N)C
  • InChi: 1S/C10H20N2O5/c1-5(16-3)7(11)9(13)12-8(10(14)15)6(2)17-4/h5-8H,11H2,1-4H3,(H,12,13)(H,14,15)/t5-,6-,7+,8+/m1/s1
  • InChiKey: YXWZKYGGDWGRIX-NGJRWZKOSA-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
Trypanosoma brucei PAB1-binding protein , putative 0.0027 0.266 0.2319
Plasmodium falciparum ataxin-2 like protein, putative 0.0027 0.266 0.5
Plasmodium vivax ataxin-2 like protein, putative 0.0027 0.266 0.5
Entamoeba histolytica deoxycytidyl transferase, putative 0.0021 0.0901 0.5
Mycobacterium tuberculosis Possible DNA-damage-inducible protein P DinP (DNA polymerase V) (pol IV 2) (DNA nucleotidyltransferase (DNA-directed)) 0.0021 0.0901 0.5
Leishmania major DNA polymerase eta, putative 0.0034 0.4524 0.4775
Plasmodium falciparum ataxin-2 like protein, putative 0.0027 0.266 0.5
Trypanosoma brucei DNA polymerase eta, putative 0.0048 0.8487 1
Loa Loa (eye worm) pigment dispersing factor receptor c 0.0054 1 1
Leishmania major hypothetical protein, conserved 0.0027 0.266 0.2319
Echinococcus multilocularis dna polymerase eta 0.0048 0.8487 1
Toxoplasma gondii ImpB/MucB/SamB family protein 0.0034 0.4524 1
Trypanosoma cruzi DNA polymerase eta, putative 0.0034 0.4524 0.4775
Mycobacterium tuberculosis Conserved hypothetical protein 0.0021 0.0901 0.5
Giardia lamblia DINP protein human, muc B family 0.0021 0.0901 0.5
Leishmania major DNA polymerase eta, putative 0.0048 0.8487 1
Echinococcus granulosus dna polymerase eta 0.0048 0.8487 1
Brugia malayi ImpB/MucB/SamB family protein 0.0048 0.8487 0.8487
Brugia malayi latrophilin 2 splice variant baaae 0.0037 0.5303 0.5303
Mycobacterium ulcerans DNA polymerase IV 0.0021 0.0901 0.5
Trypanosoma cruzi DNA polymerase eta, putative 0.0048 0.8487 1
Trichomonas vaginalis DNA polymerase eta, putative 0.0021 0.0901 0.5
Brugia malayi hypothetical protein 0.0027 0.266 0.266
Mycobacterium ulcerans DNA polymerase IV 0.0021 0.0901 0.5
Brugia malayi Calcitonin receptor-like protein seb-1 0.0054 1 1
Loa Loa (eye worm) hypothetical protein 0.0027 0.266 0.1934
Loa Loa (eye worm) hypothetical protein 0.0037 0.5303 0.4837
Schistosoma mansoni DNA polymerase eta 0.0048 0.8487 1
Trypanosoma cruzi PAB1-binding protein , putative 0.0027 0.266 0.2319
Trypanosoma cruzi PAB1-binding protein , putative 0.0027 0.266 0.2319
Trichomonas vaginalis DNA polymerase IV / kappa, putative 0.0021 0.0901 0.5
Brugia malayi ImpB/MucB/SamB family protein 0.0021 0.0901 0.0901
Loa Loa (eye worm) hypothetical protein 0.0048 0.8487 0.8338
Schistosoma mansoni hypothetical protein 0.0037 0.5303 0.5802
Loa Loa (eye worm) hypothetical protein 0.0054 1 1

Activities

Activity type Activity value Assay description Source Reference
Activity (functional) Antimalarial activity against Plasmodium berghei infected in mouse assessed as increase of survival time of host ChEMBL. 376849
Activity (functional) Antimalarial activity against Plasmodium berghei infected in mouse assessed as increase of survival time of host at 640 mg/kg ChEMBL. 376849

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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