Detailed information for compound 1451295

Basic information

Technical information
  • TDR Targets ID: 1451295
  • Name: (2-oxo-2-thiophen-2-ylethyl) 2-(thiophene-2-c arbonylamino)acetate
  • MW: 309.361 | Formula: C13H11NO4S2
  • H donors: 1 H acceptors: 3 LogP: 2.56 Rotable bonds: 8
    Rule of 5 violations (Lipinski): 1
  • SMILES: O=C(CNC(=O)c1cccs1)OCC(=O)c1cccs1
  • InChi: 1S/C13H11NO4S2/c15-9(10-3-1-5-19-10)8-18-12(16)7-14-13(17)11-4-2-6-20-11/h1-6H,7-8H2,(H,14,17)
  • InChiKey: WRJMWPZDOPULMY-UHFFFAOYSA-N  


Substructure search Similarity search

Network

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Synonyms

  • [2-oxo-2-(2-thienyl)ethyl] 2-(thiophene-2-carbonylamino)acetate
  • 2-[[oxo-(2-thienyl)methyl]amino]acetic acid [2-oxo-2-(2-thienyl)ethyl] ester
  • 2-(thiophene-2-carbonylamino)acetic acid [2-keto-2-(2-thienyl)ethyl] ester
  • (2-oxo-2-thiophen-2-yl-ethyl) 2-(thiophen-2-ylcarbonylamino)ethanoate
  • ZINC04388529
  • BAS 06811322
  • ST062151
  • MLS000075861
  • SMR000013956
  • [(Thiophene-2-carbonyl)-amino]-acetic acid 2-oxo-2-thiophen-2-yl-ethyl ester

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Homo sapiens ataxin 2 Starlite/ChEMBL No 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
Leishmania major hypothetical protein, conserved 0.003 0.037 0.5
Brugia malayi hypothetical protein 0.003 0.037 0.037
Mycobacterium ulcerans hypothetical protein 0.0152 0.5463 1
Plasmodium falciparum ataxin-2 like protein, putative 0.003 0.037 1
Trypanosoma brucei PAB1-binding protein , putative 0.003 0.037 0.5
Mycobacterium tuberculosis Adenosylmethionine-8-amino-7-oxononanoate aminotransferase BioA 0.0152 0.5463 1
Mycobacterium tuberculosis Probable aminotransferase 0.0152 0.5463 1
Wolbachia endosymbiont of Brugia malayi acetylornithine transaminase protein 0.0022 0 0.5
Echinococcus granulosus ornithine aminotransferase 0.0022 0 0.5
Toxoplasma gondii LsmAD domain-containing protein 0.003 0.037 1
Chlamydia trachomatis glutamate-1-semialdehyde-2,1-aminomutase 0.0022 0 0.5
Mycobacterium ulcerans adenosylmethionine-8-amino-7-oxononanoate aminotransferase 0.0152 0.5463 1
Plasmodium falciparum ataxin-2 like protein, putative 0.003 0.037 1
Mycobacterium leprae PROBABLE ADENOSYLMETHIONINE-8-AMINO-7-OXONONANOATE AMINOTRANSFERASE BIOA 0.0152 0.5463 1
Echinococcus multilocularis Aminotransferase class III 0.0022 0 0.5
Plasmodium vivax ataxin-2 like protein, putative 0.003 0.037 1
Echinococcus multilocularis ornithine aminotransferase 0.0022 0 0.5
Onchocerca volvulus 0.026 1 0.5
Schistosoma mansoni ornithine--oxo-acid transaminase 0.0022 0 0.5
Trypanosoma cruzi PAB1-binding protein , putative 0.003 0.037 0.5
Loa Loa (eye worm) pax transcription factor protein 2 0.026 1 1
Echinococcus multilocularis ornithine aminotransferase 0.0022 0 0.5
Trypanosoma cruzi PAB1-binding protein , putative 0.003 0.037 0.5
Echinococcus granulosus Aminotransferase class III 0.0022 0 0.5
Trichomonas vaginalis acetylornithine aminotransferase, putative 0.0152 0.5463 0.5

Activities

Activity type Activity value Assay description Source Reference
Potency (functional) 1 uM PubChem BioAssay. qHTS for Inhibitors of ATXN expression. (Class of assay: confirmatory) ChEMBL. No reference
Potency (functional) = 79.4328 um PUBCHEM_BIOASSAY: qHTS Assay for Inhibitors of DNA Polymerase Beta. (Class of assay: confirmatory) 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

Bibliographic References

No literature references available for this target.

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