Detailed information for compound 458263

Basic information

Technical information
  • TDR Targets ID: 458263
  • Name: 2-methylsulfanyl-3-phenylthieno[2,3-d]pyrimid in-4-one
  • MW: 274.361 | Formula: C13H10N2OS2
  • H donors: 0 H acceptors: 1 LogP: 3.39 Rotable bonds: 2
    Rule of 5 violations (Lipinski): 1
  • SMILES: CSc1nc2sccc2c(=O)n1c1ccccc1
  • InChi: 1S/C13H10N2OS2/c1-17-13-14-11-10(7-8-18-11)12(16)15(13)9-5-3-2-4-6-9/h2-8H,1H3
  • InChiKey: DQQDQZYWYOJTBT-UHFFFAOYSA-N  


Substructure search Similarity search

Network

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Synonyms

  • 2-methylsulfanyl-3-phenyl-thieno[2,3-d]pyrimidin-4-one
  • 2-(methylthio)-3-phenyl-4-thieno[2,3-d]pyrimidinone
  • 2-(methylthio)-3-phenyl-thieno[2,3-d]pyrimidin-4-one
  • 2-methylsulfanyl-3-phenylthieno[3,2-e]pyrimidin-4-one
  • 2-methylsulfanyl-3-phenyl-thieno[3,2-e]pyrimidin-4-one
  • 2-(methylthio)-3-phenyl-4-thieno[3,2-e]pyrimidinone
  • 2-(methylthio)-3-phenyl-thieno[3,2-e]pyrimidin-4-one
  • ZINC06580557
  • T5433742

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
Echinococcus multilocularis presenilin enhancer 2 0.2944 0.2035 0.1342
Schistosoma mansoni subfamily A22A unassigned peptidase (A22 family) 0.3137 0.2203 0.1889
Trichomonas vaginalis Clan AD, family A22, presenilin-like aspartic peptidase 0.3137 0.2203 1
Leishmania major presenilin-like aspartic peptidase, putative,presenilin-like aspartic peptidase, clan AD, family A22A, putative 0.3137 0.2203 1
Entamoeba histolytica presenilin 1 peptidase, putative 0.3137 0.2203 0.5
Echinococcus granulosus presenilin 0.3137 0.2203 0.1524
Echinococcus multilocularis gamma secretase subunit aph 1 1.2078 1 1
Trypanosoma cruzi Aph-1 protein, putative 0.4706 0.3571 1
Echinococcus multilocularis presenilin 0.3137 0.2203 0.1524
Loa Loa (eye worm) gamma-secretase subunit pen-2 0.2944 0.2035 0.2035
Brugia malayi hypothetical protein 0.1529 0.08 0.0392
Schistosoma mansoni gamma-secretase subunit aph-1 1.2078 1 1
Loa Loa (eye worm) hypothetical protein 0.1224 0.0535 0.0535
Loa Loa (eye worm) gamma-secretase subunit aph-1 1.2078 1 1
Loa Loa (eye worm) hypothetical protein 0.2278 0.1454 0.1454
Brugia malayi Amyloid A4 extracellular domain containing protein 0.2891 0.1988 0.1633
Toxoplasma gondii hypothetical protein 0.1099 0.0425 1
Trypanosoma brucei Aph-1 protein, putative 0.4706 0.3571 1
Loa Loa (eye worm) hypothetical protein 0.1529 0.08 0.08
Trichomonas vaginalis Clan AD, family A22, presenilin-like aspartic peptidase 0.3137 0.2203 1
Trypanosoma brucei presenilin-like aspartic peptidase, putative 0.3137 0.2203 0.5892
Echinococcus granulosus gamma secretase subunit aph 1 1.2078 1 1
Echinococcus granulosus presenilin enhancer 2 0.2944 0.2035 0.1342
Trichomonas vaginalis Clan AD, family A22, presenilin-like aspartic peptidase 0.3137 0.2203 1
Schistosoma mansoni hypothetical protein 0.1529 0.08 0.0431
Loa Loa (eye worm) presenilin spe-4 0.1099 0.0425 0.0425
Brugia malayi Presenilin family protein 0.3137 0.2203 0.1856
Trypanosoma cruzi Aph-1 protein, putative 0.4706 0.3571 1
Brugia malayi hypothetical protein 0.1529 0.08 0.0392
Brugia malayi gamma-secretase subunit pen-2 0.2944 0.2035 0.1681

Activities

Activity type Activity value Assay description Source Reference
Activity (functional) 0 Inhibition of TNFalpha-induced necroptosis in FADD-deficient Jurkat T cells ChEMBL. 17270434

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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