Detailed information for compound 1542224

Basic information

Technical information
  • TDR Targets ID: 1542224
  • Name: N-(2,5-dimethylphenyl)-2-[(4-methyl-1,3-thiaz ol-2-yl)sulfanyl]acetamide
  • MW: 292.42 | Formula: C14H16N2OS2
  • H donors: 1 H acceptors: 2 LogP: 3.83 Rotable bonds: 5
    Rule of 5 violations (Lipinski): 1
  • SMILES: O=C(Nc1cc(C)ccc1C)CSc1scc(n1)C
  • InChi: 1S/C14H16N2OS2/c1-9-4-5-10(2)12(6-9)16-13(17)8-19-14-15-11(3)7-18-14/h4-7H,8H2,1-3H3,(H,16,17)
  • InChiKey: PZXZJSPFAMYHMS-UHFFFAOYSA-N  


Substructure search Similarity search

Network

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Synonyms

  • N-(2,5-dimethylphenyl)-2-(4-methylthiazol-2-yl)sulfanyl-acetamide
  • N-(2,5-dimethylphenyl)-2-[(4-methyl-2-thiazolyl)thio]acetamide
  • N-(2,5-dimethylphenyl)-2-[(4-methylthiazol-2-yl)thio]acetamide
  • N-(2,5-dimethylphenyl)-2-[(4-methyl-1,3-thiazol-2-yl)sulfanyl]ethanamide
  • T5391836
  • ZINC03413929

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
Toxoplasma gondii LsmAD domain-containing protein 0.0051 0 0.5
Schistosoma mansoni tar DNA-binding protein 0.0137 0.3392 0.3619
Brugia malayi Latrophilin receptor protein 2 0.0096 0.1797 0.1797
Schistosoma mansoni tar DNA-binding protein 0.0137 0.3392 0.3619
Loa Loa (eye worm) RNA recognition domain-containing protein domain-containing protein 0.0137 0.3392 0.3392
Schistosoma mansoni tar DNA-binding protein 0.0137 0.3392 0.3619
Brugia malayi RNA binding protein 0.0137 0.3392 0.3392
Loa Loa (eye worm) pigment dispersing factor receptor c 0.0305 1 1
Brugia malayi Calcitonin receptor-like protein seb-1 0.0305 1 1
Schistosoma mansoni tar DNA-binding protein 0.0137 0.3392 0.3619
Brugia malayi TAR-binding protein 0.0137 0.3392 0.3392
Leishmania major hypothetical protein, conserved 0.0051 0 0.5
Plasmodium falciparum ataxin-2 like protein, putative 0.0051 0 0.5
Loa Loa (eye worm) TAR-binding protein 0.0137 0.3392 0.3392
Brugia malayi RNA recognition motif domain containing protein 0.0137 0.3392 0.3392
Schistosoma mansoni hypothetical protein 0.0208 0.6203 1
Loa Loa (eye worm) latrophilin receptor protein 2 0.0096 0.1797 0.1797
Echinococcus multilocularis tar DNA binding protein 0.0137 0.3392 1
Trypanosoma cruzi PAB1-binding protein , putative 0.0051 0 0.5
Brugia malayi calcium-independent alpha-latrotoxin receptor 2, putative 0.0096 0.1797 0.1797
Plasmodium vivax ataxin-2 like protein, putative 0.0051 0 0.5
Trypanosoma brucei PAB1-binding protein , putative 0.0051 0 0.5
Schistosoma mansoni tar DNA-binding protein 0.0137 0.3392 0.3619
Trypanosoma cruzi PAB1-binding protein , putative 0.0051 0 0.5
Loa Loa (eye worm) hypothetical protein 0.0096 0.1797 0.1797
Loa Loa (eye worm) hypothetical protein 0.0305 1 1
Loa Loa (eye worm) RNA binding protein 0.0137 0.3392 0.3392
Plasmodium falciparum ataxin-2 like protein, putative 0.0051 0 0.5
Loa Loa (eye worm) hypothetical protein 0.0208 0.6203 0.6203
Echinococcus granulosus tar DNA binding protein 0.0137 0.3392 1
Brugia malayi latrophilin 2 splice variant baaae 0.0208 0.6203 0.6203

Activities

Activity type Activity value Assay description Source Reference
Potency (functional) 11.6891 uM PUBCHEM_BIOASSAY: Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 96 hour incubation. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID488745, AID488752, AID488774, AID504848, AID504850] ChEMBL. No reference
Potency (functional) 22.3872 uM PubChem BioAssay. qHTS of TDP-43 Inhibitors. (Class of assay: confirmatory) ChEMBL. No reference
Potency (functional) 56.2341 uM PUBCHEM_BIOASSAY: qHTS for Inhibitors of Polymerase Iota. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID588623] ChEMBL. No reference
Potency (functional) 89.1251 uM PUBCHEM_BIOASSAY: HTS for Inhibitors of HP1-beta Chromodomain Interactions with Methylated Histone Tails. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID488962] ChEMBL. No reference

Phenotypes

Whole-cell/tissue/organism interactions

Species name Source Reference Is orphan
Plasmodium falciparum ChEMBL23

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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