Detailed information for compound 896712

Basic information

Technical information
  • TDR Targets ID: 896712
  • Name: N,N'-bis(4-amino-2-chlorophenyl)benzene-1,4-d icarboxamide
  • MW: 415.273 | Formula: C20H16Cl2N4O2
  • H donors: 4 H acceptors: 2 LogP: 3.49 Rotable bonds: 6
    Rule of 5 violations (Lipinski): 1
  • SMILES: Nc1ccc(c(c1)Cl)NC(=O)c1ccc(cc1)C(=O)Nc1ccc(cc1Cl)N
  • InChi: 1S/C20H16Cl2N4O2/c21-15-9-13(23)5-7-17(15)25-19(27)11-1-2-12(4-3-11)20(28)26-18-8-6-14(24)10-16(18)22/h1-10H,23-24H2,(H,25,27)(H,26,28)
  • InChiKey: RBFIKZHWFSXFSR-UHFFFAOYSA-N  


Substructure search Similarity search

Network

Hover on a compound node to display the structore

Synonyms

  • N,N'-bis(4-amino-2-chloro-phenyl)terephthalamide
  • N,N'-bis(4-amino-2-chlorophenyl)terephthalamide
  • N,N'-bis(4-amino-2-chloro-phenyl)benzene-1,4-dicarboxamide
  • Oprea1_076243
  • ZINC00639188
  • BAS 00411781
  • N,N'-Bis-(4-amino-2-chloro-phenyl)-terephthalamide
  • ST5228377

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
Leishmania major ion transport protein-like protein 0.0107 0 0.5
Loa Loa (eye worm) hypothetical protein 0.0447 0.707 0.7067
Loa Loa (eye worm) hypothetical protein 0.0119 0.0266 0.0255
Trypanosoma cruzi ion transport protein, putative 0.0107 0 0.5
Echinococcus multilocularis potassium voltage gated channel subfamily A 0.0559 0.9394 0.9006
Schistosoma mansoni hypothetical protein 0.0294 0.3905 0.1883
Schistosoma mansoni calcium-activated potassium channel 0.0294 0.3905 0.1883
Trichomonas vaginalis glucosylceramidase, putative 0.026 0.3199 1
Loa Loa (eye worm) hypothetical protein 0.0588 1 1
Trichomonas vaginalis glucosylceramidase, putative 0.026 0.3199 1
Echinococcus granulosus potassium voltage gated channel protein 0.0588 1 1
Trichomonas vaginalis glucosylceramidase, putative 0.026 0.3199 1
Trichomonas vaginalis glucosylceramidase, putative 0.026 0.3199 1
Loa Loa (eye worm) hypothetical protein 0.0294 0.3905 0.3898
Onchocerca volvulus 0.0447 0.707 1
Loa Loa (eye worm) hypothetical protein 0.0447 0.707 0.7067
Trichomonas vaginalis glucosylceramidase, putative 0.026 0.3199 1
Trichomonas vaginalis glucosylceramidase, putative 0.018 0.1529 0.1027
Echinococcus multilocularis potassium voltage gated channel protein 0.0588 1 1
Trichomonas vaginalis glucosylceramidase, putative 0.018 0.1529 0.1027
Echinococcus granulosus potassium voltage gated channel subfamily A 0.0588 1 1
Brugia malayi hypothetical protein 0.0447 0.707 0.5692
Trypanosoma cruzi ion transport protein, putative 0.0107 0 0.5
Schistosoma mansoni voltage-gated potassium channel 0.0588 1 1
Trichomonas vaginalis glucosylceramidase, putative 0.026 0.3199 1
Schistosoma mansoni voltage-gated potassium channel 0.0588 1 1
Loa Loa (eye worm) O-glycosyl hydrolase family 30 protein 0.026 0.3199 0.3191

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.

If you have references for this compound, please enter them in a user comment (below) or Contact us.