Detailed information for compound 321634

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 442.445 | Formula: C20H18N4O6S
  • H donors: 3 H acceptors: 5 LogP: 3.21 Rotable bonds: 8
    Rule of 5 violations (Lipinski): 1
  • SMILES: COc1ccc(cc1)Nc1ccc(cc1C(=O)Nc1ccc(cc1)S(=O)(=O)N)[N+](=O)[O-]
  • InChi: 1S/C20H18N4O6S/c1-30-16-7-2-13(3-8-16)22-19-11-6-15(24(26)27)12-18(19)20(25)23-14-4-9-17(10-5-14)31(21,28)29/h2-12,22H,1H3,(H,23,25)(H2,21,28,29)
  • InChiKey: NBVXVHCXPKXTFY-UHFFFAOYSA-N  


Substructure search Similarity search

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
Schistosoma mansoni Neurotrimin precursor (hNT) 0.0163 0.1429 0.6038
Echinococcus multilocularis neuroglian 0.0201 0.2248 0.4662
Echinococcus granulosus twitchin 0.0201 0.2248 0.0956
Loa Loa (eye worm) TK/KIN16 protein kinase 0.0223 0.2718 0.7338
Loa Loa (eye worm) hypothetical protein 0.0207 0.2367 0.5338
Echinococcus multilocularis roundabout 2 0.0244 0.3186 1
Loa Loa (eye worm) hypothetical protein 0.0244 0.3186 1
Schistosoma mansoni nephrin 0.0201 0.2248 0.9498
Echinococcus granulosus neuroglian 0.0201 0.2248 0.0956
Schistosoma mansoni cell adhesion molecule 0.0207 0.2367 1
Brugia malayi Immunoglobulin I-set domain containing protein 0.0223 0.2718 1
Echinococcus granulosus neurotracting:lsamp:neurotrimin:obcam 0.0207 0.2367 0.1094
Loa Loa (eye worm) hypothetical protein 0.0244 0.3186 1
Schistosoma mansoni vesicular amine transporter 0.0163 0.1429 0.6038
Echinococcus granulosus roundabout 2 0.0244 0.3186 0.205
Schistosoma mansoni defective proboscis extension response (dpr)-related 0.0163 0.1429 0.6038

Activities

Activity type Activity value Assay description Source Reference
Efficacy (functional) = 1 % Percent efficacy of the compound for inhibition of glucose stimulated insulin release from beta TC6 cells ChEMBL. 15501029
Efficacy (functional) = 1 % Percent efficacy of the compound for inhibition of glucose stimulated insulin release from beta TC6 cells ChEMBL. 15501029
IC50 (functional) NS 0 uM inhibitory concentration required for repolarisation of beta cell membrane potential in presence of 10 mM glucose ChEMBL. 15501029
IC50 (functional) = 26.62 uM Concentration required for inhibition of glucose stimulated insulin release from beta TC6 cells ChEMBL. 15501029
IC50 (functional) = 26.62 uM Concentration required for inhibition of glucose stimulated insulin release from beta TC6 cells ChEMBL. 15501029

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

No external resources registered for this compound

Bibliographic References

1 literature reference was collected for this gene.

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