Detailed information for compound 1099949

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 374.411 | Formula: C18H18N2O5S
  • H donors: 2 H acceptors: 3 LogP: 1.95 Rotable bonds: 5
    Rule of 5 violations (Lipinski): 1
  • SMILES: CCOC1Oc2ccccc2C(=O)/C/1=C\Nc1cccc(c1)S(=O)(=O)N
  • InChi: 1S/C18H18N2O5S/c1-2-24-18-15(17(21)14-8-3-4-9-16(14)25-18)11-20-12-6-5-7-13(10-12)26(19,22)23/h3-11,18,20H,2H2,1H3,(H2,19,22,23)/b15-11+
  • InChiKey: PCLVYHGTWPWKOS-RVDMUPIBSA-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 hypothetical protein 0.0362 1 1
Schistosoma mansoni hypothetical protein 0.0309 0.8184 0.7953
Echinococcus granulosus endonuclease exonuclease phosphatase 0.02 0.4478 0.0231
Echinococcus multilocularis endonuclease exonuclease phosphatase 0.02 0.4478 0.0231
Echinococcus multilocularis geminin 0.0362 1 1
Schistosoma mansoni 23-cyclic-nucleotide 2-phosphodiesterase 0.0167 0.336 0.2514
Schistosoma mansoni 23-cyclic-nucleotide 2-phosphodiesterase 0.0167 0.3344 0.2496
Toxoplasma gondii 5'-nucleotidase, C-terminal domain-containing protein 0.0167 0.336 1
Treponema pallidum 5'-nucleotidase (ushA) 0.0167 0.336 0.5
Schistosoma mansoni alkaline phosphatase 0.0196 0.4348 0.3628
Schistosoma mansoni hypothetical protein 0.0362 1 1
Schistosoma mansoni alkaline phosphatase 0.0196 0.4348 0.3628

Activities

Activity type Activity value Assay description Source Reference
Inhibition (binding) = 0 % Inhibition of human Ecto-5'-NT expressed in african green monkey COS7 cells using AMP as substrate at 0.1 mM preincubated for 10 mins measured after 10 mins ChEMBL. 23831808
Inhibition (binding) = 30.08 % Inhibition of rat Ecto-5'-nucleotidase transfected in COS7 cells at 1 mM preincubated for 10 mins followed by AMP addition measured after 10 mins ChEMBL. 27054295
Ki (binding) = 33.5 uM Inhibition of bovine intestinal alkaline phosphatase using p-NPP as substrate treated 10 mins before substrate addition measured after 30 mins by spectrophotometric assay ChEMBL. 23831808
Ki (binding) = 41 uM Inhibition of bovine kidney intestinal alkaline phosphatase using p-NPP as substrate treated 10 mins before substrate addition measured after 30 mins by spectrophotometric assay ChEMBL. 23831808

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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