Detailed information for compound 1673468

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 475.624 | Formula: C23H29N3O4S2
  • H donors: 1 H acceptors: 4 LogP: 5.5 Rotable bonds: 12
    Rule of 5 violations (Lipinski): 1
  • SMILES: CCCCOC(=O)NS(=O)(=O)c1sc(cc1c1cccc(c1)Cn1cccn1)CC(C)C
  • InChi: 1S/C23H29N3O4S2/c1-4-5-12-30-23(27)25-32(28,29)22-21(15-20(31-22)13-17(2)3)19-9-6-8-18(14-19)16-26-11-7-10-24-26/h6-11,14-15,17H,4-5,12-13,16H2,1-3H3,(H,25,27)
  • InChiKey: KSSUPHQPSJAPMI-UHFFFAOYSA-N  

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
Giardia lamblia Histone acetyltransferase GCN5 0.0039 0.0284 0.5
Echinococcus granulosus histone acetyltransferase KAT2B 0.014 0.9627 1
Echinococcus multilocularis tar DNA binding protein 0.0063 0.2512 0.2512
Schistosoma mansoni tar DNA-binding protein 0.0063 0.2512 0.2512
Schistosoma mansoni gcn5proteinral control of amino-acid synthesis 5-like 2 gcnl2 0.0144 1 1
Brugia malayi RNA binding protein 0.0063 0.2512 0.2512
Echinococcus granulosus aldehyde dehydrogenase mitochondrial 0.006 0.2271 0.2359
Trichomonas vaginalis cat eye syndrome critical region protein 2, cscr2, putative 0.0042 0.061 0.5
Schistosoma mansoni tar DNA-binding protein 0.0063 0.2512 0.2512
Mycobacterium ulcerans aldehyde dehydrogenase 0.006 0.2271 0.5
Plasmodium vivax histone acetyltransferase GCN5, putative 0.0042 0.061 0.5
Schistosoma mansoni tar DNA-binding protein 0.0063 0.2512 0.2512
Trichomonas vaginalis bromodomain-containing protein, putative 0.0042 0.061 0.5
Toxoplasma gondii aldehyde dehydrogenase 0.006 0.2271 1
Plasmodium falciparum histone acetyltransferase GCN5 0.0039 0.0284 0.5
Echinococcus granulosus histone acetyltransferase KAT2B 0.0042 0.061 0.0634
Brugia malayi TAR-binding protein 0.0063 0.2512 0.2512
Echinococcus granulosus tar DNA binding protein 0.0063 0.2512 0.2609
Schistosoma mansoni aldehyde dehydrogenase 0.006 0.2271 0.2271
Echinococcus multilocularis aldehyde dehydrogenase, mitochondrial 0.006 0.2271 0.2271
Schistosoma mansoni tar DNA-binding protein 0.0063 0.2512 0.2512
Loa Loa (eye worm) acetyltransferase 0.0144 1 1
Mycobacterium tuberculosis Probable aldehyde dehydrogenase 0.006 0.2271 0.5
Leishmania major aldehyde dehydrogenase, mitochondrial precursor 0.006 0.2271 0.5
Echinococcus multilocularis gcn5proteinral control of amino acid synthesis 0.0144 1 1
Mycobacterium ulcerans aldehyde dehydrogenase 0.006 0.2271 0.5
Mycobacterium ulcerans aldehyde dehydrogenase 0.006 0.2271 0.5
Brugia malayi RNA recognition motif domain containing protein 0.0063 0.2512 0.2512
Entamoeba histolytica acetyltransferase, GNAT family 0.0039 0.0284 1
Schistosoma mansoni tar DNA-binding protein 0.0063 0.2512 0.2512
Schistosoma mansoni aldehyde dehydrogenase 0.006 0.2271 0.2271

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.

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