Detailed information for compound 1065531

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 355.813 | Formula: C17H22ClNO5
  • H donors: 0 H acceptors: 1 LogP: 1.6 Rotable bonds: 9
    Rule of 5 violations (Lipinski): 1
  • SMILES: COCCN(Cc1cc(=O)oc2c1cc(Cl)c(c2)OC)CCOC
  • InChi: 1S/C17H22ClNO5/c1-21-6-4-19(5-7-22-2)11-12-8-17(20)24-15-10-16(23-3)14(18)9-13(12)15/h8-10H,4-7,11H2,1-3H3
  • InChiKey: SYCBXVQNWIEAMH-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
Brugia malayi Calcitonin receptor-like protein seb-1 0.0048 0.0935 0.1368
Mycobacterium ulcerans adenosylmethionine-8-amino-7-oxononanoate aminotransferase 0.0147 0.699 0.5
Mycobacterium ulcerans hypothetical protein 0.0147 0.699 0.5
Mycobacterium leprae PROBABLE ADENOSYLMETHIONINE-8-AMINO-7-OXONONANOATE AMINOTRANSFERASE BIOA 0.0147 0.699 0.5
Loa Loa (eye worm) hypothetical protein 0.0048 0.0935 0.1368
Schistosoma mansoni hypothetical protein 0.0196 1 1
Loa Loa (eye worm) pigment dispersing factor receptor c 0.0048 0.0935 0.1368
Trichomonas vaginalis acetylornithine aminotransferase, putative 0.0147 0.699 0.5
Loa Loa (eye worm) hypothetical protein 0.0144 0.6834 1
Mycobacterium tuberculosis Adenosylmethionine-8-amino-7-oxononanoate aminotransferase BioA 0.0147 0.699 0.5
Brugia malayi Muscleblind-like protein 0.0144 0.6834 1
Schistosoma mansoni hypothetical protein 0.0196 1 1
Echinococcus multilocularis geminin 0.0196 1 1
Loa Loa (eye worm) hypothetical protein 0.0144 0.6834 1
Brugia malayi Corticotropin releasing factor receptor 2 precursor, putative 0.0048 0.0935 0.1368
Mycobacterium tuberculosis Probable aminotransferase 0.0147 0.699 0.5

Activities

Activity type Activity value Assay description Source Reference
Potency (functional) 8.9125 uM PUBCHEM_BIOASSAY: qHTS for Inhibitors of TGF-b: Cytotox Counterscreen. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID588855, AID588860] ChEMBL. No reference
Potency (functional) 25.1189 uM PubChem BioAssay. qHTS of TDP-43 Inhibitors. (Class of assay: confirmatory) ChEMBL. No reference
Potency (functional) 28.1838 uM PubChem BioAssay. qHTS for Antagonist of cAMP-regulated guanine nucleotide exchange factor 2 (EPAC2): primary screen. (Class of assay: confirmatory) ChEMBL. No reference

Phenotypes

Whole-cell/tissue/organism interactions

Species name Source Reference Is orphan
Homo sapiens 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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