Detailed information for compound 819069

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 399.874 | Formula: C20H22ClN5O2
  • H donors: 1 H acceptors: 3 LogP: 1.5 Rotable bonds: 6
    Rule of 5 violations (Lipinski): 1
  • SMILES: CC(=O)NCc1nnc2n1CCN(CC2)Cc1ccc(o1)c1cccc(c1)Cl
  • InChi: 1S/C20H22ClN5O2/c1-14(27)22-12-20-24-23-19-7-8-25(9-10-26(19)20)13-17-5-6-18(28-17)15-3-2-4-16(21)11-15/h2-6,11H,7-10,12-13H2,1H3,(H,22,27)
  • InChiKey: WQOOONCVCPWVQZ-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
Loa Loa (eye worm) GTP-binding regulatory protein Gs alpha-S chain 0.0045 1 1
Loa Loa (eye worm) hypothetical protein 0.0013 0.0803 0.0149
Trichomonas vaginalis rotamase, putative 0.0033 0.6532 1
Echinococcus multilocularis musashi 0.0027 0.4724 0.4263
Schistosoma mansoni Guanine nucleotide-binding protein G(s) subunit alpha (Adenylate cyclase-stimulating G alpha protein) 0.0045 1 1
Brugia malayi Intermediate filament tail domain containing protein 0.0027 0.4724 0.4001
Trypanosoma cruzi peptidyl-prolyl cis-trans isomerase 0.0032 0.6311 1
Toxoplasma gondii peptidylprolyl isomerase 0.0032 0.6311 1
Echinococcus granulosus lamin dm0 0.0027 0.4724 0.4263
Entamoeba histolytica peptidyl-prolyl cis-trans isomerase, putative 0.0032 0.6311 0.5
Loa Loa (eye worm) hypothetical protein 0.0026 0.4586 0.42
Schistosoma mansoni rotamase 0.0033 0.6532 0.3427
Trypanosoma brucei peptidyl-prolyl cis-trans isomerase/rotamase, putative 0.0032 0.6311 1
Echinococcus granulosus intermediate filament protein 0.0027 0.4724 0.4263
Schistosoma mansoni Guanine nucleotide-binding protein G(s) subunit alpha (Adenylate cyclase-stimulating G alpha protein) 0.0045 1 1
Brugia malayi Pin1-type peptidyl-prolyl cis-trans isomerase, BmPin1 0.0033 0.6532 0.6057
Echinococcus granulosus guanine nucleotide binding protein Gs subunit 0.0045 1 1
Trypanosoma cruzi peptidyl-prolyl cis-trans isomerase 0.0032 0.6311 1
Trichomonas vaginalis conserved hypothetical protein 0.0033 0.6532 1
Loa Loa (eye worm) intermediate filament protein 0.0027 0.4724 0.4349
Echinococcus multilocularis lamin 0.0027 0.4724 0.4263
Schistosoma mansoni Guanine nucleotide-binding protein G(s) subunit alpha (Adenylate cyclase-stimulating G alpha protein) 0.0045 1 1
Echinococcus multilocularis lamin dm0 0.0027 0.4724 0.4263
Loa Loa (eye worm) cytoplasmic intermediate filament protein 0.0014 0.1206 0.058
Echinococcus granulosus lamin 0.0027 0.4724 0.4263
Onchocerca volvulus 0.0027 0.4724 0.5
Echinococcus multilocularis guanine nucleotide binding protein G(s) subunit 0.0045 1 1
Loa Loa (eye worm) Pin1-type peptidyl-prolyl cis-trans isomerase 0.0033 0.6532 0.6285
Onchocerca volvulus 0.0027 0.4724 0.5
Echinococcus granulosus expressed protein 0.0033 0.6532 0.6229
Loa Loa (eye worm) intermediate filament tail domain-containing protein 0.0027 0.4724 0.4349
Leishmania major peptidyl-prolyl cis-trans isomerase/rotamase, putative,PPIase, putative 0.0032 0.6311 1
Echinococcus multilocularis expressed protein 0.0033 0.6532 0.6229
Loa Loa (eye worm) hypothetical protein 0.0027 0.4724 0.4349
Wolbachia endosymbiont of Brugia malayi parvulin-like peptidyl-prolyl isomerase, PPID 0.001 0 0.5
Brugia malayi intermediate filament protein 0.0027 0.4724 0.4001
Echinococcus multilocularis guanine nucleotide binding protein G(s) subunit 0.0045 1 1
Echinococcus granulosus guanine nucleotide binding protein Gs subunit 0.0045 1 1

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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