Detailed information for compound 416447

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 484.959 | Formula: C22H21ClN6O3S
  • H donors: 3 H acceptors: 4 LogP: 3.64 Rotable bonds: 3
    Rule of 5 violations (Lipinski): 1
  • SMILES: N#Cc1ncc2nc1OCCCCCOc1c(NC(=O)N2)cc(Cl)c(c1)NCc1cscc1
  • InChi: 1S/C22H21ClN6O3S/c23-15-8-17-19(9-16(15)25-11-14-4-7-33-13-14)31-5-2-1-3-6-32-21-18(10-24)26-12-20(28-21)29-22(30)27-17/h4,7-9,12-13,25H,1-3,5-6,11H2,(H2,27,28,29,30)
  • InChiKey: FJNOQFHWHVUIOZ-UHFFFAOYSA-N  

Network

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Synonyms

No synonyms found for this compound

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Homo sapiens checkpoint kinase 1 Starlite/ChEMBL References

Predicted pathogen targets for this compound

By orthology
Species Potential target Known druggable target/s Ortholog Group
Loa Loa (eye worm) CAMK/CAMKL/CHK1 protein kinase Get druggable targets OG5_130454 All targets in OG5_130454
Brugia malayi Protein kinase domain containing protein Get druggable targets OG5_130454 All targets in OG5_130454
Schistosoma japonicum Serine/threonine-protein kinase Chk1, putative Get druggable targets OG5_130454 All targets in OG5_130454
Schistosoma mansoni serine/threonine protein kinase Get druggable targets OG5_130454 All targets in OG5_130454

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) low-density lipoprotein receptor repeat class B containing protein 0.0507 0.0683 0.0683
Brugia malayi Kringle domain containing protein 0.1262 1 1
Schistosoma mansoni subfamily S1A unassigned peptidase (S01 family) 0.0631 0.2209 0.2209
Loa Loa (eye worm) hypothetical protein 0.0507 0.0683 0.0683
Toxoplasma gondii kringle domain-containing protein 0.1262 1 0.5
Loa Loa (eye worm) hypothetical protein 0.1059 0.75 0.75
Onchocerca volvulus 0.1059 0.75 0.7317
Schistosoma mansoni subfamily S1A unassigned peptidase (S01 family) 0.0461 0.0116 0.0116
Loa Loa (eye worm) DOMON domain-containing protein 0.093 0.5909 0.5909
Schistosoma mansoni hypothetical protein 0.1262 1 1
Schistosoma mansoni hypothetical protein 0.093 0.5909 0.5909
Leishmania major hypothetical protein, conserved 0.1262 1 0.5
Onchocerca volvulus 0.093 0.5909 0.5609
Plasmodium falciparum cysteine repeat modular protein 1 0.1262 1 0.5
Echinococcus multilocularis tissue type plasminogen activator 0.1262 1 1
Brugia malayi SEA domain containing protein 0.093 0.5909 0.5609
Onchocerca volvulus 0.1262 1 1
Onchocerca volvulus 0.093 0.5909 0.5609
Onchocerca volvulus 0.093 0.5909 0.5609
Loa Loa (eye worm) hypothetical protein 0.093 0.5909 0.5909
Echinococcus granulosus tissue type plasminogen activator 0.1262 1 1
Plasmodium vivax cysteine repeat modular protein 1, putative 0.1262 1 0.5
Trypanosoma cruzi hypothetical protein, conserved 0.1262 1 0.5
Loa Loa (eye worm) hypothetical protein 0.0621 0.2092 0.2092
Onchocerca volvulus 0.093 0.5909 0.5609
Loa Loa (eye worm) TK/ROR protein kinase 0.1262 1 1
Loa Loa (eye worm) hypothetical protein 0.1262 1 1
Brugia malayi Muscle positioning protein 4 0.1059 0.75 0.7317

Activities

Activity type Activity value Assay description Source Reference
IC50 (binding) = 162 nM Inhibition of recombinant Chk1 ChEMBL. 17352464
IC50 (binding) = 162 nM Inhibition of recombinant Chk1 ChEMBL. 17352464

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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