Detailed information for compound 1793918

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 463.837 | Formula: C22H17ClF3N3O3
  • H donors: 0 H acceptors: 3 LogP: 4.65 Rotable bonds: 6
    Rule of 5 violations (Lipinski): 1
  • SMILES: O=C(N(c1ccc(cc1)C(F)(F)F)C)Cn1c(=O)oc2c1cc(cc2)c1cccnc1.Cl
  • InChi: 1S/C22H16F3N3O3.ClH/c1-27(17-7-5-16(6-8-17)22(23,24)25)20(29)13-28-18-11-14(15-3-2-10-26-12-15)4-9-19(18)31-21(28)30;/h2-12H,13H2,1H3;1H
  • InChiKey: NDOVHEKEGYMRBZ-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
Onchocerca volvulus Transient receptor potential cation channel trpm homolog 0.0067 0 0.5
Echinococcus multilocularis transient receptor potential cation channel 0.0067 1 1
Schistosoma mansoni transient receptor potential channel 0.0067 0.0004 0.0004
Toxoplasma gondii transporter, cation channel family protein 0.0067 0 0.5
Loa Loa (eye worm) hypothetical protein 0.0067 1 1
Toxoplasma gondii 3'5'-cyclic nucleotide phosphodiesterase domain-containing protein 0.0067 0 0.5
Toxoplasma gondii 3'5'-cyclic nucleotide phosphodiesterase domain-containing protein 0.0067 0 0.5
Onchocerca volvulus 0.0067 0 0.5
Toxoplasma gondii transporter, cation channel family protein 0.0067 0 0.5
Echinococcus multilocularis short transient receptor potential channel 6 0.0067 0.9996 0.9996
Schistosoma mansoni transient receptor potential channel 0.0067 0.9996 1
Leishmania major hypothetical protein, unknown function 0.0067 0 0.5
Toxoplasma gondii hypothetical protein 0.0067 0 0.5
Trypanosoma brucei Voltage-dependent calcium channel subunit, putative 0.0067 0 0.5
Schistosoma mansoni transient receptor potential channel 0.0067 0.0004 0.0004
Trypanosoma cruzi inositol 1,4,5-trisphosphate receptor, putative 0.0067 0 0.5
Echinococcus granulosus transient receptor potential cation channel 0.0067 0.0004 0.0004
Leishmania major calcium channel protein, putative,ion transporter, putative 0.0067 0 0.5
Leishmania major hypothetical protein, conserved 0.0067 0 0.5
Toxoplasma gondii transporter, cation channel family protein 0.0067 0 0.5
Trichomonas vaginalis voltage and ligand gated potassium channel, putative 0.0067 0 0.5
Trypanosoma cruzi Voltage-dependent calcium channel subunit, putative 0.0067 0 0.5
Echinococcus multilocularis transient receptor potential cation channel 0.0067 1 1
Trypanosoma brucei inositol 1,4,5-trisphosphate receptor 0.0067 0 0.5
Onchocerca volvulus Transient receptor potential cation channel trpm homolog 0.0067 0 0.5
Loa Loa (eye worm) hypothetical protein 0.0067 0.0004 0.0004
Echinococcus multilocularis transient receptor potential cation channel 0.0067 0.0004 0.0004
Echinococcus granulosus short transient receptor potential channel 6 0.0067 0.9996 0.9996
Toxoplasma gondii hypothetical protein 0.0067 0 0.5
Echinococcus granulosus transient receptor potential cation channel 0.0067 0.0004 0.0004
Loa Loa (eye worm) hypothetical protein 0.0067 0.0004 0.0004
Echinococcus granulosus transient receptor potential cation channel 0.0067 1 1
Trichomonas vaginalis voltage and ligand gated potassium channel, putative 0.0067 0 0.5

Activities

Activity type Activity value Assay description Source Reference
Activity (ADMET) Neurotoxicity in ddY mouse assessed as elongation of hexobarbital-induced sleep at 300 mg/kg, po after 1 hr relative to diazepam ChEMBL. 24050790
Activity (ADMET) Neurotoxicity in ddY mouse assessed as reduction in locomotor activity at 10 to 100 mg/kg, po after 1 hr ChEMBL. 24050790
Activity (ADMET) Neurotoxicity in ddY mouse assessed as motor impairment at 10 to 100 mg/kg, po after 1 hr by horizontal rotarod test ChEMBL. 24050790

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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