Detailed information for compound 602143

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 457.569 | Formula: C30H27N5
  • H donors: 0 H acceptors: 3 LogP: 5.32 Rotable bonds: 5
    Rule of 5 violations (Lipinski): 1
  • SMILES: N#Cc1ccc2c(c1)CCN(CC2)CCCn1c(nc2c1cncc2)c1ccc2c(c1)cccc2
  • InChi: 1S/C30H27N5/c31-20-22-6-7-24-11-16-34(17-12-26(24)18-22)14-3-15-35-29-21-32-13-10-28(29)33-30(35)27-9-8-23-4-1-2-5-25(23)19-27/h1-2,4-10,13,18-19,21H,3,11-12,14-17H2
  • InChiKey: SPWSADJQRHPLPO-UHFFFAOYSA-N  


Substructure search Similarity search

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
Entamoeba histolytica hypothetical protein 0.0003 0.0037 0.038
Trypanosoma cruzi myosin heavy chain kinase A, putative 0.0067 0.3631 1
Trypanosoma brucei myosin heavy chain kinase A, putative 0.0067 0.3631 1
Trichomonas vaginalis TKL family protein kinase 0.0004 0.0069 1
Leishmania major myosin heavy chain kinase c-like protein 0.0019 0.0963 0.2651
Schistosoma mansoni protein kinase 0.0179 1 1
Trichomonas vaginalis conserved hypothetical protein 0.0003 0.0037 0.5329
Trypanosoma cruzi myosin heavy chain kinase A, putative 0.0067 0.3631 1
Trichomonas vaginalis conserved hypothetical protein 0.0004 0.0069 1
Entamoeba histolytica hypothetical protein, conserved 0.0019 0.0963 1
Schistosoma mansoni eukaryotic elongation factor 2 kinase (eef-2 kinase) 0.0067 0.3631 0.3631
Echinococcus multilocularis dual specificity testis specific protein kinase 0.0179 1 1
Loa Loa (eye worm) hypothetical protein 0.0067 0.3631 1
Entamoeba histolytica protein kinase, putative 0.0019 0.0963 1
Echinococcus granulosus Microtubule-associated serine/threonine-protein kinase 0.0003 0.0031 0.0031
Trichomonas vaginalis TKL family protein kinase 0.0003 0.0037 0.5329
Schistosoma mansoni MAGUK homolog 0.0003 0.0031 0.0031
Entamoeba histolytica hypothetical protein 0.0019 0.0963 1
Trichomonas vaginalis TKL family protein kinase 0.0004 0.0069 1
Echinococcus multilocularis eukaryotic elongation factor 2 kinase 0.0067 0.3631 0.3631
Leishmania major elongation factor-2 kinase-like protein 0.0019 0.0963 0.2651
Echinococcus multilocularis microtubule associated serine:threonine protein 0.0003 0.0031 0.0031
Trichomonas vaginalis conserved hypothetical protein 0.0003 0.0037 0.5329
Schistosoma mansoni elongation factor 2 kinase 0.0019 0.0963 0.0963
Trichomonas vaginalis TK family protein kinase 0.0004 0.0069 1
Trichomonas vaginalis conserved hypothetical protein 0.0004 0.0069 1
Entamoeba histolytica protein kinase, putative 0.0003 0.0037 0.038
Schistosoma mansoni protein kinase 0.0179 1 1
Plasmodium falciparum conserved Plasmodium protein, unknown function 0.0002 0 0.5
Entamoeba histolytica hypothetical protein 0.0019 0.0963 1
Entamoeba histolytica hypothetical protein 0.0019 0.0963 1
Trypanosoma brucei myosin heavy chain kinase A, putative 0.0067 0.3631 1
Plasmodium vivax hypothetical protein, conserved 0.0002 0 0.5
Plasmodium vivax ubiquitin-protein ligase, putative 0.0002 0 0.5
Entamoeba histolytica protein kinase, putative 0.0019 0.0963 1
Brugia malayi MHCK/EF2 kinase domain family protein 0.0067 0.3631 1
Entamoeba histolytica hypothetical protein 0.0019 0.0963 1
Toxoplasma gondii Sel1 repeat-containing protein 0.0002 0 0.5
Echinococcus granulosus peripheral plasma membrane protein CASK 0.0003 0.0031 0.0031
Entamoeba histolytica hypothetical protein, conserved 0.0019 0.0963 1
Plasmodium falciparum ubiquitin-protein ligase, putative 0.0002 0 0.5
Plasmodium falciparum ubiquitin-protein ligase, putative 0.0002 0 0.5
Toxoplasma gondii Sel1 repeat-containing protein 0.0002 0 0.5
Entamoeba histolytica hypothetical protein, conserved 0.0019 0.0963 1
Trichomonas vaginalis conserved hypothetical protein 0.0003 0.0037 0.5329
Toxoplasma gondii Sel1 repeat-containing protein 0.0002 0 0.5
Entamoeba histolytica hypothetical protein 0.0019 0.0963 1
Entamoeba histolytica hypothetical protein 0.0019 0.0963 1
Toxoplasma gondii Sel1 repeat-containing protein 0.0002 0 0.5
Entamoeba histolytica elongation factor-2 kinase, putative 0.0019 0.0963 1
Loa Loa (eye worm) AGC/MAST/MAST protein kinase 0.0003 0.0031 0.0085
Trichomonas vaginalis CAMK family protein kinase 0.0003 0.0037 0.5329
Entamoeba histolytica hypothetical protein 0.0019 0.0963 1
Leishmania major myosin heavy chain kinase a-like protein 0.0067 0.3631 1
Onchocerca volvulus 0.0003 0.0031 1
Echinococcus granulosus eukaryotic elongation factor 2 kinase 0.0067 0.3631 0.3631
Trichomonas vaginalis TKL family protein kinase 0.0003 0.0037 0.5329
Schistosoma mansoni elongation factor 2 kinase 0.0019 0.0963 0.0963
Plasmodium vivax ubiquitin-protein ligase, putative 0.0002 0 0.5
Leishmania major related to elongation factor-2 kinase efk-1b isoform-like protein 0.0019 0.0963 0.2651
Trichomonas vaginalis TKL family protein kinase 0.0003 0.0037 0.5329
Entamoeba histolytica hypothetical protein 0.0019 0.0963 1
Echinococcus multilocularis peripheral plasma membrane protein CASK 0.0003 0.0031 0.0031

Activities

Activity type Activity value Assay description Source Reference
Inhibition (functional) = 4 % GSK_TCMDC: Inhibition of Plasmodium falciparum 3D7 LDH activity, using an LDH reporter assay. Test compounds present at 2uM ChEMBL. 20485427
Inhibition (functional) = 10.45 % ST_JUDE_LEISH: Cytotoxicity at 2uM final concentration against transgenic Leishmania Mexicana promastigotes LmGT2 that are glucose transport deficient and complemented with the L. Mexicana glucose transporter 2. Activity is measured by by DNA content using SYBR green in vitro ChEMBL. No reference
Inhibition (functional) = 15.05 % ST_JUDE_LEISH: Cytotoxicity at 2uM final concentration against transgenic Leishmania Mexicana promastigotes LmGLUT1 that are glucose transport deficient and complemented with the human glucose transporter GLUT1. Activity is measured by DNA content using SYBR green in vitro ChEMBL. No reference
Inhibition (functional) = 16.1 % ST_JUDE_LEISH: Cytotoxicity at 2uM final concentration against transgenic Leishmania Mexicana promastigotes LmPfHT that are glucose transport deficient and complemented with the Plasmodium falciparum hexose transporter. Activity is measured by by DNA content using SYBR green in vitro ChEMBL. No reference
Inhibition (functional) = 38 % GSK_TCMDC: Percent inhibition of human HepG2 cell line. Test compounds present at 10uM. ChEMBL. 20485427
Inhibition (functional) = 97 % GSK_TCMDC: Inhibition of Plasmodium falciparum Dd2 in whole red blood cells, using parasite LDH activity as an index of growth. Test compounds present at 2uM ChEMBL. 20485427
Inhibition (functional) = 100 % GSK_TCMDC: Inhibition of Plasmodium falciparum 3D7 in whole red blood cells, using parasite LDH activity as an index of growth. Test compounds present at 2uM ChEMBL. 20485427
Inhibition frequency index (IFI) (functional) = 5.67 Inhibition Frequency Index (IFI) GSK. 20485427
Percent growth inhibition (functional) = 4 % Percent inhibition of P. falciparum lactate dehydrogenase activity (at 2 uM) GSK. 20485427
Percent growth inhibition (functional) = 38 % Percent inhibition of HepG2 growth (at 10 uM) GSK. 20485427
Percent growth inhibition (functional) = 97 % Percent inhibition of P. falciparum Dd2 growth (at 2 uM) GSK. 20485427
Percent growth inhibition (functional) = 102 % Percent inhibition of P. falciparum 3D7 growth (at 2 uM) GSK. 20485427
XC50 (functional) = 6.7 XC50 determination of P. falciparum 3D7 growth GSK. 20485427
XC50 (functional) = 0.19795 uM GSK_TCMDC: Inhibition of Plasmodium falciparum 3D7 in whole erythrocytes, using parasite LDH activity as an index of growth. ChEMBL. 20485427

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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