Detailed information for compound 602246

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 462.582 | Formula: C26H27FN4OS
  • H donors: 1 H acceptors: 1 LogP: 3.99 Rotable bonds: 7
    Rule of 5 violations (Lipinski): 1
  • SMILES: Fc1ccc2c(c1)n(CCN1CCC(CC1)NCc1scc(c1)c1ccccc1)c(=O)cn2
  • InChi: 1S/C26H27FN4OS/c27-21-6-7-24-25(15-21)31(26(32)17-29-24)13-12-30-10-8-22(9-11-30)28-16-23-14-20(18-33-23)19-4-2-1-3-5-19/h1-7,14-15,17-18,22,28H,8-13,16H2
  • InChiKey: WDUOIMBQPUHECT-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
Schistosoma mansoni transcription factor LCR-F1 0.0037 0.0427 0.1315
Echinococcus multilocularis Basic leucine zipper (bZIP) transcription 0.0037 0.0427 0.0427
Loa Loa (eye worm) hypothetical protein 0.0051 0.0854 0.1387
Schistosoma mansoni intermediate filament proteins 0.0083 0.1835 0.5658
Plasmodium vivax ataxin-2 like protein, putative 0.0052 0.0878 0.5
Brugia malayi intermediate filament protein 0.0083 0.1835 0.5193
Plasmodium falciparum ataxin-2 like protein, putative 0.0052 0.0878 0.5
Schistosoma mansoni tar DNA-binding protein 0.0129 0.3243 1
Echinococcus granulosus lamin dm0 0.0083 0.1835 0.1835
Loa Loa (eye worm) hypothetical protein 0.0052 0.0878 0.1475
Echinococcus multilocularis musashi 0.0083 0.1835 0.1835
Schistosoma mansoni tar DNA-binding protein 0.0129 0.3243 1
Onchocerca volvulus 0.0083 0.1835 1
Echinococcus multilocularis lamin 0.0083 0.1835 0.1835
Schistosoma mansoni lamin 0.0083 0.1835 0.5658
Entamoeba histolytica hypothetical protein 0.0037 0.0427 0.5
Echinococcus multilocularis tumor protein p63 0.0348 1 1
Entamoeba histolytica hypothetical protein 0.0037 0.0427 0.5
Toxoplasma gondii LsmAD domain-containing protein 0.0052 0.0878 0.5
Echinococcus granulosus tar DNA binding protein 0.0129 0.3243 0.3243
Loa Loa (eye worm) TAR-binding protein 0.0129 0.3243 1
Trypanosoma brucei PAB1-binding protein , putative 0.0052 0.0878 0.5
Entamoeba histolytica hypothetical protein 0.0037 0.0427 0.5
Echinococcus granulosus lamin 0.0083 0.1835 0.1835
Brugia malayi hypothetical protein 0.0037 0.0427 0.0385
Trypanosoma cruzi PAB1-binding protein , putative 0.0052 0.0878 0.5
Loa Loa (eye worm) intermediate filament tail domain-containing protein 0.0083 0.1835 0.4923
Brugia malayi hypothetical protein 0.0052 0.0878 0.1927
Brugia malayi cytoplasmic intermediate filament protein 0.0044 0.0651 0.1152
Plasmodium falciparum ataxin-2 like protein, putative 0.0052 0.0878 0.5
Loa Loa (eye worm) MH2 domain-containing protein 0.0127 0.3183 0.9784
Brugia malayi TAR-binding protein 0.0129 0.3243 1
Brugia malayi RNA binding protein 0.0129 0.3243 1
Entamoeba histolytica hypothetical protein 0.0037 0.0427 0.5
Brugia malayi RNA recognition motif domain containing protein 0.0129 0.3243 1
Schistosoma mansoni hypothetical protein 0.0037 0.0427 0.1315
Loa Loa (eye worm) hypothetical protein 0.0081 0.1788 0.4755
Echinococcus granulosus cytoplasmic intermediate filament protein 0.004 0.0516 0.0516
Schistosoma mansoni tar DNA-binding protein 0.0129 0.3243 1
Schistosoma mansoni cellular tumor antigen P53 0.0051 0.0854 0.2633
Echinococcus multilocularis cytoplasmic intermediate filament protein 0.004 0.0516 0.0516
Loa Loa (eye worm) RNA binding protein 0.0129 0.3243 1
Schistosoma mansoni tar DNA-binding protein 0.0129 0.3243 1
Echinococcus granulosus Basic leucine zipper bZIP transcription 0.0037 0.0427 0.0427
Trypanosoma cruzi PAB1-binding protein , putative 0.0052 0.0878 0.5
Brugia malayi Intermediate filament tail domain containing protein 0.0083 0.1835 0.5193
Onchocerca volvulus 0.0083 0.1835 1
Loa Loa (eye worm) hypothetical protein 0.0083 0.1835 0.4923
Loa Loa (eye worm) RNA recognition domain-containing protein domain-containing protein 0.0129 0.3243 1
Leishmania major hypothetical protein, conserved 0.0052 0.0878 0.5
Loa Loa (eye worm) intermediate filament protein 0.0083 0.1835 0.4923
Schistosoma mansoni tar DNA-binding protein 0.0129 0.3243 1
Echinococcus granulosus intermediate filament protein 0.0083 0.1835 0.1835
Brugia malayi MH2 domain containing protein 0.0127 0.3183 0.9795
Schistosoma mansoni lamin 0.0083 0.1835 0.5658
Echinococcus multilocularis lamin dm0 0.0083 0.1835 0.1835
Echinococcus multilocularis tar DNA binding protein 0.0129 0.3243 0.3243
Loa Loa (eye worm) cytoplasmic intermediate filament protein 0.0044 0.0651 0.0656
Loa Loa (eye worm) hypothetical protein 0.004 0.0516 0.0168
Loa Loa (eye worm) transcription factor SMAD2 0.0127 0.3183 0.9784

Activities

Activity type Activity value Assay description Source Reference
IC50 (functional) > 23000 nM ST_JUDE_LEISH: Cytotoxicity 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
IC50 (functional) > 23000 nM ST_JUDE_LEISH: Cytotoxicity 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
IC50 (functional) > 23000 nM ST_JUDE_LEISH: Cytotoxicity 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) = 0 % GSK_TCMDC: Inhibition of Plasmodium falciparum 3D7 LDH activity, using an LDH reporter assay. Test compounds present at 2uM ChEMBL. 20485427
Inhibition (functional) = 0 % GSK_TCMDC: Percent inhibition of human HepG2 cell line. Test compounds present at 10uM. ChEMBL. 20485427
Inhibition (functional) = 14 % 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) = 28.44 % 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) = 32.42 % 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) = 48.55 % 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) = 91 % 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) = 10.34 Inhibition Frequency Index (IFI) GSK. 20485427
Percent growth inhibition (functional) = -5 % Percent inhibition of HepG2 growth (at 10 uM) GSK. 20485427
Percent growth inhibition (functional) = -2 % Percent inhibition of P. falciparum lactate dehydrogenase activity (at 2 uM) GSK. 20485427
Percent growth inhibition (functional) = 14 % Percent inhibition of P. falciparum Dd2 growth (at 2 uM) GSK. 20485427
Percent growth inhibition (functional) = 91 % Percent inhibition of P. falciparum 3D7 growth (at 2 uM) GSK. 20485427
XC50 (functional) = 6.06 XC50 determination of P. falciparum 3D7 growth GSK. 20485427
XC50 (functional) = 0.86255 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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