Detailed information for compound 600235

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 505.051 | Formula: C29H33ClN4O2
  • H donors: 1 H acceptors: 3 LogP: 5.41 Rotable bonds: 7
    Rule of 5 violations (Lipinski): 2
  • SMILES: COc1ccc2c(c1)c(ccn2)C(=O)NC1CCC(CC1)CCN1CCc2c(C1)ccc(c2)C#N.Cl
  • InChi: 1S/C29H32N4O2.ClH/c1-35-25-8-9-28-27(17-25)26(10-13-31-28)29(34)32-24-6-3-20(4-7-24)11-14-33-15-12-22-16-21(18-30)2-5-23(22)19-33;/h2,5,8-10,13,16-17,20,24H,3-4,6-7,11-12,14-15,19H2,1H3,(H,32,34);1H
  • InChiKey: ZXZDZAYEQIGHEH-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
Brugia malayi hypothetical protein 0.0025 0.1625 0.1505
Loa Loa (eye worm) hypothetical protein 0.0043 0.4581 0.4769
Schistosoma mansoni histone-lysine n-methyltransferase setb1 0.0017 0.0294 0.0366
Echinococcus multilocularis fetal alzheimer antigen, falz 0.0023 0.1214 0.1287
Loa Loa (eye worm) intermediate filament protein 0.0026 0.1741 0.161
Echinococcus multilocularis lamin 0.0026 0.1741 0.2026
Onchocerca volvulus 0.0026 0.1741 0.5
Schistosoma mansoni bromodomain containing protein 0.0064 0.8037 1
Loa Loa (eye worm) hypothetical protein 0.0026 0.1662 0.1522
Echinococcus granulosus bromodomain adjacent to zinc finger domain 0.0061 0.7437 1
Loa Loa (eye worm) hypothetical protein 0.0025 0.1625 0.1481
Schistosoma mansoni intermediate filament proteins 0.0026 0.1741 0.2166
Echinococcus granulosus zinc finger protein 0.002 0.0717 0.0592
Trypanosoma cruzi PAB1-binding protein , putative 0.0025 0.1625 1
Echinococcus multilocularis zinc finger protein 0.002 0.0717 0.0592
Schistosoma mansoni methyl-cpg binding protein mbd 0.0017 0.0294 0.0366
Schistosoma mansoni acetyl-CoA C-acetyltransferase 0.0023 0.1214 0.151
Echinococcus granulosus bromodomain adjacent to zinc finger domain 0.0037 0.3456 0.4427
Loa Loa (eye worm) bromodomain containing protein 0.0018 0.0397 0.0114
Echinococcus granulosus lamin dm0 0.0026 0.1741 0.2026
Plasmodium falciparum ataxin-2 like protein, putative 0.0025 0.1625 0.5
Schistosoma mansoni methyl-cpg binding protein mbd 0.0017 0.0294 0.0366
Echinococcus multilocularis lamin dm0 0.0026 0.1741 0.2026
Loa Loa (eye worm) intermediate filament tail domain-containing protein 0.0026 0.1741 0.161
Brugia malayi Intermediate filament tail domain containing protein 0.0026 0.1741 0.1623
Schistosoma mansoni zinc finger protein 0.002 0.0717 0.0891
Echinococcus granulosus intermediate filament protein 0.0026 0.1741 0.2026
Trypanosoma brucei PAB1-binding protein , putative 0.0025 0.1625 1
Echinococcus multilocularis musashi 0.0026 0.1741 0.2026
Echinococcus multilocularis bromodomain adjacent to zinc finger domain 0.0061 0.7437 1
Loa Loa (eye worm) hypothetical protein 0.0039 0.3864 0.3972
Echinococcus granulosus fetal alzheimer antigen falz 0.0023 0.1214 0.1287
Brugia malayi intermediate filament protein 0.0026 0.1741 0.1623
Loa Loa (eye worm) hypothetical protein 0.0026 0.1741 0.161
Brugia malayi PHD-finger family protein 0.0025 0.161 0.149
Toxoplasma gondii LsmAD domain-containing protein 0.0025 0.1625 0.5
Loa Loa (eye worm) hypothetical protein 0.0041 0.4261 0.4413
Loa Loa (eye worm) hypothetical protein 0.0072 0.9283 1
Echinococcus multilocularis bromodomain adjacent to zinc finger domain 0.0037 0.3456 0.4427
Plasmodium falciparum ataxin-2 like protein, putative 0.0025 0.1625 0.5
Schistosoma mansoni lamin 0.0026 0.1741 0.2166
Onchocerca volvulus 0.0026 0.1741 0.5
Schistosoma mansoni histone-lysine n-methyltransferase setb1 0.0017 0.0294 0.0366
Schistosoma mansoni lamin 0.0026 0.1741 0.2166
Brugia malayi Bromodomain containing protein 0.0039 0.3853 0.3765
Schistosoma mansoni hypothetical protein 0.0021 0.0894 0.1112
Loa Loa (eye worm) PHD-finger family protein 0.0021 0.0894 0.0667
Plasmodium vivax ataxin-2 like protein, putative 0.0025 0.1625 0.5
Echinococcus granulosus lamin 0.0026 0.1741 0.2026
Leishmania major hypothetical protein, conserved 0.0025 0.1625 1
Trypanosoma cruzi PAB1-binding protein , putative 0.0025 0.1625 1

Activities

Activity type Activity value Assay description Source Reference
Inhibition (functional) = 1 % 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) = 1 % GSK_TCMDC: Inhibition of Plasmodium falciparum 3D7 LDH activity, using an LDH reporter assay. Test compounds present at 2uM ChEMBL. 20485427
Inhibition (functional) = 5.23 % 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) = 6.71 % 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) = 7.23 % 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) = 12 % 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 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) = 0.72 Inhibition Frequency Index (IFI) GSK. 20485427
Percent growth inhibition (functional) = 1 % Percent inhibition of P. falciparum Dd2 growth (at 2 uM) GSK. 20485427
Percent growth inhibition (functional) = 1 % Percent inhibition of P. falciparum lactate dehydrogenase activity (at 2 uM) GSK. 20485427
Percent growth inhibition (functional) = 12 % Percent inhibition of HepG2 growth (at 10 uM) GSK. 20485427
Percent growth inhibition (functional) = 97 % Percent inhibition of P. falciparum 3D7 growth (at 2 uM) GSK. 20485427
XC50 (functional) = 5.94 XC50 determination of P. falciparum 3D7 growth GSK. 20485427
XC50 (functional) = 1.15543 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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