Detailed information for compound 596756

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 604.781 | Formula: C38H44N4O3
  • H donors: 2 H acceptors: 3 LogP: 6.9 Rotable bonds: 14
    Rule of 5 violations (Lipinski): 2
  • SMILES: C=CCc1cc(C2CCN(CC2)CCCCNC(=O)c2ccc(cc2)c2ccc(cc2)C#N)c(c2c1CCCC2)OCC(=O)N
  • InChi: 1S/C38H44N4O3/c1-2-7-32-24-35(37(45-26-36(40)43)34-9-4-3-8-33(32)34)30-18-22-42(23-19-30)21-6-5-20-41-38(44)31-16-14-29(15-17-31)28-12-10-27(25-39)11-13-28/h2,10-17,24,30H,1,3-9,18-23,26H2,(H2,40,43)(H,41,44)
  • InChiKey: DSNFATNYGKVXFK-UHFFFAOYSA-N  

Network

Hover on a compound node to display the structore

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
Echinococcus multilocularis aldo keto reductase 0.0317 1 1
Loa Loa (eye worm) oxidoreductase 0.0317 1 1
Onchocerca volvulus 0.0092 0.1647 0.1647
Echinococcus granulosus aldo keto reductase family 1 member B4 0.0317 1 1
Leishmania major aldo-keto reductase-like protein 0.0317 1 1
Mycobacterium tuberculosis Probable oxidoreductase 0.0317 1 1
Echinococcus multilocularis aldo keto reductase family 1, member B4 0.0317 1 1
Trichomonas vaginalis aldo-keto reductase, putative 0.0317 1 1
Trichomonas vaginalis aldo-keto reductase, putative 0.0317 1 1
Leishmania major prostaglandin f2-alpha synthase/D-arabinose dehydrogenase 0.0317 1 1
Trypanosoma cruzi aldo/keto reductase, putative 0.0317 1 1
Brugia malayi oxidoreductase, aldo/keto reductase family protein 0.0317 1 1
Trichomonas vaginalis dihydrodiol dehydrogenase, putative 0.0317 1 1
Echinococcus multilocularis aldo keto reductase family 1, member B4 0.0317 1 1
Trichomonas vaginalis aldo-keto reductase, putative 0.0317 1 1
Loa Loa (eye worm) oxidoreductase 0.0317 1 1
Trichomonas vaginalis aldo-keto reductase, putative 0.0317 1 1
Mycobacterium leprae Conserved hypothetical protein 0.0225 0.6594 0.5922
Loa Loa (eye worm) oxidoreductase 0.0317 1 1
Echinococcus multilocularis aldehyde reductase 0.0225 0.6594 0.6594
Echinococcus multilocularis aldo keto reductase 0.0317 1 1
Echinococcus multilocularis aldo keto reductase 0.0317 1 1
Echinococcus multilocularis aldo keto reductase family 1, member B4 0.0317 1 1
Plasmodium vivax oxidoreductase, aldo/keto reductase domain containing protein 0.0092 0.1647 0.5
Mycobacterium leprae PROBABLE OXIDOREDUCTASE 0.0317 1 1
Schistosoma mansoni potassium channel beta 0.0092 0.1647 0.1647
Trypanosoma cruzi aldo-keto reductase 0.0317 1 1
Trichomonas vaginalis dihydrodiol dehydrogenase, putative 0.0317 1 1
Giardia lamblia Aldose reductase 0.0317 1 0.5
Echinococcus multilocularis aldo keto reductase family 1, member B4 0.0317 1 1
Loa Loa (eye worm) oxidoreductase 0.0317 1 1
Trichomonas vaginalis aldo-keto reductase, putative 0.0317 1 1
Brugia malayi oxidoreductase, aldo/keto reductase family protein 0.0317 1 1
Echinococcus granulosus aldo keto reductase 0.0317 1 1
Giardia lamblia Aldose reductase 0.0317 1 0.5
Echinococcus granulosus hypothetical protein 0.0317 1 1
Entamoeba histolytica aldose reductase, putative 0.0317 1 1
Trichomonas vaginalis aldo/keto reductase, putative 0.0317 1 1
Entamoeba histolytica aldose reductase, putative 0.0317 1 1
Trichomonas vaginalis dihydrodiol dehydrogenase, putative 0.0317 1 1
Echinococcus multilocularis aldo keto reductase family 1, member B4 0.0317 1 1
Entamoeba histolytica aldose reductase, putative 0.0317 1 1
Schistosoma mansoni pol-related 0.0317 1 1
Echinococcus granulosus aldo keto reductase family 1 member B4 0.0317 1 1
Trichomonas vaginalis aldo/keto reductase, putative 0.0317 1 1
Echinococcus granulosus aldehyde reductase 0.0225 0.6594 0.6594
Loa Loa (eye worm) oxidoreductase 0.0317 1 1
Mycobacterium ulcerans oxidoreductase 0.0317 1 1
Echinococcus multilocularis aldo keto reductase family 1, member B4 0.0317 1 1
Echinococcus granulosus aldo keto reductase family 1 member B4 0.0317 1 1
Brugia malayi NADH-dependent xylose reductase 0.0092 0.1647 0.1647
Onchocerca volvulus 0.0317 1 1
Toxoplasma gondii aldose reductase, putative 0.0317 1 1
Trichomonas vaginalis aldo-keto reductase, putative 0.0317 1 1
Echinococcus multilocularis aldo keto reductase family 1, member B4 0.0317 1 1
Loa Loa (eye worm) glutamate-cysteine ligase modifier subunit 0.0092 0.1647 0.1647
Plasmodium vivax aldehyde reductase, putative 0.0092 0.1647 0.5
Schistosoma mansoni aldo-keto reductase 0.0317 1 1
Plasmodium falciparum aldehyde reductase, putative 0.0092 0.1647 0.5
Echinococcus granulosus voltage gated potassium channel subunit 0.0092 0.1647 0.1647
Trichomonas vaginalis aldo-keto reductase, putative 0.0317 1 1
Loa Loa (eye worm) hypothetical protein 0.0317 1 1
Brugia malayi oxidoreductase, aldo/keto reductase family protein 0.0317 1 1
Plasmodium falciparum aldo-keto reductase, putative 0.0092 0.1647 0.5
Onchocerca volvulus 0.0317 1 1
Onchocerca volvulus 0.0317 1 1
Echinococcus granulosus aldo keto reductase family 1 member B4 0.0317 1 1
Leishmania major aldehyde reductase, putative,oxidoreductase, putative 0.0317 1 1
Echinococcus granulosus aldo keto reductase family 1 member B4 0.0317 1 1
Onchocerca volvulus 0.0317 1 1
Trichomonas vaginalis aldo-keto reductase, putative 0.0317 1 1
Trypanosoma brucei aldo-keto reductase, putative 0.0317 1 1
Echinococcus multilocularis aldo keto reductase family 1, member B4 0.0317 1 1
Echinococcus multilocularis aldo keto reductase family 1, member B4 0.0317 1 1
Schistosoma mansoni aldo-keto reductase 0.0317 1 1
Echinococcus granulosus aldo keto reductase 0.0317 1 1
Echinococcus multilocularis aldo keto reductase family 1, member B4 0.0317 1 1
Echinococcus granulosus aldo keto reductase 0.0317 1 1
Echinococcus multilocularis aldo keto reductase family 1, member B4 0.0317 1 1
Echinococcus multilocularis aldo keto reductase 0.0317 1 1
Echinococcus granulosus aldo keto reductase family 1 member B4 0.0317 1 1
Trypanosoma brucei prostaglandin f synthase 0.0317 1 1
Trichomonas vaginalis aldo/keto reductase, putative 0.0317 1 1
Onchocerca volvulus 0.0317 1 1
Trichomonas vaginalis aldo-keto reductase, putative 0.0317 1 1
Leishmania major prostaglandin f synthase, putative 0.0317 1 1
Echinococcus granulosus aldo keto reductase family 1 member B4 0.0317 1 1
Brugia malayi glutamate-cysteine ligase modifier subunit 0.0092 0.1647 0.1647
Trichomonas vaginalis aldo-keto reductase, putative 0.0317 1 1
Echinococcus granulosus aldo keto reductase family 1 member B4 0.0317 1 1
Echinococcus multilocularis voltage gated potassium channel subunit 0.0092 0.1647 0.1647
Onchocerca volvulus 0.0317 1 1
Echinococcus granulosus aldo keto reductase family 1 member B4 0.0317 1 1
Trichomonas vaginalis aldo-keto reductase, putative 0.0317 1 1
Trichomonas vaginalis aldo-keto reductase, putative 0.0317 1 1
Echinococcus granulosus aldo keto reductase family 1, member B4 0.0092 0.1647 0.1647

Activities

Activity type Activity value Assay description Source 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) = 0.81 % 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) = 2.67 % 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) = 3.22 % 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) = 43 % GSK_TCMDC: Percent inhibition of human HepG2 cell line. Test compounds present at 10uM. ChEMBL. 20485427
Inhibition (functional) = 92 % 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) = 8.33 Inhibition Frequency Index (IFI) GSK. 20485427
Percent growth inhibition (functional) = -6 % Percent inhibition of P. falciparum lactate dehydrogenase activity (at 2 uM) GSK. 20485427
Percent growth inhibition (functional) = 43 % Percent inhibition of HepG2 growth (at 10 uM) GSK. 20485427
Percent growth inhibition (functional) = 92 % Percent inhibition of P. falciparum Dd2 growth (at 2 uM) GSK. 20485427
Percent growth inhibition (functional) = 101 % Percent inhibition of P. falciparum 3D7 growth (at 2 uM) GSK. 20485427
XC50 (functional) = 6.1 XC50 determination of P. falciparum 3D7 growth GSK. 20485427
XC50 (functional) = 0.79939 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.

If you have references for this compound, please enter them in a user comment (below) or Contact us.