Detailed information for compound 602066

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 393.396 | Formula: C20H19N5O4
  • H donors: 5 H acceptors: 4 LogP: 2 Rotable bonds: 6
    Rule of 5 violations (Lipinski): 1
  • SMILES: OC(=O)/C=C\C(=O)O.NC(=N)NN=Cc1c[nH]c2c1cc(cc2)c1ccccc1
  • InChi: 1S/C16H15N5.C4H4O4/c17-16(18)21-20-10-13-9-19-15-7-6-12(8-14(13)15)11-4-2-1-3-5-11;5-3(6)1-2-4(7)8/h1-10,19H,(H4,17,18,21);1-2H,(H,5,6)(H,7,8)/b;2-1-
  • InChiKey: MEQAHNJQKZBBIZ-BTJKTKAUSA-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 protein tyrosine phosphatase, putative 0.0253 1 1
Schistosoma mansoni rab6-interacting 0.0039 0.124 0.1363
Giardia lamblia Low molecular weight protein-tyrosine-phosphatase 0.0253 1 1
Schistosoma mansoni rab6-interacting 0.0039 0.124 0.1363
Trichomonas vaginalis low molecular weight protein tyrosine phosphatase, putative 0.0253 1 0.5
Echinococcus granulosus Polycystic kidney disease protein 0.0039 0.124 0.1305
Trichomonas vaginalis low molecular weight protein-tyrosine-phosphatase, putative 0.0253 1 0.5
Schistosoma mansoni lipoxygenase 0.0231 0.9098 1
Loa Loa (eye worm) phosphotyrosine protein phosphatase 0.0253 1 1
Onchocerca volvulus 0.0253 1 1
Trichomonas vaginalis low molecular weight protein-tyrosine-phosphatase, putative 0.0253 1 0.5
Echinococcus multilocularis RUN 0.0039 0.124 0.1305
Trichomonas vaginalis low molecular weight protein tyrosine phosphatase, putative 0.0253 1 0.5
Leishmania major ATP-binding cassette protein subfamily G, member 4, putative 0.001 0.0061 0.5
Brugia malayi Doublecortin family protein 0.0039 0.124 0.124
Echinococcus granulosus lipoxygenase domain containing protein 0.0039 0.124 0.1305
Schistosoma mansoni hypothetical protein 0.0039 0.124 0.1363
Schistosoma mansoni loxhd1 0.0039 0.124 0.1363
Brugia malayi hypothetical protein 0.0039 0.124 0.124
Schistosoma mansoni ATP-binding cassette sub-family g2 (white protein) (abcg2) 0.001 0.0061 0.0067
Echinococcus multilocularis lipoxygenase domain containing protein 0.0039 0.124 0.1305
Echinococcus granulosus lipoxygenase domain containing protein 0.0039 0.124 0.1305
Trichomonas vaginalis low molecular weight protein tyrosine phosphatase, putative 0.0253 1 0.5
Echinococcus multilocularis arachidonate 5 lipoxygenase 0.0231 0.9098 1
Mycobacterium tuberculosis Phosphotyrosine protein phosphatase PtpA (protein-tyrosine-phosphatase) (PTPase) (LMW phosphatase) 0.0253 1 0.5
Loa Loa (eye worm) hypothetical protein 0.0039 0.124 0.124
Schistosoma mansoni lipoxygenase 0.0162 0.6259 0.6879
Mycobacterium ulcerans phosphotyrosine protein phosphatase PtpA 0.0253 1 1
Loa Loa (eye worm) doublecortin family protein 0.0039 0.124 0.124
Trypanosoma cruzi ABC transporter, putative 0.001 0.0061 0.5
Plasmodium vivax multidomain scavenger receptor, putative 0.0039 0.124 1
Echinococcus granulosus arachidonate 5 lipoxygenase 0.0231 0.9098 1
Echinococcus multilocularis Polycystic kidney disease protein 0.0039 0.124 0.1305
Schistosoma mansoni polycystin 1-related 0.0039 0.124 0.1363
Entamoeba histolytica protein tyrosine phosphatase, putative 0.0253 1 1
Echinococcus multilocularis lipoxygenase domain containing protein 0.0039 0.124 0.1305
Trypanosoma cruzi ATP-binding cassette protein, putative 0.001 0.0061 0.5
Toxoplasma gondii ATP-binding cassette G family transporter ABCG84 0.001 0.0061 0.5
Trypanosoma brucei ABC transporter, putative 0.001 0.0061 0.5
Leishmania major ATP-binding cassette protein subfamily G, member 6, putative 0.001 0.0061 0.5
Trichomonas vaginalis low molecular weight protein-tyrosine-phosphatase, putative 0.0253 1 0.5
Plasmodium falciparum LCCL domain-containing protein 0.0039 0.124 1
Brugia malayi hypothetical protein 0.0039 0.124 0.124
Trypanosoma brucei ATP-binding cassette protein, putative 0.001 0.0061 0.5
Loa Loa (eye worm) hypothetical protein 0.0039 0.124 0.124
Echinococcus granulosus RUN 0.0039 0.124 0.1305

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) = 0.13 % 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) = 0.57 % 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) = 1.34 % 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 % GSK_TCMDC: Percent inhibition of human HepG2 cell line. Test compounds present at 10uM. ChEMBL. 20485427
Inhibition (functional) = 61 % 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) = 84 % 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) = 3.68 Inhibition Frequency Index (IFI) GSK. 20485427
Percent growth inhibition (functional) = -2 % Percent inhibition of P. falciparum lactate dehydrogenase activity (at 2 uM) GSK. 20485427
Percent growth inhibition (functional) = 15 % Percent inhibition of HepG2 growth (at 10 uM) GSK. 20485427
Percent growth inhibition (functional) = 61 % Percent inhibition of P. falciparum Dd2 growth (at 2 uM) GSK. 20485427
Percent growth inhibition (functional) = 84 % Percent inhibition of P. falciparum 3D7 growth (at 2 uM) GSK. 20485427
XC50 (functional) = 6.28 XC50 determination of P. falciparum 3D7 growth GSK. 20485427
XC50 (functional) = 0.52769 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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