Detailed information for compound 258607

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 695.807 | Formula: C31H53N9O9
  • H donors: 8 H acceptors: 9 LogP: -1.61 Rotable bonds: 26
    Rule of 5 violations (Lipinski): 3
  • SMILES: CC[C@@H]([C@@H](C(=O)N[C@H](C(=O)N)C)NC(=O)[C@H]1CCCN1C(=O)CNC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](C(C)C)NC(=O)C)CCC(=O)N)C)C
  • InChi: 1S/C31H53N9O9/c1-8-16(4)25(31(49)35-17(5)26(33)44)39-29(47)21-10-9-13-40(21)23(43)14-34-27(45)18(6)36-28(46)20(11-12-22(32)42)38-30(48)24(15(2)3)37-19(7)41/h15-18,20-21,24-25H,8-14H2,1-7H3,(H2,32,42)(H2,33,44)(H,34,45)(H,35,49)(H,36,46)(H,37,41)(H,38,48)(H,39,47)/t16-,17-,18-,20-,21+,24-,25-/m0/s1
  • InChiKey: YHVDSQHTZCEKFM-UREIEYMMSA-N  

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
Echinococcus multilocularis jun protein 0.0084 0.1347 0.4125
Entamoeba histolytica Niemann-Pick C1 protein, putative 0.01 0.1864 0.5
Echinococcus granulosus acetylcholinesterase 0.0135 0.3035 0.9296
Schistosoma mansoni niemann-pick C1 (NPC1) 0.0101 0.1914 0.1914
Loa Loa (eye worm) hypothetical protein 0.0052 0.0315 0.1039
Brugia malayi bZIP transcription factor family protein 0.0084 0.1347 0.4437
Loa Loa (eye worm) hypothetical protein 0.0081 0.1271 0.4189
Echinococcus multilocularis acetylcholinesterase 0.0135 0.3035 0.9296
Echinococcus granulosus Basic leucine zipper bZIP transcription factor 0.0084 0.1347 0.4125
Loa Loa (eye worm) hypothetical protein 0.0135 0.3035 1
Echinococcus multilocularis expressed conserved protein 0.0094 0.1666 0.5102
Echinococcus multilocularis protein dispatched 1 0.0049 0.0198 0.0606
Loa Loa (eye worm) hypothetical protein 0.0135 0.3035 1
Schistosoma mansoni jun-related protein 0.0068 0.0832 0.0832
Echinococcus granulosus Niemann Pick C1 protein 0.0142 0.3265 1
Echinococcus multilocularis Basic leucine zipper (bZIP) transcription factor 0.0084 0.1347 0.4125
Schistosoma mansoni hypothetical protein 0.0068 0.0832 0.0832
Echinococcus granulosus jun protein 0.0084 0.1347 0.4125
Schistosoma mansoni family S9 non-peptidase homologue (S09 family) 0.0135 0.3035 0.3035
Loa Loa (eye worm) hypothetical protein 0.01 0.1864 0.6141
Brugia malayi Carboxylesterase family protein 0.0135 0.3035 1
Echinococcus multilocularis Niemann Pick C1 protein 0.0142 0.3265 1
Echinococcus granulosus Niemann Pick C1 protein 0.01 0.1864 0.5709
Loa Loa (eye worm) acetylcholinesterase 1 0.0135 0.3035 1
Echinococcus granulosus carboxylesterase 5A 0.0135 0.3035 0.9296
Onchocerca volvulus 0.0066 0.0757 0.5
Echinococcus granulosus expressed conserved protein 0.0094 0.1666 0.5102
Loa Loa (eye worm) carboxylesterase 0.0135 0.3035 1
Echinococcus granulosus acetylcholinesterase 0.0135 0.3035 0.9296
Echinococcus multilocularis carboxylesterase 5A 0.0135 0.3035 0.9296
Brugia malayi hypothetical protein 0.0066 0.0757 0.2493
Trichomonas vaginalis conserved hypothetical protein 0.0043 0 0.5
Brugia malayi Carboxylesterase family protein 0.0135 0.3035 1
Echinococcus multilocularis Niemann Pick C1 protein 0.01 0.1864 0.5709
Brugia malayi Niemann-Pick C1 protein precursor 0.01 0.1864 0.6141
Echinococcus multilocularis acetylcholinesterase 0.0135 0.3035 0.9296

Activities

Activity type Activity value Assay description Source Reference
IC50 (binding) = 2500 uM In vitro inhibition of human Cyclophillin A/protein interaction. ChEMBL. 12431052
IC50 (binding) = 2500 uM In vitro inhibition of human Cyclophillin A/protein interaction. ChEMBL. 12431052

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

No external resources registered for this compound

Bibliographic References

1 literature reference was collected for this gene.

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