Detailed information for compound 1568683

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 660.772 | Formula: C33H42F2N4O6S
  • H donors: 3 H acceptors: 6 LogP: 4.23 Rotable bonds: 17
    Rule of 5 violations (Lipinski): 2
  • SMILES: CCCN(C(=O)c1cc(cc(c1)c1ncco1)C(=O)N[C@H]([C@@H]([C@@H]1NC[C@@H](C1)S(=O)(=O)CCC)O)Cc1cc(F)cc(c1)F)CCC
  • InChi: 1S/C33H42F2N4O6S/c1-4-8-39(9-5-2)33(42)24-16-22(15-23(17-24)32-36-7-10-45-32)31(41)38-29(14-21-12-25(34)18-26(35)13-21)30(40)28-19-27(20-37-28)46(43,44)11-6-3/h7,10,12-13,15-18,27-30,37,40H,4-6,8-9,11,14,19-20H2,1-3H3,(H,38,41)/t27-,28-,29+,30-/m1/s1
  • InChiKey: YDOMJVDTZBDVFM-GKIKGMKOSA-N  


Substructure search Similarity search

Network

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Synonyms

No synonyms found for this compound

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Homo sapiens beta-site APP-cleaving enzyme 1 Starlite/ChEMBL References

Predicted pathogen targets for this compound

By orthology
Species Potential target Known druggable target/s Ortholog Group
Schistosoma mansoni memapsin-2 (A01 family) Get druggable targets OG5_135830 All targets in OG5_135830
Schistosoma japonicum ko:K07747 beta-site APP-cleaving enzyme 2 (memapsin 1) [EC3.4.23.45], putative Get druggable targets OG5_135830 All targets in OG5_135830
By sequence similarity to non orthologous known druggable targets
Species Potential target Known druggable target Length Alignment span Identity
Plasmodium falciparum plasmepsin VII beta-site APP-cleaving enzyme 1 401 aa 352 aa 21.3 %
Obtained from network model

Ranking Plot

Putative Targets List

Species Potential target Raw Global Species
Plasmodium falciparum plasmepsin VI 0.0021 0 0.5
Loa Loa (eye worm) hypothetical protein 0.0021 0 0.5
Loa Loa (eye worm) aspartyl protease 6 0.0021 0 0.5
Plasmodium vivax aspartyl protease, putative 0.0021 0 0.5
Loa Loa (eye worm) hypothetical protein 0.0021 0 0.5
Plasmodium vivax aspartyl proteinase, putative 0.0021 0 0.5
Plasmodium vivax aspartyl protease, putative 0.0021 0 0.5
Toxoplasma gondii aspartyl protease ASP1 0.0021 0 0.5
Plasmodium vivax aspartyl protease, putative 0.0021 0 0.5
Plasmodium falciparum plasmepsin V 0.0021 0 0.5
Plasmodium falciparum plasmepsin IX 0.0021 0 0.5
Plasmodium falciparum plasmepsin VII 0.0021 0 0.5
Plasmodium falciparum plasmepsin I 0.0021 0 0.5
Brugia malayi Eukaryotic aspartyl protease family protein 0.0021 0 0.5
Plasmodium vivax aspartyl proteinase, putative 0.0021 0 0.5
Plasmodium falciparum plasmepsin X 0.0021 0 0.5
Onchocerca volvulus 0.0317 0.5912 1
Brugia malayi aspartic protease BmAsp-1, identical 0.0021 0 0.5
Toxoplasma gondii eukaryotic aspartyl protease superfamily protein 0.0021 0 0.5
Toxoplasma gondii aspartyl proteinase (eimepsin), putative 0.0021 0 0.5
Trichomonas vaginalis Clan AA, family A1, cathepsin D-like aspartic peptidase 0.0021 0 0.5
Plasmodium falciparum plasmepsin IV 0.0021 0 0.5
Toxoplasma gondii aspartyl protease 0.0021 0 0.5
Plasmodium vivax plasmepsin IV, putative 0.0021 0 0.5
Echinococcus multilocularis cathepsin d (lysosomal aspartyl protease) 0.0021 0 0.5
Plasmodium falciparum plasmepsin VIII, putative 0.0021 0 0.5
Echinococcus granulosus cathepsin d lysosomal aspartyl protease 0.0021 0 0.5
Brugia malayi aspartic protease BmAsp-2, identical 0.0021 0 0.5
Toxoplasma gondii aspartyl protease ASP3 0.0021 0 0.5
Brugia malayi Pepsin A precursor 0.0021 0 0.5
Loa Loa (eye worm) aspartic protease BmAsp-2 0.0021 0 0.5
Brugia malayi hypothetical protein 0.0021 0 0.5
Plasmodium falciparum plasmepsin III 0.0021 0 0.5
Loa Loa (eye worm) aspartic protease BmAsp-1 0.0021 0 0.5
Plasmodium vivax plasmepsin V, putative 0.0021 0 0.5
Plasmodium falciparum plasmepsin II 0.0021 0 0.5
Loa Loa (eye worm) hypothetical protein 0.0021 0 0.5
Brugia malayi hypothetical protein 0.0021 0 0.5

Activities

Activity type Activity value Assay description Source Reference
IC50 (binding) = 68 nM Inhibition of BACE-1 in human HEK293 cells overexpressing APP 695 swedish mutation assessed as inhibition of amyloid beta (1 to 40) production by immunoprecipitation assay ChEMBL. 21974952

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.