Detailed information for compound 917520

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 709.872 | Formula: C38H55N5O8
  • H donors: 6 H acceptors: 7 LogP: 5.73 Rotable bonds: 25
    Rule of 5 violations (Lipinski): 3
  • SMILES: CC(C[C@H](C(=O)N[C@H](C(=O)N[C@@H](C(=O)N[C@H](C(=O)O)Cc1ccccc1)CC(C)C)Cc1ccccc1)NC(=O)[C@@H](NC(=O)OC(C)(C)C)C)C
  • InChi: 1S/C38H55N5O8/c1-23(2)19-28(40-32(44)25(5)39-37(50)51-38(6,7)8)33(45)42-30(21-26-15-11-9-12-16-26)35(47)41-29(20-24(3)4)34(46)43-31(36(48)49)22-27-17-13-10-14-18-27/h9-18,23-25,28-31H,19-22H2,1-8H3,(H,39,50)(H,40,44)(H,41,47)(H,42,45)(H,43,46)(H,48,49)/t25-,28+,29+,30-,31-/m0/s1
  • InChiKey: MJBDSSQEKPWUKT-KAVNOODHSA-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 formyl peptide receptor 1 Starlite/ChEMBL References

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
Loa Loa (eye worm) hypothetical protein 0.0912 1 1
Onchocerca volvulus Glutaminyl cyclase homolog 0.0912 1 1
Trichomonas vaginalis conserved hypothetical protein 0.0207 0 0.5
Trypanosoma cruzi glutaminyl cyclase, putative 0.0207 0 0.5
Trichomonas vaginalis Clan MH, family M28, aminopeptidase S-like metallopeptidase 0.0207 0 0.5
Trichomonas vaginalis conserved hypothetical protein 0.0207 0 0.5
Mycobacterium tuberculosis Conserved protein 0.0207 0 0.5
Toxoplasma gondii peptidase, M28 family protein 0.0207 0 0.5
Schistosoma mansoni glutaminyl cyclase (M28 family) 0.0912 1 1
Toxoplasma gondii hypothetical protein 0.0207 0 0.5
Leishmania major hypothetical protein, conserved 0.0207 0 0.5
Trypanosoma brucei glutaminyl cyclase, putative 0.0207 0 0.5
Trichomonas vaginalis conserved hypothetical protein 0.0207 0 0.5
Mycobacterium ulcerans hypothetical protein 0.0207 0 0.5
Leishmania major glutaminyl cyclase, putative 0.0207 0 0.5
Trypanosoma cruzi glutaminyl cyclase, putative 0.0207 0 0.5
Echinococcus granulosus glutaminyl peptide cyclotransferase 0.0912 1 1
Mycobacterium ulcerans lipoprotein aminopeptidase LpqL 0.0207 0 0.5
Mycobacterium tuberculosis Probable lipoprotein aminopeptidase LpqL 0.0207 0 0.5
Echinococcus multilocularis glutaminyl peptide cyclotransferase 0.0912 1 1

Activities

Activity type Activity value Assay description Source Reference
Activity (binding) Agonist activity at formyl peptide receptor in human HL60 cells at 10 uM by Fura-2 method ChEMBL. 25035262
Kd (functional) = 170 nM Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins prior to fMLP challenge by Fura-2 method ChEMBL. 25035262

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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