Detailed information for compound 317013

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 827.935 | Formula: C42H58FN5O11
  • H donors: 3 H acceptors: 8 LogP: 4.35 Rotable bonds: 10
    Rule of 5 violations (Lipinski): 2
  • SMILES: CC[C@H]1OC(=O)[C@@](C)(F)C(=O)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@@H]([C@H]2O)N(C)C)[C@](C[C@H](C(=O)[C@@H]([C@@H]2[C@]1(C)OC(=O)N2)C)C)(C)OC(=O)NCc1ccc(cc1)c1ccncn1
  • InChi: 1S/C42H58FN5O11/c1-11-30-42(8)33(47-39(54)59-42)24(4)31(49)22(2)19-40(6,58-38(53)45-20-26-12-14-27(15-13-26)28-16-17-44-21-46-28)35(25(5)34(51)41(7,43)37(52)56-30)57-36-32(50)29(48(9)10)18-23(3)55-36/h12-17,21-25,29-30,32-33,35-36,50H,11,18-20H2,1-10H3,(H,45,53)(H,47,54)/t22-,23-,24+,25+,29+,30-,32-,33-,35-,36+,40-,41+,42-/m1/s1
  • InChiKey: LVEGPEBVHDWCQQ-IWBSLHARSA-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
Echinococcus granulosus adenosine kinase 0.124 1 0.5
Leishmania major adenosine kinase, putative 0.124 1 0.5
Trypanosoma cruzi adenosine kinase, putative 0.124 1 0.5
Trypanosoma cruzi adenosine kinase, putative 0.124 1 0.5
Toxoplasma gondii kinase, pfkB family protein 0.124 1 0.5
Schistosoma mansoni adenosine kinase 0.124 1 0.5
Schistosoma mansoni adenosine kinase 0.124 1 0.5
Onchocerca volvulus 0.1099 0 0.5
Echinococcus multilocularis adenosine kinase 0.124 1 0.5
Trypanosoma brucei adenosine kinase, putative 0.124 1 0.5
Trypanosoma brucei adenosine kinase, putative 0.124 1 0.5
Loa Loa (eye worm) hypothetical protein 0.124 1 0.5

Activities

Activity type Activity value Assay description Source Reference
MIC (functional) = 0.03 ug ml-1 Minimum inhibitory concentrationof the compound against erythromycin-susceptible Streptococcus pneumoniae was determined ChEMBL. 15686880
MIC (functional) = 0.06 ug ml-1 Minimum inhibitory concentrationof the compound against 3 erythromycin-susceptible Streptococcus pneumoniae OC4051 with an erm(B)-ribosomal methylase-mediated resistance was determined ChEMBL. 15686880
MIC (functional) = 0.12 ug ml-1 Minimum inhibitory concentrationof the compound against erythromycin-susceptible Staphylococcus aureus Smith OC4172 was determined ChEMBL. 15686880
MIC (functional) = 0.12 ug ml-1 Minimum inhibitory concentrationof the compound against 3 erythromycin-susceptible Streptococcus pneumoniae OC4421 with an mef(A) efflux-mediated resistance was determined ChEMBL. 15686880
MIC (functional) = 4 ug ml-1 Minimum inhibitory concentrationof the compound against erythromycin-susceptible Staphylococcusaureus Smith OC4172 in 50% mouse serum was determined ChEMBL. 15686880
MIC (functional) = 4 ug ml-1 Minimum inhibitory concentrationof the compound against Haemophilus influenzae OC4882 was determined ChEMBL. 15686880
MIC (functional) = 4 ug ml-1 Minimum inhibitory concentrationof the compound against erythromycin-susceptible Staphylococcusaureus Smith OC4172 in 50% mouse serum was determined ChEMBL. 15686880
MIC (functional) = 16 ug ml-1 Minimum inhibitory concentrationof the compound againstEnterococcus faecalis ATCC51299 with an erm(B)-encoded ribosomalmethylase was determined ChEMBL. 15686880

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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