Detailed information for compound 306739

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 343.375 | Formula: C22H17NO3
  • H donors: 2 H acceptors: 3 LogP: 4.89 Rotable bonds: 6
    Rule of 5 violations (Lipinski): 1
  • SMILES: O=C(Nc1ccccc1C(=O)O)/C=C/c1ccc(cc1)c1ccccc1
  • InChi: 1S/C22H17NO3/c24-21(23-20-9-5-4-8-19(20)22(25)26)15-12-16-10-13-18(14-11-16)17-6-2-1-3-7-17/h1-15H,(H,23,24)(H,25,26)/b15-12+
  • InChiKey: AIGCPSYTABFABO-NTCAYCPXSA-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 leukotriene B4 receptor Starlite/ChEMBL No 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
Trichomonas vaginalis geranylgeranyl pyrophosphate synthase, putative 0.0207 1 0.5
Echinococcus multilocularis farnesyl pyrophosphate synthase 0.0207 1 1
Mycobacterium ulcerans geranylgeranyl pyrophosphate synthase 0.0207 1 1
Treponema pallidum octaprenyl-diphosphate synthase 0.0052 0 0.5
Wolbachia endosymbiont of Brugia malayi geranylgeranyl pyrophosphate synthase 0.0052 0 0.5
Schistosoma mansoni farnesyl pyrophosphate synthase 0.0207 1 1
Wolbachia endosymbiont of Brugia malayi geranylgeranyl pyrophosphate synthase 0.0052 0 0.5
Trypanosoma cruzi farnesyl pyrophosphate synthase 0.0207 1 1
Toxoplasma gondii polyprenyl synthetase superfamily protein 0.0207 1 1
Mycobacterium tuberculosis Probable geranylgeranyl pyrophosphate synthetase IdsA2 (ggppsase) (GGPP synthetase) (geranylgeranyl diphosphate synthase) 0.0207 1 1
Leishmania major farnesyl pyrophosphate synthase 0.0207 1 1
Entamoeba histolytica geranylgeranyl pyrophosphate synthase, putative 0.0052 0 0.5
Trichomonas vaginalis geranylgeranyl pyrophosphate synthase, putative 0.0207 1 0.5
Plasmodium vivax geranylgeranyl pyrophosphate synthase 0.0207 1 1
Loa Loa (eye worm) polyprenyl synthetase 0.0207 1 1
Mycobacterium ulcerans geranylgeranyl pyrophosphate synthase 0.0207 1 1
Chlamydia trachomatis geranylgeranyl pyrophosphate synthase 0.0052 0 0.5
Entamoeba histolytica geranylgeranyl pyrophosphate synthetase, putative 0.0052 0 0.5
Trypanosoma cruzi farnesyl pyrophosphate synthase, putative 0.0207 1 1
Trichomonas vaginalis geranylgeranyl diphosphate synthase, putative 0.0207 1 0.5
Giardia lamblia Farnesyl diphosphate synthase 0.0207 1 0.5
Plasmodium falciparum geranylgeranyl pyrophosphate synthase, putative 0.0207 1 1
Trypanosoma brucei farnesyl pyrophosphate synthase 0.0207 1 1
Echinococcus granulosus farnesyl pyrophosphate synthase 0.0207 1 1
Entamoeba histolytica bifunctional short chain isoprenyl diphosphate synthase, putative 0.0052 0 0.5
Mycobacterium leprae PROBABLE POLYPRENYL-DIPHOSPHATE SYNTHASE GRCC1 (POLYPRENYL PYROPHOSPHATE SYNTHETASE) 0.0052 0 0.5

Activities

Activity type Activity value Assay description Source Reference
IC50 (binding) = 830 nM In vitro binding affinity towards LTB4 receptor determined by measuring the displacement of [3H]-LTB4 from isolated neutrophils ChEMBL. No reference
IC50 (binding) = 830 nM In vitro binding affinity towards LTB4 receptor determined by measuring the displacement of [3H]-LTB4 from isolated neutrophils ChEMBL. No reference
IC50 (functional) = 3417 nM In vitro inhibition of LTB4 induced neutrophil aggregation was determined ChEMBL. No reference
IC50 (functional) = 3417 nM In vitro inhibition of LTB4 induced neutrophil aggregation was determined ChEMBL. No reference

Phenotypes

Whole-cell/tissue/organism interactions

Species name Source Reference Is orphan
Homo sapiens ChEMBL23

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

No literature references available for this target.

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