Detailed information for compound 216312

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 283.345 | Formula: C16H13NO2S
  • H donors: 1 H acceptors: 3 LogP: 2.79 Rotable bonds: 1
    Rule of 5 violations (Lipinski): 1
  • SMILES: N#Cc1ccccc1C#CCC1(C)SC(=O)C(=C1O)C
  • InChi: 1S/C16H13NO2S/c1-11-14(18)16(2,20-15(11)19)9-5-8-12-6-3-4-7-13(12)10-17/h3-4,6-7,18H,9H2,1-2H3
  • InChiKey: ZSLPDNDSYQTVFQ-UHFFFAOYSA-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
Plasmodium falciparum protein farnesyltransferase subunit alpha 0.0185 0.2147 0.5
Schistosoma mansoni geranylgeranyl transferase type I beta subunit 0.0231 0.3148 0.4054
Loa Loa (eye worm) prenyltransferase and squalene oxidase repeat family protein 0.0231 0.3148 0.133
Brugia malayi hypothetical protein 0.0426 0.7439 0.7439
Echinococcus multilocularis geranylgeranyl transferase type I beta subunit 0.0231 0.3148 0.1275
Plasmodium vivax prenyltransferase alpha subunit, putative 0.0185 0.2147 0.5
Loa Loa (eye worm) hypothetical protein 0.0294 0.4536 0.3175
Brugia malayi hypoxia-induced factor 1 0.0271 0.4036 0.4036
Toxoplasma gondii hypothetical protein 0.0137 0.1091 0.5
Echinococcus granulosus jun protein 0.0542 1 1
Schistosoma mansoni jun-related protein 0.0441 0.7766 1
Echinococcus multilocularis Basic leucine zipper (bZIP) transcription factor 0.0542 1 1
Brugia malayi Prenyltransferase and squalene oxidase repeat family protein 0.0231 0.3148 0.3148
Onchocerca volvulus 0.0426 0.7439 0.5
Trichomonas vaginalis protein farnesyltransferase alpha subunit/RAB geranylgeranyl transferase alpha subunit, putative 0.0185 0.2147 0.5134
Schistosoma mansoni protein farnesyltransferase alpha subunit 0.0185 0.2147 0.2765
Schistosoma mansoni geranylgeranyl transferase type I beta subunit 0.0231 0.3148 0.4054
Trichomonas vaginalis protein farnesyltransferase alpha subunit, putative 0.0185 0.2147 0.5134
Echinococcus multilocularis jun protein 0.0542 1 1
Loa Loa (eye worm) hypoxia-induced factor 1 0.0271 0.4036 0.2509
Echinococcus granulosus Basic leucine zipper bZIP transcription factor 0.0542 1 1
Trichomonas vaginalis geranylgeranyl transferase type I beta subunit, putative 0.0231 0.3148 1
Brugia malayi Protein prenyltransferase alpha subunit repeat containing protein 0.0185 0.2147 0.2147
Echinococcus granulosus geranylgeranyl transferase type I beta subunit 0.0231 0.3148 0.1275
Brugia malayi hypothetical protein 0.0294 0.4536 0.4536
Trichomonas vaginalis protein farnesyltransferase alpha subunit, putative 0.0185 0.2147 0.5134
Schistosoma mansoni hypothetical protein 0.0441 0.7766 1
Giardia lamblia Rab geranylgeranyltransferase 0.0185 0.2147 0.5
Loa Loa (eye worm) hypothetical protein 0.0528 0.9673 1
Entamoeba histolytica geranylgeranyl transferase beta subunit 0.0231 0.3148 1

Activities

Activity type Activity value Assay description Source Reference
IC50 (binding) = 48 uM Inhibitory activity against recombinant Mycobacterium tuberculosis beta-ketoacyl-Acyl Carrier Protein synthase mtFabH condensing enzyme ChEMBL. 14698162

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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