Detailed information for compound 349988

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 359.588 | Formula: C24H41NO
  • H donors: 1 H acceptors: 1 LogP: 7.29 Rotable bonds: 18
    Rule of 5 violations (Lipinski): 1
  • SMILES: CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCNC(=O)CCC
  • InChi: 1S/C24H41NO/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-23-25-24(26)22-4-2/h8-9,11-12,14-15,17-18H,3-7,10,13,16,19-23H2,1-2H3,(H,25,26)/b9-8-,12-11-,15-14-,18-17-
  • InChiKey: FRXFHGCFWRSQGQ-GKFVBPDJSA-N  

Network

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Synonyms

No synonyms found for this compound

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Rattus norvegicus Cannabinoid CB1 receptor 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
Brugia malayi Immunoglobulin I-set domain containing protein 0.0045 0.3485 0.1525
Schistosoma mansoni tyrosine kinase 0.0101 0.9674 1
Echinococcus multilocularis neuroglian 0.0037 0.2639 0.0443
Loa Loa (eye worm) hypothetical protein 0.0042 0.3139 0.1075
Echinococcus granulosus neurotracting:lsamp:neurotrimin:obcam 0.0042 0.3139 0.1122
Echinococcus multilocularis basic fibroblast growth factor receptor 1 A 0.0101 0.9674 1
Loa Loa (eye worm) TK protein kinase 0.0104 1 1
Echinococcus multilocularis fibroblast growth factor receptor 4 0.0101 0.9674 1
Schistosoma mansoni cell adhesion molecule 0.0042 0.3139 0.3245
Echinococcus multilocularis roundabout 2 0.0045 0.3465 0.1565
Schistosoma mansoni Neurotrimin precursor (hNT) 0.0035 0.2313 0.2391
Echinococcus granulosus twitchin 0.0037 0.2639 0.0443
Loa Loa (eye worm) TK/KIN16 protein kinase 0.0045 0.3485 0.1525
Echinococcus granulosus neuroglian 0.0037 0.2639 0.0443
Echinococcus granulosus fibroblast growth factor receptor 4 0.0101 0.9674 1
Echinococcus granulosus basic fibroblast growth factor receptor 1 A 0.0101 0.9674 1
Loa Loa (eye worm) hypothetical protein 0.0045 0.3465 0.1499
Loa Loa (eye worm) hypothetical protein 0.0045 0.3465 0.1499
Schistosoma mansoni nephrin 0.0037 0.2639 0.2728
Schistosoma mansoni defective proboscis extension response (dpr)-related 0.0035 0.2313 0.2391
Echinococcus granulosus roundabout 2 0.0045 0.3465 0.1565
Schistosoma mansoni vesicular amine transporter 0.0035 0.2313 0.2391

Activities

Activity type Activity value Assay description Source Reference
EC50 (functional) = -5.5 Displacement of [35S]GTPgammaS from rat cerebellar CB1 receptor ChEMBL. 16420041
Emax (functional) = 199 % Displacement of [35S]GTPgammaS from rat cerebellar CB1 receptor ChEMBL. 16420041
Emax (functional) = 199 % Displacement of [35S]GTPgammaS from rat cerebellar CB1 receptor ChEMBL. 16420041
Log EC50 (functional) = 5.5 Displacement of [35S]GTPgammaS from rat cerebellar CB1 receptor ChEMBL. 16420041

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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