Detailed information for compound 2116351

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 553.145 | Formula: C30H30Cl3N3O
  • H donors: 1 H acceptors: 2 LogP: 8.79 Rotable bonds: 5
    Rule of 5 violations (Lipinski): 2
  • SMILES: Clc1ccc2c(c1)CCCc1c2n(nc1C(=O)NCC12CC3CC(C2)CC(C1)C3)c1ccc(cc1Cl)Cl
  • InChi: InChI=1S/C30H30Cl3N3O/c31-21-4-6-23-20(11-21)2-1-3-24-27(35-36(28(23)24)26-7-5-22(32)12-25(26)33)29(37)34-16-30-13-17-8-18(14-30)10-19(9-17)15-30/h4-7,11-12,17-19H,1-3,8-10,13-16H2,(H,34,37)
  • InChiKey: JCRLUGHPQYNAQX-UHFFFAOYSA-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
Mus musculus cannabinoid receptor 1 (brain) References
Homo sapiens cannabinoid receptor 2 (macrophage) 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) hexokinase 0.026 0.3964 0.3964
Trypanosoma brucei farnesyl pyrophosphate synthase 0.0396 0.9527 1
Mycobacterium tuberculosis Probable geranylgeranyl pyrophosphate synthetase IdsA2 (ggppsase) (GGPP synthetase) (geranylgeranyl diphosphate synthase) 0.0396 0.9527 0.5
Plasmodium falciparum geranylgeranyl pyrophosphate synthase, putative 0.0396 0.9527 1
Echinococcus granulosus farnesyl pyrophosphate synthase 0.0396 0.9527 0.9216
Loa Loa (eye worm) hexokinase 0.026 0.3964 0.3964
Trichomonas vaginalis geranylgeranyl pyrophosphate synthase, putative 0.0396 0.9527 0.5
Trypanosoma cruzi farnesyl pyrophosphate synthase, putative 0.0396 0.9527 0.9216
Echinococcus multilocularis farnesyl pyrophosphate synthase 0.0396 0.9527 0.9216
Toxoplasma gondii polyprenyl synthetase superfamily protein 0.0396 0.9527 1
Schistosoma mansoni geranylgeranyl pyrophosphate synthase 0.0407 1 1
Leishmania major farnesyl pyrophosphate synthase 0.0396 0.9527 0.9216
Onchocerca volvulus 0.026 0.3964 1
Loa Loa (eye worm) hypothetical protein 0.0177 0.0582 0.0582
Onchocerca volvulus 0.026 0.3964 1
Loa Loa (eye worm) hexokinase type II 0.026 0.3964 0.3964
Echinococcus granulosus geranylgeranyl pyrophosphate synthase 0.0407 1 1
Giardia lamblia Farnesyl diphosphate synthase 0.0396 0.9527 0.5
Trichomonas vaginalis geranylgeranyl pyrophosphate synthase, putative 0.0396 0.9527 0.5
Brugia malayi Hexokinase family protein 0.026 0.3964 0.3964
Echinococcus multilocularis geranylgeranyl pyrophosphate synthase 0.0407 1 1
Loa Loa (eye worm) geranylgeranyl pyrophosphate synthetase 0.0407 1 1
Mycobacterium ulcerans geranylgeranyl pyrophosphate synthase 0.0396 0.9527 0.5
Onchocerca volvulus 0.026 0.3964 1
Leishmania major polyprenyl synthase, putative 0.0407 1 1
Trypanosoma cruzi polyprenyl synthase, putative 0.0407 1 1
Mycobacterium ulcerans geranylgeranyl pyrophosphate synthase 0.0396 0.9527 0.5
Entamoeba histolytica hexokinase 2 0.026 0.3964 0.5
Schistosoma mansoni farnesyl pyrophosphate synthase 0.0396 0.9527 0.9216
Trypanosoma cruzi polyprenyl synthase, putative 0.0407 1 1
Plasmodium vivax geranylgeranyl pyrophosphate synthase 0.0396 0.9527 1
Brugia malayi hexokinase 0.026 0.3964 0.3964
Brugia malayi Polyprenyl synthetase family protein 0.0396 0.9527 0.9527
Loa Loa (eye worm) polyprenyl synthetase 0.0396 0.9527 0.9527
Trichomonas vaginalis geranylgeranyl diphosphate synthase, putative 0.0396 0.9527 0.5
Trypanosoma cruzi farnesyl pyrophosphate synthase 0.0396 0.9527 0.9216
Entamoeba histolytica hexokinase 1 0.026 0.3964 0.5
Treponema pallidum octaprenyl-diphosphate synthase 0.0407 1 1

Activities

Activity type Activity value Assay description Source Reference
Activity (binding) Intrinsic activity at CB1 receptor in mouse N1E-115 cells assessed as phosphorylation of ERK1/2 at 1 nM to 10 uM after 10 mins by Western blot method LITERATURE. 27240274
Activity (binding) = 108 % Antagonist activity at CB1 receptor in mouse N1E-115 cells assessed as inhibition of WIN55,212-2-induced phosphorylation of ERK1/2 by measuring phosphorylated ERK1/2 level at 1 uM preincubated for 5 mins followed by WIN55,212-2 addition measured after 10 mins by Western blot method (Rvb = 185 +/- 12%) LITERATURE. 27240274
Intrinsic activity (binding) = 98 % Intrinsic activity at CB1 receptor in mouse N1E-115 cells assessed as phosphorylation of ERK1/2 at 1 uM after 10 mins by Western blot method relative to control LITERATURE. 27240274
Ki (binding) = 13.3 nM Displacement of [3H]-CP55,940 from human CB2 receptor transfected in CHO cell membranes after 60 mins by liquid scintillation spectrometry LITERATURE. 27240274
Ki (binding) = 19.1 nM Displacement of [3H]-CP55,940 from CB1 receptor in mouse whole brain membranes after 60 mins by liquid scintillation spectrometry LITERATURE. 27240274

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.

If you have references for this compound, please enter them in a user comment (below) or Contact us.