Detailed information for compound 1054757

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 343.889 | Formula: C18H30ClNO3
  • H donors: 1 H acceptors: 0 LogP: 3.71 Rotable bonds: 2
    Rule of 5 violations (Lipinski): 1
  • SMILES: NCC[C@@H]1CC[C@@]2(CC1)OO[C@@]1(O2)C2CC3CC1CC(C2)C3.Cl
  • InChi: 1S/C18H29NO3.ClH/c19-6-3-12-1-4-17(5-2-12)20-18(22-21-17)15-8-13-7-14(10-15)11-16(18)9-13;/h12-16H,1-11,19H2;1H/t12-,13?,14?,15?,16?,17+,18-;
  • InChiKey: FJCUKQIASSDZQC-WOBFJMHOSA-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
Trichomonas vaginalis CMGC family protein kinase 0.1102 0 0.5
Trypanosoma cruzi malonyl-CoA decarboxylase, mitochondrial precursor, putative 0.611138 0.348736 1
Entamoeba histolytica protein kinase domain containing protein 0.1102 0 0.5
Leishmania major malonyl-coa decarboxylase-like protein 0.611138 0.348736 1
Plasmodium falciparum casein kinase 2, alpha subunit 0.1102 0 0.5
Trichomonas vaginalis CMGC family protein kinase 0.1102 0 0.5
Plasmodium vivax casein kinase 2, alpha subunit, putative 0.1102 0 0.5
Toxoplasma gondii CMGC kinase, CK2 family 0.1102 0 0.5
Wolbachia endosymbiont of Brugia malayi malonyl-CoA decarboxylase 1.54664 1 0.5
Echinococcus multilocularis casein kinase ii subunit alpha 0.1102 0 0.5
Trichomonas vaginalis CMGC family protein kinase 0.1102 0 0.5
Plasmodium vivax unspecified product 0.1102 0 0.5
Trichomonas vaginalis CMGC family protein kinase 0.1102 0 0.5
Trichomonas vaginalis CMGC family protein kinase 0.1102 0 0.5
Trypanosoma cruzi malonyl-CoA decarboxylase, mitochondrial precursor, putative 0.611138 0.348736 1
Echinococcus granulosus casein kinase ii subunit alpha 0.1102 0 0.5
Trichomonas vaginalis CMGC family protein kinase 0.1102 0 0.5
Brugia malayi putative malonyl-CoA decarboxylase 1.54664 1 1
Trichomonas vaginalis CMGC family protein kinase 0.1102 0 0.5
Schistosoma mansoni protein kinase 0.1102 0 0.5
Loa Loa (eye worm) hypothetical protein 1.54664 1 1
Giardia lamblia Kinase, CMGC CK2 0.1102 0 0.5
Entamoeba histolytica casein kinase, putative 0.1102 0 0.5
Trypanosoma brucei malonyl-CoA decarboxylase, mitochondrial precursor, putative 0.611138 0.348736 1

Activities

Activity type Activity value Assay description Source Reference
Activity (functional) = 99.08 % Antimalarial activity against Plasmodium berghei infected in MORO mouse assessed as reduction of parasitemia at 10 mg/kg, po ChEMBL. 17189686
IC50 (functional) = 0.15 ng/ml Antimalarial activity against chloroquine-resistant Plasmodium falciparum K1 ChEMBL. 17189686
IC50 (functional) = 0.48 ng/ml Antimalarial activity against chloroquine-sensitive Plasmodium falciparum NF54 ChEMBL. 17189686

Phenotypes

Whole-cell/tissue/organism interactions

Species name Source Reference Is orphan
Plasmodium falciparum ChEMBL23 17189686

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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