Detailed information for compound 415337

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 424.399 | Formula: C20H24O10
  • H donors: 3 H acceptors: 6 LogP: -0.38 Rotable bonds: 1
    Rule of 5 violations (Lipinski): 1
  • SMILES: O=C1O[C@@H]2[C@@]([C@@H]1C)(O)[C@@]13[C@]4(C2)O[C@H]2[C@@]3([C@@H](O)C(=O)O2)[C@@H]([C@@H](C1OC4=O)O)C(C)(C)C
  • InChi: 1S/C20H24O10/c1-6-12(23)27-7-5-17-14(25)28-11-8(21)9(16(2,3)4)18(20(11,17)19(6,7)26)10(22)13(24)29-15(18)30-17/h6-11,15,21-22,26H,5H2,1-4H3/t6-,7+,8+,9+,10+,11?,15+,17-,18+,19-,20-/m1/s1
  • InChiKey: HXSVRRZOLBFCIQ-YKWLXHBJSA-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
Homo sapiens glycine receptor, alpha 2 Starlite/ChEMBL References
Homo sapiens glycine receptor, alpha 1 Starlite/ChEMBL References

Predicted pathogen targets for this compound

By orthology
Species Potential target Known druggable target/s Ortholog Group
Echinococcus granulosus glycine receptor subunit alpha 1 Get druggable targets OG5_128286 All targets in OG5_128286
Echinococcus granulosus glycine receptor subunit alpha 1 Get druggable targets OG5_128286 All targets in OG5_128286
Loa Loa (eye worm) hypothetical protein Get druggable targets OG5_128286 All targets in OG5_128286
Echinococcus granulosus glycine receptor subunit beta Get druggable targets OG5_128286 All targets in OG5_128286
Schistosoma mansoni Cys-loop ligand gated ion channel subunit Get druggable targets OG5_128286 All targets in OG5_128286
Loa Loa (eye worm) glutamate-gated chloride channel alpha3A subunit Get druggable targets OG5_128286 All targets in OG5_128286
Schistosoma japonicum ko:K05195 glycine receptor, alpha 3, putative Get druggable targets OG5_128286 All targets in OG5_128286
Echinococcus multilocularis glycine receptor subunit alpha 1 Get druggable targets OG5_128286 All targets in OG5_128286
Schistosoma japonicum ko:K05194 glycine receptor, alpha 2, putative Get druggable targets OG5_128286 All targets in OG5_128286
Brugia malayi Cation transporter family protein Get druggable targets OG5_128286 All targets in OG5_128286
Echinococcus granulosus glycine receptor subunit alpha 1 Get druggable targets OG5_128286 All targets in OG5_128286
Echinococcus multilocularis glycine receptor subunit alpha 1 Get druggable targets OG5_128286 All targets in OG5_128286
Schistosoma mansoni Cys-loop ligand gated ion channel subunit Get druggable targets OG5_128286 All targets in OG5_128286
Echinococcus granulosus Cys loop ligand gated ion channel subunit Get druggable targets OG5_128286 All targets in OG5_128286
Echinococcus multilocularis glycine receptor subunit beta Get druggable targets OG5_128286 All targets in OG5_128286
Echinococcus granulosus glycine receptor subunit beta Get druggable targets OG5_128286 All targets in OG5_128286
Echinococcus multilocularis glycine receptor subunit beta Get druggable targets OG5_128286 All targets in OG5_128286
Schistosoma mansoni Cys-loop ligand gated ion channel subunit Get druggable targets OG5_128286 All targets in OG5_128286
Echinococcus granulosus Cys loop ligand gated ion channel subunit Get druggable targets OG5_128286 All targets in OG5_128286
Schistosoma japonicum Glycine receptor subunit alpha-3 precursor, putative Get druggable targets OG5_128286 All targets in OG5_128286
Echinococcus multilocularis Cys loop ligand gated ion channel subunit Get druggable targets OG5_128286 All targets in OG5_128286
Loa Loa (eye worm) GABA receptor subunit Get druggable targets OG5_128286 All targets in OG5_128286
Brugia malayi glutamate-gated chloride channel alpha3A subunit, putative Get druggable targets OG5_128286 All targets in OG5_128286
Loa Loa (eye worm) glutamate-gated chloride channel alpha3A subunit Get druggable targets OG5_128286 All targets in OG5_128286
Echinococcus multilocularis Cys loop ligand gated ion channel subunit Get druggable targets OG5_128286 All targets in OG5_128286
Brugia malayi glutamate-gated chloride channel alpha3A subunit, putative Get druggable targets OG5_128286 All targets in OG5_128286
Loa Loa (eye worm) hypothetical protein Get druggable targets OG5_128286 All targets in OG5_128286
Echinococcus multilocularis glycine receptor subunit alpha 1 Get druggable targets OG5_128286 All targets in OG5_128286

By sequence similarity to non orthologous known druggable targets
Species Potential target Known druggable target Length Alignment span Identity
Brugia malayi excitatory GABA receptor EXP-1A glycine receptor, alpha 1 449 aa 441 aa 29.5 %
Brugia malayi Neurotransmitter-gated ion-channel ligand binding domain containing protein glycine receptor, alpha 2 452 aa 428 aa 30.1 %

Obtained from network model

Ranking Plot


Putative Targets List


Species Potential target Raw Global Species
Echinococcus multilocularis glycine receptor subunit alpha 1 0.0145 0.0129 0.0129
Trypanosoma cruzi DNA repair and recombination helicase protein PIF7, putative 0.1385 1 0.5
Trypanosoma brucei DNA repair and recombination helicase protein PIF6 0.1385 1 0.5
Loa Loa (eye worm) hypothetical protein 0.0131 0.0019 0.1437
Entamoeba histolytica hypothetical protein, conserved 0.1385 1 0.5
Echinococcus granulosus glycine receptor subunit beta 0.0145 0.0129 0.0129
Echinococcus granulosus glycine receptor subunit beta 0.0145 0.0129 0.0129
Loa Loa (eye worm) GABA receptor subunit 0.0131 0.0019 0.1437
Entamoeba histolytica DNA repair and recombination protein, putative 0.1385 1 0.5
Echinococcus granulosus glycine receptor subunit alpha 1 0.0145 0.0129 0.0129
Leishmania major PIF1 helicase-like protein, putative,DNA repair and recombination protein, mitochondrial precursor, putative 0.1385 1 0.5
Brugia malayi Cation transporter family protein 0.0145 0.0129 1
Brugia malayi glutamate-gated chloride channel alpha3A subunit, putative 0.0131 0.0019 0.1437
Trichomonas vaginalis conserved hypothetical protein 0.1385 1 0.5
Trypanosoma cruzi DNA repair and recombination helicase protein PIF6, putative 0.1385 1 0.5
Echinococcus granulosus Cys loop ligand gated ion channel subunit 0.0145 0.0129 0.0129
Echinococcus multilocularis glycine receptor subunit beta 0.0145 0.0129 0.0129
Loa Loa (eye worm) hypothetical protein 0.0145 0.0129 1
Echinococcus multilocularis ATP dependent DNA helicase PIF1 0.1385 1 1
Echinococcus multilocularis glycine receptor subunit alpha 1 0.0145 0.0129 0.0129
Echinococcus granulosus glycine receptor subunit alpha 1 0.0145 0.0129 0.0129
Schistosoma mansoni hypothetical protein 0.1385 1 1
Loa Loa (eye worm) glutamate-gated chloride channel alpha3A subunit 0.0145 0.0129 1
Echinococcus granulosus glycine receptor subunit alpha 1 0.0145 0.0129 0.0129
Echinococcus multilocularis Cys loop ligand gated ion channel subunit 0.0145 0.0129 0.0129
Giardia lamblia Rrm3p helicase 0.1385 1 0.5
Trypanosoma brucei DNA repair and recombination helicase protein PIF7 0.1385 1 0.5
Leishmania major PIF1 helicase-like protein, putative,DNA repair and recombination protein, mitochondrial precursor, putative 0.1385 1 0.5
Echinococcus multilocularis glycine receptor subunit beta 0.0145 0.0129 0.0129
Echinococcus multilocularis glycine receptor subunit alpha 1 0.0145 0.0129 0.0129
Trypanosoma cruzi DNA repair and recombination helicase protein PIF7, putative 0.1385 1 0.5

Activities

Activity type Activity value Assay description Source Reference
IC50 (binding) = -5.4 Activity at human alpha1betaGlyR expressed in HEK293 cells by FMP assay ChEMBL. 17352465
IC50 (binding) = -5.1 Activity at human alpha1GlyR expressed in HEK293 cells by FMP assay ChEMBL. 17352465
IC50 (binding) = -4.9 Activity at human alpha2GlyR expressed in HEK293 cells by FMP assay ChEMBL. 17352465
IC50 (binding) = 4.2 uM Activity at human alpha1betaGlyR expressed in HEK293 cells by FMP assay ChEMBL. 17352465
IC50 (binding) = 4.2 uM Activity at human alpha1betaGlyR expressed in HEK293 cells by FMP assay ChEMBL. 17352465
IC50 (binding) = 6.4 uM Activity at human alpha1GlyR expressed in HEK293 cells assessed as inhibition of 300 uM glycine-induced current by whole-cell patch clamp experiment ChEMBL. 17352465
IC50 (binding) = 6.4 uM Activity at human alpha1GlyR expressed in HEK293 cells assessed as inhibition of 300 uM glycine-induced current by whole-cell patch clamp experiment ChEMBL. 17352465
IC50 (binding) = 7.1 uM Activity at human alpha1GlyR expressed in HEK293 cells by FMP assay ChEMBL. 17352465
IC50 (binding) = 7.1 uM Activity at human alpha1GlyR expressed in HEK293 cells by FMP assay ChEMBL. 17352465
IC50 (binding) = 12 uM Activity at human alpha2GlyR expressed in HEK293 cells by FMP assay ChEMBL. 17352465
IC50 (binding) = 12 uM Activity at human alpha2GlyR expressed in HEK293 cells by FMP assay ChEMBL. 17352465
Log IC50 (binding) = 4.9 Activity at human alpha2GlyR expressed in HEK293 cells by FMP assay ChEMBL. 17352465
Log IC50 (binding) = 5.1 Activity at human alpha1GlyR expressed in HEK293 cells by FMP assay ChEMBL. 17352465
Log IC50 (binding) = 5.4 Activity at human alpha1betaGlyR expressed in HEK293 cells by FMP assay ChEMBL. 17352465

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.

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