Detailed information for compound 934099

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 526.573 | Formula: C26H38O11
  • H donors: 2 H acceptors: 6 LogP: 0.27 Rotable bonds: 7
    Rule of 5 violations (Lipinski): 2
  • SMILES: COC(=O)[C@@H]1C[C@H](OC(=O)C)C(=O)[C@H]2[C@@]1(C)CC[C@@H]1[C@]2(C)C[C@H](CC1=O)[C@]1(O)[C@@H](OC)O[C@H]([C@H]1O)OC
  • InChi: 1S/C26H38O11/c1-12(27)36-17-10-15(21(31)33-4)24(2)8-7-14-16(28)9-13(11-25(14,3)19(24)18(17)29)26(32)20(30)22(34-5)37-23(26)35-6/h13-15,17,19-20,22-23,30,32H,7-11H2,1-6H3/t13-,14-,15-,17-,19-,20+,22+,23-,24-,25-,26+/m0/s1
  • InChiKey: ODBHOLKTMJCQDG-RRQPKOPKSA-N  


Substructure search Similarity search

Network

Hover on a compound node to display the structore

Synonyms

No synonyms found for this compound

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Homo sapiens opioid receptor, delta 1 Starlite/ChEMBL References
Homo sapiens opioid receptor, mu 1 Starlite/ChEMBL References
Homo sapiens opioid receptor, kappa 1 Starlite/ChEMBL References

Predicted pathogen targets for this compound

By orthology
Species Potential target Known druggable target/s Ortholog Group
Echinococcus multilocularis tm gpcr rhodopsin gpcr rhodopsin superfamily Get druggable targets OG5_139759 All targets in OG5_139759
Echinococcus granulosus tm gpcr rhodopsin Get druggable targets OG5_139759 All targets in OG5_139759
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
Trypanosoma brucei cdc2-related kinase 3 0.0095 0.0019 0.5
Leishmania major cell division related protein kinase 2,cdc2-related kinase 0.0095 0.0019 0.5
Trichomonas vaginalis CMGC family protein kinase 0.0095 0.0019 0.5
Loa Loa (eye worm) CMGC/CDK/CDC2 protein kinase 0.0095 0.0019 1
Plasmodium falciparum protein kinase 5 0.0095 0.0019 0.5
Trichomonas vaginalis CMGC family protein kinase 0.0095 0.0019 0.5
Schistosoma mansoni serine/threonine protein kinase 0.0095 0.0019 0.5
Trichomonas vaginalis CMGC family protein kinase 0.0095 0.0019 0.5
Trypanosoma cruzi cdc2-related kinase 1 0.0095 0.0019 0.5
Mycobacterium ulcerans O-methyltransferase 0.0591 0.9218 0.5
Giardia lamblia Kinase, CMGC CDK 0.0095 0.0019 0.5
Entamoeba histolytica cell division protein kinase 2, putative 0.0095 0.0019 0.5
Mycobacterium tuberculosis Probable catechol-O-methyltransferase 0.053 0.808 0.5
Brugia malayi cell division control protein 2 homolog 0.0095 0.0019 0.5
Trypanosoma cruzi cdc2-related kinase 3 0.0095 0.0019 0.5
Trypanosoma cruzi cdc2-related kinase 3 0.0095 0.0019 0.5
Plasmodium vivax protein kinase Crk2 0.0095 0.0019 0.5
Loa Loa (eye worm) CMGC/CDK/CDK5 protein kinase 0.0095 0.0019 1
Echinococcus multilocularis tm gpcr rhodopsin gpcr rhodopsin superfamily 0.0634 1 1
Loa Loa (eye worm) CMGC/CDK/CDC2 protein kinase 0.0095 0.0019 1
Schistosoma mansoni serine/threonine protein kinase 0.0095 0.0019 0.5
Trypanosoma cruzi cdc2-related kinase 1 0.0095 0.0019 0.5
Toxoplasma gondii cell-cycle-associated protein kinase CDK, putative 0.0095 0.0019 0.5
Leishmania major cell division protein kinase 2,cdc2-related kinase 0.0095 0.0019 0.5
Trypanosoma brucei cdc2-related kinase 1 0.0095 0.0019 0.5
Entamoeba histolytica cell division protein kinase 2, putative 0.0095 0.0019 0.5
Brugia malayi Protein kinase domain containing protein 0.0095 0.0019 0.5
Giardia lamblia Kinase, CMGC CDK 0.0095 0.0019 0.5

Activities

Activity type Activity value Assay description Source Reference
Ki (binding) = 7020 nM Displacement of [125I]IOXY from human kappa opioid receptor expressed in CHO cells ChEMBL. 17580847
Ki (binding) > 10000 nM Displacement of [125I]IOXY from human mu opioid receptor expressed in CHO cells ChEMBL. 17580847
Ki (binding) > 10000 nM Displacement of [125I]IOXY from human delta opioid receptor expressed in CHO cells ChEMBL. 17580847
Ki (functional) > 1.9 uM Antagonist activity at kappa opioid receptor by [35S]GTPgammaS binding assay ChEMBL. 19099466
Ki (functional) > 1.9 uM Antagonist activity at mu opioid receptor (unknown origin) by [35S]GTPgammaS binding assay ChEMBL. 23548164

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

3 literature references were collected for this gene.

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