Detailed information for compound 931171

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 321.416 | Formula: C20H23N3O
  • H donors: 1 H acceptors: 1 LogP: 3.36 Rotable bonds: 5
    Rule of 5 violations (Lipinski): 1
  • SMILES: c1ccc(cc1)CC[C@H]1OCCN(C1)Cc1nc2c([nH]1)cccc2
  • InChi: 1S/C20H23N3O/c1-2-6-16(7-3-1)10-11-17-14-23(12-13-24-17)15-20-21-18-8-4-5-9-19(18)22-20/h1-9,17H,10-15H2,(H,21,22)/t17-/m1/s1
  • InChiKey: JVQBISWUXRKBAJ-QGZVFWFLSA-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 dopamine receptor D4 Starlite/ChEMBL References
Homo sapiens dopamine receptor D3 Starlite/ChEMBL References
Homo sapiens cytochrome P450, family 2, subfamily D, polypeptide 6 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
Species Potential target Known druggable target Length Alignment span Identity
Brugia malayi hypothetical protein dopamine receptor D3 400 aa 392 aa 19.9 %
Brugia malayi cytochrome P450 cytochrome P450, family 2, subfamily D, polypeptide 6 497 aa 425 aa 32.0 %

Obtained from network model

Ranking Plot


Putative Targets List


Species Potential target Raw Global Species
Echinococcus granulosus fructose 16 bisphosphatase 1 0.0656 1 0.5
Loa Loa (eye worm) fructose-1,6-bisphosphatase 0.0656 1 0.5
Toxoplasma gondii fructose-bisphospatase II 0.0656 1 1
Trypanosoma cruzi fructose-1,6-bisphosphatase, cytosolic, putative 0.0656 1 1
Schistosoma mansoni fructose-16-bisphosphatase-related 0.0656 1 0.5
Echinococcus multilocularis fructose 1,6 bisphosphatase 1 0.0656 1 0.5
Trypanosoma cruzi fructose-1,6-bisphosphatase, cytosolic, putative 0.0656 1 1
Trypanosoma brucei fructose-1,6-bisphosphatase 0.0656 1 1
Leishmania major 0.0656 1 0.5

Activities

Activity type Activity value Assay description Source Reference
IC50 (binding) = 0.18 uM Inhibition of human dopamine D4 receptor ChEMBL. 25221667
IC50 (ADMET) = 18 uM Inhibition of human CYP2D6 by electrospray ionization ChEMBL. 25221667
IC50 (ADMET) > 30 uM Inhibition of human CYP1A2 by electrospray ionization ChEMBL. 25221667
IC50 (ADMET) > 30 uM Inhibition of human CYP2C9 by electrospray ionization ChEMBL. 25221667
IC50 (ADMET) > 30 uM Inhibition of human CYP3A4 by electrospray ionization ChEMBL. 25221667
IC50 (binding) = 46.2 uM Inhibition of human dopamine D3 receptor ChEMBL. 25221667
IC50 (binding) > 100 uM Inhibition of human dopamine D1 receptor ChEMBL. 25221667
IC50 (binding) > 100 uM Inhibition of human dopamine D2 receptor ChEMBL. 25221667
Ki (binding) = 0.07 uM Inhibition of human dopamine D4 receptor ChEMBL. 25221667
Ki (binding) = 15.7 uM Inhibition of human dopamine D3 receptor ChEMBL. 25221667
Ki (binding) > 100 uM Inhibition of human dopamine D1 receptor ChEMBL. 25221667
Ki (binding) > 100 uM Inhibition of human dopamine D2 receptor ChEMBL. 25221667

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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