Detailed information for compound 1896954
Basic information
Technical information
- Name: Unnamed compound
- MW: 375.934 | Formula: C25H26ClN
-
H donors: 0
H acceptors: 0
LogP: 6.35
Rotable bonds: 5
Rule of 5 violations (Lipinski): 1 - SMILES: c1ccc(cc1)CN1CCC(=CC1)c1ccccc1Cc1ccccc1.Cl
- InChi: 1S/C25H25N.ClH/c1-3-9-21(10-4-1)19-24-13-7-8-14-25(24)23-15-17-26(18-16-23)20-22-11-5-2-6-12-22;/h1-15H,16-20H2;1H
- InChiKey: QGDOEHKNOQAMJG-UHFFFAOYSA-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 |
|---|---|---|---|---|
| Echinococcus multilocularis | gamma secretase subunit aph 1 | 0.026 | 0.4825 | 0.4283 |
| Trypanosoma brucei | proteasome beta 6 subunit | 0.0133 | 0.0949 | 0.0949 |
| Trypanosoma cruzi | proteasome subunit beta type-5, putative | 0.0431 | 1 | 1 |
| Loa Loa (eye worm) | proteasome A-type and B-type family protein | 0.0431 | 1 | 1 |
| Loa Loa (eye worm) | gamma-secretase subunit aph-1 | 0.026 | 0.4825 | 0.4283 |
| Schistosoma mansoni | proteasome catalytic subunit 3 (T01 family) | 0.0431 | 1 | 1 |
| Plasmodium vivax | proteasome subunit beta type-5, putative | 0.0431 | 1 | 1 |
| Brugia malayi | gamma-secretase subunit aph-1 | 0.026 | 0.4825 | 0.4283 |
| Plasmodium falciparum | proteasome subunit beta type-5 | 0.0431 | 1 | 1 |
| Mycobacterium tuberculosis | Proteasome beta subunit PrcB; assembles with alpha subunit PrcA. | 0.0431 | 1 | 0.5 |
| Schistosoma mansoni | gamma-secretase subunit aph-1 | 0.026 | 0.4825 | 0.4283 |
| Trypanosoma cruzi | proteasome beta 6 subunit, putative | 0.0133 | 0.0949 | 0.0949 |
| Echinococcus granulosus | proteasome prosome macropain | 0.0431 | 1 | 1 |
| Toxoplasma gondii | proteasome subunit beta type, putative | 0.0431 | 1 | 1 |
| Trypanosoma cruzi | proteasome beta 6 subunit, putative | 0.0133 | 0.0949 | 0.0949 |
| Entamoeba histolytica | proteasome subunit beta type 5 precursor, putative | 0.0431 | 1 | 1 |
| Mycobacterium leprae | proteasome (beta subunit) PrcB | 0.0431 | 1 | 0.5 |
| Echinococcus granulosus | gamma secretase subunit aph 1 | 0.026 | 0.4825 | 0.4283 |
| Mycobacterium ulcerans | proteasome PrcB | 0.0431 | 1 | 0.5 |
| Trypanosoma cruzi | proteasome subunit beta type-5, putative | 0.0431 | 1 | 1 |
| Giardia lamblia | Proteasome subunit beta type 5 precursor | 0.0431 | 1 | 1 |
| Leishmania major | proteasome beta 5 subunit, putative | 0.0431 | 1 | 1 |
| Trypanosoma brucei | proteasome subunit beta type-5, putative | 0.0431 | 1 | 1 |
| Echinococcus multilocularis | proteasome (prosome, macropain) | 0.0431 | 1 | 1 |
| Trichomonas vaginalis | Family T1, proteasome beta subunit, threonine peptidase | 0.0431 | 1 | 1 |
Activities
| Activity type | Activity value | Assay description | Source | Reference |
|---|---|---|---|---|
| ED50 (functional) | > 20 mg kg-1 | Antidepressant activity in ip dosed CD1 mouse assessed as inhibition of tetrabenazine methanesulfonate-induced reserpine like behavior administered 30 mins before tetrabenazine methanesulfonate challenge measured after 30 mins | ChEMBL. | 533882 |
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.
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
- ChEMBL: CHEMBL3250709
Bibliographic References
No literature references available for this target.
If you have references for this compound, please enter them in a user comment (below) or Contact us.