Detailed information for compound 1503881

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 607.662 | Formula: C32H33N9O4
  • H donors: 2 H acceptors: 5 LogP: 2.32 Rotable bonds: 9
    Rule of 5 violations (Lipinski): 2
  • SMILES: COc1c(/C=C/C(=O)N2N=Cc3c([C@@H]2c2cnc(nc2)N2CCOCC2)cccc3)cc(cc1OC)Cc1cnc(nc1N)N
  • InChi: 1S/C32H33N9O4/c1-43-26-15-20(14-23-16-35-31(34)39-30(23)33)13-21(29(26)44-2)7-8-27(42)41-28(25-6-4-3-5-22(25)19-38-41)24-17-36-32(37-18-24)40-9-11-45-12-10-40/h3-8,13,15-19,28H,9-12,14H2,1-2H3,(H4,33,34,35,39)/b8-7+/t28-/m0/s1
  • InChiKey: YTQNXENPQFRJGI-YIXADMSASA-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 voltage dependent calcium channel 0.0705 0.9978 1
Schistosoma mansoni high voltage-activated calcium channel Cav1 0.0705 0.9978 1
Echinococcus multilocularis voltage dependent calcium channel type d subunit 0.0705 0.9978 1
Toxoplasma gondii transporter, cation channel family protein 0.0246 0.0604 1
Echinococcus granulosus voltage dependent calcium channel 0.0705 0.9978 1
Echinococcus multilocularis voltage dependent L type calcium channel subunit 0.0705 0.9978 1
Echinococcus granulosus voltage dependent L type calcium channel subunit|voltage dependent calcium channel 0.0705 0.9978 1
Echinococcus granulosus retinoic acid receptor rxr beta a 0.0426 0.429 0.3931
Loa Loa (eye worm) nuclear receptor nhr-7B 0.0675 0.9364 0.9384
Echinococcus multilocularis voltage dependent calcium channel 0.0705 0.9978 1
Trypanosoma brucei Voltage-dependent calcium channel subunit, putative 0.0246 0.0604 0.5
Loa Loa (eye worm) voltage-dependent calcium channel 0.0246 0.0604 0.0606
Brugia malayi Voltage-gated calcium channel, L-type, alpha subunit. C. elegans egl-19 ortholog 0.0705 0.9978 1
Loa Loa (eye worm) hypothetical protein 0.0246 0.0604 0.0606
Echinococcus granulosus voltage dependent calcium channel type d subunit|voltage dependent calcium channel alpha 1 0.0705 0.9978 1
Loa Loa (eye worm) hypothetical protein 0.0647 0.8796 0.8815
Echinococcus multilocularis voltage dependent calcium channel type d subunit 0.0705 0.9978 1
Trypanosoma cruzi Voltage-dependent calcium channel subunit, putative 0.0246 0.0604 0.5
Schistosoma mansoni voltage-gated cation channel 0.0705 0.9978 1
Echinococcus granulosus voltage dependent calcium channel type d subunit|voltage dependent calcium channel|voltage dependent L type calcium channel subu 0.0705 0.9978 1
Echinococcus multilocularis voltage dependent L type calcium channel subunit 0.0705 0.9978 1
Loa Loa (eye worm) calcium channel 0.0705 0.9978 1
Schistosoma mansoni high voltage-activated calcium channel Cav2A 0.0705 0.9978 1
Loa Loa (eye worm) hypothetical protein 0.0705 0.9978 1

Activities

Activity type Activity value Assay description Source Reference
Activity (binding) = 75.6 % Activity of human DHFR at 52 uM ChEMBL. 19546364

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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