Detailed information for compound 202966

Basic information

Technical information
  • TDR Targets ID: 202966
  • Name: 5-ethyl-4-phenylpyridazino[4,3-b]indol-3-amin e
  • MW: 288.346 | Formula: C18H16N4
  • H donors: 1 H acceptors: 2 LogP: 2.93 Rotable bonds: 2
    Rule of 5 violations (Lipinski): 1
  • SMILES: CCn1c2ccccc2c2c1c(c1ccccc1)c(N)nn2
  • InChi: 1S/C18H16N4/c1-2-22-14-11-7-6-10-13(14)16-17(22)15(18(19)21-20-16)12-8-4-3-5-9-12/h3-11H,2H2,1H3,(H2,19,21)
  • InChiKey: KOMPIQYPXFYNRB-UHFFFAOYSA-N  


Substructure search Similarity search

Network

Hover on a compound node to display the structore

Synonyms

  • 5-ethyl-4-phenyl-pyridazino[4,3-b]indol-3-amine
  • 5-ethyl-4-phenyl-3-pyridazino[4,3-b]indolamine
  • (5-ethyl-4-phenyl-pyridazino[4,3-b]indol-3-yl)amine
  • 5-ethyl-4-phenylpyridazino[5,6-b]indol-3-amine
  • 5-ethyl-4-phenyl-pyridazino[5,6-b]indol-3-amine
  • 5-ethyl-4-phenyl-3-pyridazino[5,6-b]indolamine
  • (5-ethyl-4-phenyl-pyridazino[5,6-b]indol-3-yl)amine
  • 5H-Pyridazino[4,3-b]indol-3-amine, 5-ethyl-4-phenyl-
  • AIDS-212351
  • AIDS212351

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 Mitotic checkpoint protein PRCC, C terminal 0.0123 0.5227 0.9197
Onchocerca volvulus Protein ultraspiracle homolog 0.001 0 0.5
Echinococcus multilocularis thyroid hormone receptor alpha 0.0132 0.5683 1
Schistosoma mansoni thyroid hormone receptor 0.0132 0.5683 1
Onchocerca volvulus Steroid hormone receptor family member cnr14 homolog 0.001 0 0.5
Loa Loa (eye worm) follicle stimulating hormone receptor 0.0225 1 1
Schistosoma mansoni thyroid hormone receptor 0.0132 0.5683 1
Echinococcus granulosus Mitotic checkpoint protein PRCC C terminal 0.0123 0.5227 1
Onchocerca volvulus Bile acid receptor homolog 0.001 0 0.5
Schistosoma mansoni hypothetical protein 0.0123 0.5227 0.9197
Onchocerca volvulus 0.001 0 0.5

Activities

Activity type Activity value Assay description Source Reference
IC50 (binding) uM Inhibitory activity of compound against Monoamine oxidase A isolated from rat liver mitochondria using [14C]-5-HT creatinine sulfate; NI denotes no inhibition at 1000 uM ChEMBL. 15189042
IC50 (binding) NI 0 uM Inhibitory activity of compound against Monoamine oxidase A isolated from rat liver mitochondria using [14C]-5-HT creatinine sulfate; NI denotes no inhibition at 1000 uM ChEMBL. 15189042
IC50 (binding) = 72 uM Inhibition of Monoamine oxidase B from rat liver mitochondria ChEMBL. 15189042
IC50 (binding) = 72 uM Inhibition of Monoamine oxidase B from rat liver mitochondria ChEMBL. 15189042
Inhibition (functional) = 0 % In vitro inhibition of Mycobacterium tuberculosis H37Rv, determined at 2 ug/mL ChEMBL. 15189042
Inhibition (functional) = 0 % In vitro inhibition of Mycobacterium tuberculosis H37Rv, determined at 0.2 ug/mL ChEMBL. 15189042
Inhibition (functional) = 0 % In vitro inhibition of Mycobacterium tuberculosis H37Rv, determined at 2 ug/mL ChEMBL. 15189042
Inhibition (functional) = 0 % In vitro inhibition of Mycobacterium tuberculosis H37Rv, determined at 0.2 ug/mL ChEMBL. 15189042
Inhibition (functional) = 40.3 % In vitro inhibition of Mycobacterium tuberculosis H37Rv, determined at 20 ug/mL ChEMBL. 15189042
Inhibition (functional) = 40.3 % In vitro inhibition of Mycobacterium tuberculosis H37Rv, determined at 20 ug/mL ChEMBL. 15189042

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.

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