Detailed information for compound 631120

Basic information

Technical information
  • TDR Targets ID: 631120
  • Name: 1-(4-methoxyphenyl)-N-(phenylmethyl)methanami ne
  • MW: 227.302 | Formula: C15H17NO
  • H donors: 1 H acceptors: 0 LogP: 2.76 Rotable bonds: 5
    Rule of 5 violations (Lipinski): 1
  • SMILES: COc1ccc(cc1)CNCc1ccccc1
  • InChi: 1S/C15H17NO/c1-17-15-9-7-14(8-10-15)12-16-11-13-5-3-2-4-6-13/h2-10,16H,11-12H2,1H3
  • InChiKey: WZUBICZIDUTTNJ-UHFFFAOYSA-N  

Network

Hover on a compound node to display the structore

Synonyms

  • benzyl-(4-methoxybenzyl)amine
  • CBMicro_047998
  • BAS 04444873
  • Benzyl-(4-methoxy-benzyl)-amine
  • Oprea1_083007
  • CBMicro_025161
  • Oprea1_365043
  • EU-0041317
  • ST5019998
  • BIM-0025008.P001

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
Mycobacterium ulcerans UDP-galactopyranose mutase Glf 0.0583 0.7088 1
Entamoeba histolytica fructose-1,6-bisphosphate aldolase, putative 0.0299 0.3329 0.5
Brugia malayi O-Glycosyl hydrolase family 30 protein 0.0258 0.2786 1
Trichomonas vaginalis fructose-bisphosphate aldolase, putative 0.0299 0.3329 1
Loa Loa (eye worm) pigment dispersing factor receptor c 0.01 0.0687 0.1659
Treponema pallidum fructose-bisphosphate aldolase 0.0299 0.3329 0.5
Trichomonas vaginalis glucosylceramidase, putative 0.0258 0.2786 0.684
Echinococcus multilocularis diuretic hormone 44 receptor GPRdih2 0.0185 0.1815 0.1656
Mycobacterium tuberculosis UDP-galactopyranose mutase Glf (UDP-GALP mutase) (NAD+-flavin adenine dinucleotide-requiring enzyme) 0.0583 0.7088 1
Mycobacterium ulcerans fructose-bisphosphate aldolase 0.0146 0.1303 0.1612
Trichomonas vaginalis fructose-bisphosphate aldolase, putative 0.0299 0.3329 1
Trichomonas vaginalis fructose-bisphosphate aldolase, putative 0.0299 0.3329 1
Trichomonas vaginalis fructose-bisphosphate aldolase, putative 0.0299 0.3329 1
Trichomonas vaginalis fructose-bisphosphate aldolase, putative 0.0299 0.3329 1
Trichomonas vaginalis glucosylceramidase, putative 0.0179 0.1731 0.0703
Mycobacterium leprae Probable UDP-galactopyranose mutase Glf (UDP-galp mutase) (NAD+-flavin adenine dinucleotide-requiring enzyme) 0.0583 0.7088 1
Trichomonas vaginalis glucosylceramidase, putative 0.0258 0.2786 0.684
Schistosoma mansoni aldehyde dehydrogenase 0.0062 0.0191 0.7066
Loa Loa (eye worm) hypothetical protein 0.0234 0.2468 0.8738
Onchocerca volvulus Glucosylceramidase homolog 0.0169 0.161 1
Mycobacterium tuberculosis Probable fructose-bisphosphate aldolase Fba 0.0146 0.1303 0.1612
Brugia malayi Corticotropin releasing factor receptor 2 precursor, putative 0.0253 0.2717 0.9753
Entamoeba histolytica fructose-1,6-bisphosphate aldolase, putative 0.0299 0.3329 0.5
Echinococcus multilocularis survival motor neuron protein 1 0.0234 0.2468 0.2322
Leishmania major aldehyde dehydrogenase, mitochondrial precursor 0.0062 0.0191 0.5
Trichomonas vaginalis glucosylceramidase, putative 0.0258 0.2786 0.684
Toxoplasma gondii aldehyde dehydrogenase 0.0062 0.0191 0.5
Trichomonas vaginalis glucosylceramidase, putative 0.0179 0.1731 0.0703
Trichomonas vaginalis fructose-bisphosphate aldolase, putative 0.0299 0.3329 1
Loa Loa (eye worm) hypothetical protein 0.0253 0.2717 0.9726
Trichomonas vaginalis fructose-bisphosphate aldolase, putative 0.0299 0.3329 1
Echinococcus granulosus diuretic hormone 44 receptor GPRdih2 0.0185 0.1815 0.7131
Trichomonas vaginalis glucosylceramidase, putative 0.0258 0.2786 0.684
Trichomonas vaginalis fructose-bisphosphate aldolase, putative 0.0299 0.3329 1
Loa Loa (eye worm) O-glycosyl hydrolase family 30 protein 0.0258 0.2786 1
Trichomonas vaginalis glucosylceramidase, putative 0.0258 0.2786 0.684
Trichomonas vaginalis glucosylceramidase, putative 0.0258 0.2786 0.684
Brugia malayi latrophilin 2 splice variant baaae 0.0068 0.027 0.0968
Echinococcus granulosus survival motor neuron protein 1 0.0234 0.2468 1
Brugia malayi Calcitonin receptor-like protein seb-1 0.01 0.0687 0.2467
Brugia malayi hypothetical protein 0.0234 0.2468 0.886
Giardia lamblia Fructose-bisphosphate aldolase 0.0299 0.3329 0.5
Schistosoma mansoni aldehyde dehydrogenase 0.0062 0.0191 0.7066
Schistosoma mansoni hypothetical protein 0.0068 0.027 1

Activities

No activities found for this compound.

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

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.