Detailed information for compound 1495235

Basic information

Technical information
  • TDR Targets ID: 1495235
  • Name: N-[di(phenyl)methyl]pyridin-3-amine
  • MW: 260.333 | Formula: C18H16N2
  • H donors: 1 H acceptors: 1 LogP: 4.03 Rotable bonds: 4
    Rule of 5 violations (Lipinski): 1
  • SMILES: c1ccc(cc1)C(c1ccccc1)Nc1cccnc1
  • InChi: 1S/C18H16N2/c1-3-8-15(9-4-1)18(16-10-5-2-6-11-16)20-17-12-7-13-19-14-17/h1-14,18,20H
  • InChiKey: KALZXZXWVYADFD-UHFFFAOYSA-N  

Network

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Synonyms

  • N-[di(phenyl)methyl]-3-pyridinamine
  • di(phenyl)methyl-(3-pyridyl)amine
  • NSC118961

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Homo sapiens glucagon-like peptide 1 receptor Starlite/ChEMBL No 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
Loa Loa (eye worm) pigment dispersing factor receptor c glucagon-like peptide 1 receptor 463 aa 388 aa 25.8 %

Obtained from network model

Ranking Plot


Putative Targets List


Species Potential target Raw Global Species
Loa Loa (eye worm) hypothetical protein 0.006 0.3138 0.3138
Loa Loa (eye worm) pigment dispersing factor receptor c 0.006 0.3138 0.3138
Loa Loa (eye worm) hypothetical protein 0.0102 1 1
Brugia malayi Hypothetical tyrosinase-like protein C02C2.1 in chromosome III 0.0102 1 1
Brugia malayi Hypothetical tyrosinase-like protein F21C3.2 in chromosome I 0.0102 1 1
Brugia malayi Corticotropin releasing factor receptor 2 precursor, putative 0.006 0.3138 0.3138
Schistosoma mansoni tyrosinase precursor 0.0102 1 1
Brugia malayi Hypothetical tyrosinase-like protein C02C2.1 in chromosome III 0.0102 1 1
Onchocerca volvulus 0.0102 1 0.5
Loa Loa (eye worm) cytochrome P450 family protein 0.0072 0.5036 0.5036
Loa Loa (eye worm) hypothetical protein 0.0102 1 1
Schistosoma mansoni tyrosinase precursor 0.0102 1 1
Brugia malayi Cytochrome P450 family protein 0.0072 0.5036 0.5036
Brugia malayi Hypothetical tyrosinase-like protein C02C2.1 in chromosome III 0.0102 1 1
Loa Loa (eye worm) ShTK domain-containing protein 0.0102 1 1
Brugia malayi Common central domain of tyrosinase family protein 0.0102 1 1
Onchocerca volvulus 0.0102 1 0.5
Loa Loa (eye worm) ShTK domain-containing protein 0.0102 1 1
Loa Loa (eye worm) tyrosinase 1 0.0102 1 1
Onchocerca volvulus 0.0102 1 0.5
Brugia malayi Calcitonin receptor-like protein seb-1 0.006 0.3138 0.3138
Onchocerca volvulus 0.0102 1 0.5

Activities

Activity type Activity value Assay description Source Reference
AC50 (binding) = 32.964 uM PUBCHEM_BIOASSAY: Fluorescence Polarization with Cer CAL-PDZ Measured in Biochemical System Using Plate Reader - 2109-01_Inhibitor_Dose_CherryPick_Activity. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID504435] ChEMBL. No reference
Potency (functional) 7.9433 uM PubChem BioAssay. qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode). (Class of assay: confirmatory) ChEMBL. No reference
Potency (functional) 112.2018 uM PUBCHEM_BIOASSAY: HTS for Inhibitors of HP1-beta Chromodomain Interactions with Methylated Histone Tails. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID488962] ChEMBL. No reference

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.

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