Detailed information for compound 62610

Basic information

Technical information
  • TDR Targets ID: 62610
  • Name: 4-(3-amino-1H-1,2,4-triazol-5-yl)-N,N-dimethy lpyridin-2-amine
  • MW: 204.232 | Formula: C9H12N6
  • H donors: 2 H acceptors: 3 LogP: 0.69 Rotable bonds: 2
    Rule of 5 violations (Lipinski): 1
  • SMILES: CN(c1nccc(c1)c1n[nH]c(n1)N)C
  • InChi: 1S/C9H12N6/c1-15(2)7-5-6(3-4-11-7)8-12-9(10)14-13-8/h3-5H,1-2H3,(H3,10,12,13,14)
  • InChiKey: LJSSPQRYKZTFBZ-UHFFFAOYSA-N  


Substructure search Similarity search

Network

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Synonyms

  • 4-(3-amino-1H-1,2,4-triazol-5-yl)-N,N-dimethyl-pyridin-2-amine
  • 4-(3-amino-1H-1,2,4-triazol-5-yl)-N,N-dimethyl-2-pyridinamine
  • 4-(3-azanyl-1H-1,2,4-triazol-5-yl)-N,N-dimethyl-pyridin-2-amine
  • [4-(3-amino-1H-1,2,4-triazol-5-yl)-2-pyridyl]-dimethyl-amine
  • 4-(5-amino-2H-1,2,4-triazol-3-yl)-N,N-dimethylpyridin-2-amine
  • 4-(5-amino-2H-1,2,4-triazol-3-yl)-N,N-dimethyl-pyridin-2-amine
  • 4-(5-amino-2H-1,2,4-triazol-3-yl)-N,N-dimethyl-2-pyridinamine
  • [4-(5-amino-2H-1,2,4-triazol-3-yl)-2-pyridyl]-dimethyl-amine

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
Giardia lamblia Hypothetical protein 0.0065 0.0396 0.5
Echinococcus multilocularis 6 phosphofructo 2 kinase:fructose 2 0.011 1 0.5
Trypanosoma brucei 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase, putative 0.011 1 1
Loa Loa (eye worm) hypothetical protein 0.011 1 1
Loa Loa (eye worm) hypothetical protein 0.0108 0.9604 0.9604
Entamoeba histolytica phosphoglycerate mutase family protein, putative 0.0065 0.0396 0.5
Trypanosoma cruzi 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase, putative 0.011 1 1
Onchocerca volvulus 0.011 1 0.5
Schistosoma mansoni 6-phosphofructokinase 0.011 1 0.5
Leishmania major 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase, putative 0.011 1 1
Mycobacterium ulcerans hypothetical protein 0.0065 0.0396 0.5
Giardia lamblia Hypothetical protein 0.0065 0.0396 0.5
Mycobacterium ulcerans fructose-2,6-bisphosphatase GpmB 0.0065 0.0396 0.5
Trypanosoma cruzi 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase, putative 0.011 1 1

Activities

Activity type Activity value Assay description Source Reference
-Log KB (functional) = 5.59 % In vitro Histamine H2 receptor antagonist activity in the histamine-stimulated guinea pig right atrium ChEMBL. 2894467
-Log KB (functional) = 5.59 % In vitro Histamine H2 receptor antagonist activity in the histamine-stimulated guinea pig right atrium ChEMBL. 2894467
Activity (ADMET) = -1.17 Log (Cbrain/Cblood) in rats ChEMBL. 2894467
Inhibition (functional) = 48 % Maximum percent inhibition of acid output in pentagastrin-stimulated Heidenhain pouch dog following 1 mg/kg i.v. administration. ChEMBL. 2866245
Inhibition (functional) = 80 % Maximum percent inhibition of acid output in pentagastrin-stimulated Heidenhain pouch dog at dose (5 mg/kg) administered intravenously ChEMBL. 2866245
KB (functional) = 0.00000319 Dissociation constant of H2 receptor antagonist activity against guinea pig atrium ChEMBL. 2866245
KB (functional) = 0.00000319 Dissociation constant of H2 receptor antagonist activity against guinea pig atrium ChEMBL. 2866245
Log BB (ADMET) = -1.17 logBB, log(C brain/C blood) ChEMBL. 8941388

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

3 literature references were collected for this gene.

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