Detailed information for compound 1781917

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 370.34 | Formula: C17H21Cl2N3S
  • H donors: 1 H acceptors: 1 LogP: 6.84 Rotable bonds: 8
    Rule of 5 violations (Lipinski): 1
  • SMILES: CCCCCC/C(=N/Nc1scc(n1)c1ccc(cc1Cl)Cl)/C
  • InChi: 1S/C17H21Cl2N3S/c1-3-4-5-6-7-12(2)21-22-17-20-16(11-23-17)14-9-8-13(18)10-15(14)19/h8-11H,3-7H2,1-2H3,(H,20,22)/b21-12+
  • InChiKey: UIPIYIDCDOEEIM-CIAFOILYSA-N  


Substructure search Similarity search

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
Plasmodium falciparum hydroxymethyldihydropterin pyrophosphokinase-dihydropteroate synthase 0.7631 0.2426 0.5
Mycobacterium ulcerans 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase 3.1175 1 1
Schistosoma mansoni integrin alpha 0.0164 0.0024 0.5
Loa Loa (eye worm) integrin alpha pat-2 0.0253 0.0052 1
Loa Loa (eye worm) hypothetical protein 0.0129 0.0012 0.2358
Mycobacterium ulcerans flavin-containing monoamine oxidase AofH 0.059 0.0161 0.004
Plasmodium vivax hydroxymethylpterin pyrophosphokinase-dihydropteroate synthetase, putative 0.7631 0.2426 0.5
Loa Loa (eye worm) hypothetical protein 0.0124 0.0011 0.2068
Echinococcus multilocularis integrin alpha 3 0.0126 0.0011 0.5
Mycobacterium tuberculosis Probable flavin-containing monoamine oxidase AofH (amine oxidase) (MAO) 0.0549 0.0147 0.0034
Echinococcus granulosus integrin alpha 3 0.0126 0.0011 0.5
Leishmania major methionine synthase, putative 0.0468 0.0121 0.5
Brugia malayi Integrin alpha pat-2 precursor 0.0164 0.0024 1
Chlamydia trachomatis bifunctional 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase/dihydropteroate synthase 0.7631 0.2426 0.5
Toxoplasma gondii dihydropteroate synthase 0.7631 0.2426 0.5
Mycobacterium tuberculosis 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase FolK (7,8-dihydro-6-hydroxymethylpterin-pyrophosphokinase) ( 2.4012 0.7696 1
Mycobacterium ulcerans flavin-containing monoamine oxidase AofH 0.059 0.0161 0.004

Activities

Activity type Activity value Assay description Source Reference
MIC (functional) = 2 ug ml-1 Anticandida activity against Candida albicans clinical isolate assessed as growth inhibition after 24 hrs by broth microdilution method ChEMBL. 23702472
MIC (functional) > 256 ug ml-1 Antibacterial activity against Escherichia coli assessed as growth inhibition after 18 to 22 hrs by broth microdilution method ChEMBL. 23702472

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.
 
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External resources for this compound

Bibliographic References

No literature references available for this target.

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