Detailed information for compound 1703566

Basic information

Technical information
  • TDR Targets ID: 1703566
  • Name: [5-[(4-bromophenyl)sulfinylmethyl]furan-2-yl] -(4-cyclohexylpiperazin-1-yl)methanone
  • MW: 479.43 | Formula: C22H27BrN2O3S
  • H donors: 0 H acceptors: 2 LogP: 3.85 Rotable bonds: 6
    Rule of 5 violations (Lipinski): 1
  • SMILES: O=C(c1ccc(o1)CS(=O)c1ccc(cc1)Br)N1CCN(CC1)C1CCCCC1
  • InChi: 1S/C22H27BrN2O3S/c23-17-6-9-20(10-7-17)29(27)16-19-8-11-21(28-19)22(26)25-14-12-24(13-15-25)18-4-2-1-3-5-18/h6-11,18H,1-5,12-16H2
  • InChiKey: XMIFLNOIWIZEJP-UHFFFAOYSA-N  


Substructure search Similarity search

Network

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Synonyms

  • [5-[(4-bromophenyl)sulfinylmethyl]-2-furyl]-(4-cyclohexylpiperazin-1-yl)methanone
  • [5-[(4-bromophenyl)sulfinylmethyl]-2-furyl]-(4-cyclohexyl-1-piperazinyl)methanone

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Homo sapiens GNAS complex locus Starlite/ChEMBL No references

Predicted pathogen targets for this compound

By orthology
Species Potential target Known druggable target/s Ortholog Group
Echinococcus granulosus guanine nucleotide binding protein Gs subunit Get druggable targets OG5_131088 All targets in OG5_131088
Brugia malayi GTP-binding regulatory protein Gs alpha-S chain, putative Get druggable targets OG5_131088 All targets in OG5_131088
Schistosoma mansoni Guanine nucleotide-binding protein G(s) subunit alpha (Adenylate cyclase-stimulating G alpha protein) Get druggable targets OG5_131088 All targets in OG5_131088
Schistosoma mansoni Guanine nucleotide-binding protein G(s) subunit alpha (Adenylate cyclase-stimulating G alpha protein) Get druggable targets OG5_131088 All targets in OG5_131088
Echinococcus granulosus guanine nucleotide binding protein Gs subunit Get druggable targets OG5_131088 All targets in OG5_131088
Echinococcus multilocularis guanine nucleotide binding protein G(s) subunit Get druggable targets OG5_131088 All targets in OG5_131088
Schistosoma mansoni Guanine nucleotide-binding protein G(s) subunit alpha (Adenylate cyclase-stimulating G alpha protein) Get druggable targets OG5_131088 All targets in OG5_131088
Echinococcus multilocularis guanine nucleotide binding protein G(s) subunit Get druggable targets OG5_131088 All targets in OG5_131088
Loa Loa (eye worm) GTP-binding regulatory protein Gs alpha-S chain Get druggable targets OG5_131088 All targets in OG5_131088
Schistosoma japonicum ko:K04632 guanine nucleotide binding protein (G protein), alpha stimulating, putative Get druggable targets OG5_131088 All targets in OG5_131088
By sequence similarity to non orthologous known druggable targets
Species Potential target Known druggable target Length Alignment span Identity
Schistosoma mansoni GTP-binding protein alpha subunit gna GNAS complex locus 394 aa 450 aa 28.7 %
Obtained from network model

Ranking Plot

Putative Targets List

Species Potential target Raw Global Species
Echinococcus multilocularis ubiquinone biosynthesis monooxygenase COQ6 0.0095 0.5 0.5
Mycobacterium ulcerans membrane-associated oxidoreductase 0.0095 0.5 0.5
Mycobacterium tuberculosis Possible oxidoreductase 0.0095 0.5 0.5
Toxoplasma gondii FAD binding domain-containing protein 0.0095 0.5 0.5
Mycobacterium tuberculosis Probable oxidoreductase 0.0095 0.5 0.5
Mycobacterium ulcerans hypothetical protein 0.0095 0.5 0.5
Mycobacterium ulcerans hypothetical protein 0.0095 0.5 0.5
Mycobacterium ulcerans oxidoreductase 0.0095 0.5 0.5
Loa Loa (eye worm) hypothetical protein 0.0095 0.5 0.5
Plasmodium vivax FAD-dependent monooxygenase, putative 0.0095 0.5 0.5
Plasmodium falciparum FAD-dependent monooxygenase, putative 0.0095 0.5 0.5
Leishmania major hypothetical protein, conserved 0.0095 0.5 0.5
Mycobacterium leprae possibleputative FAD-linked oxidoreductase 0.0095 0.5 0.5
Trypanosoma brucei kynurenine 3-monooxygenase, putative 0.0095 0.5 0.5
Mycobacterium ulcerans oxidoreductase GMC-type 0.0095 0.5 0.5
Trypanosoma cruzi Monooxygenase, putative 0.0095 0.5 0.5
Mycobacterium ulcerans FAD-linked oxidoreductase 0.0095 0.5 0.5
Mycobacterium tuberculosis Possible oxidoreductase 0.0095 0.5 0.5
Leishmania major hypothetical protein, conserved 0.0095 0.5 0.5
Mycobacterium ulcerans hypothetical protein 0.0095 0.5 0.5
Mycobacterium ulcerans oxidoreductase 0.0095 0.5 0.5
Toxoplasma gondii FAD binding domain-containing protein 0.0095 0.5 0.5
Echinococcus granulosus protein MICAL 3 0.0095 0.5 0.5
Trypanosoma brucei Monooxygenase, putative 0.0095 0.5 0.5
Plasmodium vivax hypothetical protein, conserved 0.0095 0.5 0.5
Echinococcus multilocularis protein MICAL 3 0.0095 0.5 0.5
Schistosoma mansoni hypothetical protein 0.0095 0.5 0.5
Mycobacterium tuberculosis Probable oxidoreductase 0.0095 0.5 0.5
Trypanosoma cruzi hypothetical protein, conserved 0.0095 0.5 0.5
Mycobacterium ulcerans FAD-dependent oxidoreductase 0.0095 0.5 0.5
Echinococcus granulosus ubiquinone biosynthesis monooxygenase COQ6 0.0095 0.5 0.5
Schistosoma mansoni monoxygenase 0.0095 0.5 0.5
Mycobacterium tuberculosis Possible oxidoreductase 0.0095 0.5 0.5
Wolbachia endosymbiont of Brugia malayi 2-polyprenyl-6-methoxyphenol 4-hydroxylase 0.0095 0.5 0.5

Activities

Activity type Activity value Assay description Source Reference
Potency (functional) 1.2589 uM PubChem BioAssay. qHTS for Agonist of gsp, the Etiologic Mutation Responsible for Fibrous Dysplasia/McCune-Albright Syndrome: qHTS. (Class of assay: confirmatory) 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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