Detailed information for compound 1751643

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 482.567 | Formula: C26H27FN2O4S
  • H donors: 1 H acceptors: 3 LogP: 3.96 Rotable bonds: 5
    Rule of 5 violations (Lipinski): 1
  • SMILES: OC[C@H]1[C@H]2CCN([C@H]2c2c(N1C)ccc(c2)c1ccc(cc1)OC)S(=O)(=O)c1ccc(cc1)F
  • InChi: 1S/C26H27FN2O4S/c1-28-24-12-5-18(17-3-8-20(33-2)9-4-17)15-23(24)26-22(25(28)16-30)13-14-29(26)34(31,32)21-10-6-19(27)7-11-21/h3-12,15,22,25-26,30H,13-14,16H2,1-2H3/t22-,25+,26-/m1/s1
  • InChiKey: GNSHHRJMKAZSTL-ZSQFBXSQSA-N  

Network

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Synonyms

No synonyms found for this compound

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Homo sapiens paired box 8 Starlite/ChEMBL No references

Predicted pathogen targets for this compound

By orthology
Species Potential target Known druggable target/s Ortholog Group
Brugia malayi Pax transcription factor protein 2 Get druggable targets OG5_139945 All targets in OG5_139945
Loa Loa (eye worm) pax transcription factor protein 2 Get druggable targets OG5_139945 All targets in OG5_139945
Onchocerca volvulus Get druggable targets OG5_139945 All targets in OG5_139945

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
Loa Loa (eye worm) hypothetical protein 0.1005 0.1434 0.3428
Loa Loa (eye worm) eukaryotic-type carbonic anhydrase 0.2374 0.4184 1
Loa Loa (eye worm) eukaryotic-type carbonic anhydrase 0.1005 0.1434 0.3428
Echinococcus multilocularis carbonic anhydrase II 0.2374 0.4184 1
Schistosoma mansoni carbonic anhydrase 0.5271 1 1
Leishmania major carbonic anhydrase family protein, putative 0.5271 1 1
Trichomonas vaginalis conserved hypothetical protein 0.2279 0.3993 0.5
Brugia malayi Eukaryotic-type carbonic anhydrase family protein 0.1005 0.1434 0.3428
Echinococcus granulosus carbonic anhydrase II 0.2374 0.4184 1
Schistosoma mansoni carbonic anhydrase II (carbonate dehydratase II) 0.2374 0.4184 0.321
Brugia malayi Eukaryotic-type carbonic anhydrase family protein 0.1005 0.1434 0.3428
Trichomonas vaginalis conserved hypothetical protein 0.2279 0.3993 0.5
Mycobacterium tuberculosis Beta-carbonic anhydrase CanB 0.2992 0.5423 1
Trypanosoma brucei carbonic anhydrase-like protein 0.2374 0.4184 0.5
Trypanosoma cruzi carbonic anhydrase-like protein, putative 0.2374 0.4184 0.5
Brugia malayi Putative carbonic anhydrase 5 precursor 0.2374 0.4184 1
Brugia malayi Carbonic anhydrase like protein 2 precursor 0.1005 0.1434 0.3428
Schistosoma mansoni carbonic anhydrase II (carbonate dehydratase II) 0.2374 0.4184 0.321
Onchocerca volvulus 0.0291 0 0.5
Loa Loa (eye worm) hypothetical protein 0.1005 0.1434 0.3428
Trypanosoma cruzi carbonic anhydrase-like protein, putative 0.2374 0.4184 0.5
Mycobacterium leprae CARBONIC ANHYDRASE (CARBONATE DEHYDRATASE) (CARBONIC DEHYDRATASE) 0.5271 1 0.5
Plasmodium falciparum carbonic anhydrase 0.1005 0.1434 0.5
Toxoplasma gondii hypothetical protein 0.1005 0.1434 0.5
Brugia malayi Eukaryotic-type carbonic anhydrase family protein 0.1005 0.1434 0.3428
Mycobacterium ulcerans carbonic anhydrase 0.5271 1 1
Brugia malayi Carbonic anhydrase like protein 2 precursor 0.1005 0.1434 0.3428
Brugia malayi Eukaryotic-type carbonic anhydrase family protein 0.2374 0.4184 1
Loa Loa (eye worm) carbonic anhydrase 3 0.2374 0.4184 1
Loa Loa (eye worm) hypothetical protein 0.1005 0.1434 0.3428

Activities

Activity type Activity value Assay description Source Reference
AC50 (functional) = 8.98 uM PubChem BioAssay. HTS for PAX8 inhibitors using PAX8 luciferase reporter gene assay in RMG-I cells Measured in Cell-Based System Using Plate Reader - 7054-01_Inhibitor_Dose_CherryPick_Activity. (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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