Detailed information for compound 1683558

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 430.896 | Formula: C19H21ClF2N2O3S
  • H donors: 1 H acceptors: 3 LogP: 4.06 Rotable bonds: 8
    Rule of 5 violations (Lipinski): 1
  • SMILES: CC(C[C@@H](N(S(=O)(=O)c1ccc(cc1)Cl)Cc1ccc(c(c1)F)F)C(=O)N)C
  • InChi: 1S/C19H21ClF2N2O3S/c1-12(2)9-18(19(23)25)24(11-13-3-8-16(21)17(22)10-13)28(26,27)15-6-4-14(20)5-7-15/h3-8,10,12,18H,9,11H2,1-2H3,(H2,23,25)/t18-/m1/s1
  • InChiKey: YUXAYDYPQVQENO-GOSISDBHSA-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
Echinococcus granulosus zinc finger protein 0.002 0.0333 0.0188
Trichomonas vaginalis ap endonuclease, putative 0.002 0.0199 0.5
Schistosoma mansoni hypothetical protein 0.0022 0.0518 0.0411
Plasmodium vivax AP endonuclease (DNA-[apurinic or apyrimidinic site] lyase), putative 0.002 0.0199 0.5
Brugia malayi Bromodomain containing protein 0.004 0.3599 0.3469
Treponema pallidum exodeoxyribonuclease (exoA) 0.002 0.0199 0.5
Echinococcus multilocularis bromodomain adjacent to zinc finger domain 0.0062 0.7332 1
Echinococcus multilocularis bromodomain adjacent to zinc finger domain 0.0038 0.3186 0.4188
Loa Loa (eye worm) hypothetical protein 0.0043 0.4024 0.4348
Schistosoma mansoni bromodomain containing protein 0.0066 0.7956 1
Echinococcus multilocularis fetal alzheimer antigen, falz 0.0024 0.0851 0.0914
Brugia malayi PHD-finger family protein 0.0026 0.1264 0.1086
Trypanosoma cruzi apurinic/apyrimidinic endonuclease 0.002 0.0199 0.5
Wolbachia endosymbiont of Brugia malayi exonuclease III 0.002 0.0199 0.5
Loa Loa (eye worm) hypothetical protein 0.004 0.3611 0.3902
Giardia lamblia Endonuclease/Exonuclease/phosphatase 0.002 0.0199 0.5
Leishmania major apurinic/apyrimidinic endonuclease-redox protein 0.002 0.0199 0.5
Mycobacterium tuberculosis Probable exodeoxyribonuclease III protein XthA (exonuclease III) (EXO III) (AP endonuclease VI) 0.002 0.0199 0.5
Echinococcus granulosus bromodomain adjacent to zinc finger domain 0.0062 0.7332 1
Echinococcus granulosus bromodomain adjacent to zinc finger domain 0.0038 0.3186 0.4188
Loa Loa (eye worm) exodeoxyribonuclease III family protein 0.002 0.0199 0.0215
Loa Loa (eye worm) hypothetical protein 0.0074 0.9254 1
Echinococcus multilocularis zinc finger protein 0.002 0.0333 0.0188
Loa Loa (eye worm) PHD-finger family protein 0.0022 0.0518 0.0559
Schistosoma mansoni acetyl-CoA C-acetyltransferase 0.0024 0.0851 0.084
Entamoeba histolytica exodeoxyribonuclease III, putative 0.002 0.0199 0.5
Toxoplasma gondii exonuclease III APE 0.002 0.0199 0.5
Mycobacterium ulcerans exodeoxyribonuclease III protein XthA 0.002 0.0199 0.5
Trypanosoma brucei apurinic/apyrimidinic endonuclease, putative 0.002 0.0199 0.5
Trypanosoma cruzi apurinic/apyrimidinic endonuclease, putative 0.002 0.0199 0.5
Schistosoma mansoni zinc finger protein 0.002 0.0333 0.0173
Echinococcus granulosus fetal alzheimer antigen falz 0.0024 0.0851 0.0914
Plasmodium falciparum AP endonuclease (DNA-[apurinic or apyrimidinic site] lyase), putative 0.002 0.0199 0.5
Loa Loa (eye worm) hypothetical protein 0.0045 0.4357 0.4709
Trichomonas vaginalis ap endonuclease, putative 0.002 0.0199 0.5

Activities

No activities found for this compound.

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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