Detailed information for compound 649292

Basic information

Technical information
  • TDR Targets ID: 649292
  • Name: 2-chloro-5-[(3-nitrophenyl)sulfamoyl]-N-pheny lbenzamide
  • MW: 431.85 | Formula: C19H14ClN3O5S
  • H donors: 2 H acceptors: 5 LogP: 3.74 Rotable bonds: 7
    Rule of 5 violations (Lipinski): 1
  • SMILES: O=C(c1cc(ccc1Cl)S(=O)(=O)Nc1cccc(c1)[N+](=O)[O-])Nc1ccccc1
  • InChi: 1S/C19H14ClN3O5S/c20-18-10-9-16(12-17(18)19(24)21-13-5-2-1-3-6-13)29(27,28)22-14-7-4-8-15(11-14)23(25)26/h1-12,22H,(H,21,24)
  • InChiKey: DAKGIVDCIHCSAJ-UHFFFAOYSA-N  


Substructure search Similarity search

Network

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Synonyms

  • 2-chloro-5-[(3-nitrophenyl)sulfamoyl]-N-phenyl-benzamide
  • BAS 00131998
  • ZINC00808501
  • 2-Chloro-5-(3-nitro-phenylsulfamoyl)-N-phenyl-benzamide

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 vivax ATP-dependent Clp protease proteolytic subunit, putative 0.0091 0.2904 1
Echinococcus multilocularis peptidase Clp (S14 family) 0.0059 0.1652 0.3329
Loa Loa (eye worm) hypothetical protein 0.017 0.6067 0.6067
Wolbachia endosymbiont of Brugia malayi ATP-dependent Clp protease proteolytic subunit 0.0091 0.2904 0.5
Brugia malayi RNA binding protein 0.0142 0.4963 0.4963
Mycobacterium leprae PROBABLE ATP-DEPENDENT CLP PROTEASE PROTEOLYTIC SUBUNIT 2 CLPP2 (ENDOPEPTIDASE CLP 2) 0.0091 0.2904 1
Mycobacterium tuberculosis Probable ATP-dependent CLP protease proteolytic subunit 1 ClpP1 (endopeptidase CLP) 0.0059 0.1652 0.5
Schistosoma mansoni tar DNA-binding protein 0.0142 0.4963 1
Mycobacterium ulcerans ATP-dependent Clp protease proteolytic subunit 0.0091 0.2904 0.5
Schistosoma mansoni hypothetical protein 0.0116 0.3916 0.7891
Echinococcus multilocularis ATP dependent Clp protease proteolytic subunit 0.0091 0.2904 0.5852
Echinococcus multilocularis diuretic hormone 44 receptor GPRdih2 0.0054 0.142 0.2861
Treponema pallidum ATP-dependent Clp protease proteolytic subunit 0.0091 0.2904 1
Echinococcus granulosus GPCR family 2 0.0054 0.142 0.2861
Echinococcus granulosus peptidase Clp S14 family 0.0059 0.1652 0.3329
Schistosoma mansoni hypothetical protein 0.0054 0.142 0.2861
Mycobacterium leprae PROBABLE ATP-DEPENDENT CLP PROTEASE PROTEOLYTIC SUBUNIT 1 CLPP1 (ENDOPEPTIDASE CLP) 0.0059 0.1652 0.4744
Loa Loa (eye worm) hypothetical protein 0.0116 0.3916 0.3916
Brugia malayi TAR-binding protein 0.0142 0.4963 0.4963
Toxoplasma gondii ATP-dependent Clp endopeptidase, proteolytic subunit ClpP domain-containing protein 0.0091 0.2904 1
Loa Loa (eye worm) RNA binding protein 0.0142 0.4963 0.4963
Schistosoma mansoni hypothetical protein 0.0054 0.142 0.2861
Plasmodium falciparum ATP-dependent Clp protease proteolytic subunit 0.0091 0.2904 1
Loa Loa (eye worm) MH2 domain-containing protein 0.0268 1 1
Echinococcus multilocularis cadherin EGF LAG seven pass G type receptor 0.0054 0.142 0.2861
Echinococcus granulosus ATP dependent Clp protease proteolytic subunit 0.0091 0.2904 0.5852
Schistosoma mansoni tar DNA-binding protein 0.0142 0.4963 1
Brugia malayi Calcitonin receptor-like protein seb-1 0.017 0.6067 0.6067
Brugia malayi RNA recognition motif domain containing protein 0.0142 0.4963 0.4963
Brugia malayi calcium-independent alpha-latrotoxin receptor 2, putative 0.0054 0.142 0.142
Loa Loa (eye worm) hypothetical protein 0.0054 0.142 0.142
Loa Loa (eye worm) latrophilin receptor protein 2 0.0054 0.142 0.142
Loa Loa (eye worm) hypothetical protein 0.0091 0.2904 0.2904
Mycobacterium ulcerans ATP-dependent Clp protease proteolytic subunit 0.0091 0.2904 0.5
Mycobacterium tuberculosis Probable ATP-dependent CLP protease proteolytic subunit 2 ClpP2 (endopeptidase CLP 2) 0.0059 0.1652 0.5
Chlamydia trachomatis ATP-dependent Clp protease proteolytic subunit 0.0091 0.2904 0.5
Schistosoma mansoni tar DNA-binding protein 0.0142 0.4963 1
Chlamydia trachomatis ATP-dependent Clp protease proteolytic subunit 0.0091 0.2904 0.5
Brugia malayi latrophilin 2 splice variant baaae 0.0116 0.3916 0.3916
Schistosoma mansoni tar DNA-binding protein 0.0142 0.4963 1
Loa Loa (eye worm) TAR-binding protein 0.0142 0.4963 0.4963
Loa Loa (eye worm) transcription factor SMAD2 0.0268 1 1
Schistosoma mansoni hypothetical protein 0.0054 0.142 0.2861
Brugia malayi Probable ClpP-like protease 0.0091 0.2904 0.2904
Schistosoma mansoni hypothetical protein 0.0054 0.142 0.2861
Loa Loa (eye worm) RNA recognition domain-containing protein domain-containing protein 0.0142 0.4963 0.4963
Loa Loa (eye worm) pigment dispersing factor receptor c 0.017 0.6067 0.6067
Brugia malayi Latrophilin receptor protein 2 0.0054 0.142 0.142
Brugia malayi Corticotropin releasing factor receptor 2 precursor, putative 0.017 0.6067 0.6067
Echinococcus granulosus diuretic hormone 44 receptor GPRdih2 0.0054 0.142 0.2861
Toxoplasma gondii ATP-dependent Clp endopeptidase, proteolytic subunit ClpP domain-containing protein 0.0091 0.2904 1
Echinococcus granulosus cadherin EGF LAG seven pass G type receptor 0.0054 0.142 0.2861
Schistosoma mansoni tar DNA-binding protein 0.0142 0.4963 1
Echinococcus multilocularis GPCR, family 2 0.0054 0.142 0.2861
Echinococcus multilocularis tar DNA binding protein 0.0142 0.4963 1
Echinococcus granulosus tar DNA binding protein 0.0142 0.4963 1
Schistosoma mansoni peptidase Clp (S14 family) 0.0091 0.2904 0.5852

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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