Detailed information for compound 1606389

Basic information

Technical information
  • TDR Targets ID: 1606389
  • Name: N-[(Z)-1-(6-chloro-1H-benzimidazol-2-yl)-2-[4 -(hydroxy-oxidoamino)phenyl]ethenyl]benzamide
  • MW: 418.833 | Formula: C22H15ClN4O3
  • H donors: 2 H acceptors: 4 LogP: 4.88 Rotable bonds: 6
    Rule of 5 violations (Lipinski): 1
  • SMILES: Clc1ccc2c(c1)nc([nH]2)/C(=C/c1ccc(cc1)[N+](=O)[O-])/NC(=O)c1ccccc1
  • InChi: 1S/C22H15ClN4O3/c23-16-8-11-18-19(13-16)25-21(24-18)20(26-22(28)15-4-2-1-3-5-15)12-14-6-9-17(10-7-14)27(29)30/h1-13H,(H,24,25)(H,26,28)/b20-12-
  • InChiKey: BAIPJRVPJMGIOF-NDENLUEZSA-N  


Substructure search Similarity search

Network

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Synonyms

  • N-[1-(6-chloro-1H-benzimidazol-2-yl)-2-(4-nitrophenyl)ethenyl]benzamide
  • 4-[(Z)-2-(benzoylamino)-2-(6-chloro-1H-benzimidazol-2-yl)ethenyl]-N-hydroxybenzeneamine oxide
  • N-[(Z)-1-(6-chloro-1H-benzimidazol-2-yl)-2-(4-nitrophenyl)ethenyl]benzamide
  • N-[(Z)-1-(6-chloro-1H-benzimidazol-2-yl)-2-(4-nitrophenyl)vinyl]benzamide
  • N-[(Z)-1-(6-chloro-1H-benzimidazol-2-yl)-2-[4-(hydroxy-oxido-amino)phenyl]vinyl]benzamide
  • N-[1-(6-chloro-1H-benzimidazol-2-yl)-2-(4-nitrophenyl)vinyl]benzamide
  • 4-[(Z)-2-(benzoylamino)-2-(6-chloro-1H-benzimidazol-2-yl)vinyl]-N-hydroxy-benzeneamine oxide
  • N-[(Z)-1-(6-chloro-1H-benzimidazol-2-yl)-2-[4-(hydroxy-oxidoamino)phenyl]vinyl]benzamide
  • 4-[(Z)-2-(6-chloro-1H-benzimidazol-2-yl)-2-[(oxo-phenylmethyl)amino]vinyl]-N-hydroxybenzeneamine oxide
  • N-[(Z)-1-(6-chloro-1H-benzimidazol-2-yl)-2-[4-(hydroxy-oxido-amino)phenyl]ethenyl]benzamide
  • 4-[(Z)-2-(6-chloro-1H-benzimidazol-2-yl)-2-(phenylcarbonylamino)ethenyl]-N-hydroxy-benzeneamine oxide
  • AIDS-131679
  • AIDS131679
  • N-(1-(5-Chloro-1H-benzimidazol-2-yl)-2-(4-(hydroxy(oxido)amino)phenyl)vinyl)benzamide
  • NSC624424
  • NCI60_007365

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 multilocularis SWI:SNF matrix associated 0.1058 0.5 0.5
Plasmodium vivax SWIB/MDM2 domain-containing protein, putative 0.1058 0.5 0.5
Toxoplasma gondii DNA topoisomerase domain-containing protein 0.1058 0.5 0.5
Plasmodium falciparum SWIB/MDM2 domain-containing protein 0.1058 0.5 0.5
Loa Loa (eye worm) brahma associated protein 0.1058 0.5 0.5
Toxoplasma gondii SWIB/MDM2 domain-containing protein 0.1058 0.5 0.5
Echinococcus granulosus Upstream activation factor subunit UAF30 0.1058 0.5 0.5
Schistosoma mansoni hypothetical protein 0.1058 0.5 0.5
Plasmodium falciparum SWIB/MDM2 domain-containing protein 0.1058 0.5 0.5
Chlamydia trachomatis SWIB complex protein 0.1058 0.5 0.5
Brugia malayi brahma associated protein 60 kDa 0.1058 0.5 0.5
Echinococcus multilocularis Upstream activation factor subunit UAF30 0.1058 0.5 0.5
Schistosoma mansoni brg-1 associated factor 0.1058 0.5 0.5
Chlamydia trachomatis DNA topoisomerase I 0.1058 0.5 0.5
Brugia malayi SWIB/MDM2 domain containing protein 0.1058 0.5 0.5
Trichomonas vaginalis conserved hypothetical protein 0.1058 0.5 0.5
Echinococcus granulosus SWI:SNF matrix associated 0.1058 0.5 0.5
Echinococcus multilocularis SWI:SNF matrix associated 0.1058 0.5 0.5
Onchocerca volvulus 0.1058 0.5 0.5
Loa Loa (eye worm) SWIB/MDM2 domain-containing protein 0.1058 0.5 0.5
Schistosoma mansoni hypothetical protein 0.1058 0.5 0.5
Schistosoma mansoni hypothetical protein 0.1058 0.5 0.5
Plasmodium vivax hypothetical protein, conserved 0.1058 0.5 0.5
Echinococcus multilocularis SWI:SNF matrix associated 0.1058 0.5 0.5

Activities

Activity type Activity value Assay description Source Reference
GI50 (functional) -4.858 PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the UO-31 Renal cell line. (Class of assay: confirmatory) ChEMBL. No reference
GI50 (functional) -4.854 PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the HOP-92 Non-Small Cell Lung cell line. (Class of assay: confirmatory) ChEMBL. No reference
GI50 (functional) -4.765 PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the HL-60(TB) Leukemia cell line. (Class of assay: confirmatory) ChEMBL. No reference
GI50 (functional) -4.754 PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the SK-MEL-5 Melanoma cell line. (Class of assay: confirmatory) ChEMBL. No reference
GI50 (functional) -4.743 PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the NCI-H23 Non-Small Cell Lung cell line. (Class of assay: confirmatory) ChEMBL. No reference
GI50 (functional) -4.719 PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the SF-539 Central Nervous System cell line. (Class of assay: confirmatory) ChEMBL. No reference
GI50 (functional) -4.685 PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the SN12C Renal cell line. (Class of assay: confirmatory) ChEMBL. No reference
GI50 (functional) -4.658 PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the ACHN Renal cell line. (Class of assay: confirmatory) ChEMBL. No reference
GI50 (functional) -4.455 PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the MALME-3M Melanoma cell line. (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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