Detailed information for compound 1585425

Basic information

Technical information
  • TDR Targets ID: 1585425
  • Name: 7-methyl-3-oxo-N-(2-phenylethyl)-4H-1,4-benzo xazine-6-sulfonamide
  • MW: 346.401 | Formula: C17H18N2O4S
  • H donors: 2 H acceptors: 3 LogP: 2.16 Rotable bonds: 5
    Rule of 5 violations (Lipinski): 1
  • SMILES: O=C1COc2c(N1)cc(c(c2)C)S(=O)(=O)NCCc1ccccc1
  • InChi: 1S/C17H18N2O4S/c1-12-9-15-14(19-17(20)11-23-15)10-16(12)24(21,22)18-8-7-13-5-3-2-4-6-13/h2-6,9-10,18H,7-8,11H2,1H3,(H,19,20)
  • InChiKey: AXLDZEPCJSEXID-UHFFFAOYSA-N  


Substructure search Similarity search

Network

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Synonyms

  • 3-keto-7-methyl-N-(2-phenylethyl)-4H-1,4-benzoxazine-6-sulfonamide
  • ZINC04512198
  • A3754/0159137
  • BAS 13090635
  • 7-Methyl-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazine-6-sulfonic acid phenethyl-amide

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Homo sapiens geminin, DNA replication inhibitor Starlite/ChEMBL No references
Homo sapiens glucagon-like peptide 1 receptor Starlite/ChEMBL No references

Predicted pathogen targets for this compound

By orthology
No druggable targets predicted by orthology data
By sequence similarity to non orthologous known druggable targets
Species Potential target Known druggable target Length Alignment span Identity
Brugia malayi Hypothetical 65.5 kDa Trp-Asp repeats containing protein F02E8.5 inchromosome X geminin, DNA replication inhibitor 209 aa 176 aa 27.8 %
Loa Loa (eye worm) pigment dispersing factor receptor c glucagon-like peptide 1 receptor 463 aa 388 aa 25.8 %
Obtained from network model

Ranking Plot

Putative Targets List

Species Potential target Raw Global Species
Loa Loa (eye worm) carboxylesterase 0.0839 1 1
Onchocerca volvulus 0.0142 0 0.5
Mycobacterium tuberculosis Carboxylesterase LipT 0.0142 0 0.5
Echinococcus granulosus acetylcholinesterase 0.0839 1 1
Schistosoma mansoni family S9 non-peptidase homologue (S09 family) 0.0839 1 1
Echinococcus multilocularis carboxylesterase 5A 0.0839 1 1
Mycobacterium ulcerans carboxylesterase, LipT 0.0142 0 0.5
Echinococcus multilocularis geminin 0.0205 0.0901 0.0901
Schistosoma mansoni hypothetical protein 0.0205 0.0901 0.0901
Schistosoma mansoni hypothetical protein 0.0205 0.0901 0.0901
Loa Loa (eye worm) acetylcholinesterase 1 0.0839 1 1
Echinococcus granulosus geminin 0.0205 0.0901 0.0901
Loa Loa (eye worm) hypothetical protein 0.0839 1 1
Echinococcus granulosus acetylcholinesterase 0.0839 1 1
Brugia malayi Carboxylesterase family protein 0.0839 1 1
Loa Loa (eye worm) hypothetical protein 0.0839 1 1
Onchocerca volvulus 0.0142 0 0.5
Mycobacterium tuberculosis POSSIBLE PARA-NITROBENZYL ESTERASE (FRAGMENT) 0.0142 0 0.5
Echinococcus granulosus carboxylesterase 5A 0.0839 1 1
Trichomonas vaginalis carboxylesterase domain containing protein, putative 0.0142 0 0.5
Echinococcus multilocularis acetylcholinesterase 0.0839 1 1
Mycobacterium tuberculosis POSSIBLE PARA-NITROBENZYL ESTERASE (FRAGMENT) 0.0142 0 0.5
Onchocerca volvulus 0.0142 0 0.5
Onchocerca volvulus 0.0142 0 0.5
Echinococcus multilocularis acetylcholinesterase 0.0839 1 1
Onchocerca volvulus 0.0142 0 0.5
Trichomonas vaginalis spcc417.12 protein, putative 0.0142 0 0.5

Activities

Activity type Activity value Assay description Source Reference
Potency (functional) 0.1458 uM PubChem BioAssay. A quantitative high throughput screen for small molecules that induce DNA re-replication in SW480 colon adenocarcinoma cells. (Class of assay: confirmatory) ChEMBL. No reference
Potency (functional) 7.9433 uM PubChem BioAssay. qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode). (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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