Detailed information for compound 1529917

Basic information

Technical information
  • TDR Targets ID: 1529917
  • Name: 3-(3-morpholin-4-ylpropyl)-2-[2-oxo-2-(4-phen ylpiperazin-1-yl)ethyl]sulfanylquinazolin-4-o ne
  • MW: 507.648 | Formula: C27H33N5O3S
  • H donors: 0 H acceptors: 2 LogP: 2.96 Rotable bonds: 9
    Rule of 5 violations (Lipinski): 2
  • SMILES: O=C(N1CCN(CC1)c1ccccc1)CSc1nc2ccccc2c(=O)n1CCCN1CCOCC1
  • InChi: 1S/C27H33N5O3S/c33-25(31-15-13-30(14-16-31)22-7-2-1-3-8-22)21-36-27-28-24-10-5-4-9-23(24)26(34)32(27)12-6-11-29-17-19-35-20-18-29/h1-5,7-10H,6,11-21H2
  • InChiKey: ZUWKJTFROLKEKS-UHFFFAOYSA-N  


Substructure search Similarity search

Network

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Synonyms

  • 3-(3-morpholinopropyl)-2-[2-oxo-2-(4-phenylpiperazin-1-yl)ethyl]sulfanyl-quinazolin-4-one
  • 3-(3-morpholinopropyl)-2-[[2-oxo-2-(4-phenyl-1-piperazinyl)ethyl]thio]-4-quinazolinone
  • 2-[[2-keto-2-(4-phenylpiperazin-1-yl)ethyl]thio]-3-(3-morpholinopropyl)quinazolin-4-one
  • 3-(3-morpholin-4-ylpropyl)-2-[2-oxo-2-(4-phenylpiperazin-1-yl)ethyl]sulfanyl-quinazolin-4-one
  • MLS000772507
  • SMR000377259
  • T5276208

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 0.0079 0.5 0.5
Plasmodium vivax hypothetical protein, conserved 0.0079 0.5 0.5
Schistosoma mansoni hypothetical protein 0.0079 0.5 0.5
Loa Loa (eye worm) SWIB/MDM2 domain-containing protein 0.0079 0.5 0.5
Schistosoma mansoni hypothetical protein 0.0079 0.5 0.5
Onchocerca volvulus 0.0079 0.5 0.5
Echinococcus multilocularis SWI:SNF matrix associated 0.0079 0.5 0.5
Echinococcus granulosus SWI:SNF matrix associated 0.0079 0.5 0.5
Trichomonas vaginalis conserved hypothetical protein 0.0079 0.5 0.5
Brugia malayi SWIB/MDM2 domain containing protein 0.0079 0.5 0.5
Chlamydia trachomatis DNA topoisomerase I 0.0079 0.5 0.5
Schistosoma mansoni brg-1 associated factor 0.0079 0.5 0.5
Brugia malayi brahma associated protein 60 kDa 0.0079 0.5 0.5
Echinococcus granulosus Upstream activation factor subunit UAF30 0.0079 0.5 0.5
Plasmodium falciparum SWIB/MDM2 domain-containing protein 0.0079 0.5 0.5
Schistosoma mansoni hypothetical protein 0.0079 0.5 0.5
Chlamydia trachomatis SWIB complex protein 0.0079 0.5 0.5
Echinococcus multilocularis Upstream activation factor subunit UAF30 0.0079 0.5 0.5
Toxoplasma gondii SWIB/MDM2 domain-containing protein 0.0079 0.5 0.5
Toxoplasma gondii DNA topoisomerase domain-containing protein 0.0079 0.5 0.5
Loa Loa (eye worm) brahma associated protein 0.0079 0.5 0.5
Plasmodium falciparum SWIB/MDM2 domain-containing protein 0.0079 0.5 0.5
Plasmodium vivax SWIB/MDM2 domain-containing protein, putative 0.0079 0.5 0.5
Echinococcus multilocularis SWI:SNF matrix associated 0.0079 0.5 0.5

Activities

Activity type Activity value Assay description Source Reference
Potency (functional) 23.1093 uM PUBCHEM_BIOASSAY: Nrf2 qHTS screen for inhibitors. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID493153, AID493163, AID504648] ChEMBL. No reference
Potency (functional) 28.1838 uM PubChem BioAssay. qHTS for Activators of Integrin-Mediated Alleviation for Muscular Dystrophy. (Class of assay: confirmatory) ChEMBL. No reference
Potency (functional) 39.8107 uM PubChem BioAssay. qHTS for Antagonist of cAMP-regulated guanine nucleotide exchange factor 3 (EPAC1): primary screen. (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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