Detailed information for compound 1455121

Basic information

Technical information
  • TDR Targets ID: 1455121
  • Name: 2-furan-2-yl-3-(4-methoxyphenyl)quinazolin-4- one
  • MW: 318.326 | Formula: C19H14N2O3
  • H donors: 0 H acceptors: 1 LogP: 3.46 Rotable bonds: 3
    Rule of 5 violations (Lipinski): 1
  • SMILES: COc1ccc(cc1)n1c(nc2c(c1=O)cccc2)c1ccco1
  • InChi: 1S/C19H14N2O3/c1-23-14-10-8-13(9-11-14)21-18(17-7-4-12-24-17)20-16-6-3-2-5-15(16)19(21)22/h2-12H,1H3
  • InChiKey: IDFKAZZRWRKHIJ-UHFFFAOYSA-N  


Substructure search Similarity search

Network

Hover on a compound node to display the structore

Synonyms

  • 2-(2-furyl)-3-(4-methoxyphenyl)quinazolin-4-one
  • 2-(2-furyl)-3-(4-methoxyphenyl)-4-quinazolinone
  • Oprea1_788015
  • ZINC00183534
  • ChemDiv3_001467
  • STOCK2S-31339
  • MLS000855929
  • SMR000286374
  • 2-Furan-2-yl-3-(4-methoxy-phenyl)-3H-quinazolin-4-one
  • BAS 01817064
  • Oprea1_378633
  • IDI1_020433
  • AE-848/82198014

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Homo sapiens K(lysine) acetyltransferase 2A Starlite/ChEMBL No references
Homo sapiens glucagon-like peptide 1 receptor Starlite/ChEMBL No references

Predicted pathogen targets for this compound

By orthology
Species Potential target Known druggable target/s Ortholog Group
Neospora caninum hypothetical protein Get druggable targets OG5_127781 All targets in OG5_127781
Plasmodium berghei histone acetyltransferase GCN5, putative Get druggable targets OG5_127781 All targets in OG5_127781
Plasmodium falciparum histone acetyltransferase GCN5 Get druggable targets OG5_127781 All targets in OG5_127781
Echinococcus granulosus histone acetyltransferase KAT2B Get druggable targets OG5_127781 All targets in OG5_127781
Theileria parva histone acetyltransferase Gcn5, putative Get druggable targets OG5_127781 All targets in OG5_127781
Plasmodium yoelii histone acetyltransferase GCN5-related Get druggable targets OG5_127781 All targets in OG5_127781
Candida albicans bromodomain protein similar to S. cerevisiae GCN5 (YGR252W) histone acetyltransferase Get druggable targets OG5_127781 All targets in OG5_127781
Echinococcus multilocularis gcn5proteinral control of amino acid synthesis Get druggable targets OG5_127781 All targets in OG5_127781
Babesia bovis histone acetyltransferase Get druggable targets OG5_127781 All targets in OG5_127781
Plasmodium knowlesi histone acetyltransferase GCN5, putative Get druggable targets OG5_127781 All targets in OG5_127781
Echinococcus granulosus histone acetyltransferase KAT2B Get druggable targets OG5_127781 All targets in OG5_127781
Schistosoma mansoni gcn5proteinral control of amino-acid synthesis 5-like 2 gcnl2 Get druggable targets OG5_127781 All targets in OG5_127781
Trichomonas vaginalis cat eye syndrome critical region protein 2, cscr2, putative Get druggable targets OG5_127781 All targets in OG5_127781
Schistosoma japonicum ko:K06062 p300/CBP-associated factor, putative Get druggable targets OG5_127781 All targets in OG5_127781
Giardia lamblia Histone acetyltransferase GCN5 Get druggable targets OG5_127781 All targets in OG5_127781
Toxoplasma gondii histone lysine acetyltransferase GCN5-B Get druggable targets OG5_127781 All targets in OG5_127781
Loa Loa (eye worm) acetyltransferase Get druggable targets OG5_127781 All targets in OG5_127781
Toxoplasma gondii histone lysine acetyltransferase GCN5-A Get druggable targets OG5_127781 All targets in OG5_127781
Cryptosporidium hominis histone acetyltransferase Get druggable targets OG5_127781 All targets in OG5_127781
Plasmodium vivax histone acetyltransferase GCN5, putative Get druggable targets OG5_127781 All targets in OG5_127781
Trichomonas vaginalis bromodomain-containing protein, putative Get druggable targets OG5_127781 All targets in OG5_127781
Candida albicans bromodomain protein similar to S. cerevisiae GCN5 (YGR252W) histone acetyltransferase Get druggable targets OG5_127781 All targets in OG5_127781
Entamoeba histolytica acetyltransferase, GNAT family Get druggable targets OG5_127781 All targets in OG5_127781
Cryptosporidium parvum GCN5 like acetylase + bromodomain Get druggable targets OG5_127781 All targets in OG5_127781
Brugia malayi acetyltransferase, GNAT family protein Get druggable targets OG5_127781 All targets in OG5_127781
Neospora caninum Bromodomain containing protein, related Get druggable targets OG5_127781 All targets in OG5_127781
By sequence similarity to non orthologous known druggable targets
Species Potential target Known druggable target Length Alignment span Identity
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) hypothetical protein 0.0079 0.1743 0.1743
Entamoeba histolytica acetyltransferase, GNAT family 0.0047 0.0441 0.5
Toxoplasma gondii histone lysine acetyltransferase GCN5-A 0.0051 0.0618 0.5
Echinococcus multilocularis tar DNA binding protein 0.0198 0.6638 1
Mycobacterium ulcerans glutaminase 0.0279 1 0.5
Brugia malayi latrophilin 2 splice variant baaae 0.0079 0.1743 0.1743
Echinococcus granulosus tar DNA binding protein 0.0198 0.6638 1
Brugia malayi acetyltransferase, GNAT family protein 0.0175 0.5705 0.5705
Brugia malayi RNA binding protein 0.0198 0.6638 0.6638
Echinococcus granulosus histone acetyltransferase KAT2B 0.017 0.5503 0.8291
Brugia malayi Calcitonin receptor-like protein seb-1 0.0115 0.3245 0.3245
Plasmodium falciparum histone acetyltransferase GCN5 0.0047 0.0441 0.5
Schistosoma mansoni gcn5proteinral control of amino-acid synthesis 5-like 2 gcnl2 0.0175 0.5705 0.5705
Plasmodium vivax histone acetyltransferase GCN5, putative 0.0051 0.0618 0.5
Schistosoma mansoni tar DNA-binding protein 0.0198 0.6638 0.6638
Loa Loa (eye worm) TAR-binding protein 0.0198 0.6638 0.6638
Giardia lamblia Histone acetyltransferase GCN5 0.0047 0.0441 0.5
Schistosoma mansoni glutaminase 0.0279 1 1
Toxoplasma gondii histone lysine acetyltransferase GCN5-B 0.0051 0.0618 0.5
Schistosoma mansoni tar DNA-binding protein 0.0198 0.6638 0.6638
Trichomonas vaginalis glutaminase, putative 0.0279 1 1
Brugia malayi TAR-binding protein 0.0198 0.6638 0.6638
Echinococcus multilocularis gcn5proteinral control of amino acid synthesis 0.0175 0.5705 0.8596
Loa Loa (eye worm) acetyltransferase 0.0175 0.5705 0.5705
Loa Loa (eye worm) hypothetical protein 0.0115 0.3245 0.3245
Schistosoma mansoni tar DNA-binding protein 0.0198 0.6638 0.6638
Loa Loa (eye worm) pigment dispersing factor receptor c 0.0115 0.3245 0.3245
Brugia malayi RNA recognition motif domain containing protein 0.0198 0.6638 0.6638
Loa Loa (eye worm) MH2 domain-containing protein 0.0233 0.8105 0.8105
Loa Loa (eye worm) RNA recognition domain-containing protein domain-containing protein 0.0198 0.6638 0.6638
Loa Loa (eye worm) glutaminase 0.0279 1 1
Echinococcus granulosus histone acetyltransferase KAT2B 0.0051 0.0618 0.093
Brugia malayi MH2 domain containing protein 0.0233 0.8105 0.8105
Schistosoma mansoni tar DNA-binding protein 0.0198 0.6638 0.6638
Loa Loa (eye worm) glutaminase 2 0.0279 1 1
Brugia malayi Corticotropin releasing factor receptor 2 precursor, putative 0.0115 0.3245 0.3245
Loa Loa (eye worm) transcription factor SMAD2 0.0233 0.8105 0.8105
Loa Loa (eye worm) RNA binding protein 0.0198 0.6638 0.6638
Schistosoma mansoni tar DNA-binding protein 0.0198 0.6638 0.6638
Schistosoma mansoni hypothetical protein 0.0079 0.1743 0.1743

Activities

Activity type Activity value Assay description Source Reference
Potency (functional) 9.285 uM PUBCHEM_BIOASSAY: Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID488752, AID488774, AID504848, AID504850] ChEMBL. No reference
Potency (functional) 12.5893 uM PubChem BioAssay. qHTS of GLP-1 Receptor Inverse Agonists (Inhibition Mode). (Class of assay: confirmatory) ChEMBL. No reference
Potency (functional) 15.8489 uM PUBCHEM_BIOASSAY: qHTS Assay for Inhibitors of GCN5L2. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID504398] ChEMBL. No reference
Potency (binding) 25.1189 uM PubChem BioAssay. qHTS Assay for Inhibitors of MBNL1-poly(CUG) RNA binding. (Class of assay: confirmatory) ChEMBL. No reference
Potency (functional) 35.4813 uM PUBCHEM_BIOASSAY: qHTS for Inhibitors of binding or entry into cells for Lassa Virus. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID463114, AID540249] ChEMBL. No reference
Potency (functional) 89.1251 uM PUBCHEM_BIOASSAY: qHTS for Inhibitors of Polymerase Iota. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID588623] ChEMBL. No reference

Phenotypes

Whole-cell/tissue/organism interactions

Species name Source Reference Is orphan
Plasmodium falciparum ChEMBL23

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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