Detailed information for compound 13526

Basic information

Technical information
  • TDR Targets ID: 13526
  • Name: 9-benzyl-8-hydroxy-1,3-dimethyl-7-propyl-2H-p urino[7,8-a]pyrimidine-4,6-dione
  • MW: 381.428 | Formula: C20H23N5O3
  • H donors: 1 H acceptors: 4 LogP: 3.05 Rotable bonds: 4
    Rule of 5 violations (Lipinski): 1
  • SMILES: CCCc1c(O)n(Cc2ccccc2)c2n(c1=O)c1C(=O)N(C)CN(c1n2)C
  • InChi: 1S/C20H23N5O3/c1-4-8-14-17(26)24(11-13-9-6-5-7-10-13)20-21-16-15(25(20)18(14)27)19(28)23(3)12-22(16)2/h5-7,9-10,26H,4,8,11-12H2,1-3H3
  • InChiKey: GMLZNSRIKGGYLC-UHFFFAOYSA-N  


Substructure search Similarity search

Network

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Synonyms

  • 8-hydroxy-1,3-dimethyl-9-(phenylmethyl)-7-propyl-2H-purino[7,8-a]pyrimidine-4,6-dione
  • 9-benzyl-8-hydroxy-1,3-dimethyl-7-propyl-2H-purino[7,8-a]pyrimidine-4,6-quinone

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
Brugia malayi Integrin alpha pat-2 precursor 0.0165 0.3448 0.1886
Loa Loa (eye worm) integrin beta-2 0.0338 1 1
Echinococcus multilocularis eukaryotic initiation factor 4A 0.0291 0.8197 1
Loa Loa (eye worm) hypothetical protein 0.0125 0.1926 0.1368
Loa Loa (eye worm) hypothetical protein 0.0291 0.8197 0.8072
Plasmodium falciparum eukaryotic initiation factor 4A 0.0291 0.8197 0.5
Giardia lamblia Translation initiation factor eIF-4A, putative 0.0291 0.8197 0.5
Schistosoma mansoni DEAD box ATP-dependent RNA helicase 0.0291 0.8197 1
Treponema pallidum ATP-dependent RNA helicase 0.0291 0.8197 0.5
Mycobacterium tuberculosis Probable cold-shock DeaD-box protein A homolog DeaD (ATP-dependent RNA helicase dead homolog) 0.0291 0.8197 1
Entamoeba histolytica DEAD/DEAH box helicase, putative 0.0291 0.8197 0.5
Echinococcus granulosus integrin alpha 3 0.0127 0.1989 0.2427
Echinococcus multilocularis integrin beta 2 0.0251 0.6682 0.8152
Trichomonas vaginalis DEAD box ATP-dependent RNA helicase, putative 0.0291 0.8197 0.5
Loa Loa (eye worm) integrin alpha pat-2 0.0255 0.6833 0.6614
Toxoplasma gondii eukaryotic initiation factor-4A, putative 0.0291 0.8197 0.5
Schistosoma mansoni DEAD box ATP-dependent RNA helicase 0.0291 0.8197 1
Echinococcus granulosus eukaryotic initiation factor 4A 0.0291 0.8197 1
Trypanosoma cruzi Eukaryotic initiation factor 4A-1 0.0291 0.8197 0.5
Echinococcus multilocularis integrin alpha 3 0.0127 0.1989 0.2427
Echinococcus granulosus eukaryotic initiation factor 4A III 0.0291 0.8197 1
Schistosoma mansoni integrin alpha 0.0165 0.3448 0.4207
Leishmania major eukaryotic initiation factor 4a, putative 0.0291 0.8197 0.5
Trichomonas vaginalis DEAD box ATP-dependent RNA helicase, putative 0.0291 0.8197 0.5
Trypanosoma brucei Eukaryotic initiation factor 4A-1 0.0291 0.8197 0.5
Leishmania major eukaryotic initiation factor 4a, putative 0.0291 0.8197 0.5
Loa Loa (eye worm) hypothetical protein 0.013 0.2105 0.156
Echinococcus multilocularis eukaryotic initiation factor 4A III 0.0291 0.8197 1
Brugia malayi eukaryotic initiation factor 4A 0.0291 0.8197 0.7767
Onchocerca volvulus Eukaryotic initiation factor 4A homolog 0.0291 0.8197 0.5
Plasmodium vivax RNA helicase-1, putative 0.0291 0.8197 0.5
Trichomonas vaginalis DEAD box ATP-dependent RNA helicase, putative 0.0291 0.8197 0.5
Trypanosoma cruzi Eukaryotic initiation factor 4A-1 0.0291 0.8197 0.5
Echinococcus granulosus integrin beta 2 0.0251 0.6682 0.8152
Schistosoma mansoni integrin beta subunit 0.0199 0.4737 0.5779

Activities

Activity type Activity value Assay description Source Reference
Inhibition (functional) = 16 % Prophylactic anti-inflammatory activity in adjuvant arthritic rat at 12.5 mg/kg in noninjected 1 degree paw ChEMBL. 2496230
Inhibition (functional) = 24 % Prophylactic antiinflammatory activity against adjuvant arthritic rat at dose of 25 mg/kg in noninjected 1 degree paw . ChEMBL. 2496230
Inhibition (functional) = 38 % Prophylactic anti-inflammatory activity in adjuvant arthritic rat at 12.5 mg/kg in noninjected 2 degree paw ChEMBL. 2496230
Inhibition (functional) = 38 % Prophylactic antiinflammatory activity against adjuvant arthritic rat at dose of 50 mg/kg in noninjected 1 degree paw . ChEMBL. 2496230
Inhibition (functional) = 45 % Antiinflammatory activity against reverse passive Arthus reaction-synovitis in rat at dose of 50 mg/kg per orally. ChEMBL. 2496230
Inhibition (functional) = 65 % Prophylactic antiinflammatory activity against adjuvant arthritic rat at dose of 25 mg/kg in noninjected 2 degree paw . ChEMBL. 2496230
Inhibition (functional) = 70 % Prophylactic antiinflammatory activity against adjuvant arthritic rat at dose of 50 mg/kg in noninjected 2 degree paw . ChEMBL. 2496230

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

1 literature reference was collected for this gene.

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