Detailed information for compound 32419

Basic information

Technical information
  • TDR Targets ID: 32419
  • Name: 5-[5-[4-(4,5-dihydro-1,3-oxazol-2-yl)-2-ethyl -6-methylphenoxy]pentyl]-3-methyl-1,2-oxazole
  • MW: 356.459 | Formula: C21H28N2O3
  • H donors: 0 H acceptors: 1 LogP: 4.5 Rotable bonds: 9
    Rule of 5 violations (Lipinski): 1
  • SMILES: CCc1cc(cc(c1OCCCCCc1onc(c1)C)C)C1=NCCO1
  • InChi: 1S/C21H28N2O3/c1-4-17-14-18(21-22-9-11-25-21)12-15(2)20(17)24-10-7-5-6-8-19-13-16(3)23-26-19/h12-14H,4-11H2,1-3H3
  • InChiKey: TZBUIPPGJLRTCG-UHFFFAOYSA-N  

Network

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Synonyms

  • 5-[5-[4-(4,5-dihydrooxazol-2-yl)-2-ethyl-6-methyl-phenoxy]pentyl]-3-methyl-isoxazole
  • 5-[5-[4-(4,5-dihydrooxazol-2-yl)-2-ethyl-6-methylphenoxy]pentyl]-3-methylisoxazole
  • 5-[5-[4-(4,5-dihydro-1,3-oxazol-2-yl)-2-ethyl-6-methyl-phenoxy]pentyl]-3-methyl-1,2-oxazole
  • 5-[5-[2-ethyl-6-methyl-4-(2-oxazolin-2-yl)phenoxy]pentyl]-3-methyl-isoxazole
  • 5-{5-[4-(4,5-Dihydro-oxazol-2-yl)-2-ethyl-6-methyl-phenoxy]-pentyl}-3-methyl-isoxazole
  • AIDS-209244
  • AIDS209244

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
Schistosoma mansoni patched 1 0.046 0.199 0.199
Mycobacterium leprae DIHYDROFOLATE REDUCTASE DFRA (DHFR) (TETRAHYDROFOLATE DEHYDROGENASE) 0.1866 1 1
Trypanosoma cruzi 3-hydroxy-3-methylglutaryl-CoA reductase 0.1118 0.5741 0.8215
Echinococcus multilocularis geminin 0.02 0.0503 0.0503
Echinococcus multilocularis Niemann Pick C1 protein 0.046 0.199 0.199
Mycobacterium ulcerans dihydrofolate reductase DfrA 0.1866 1 1
Echinococcus multilocularis dihydrofolate reductase 0.1866 1 1
Trypanosoma brucei 3-hydroxy-3-methylglutaryl-CoA reductase, putative 0.1118 0.5741 0.8215
Loa Loa (eye worm) dihydrofolate reductase 0.1866 1 1
Chlamydia trachomatis dihydrofolate reductase 0.1866 1 0.5
Echinococcus granulosus Niemann Pick C1 protein 0.046 0.199 0.199
Brugia malayi thymidylate synthase 0.0434 0.1842 0.1842
Loa Loa (eye worm) thymidylate synthase 0.0434 0.1842 0.1842
Toxoplasma gondii bifunctional dihydrofolate reductase-thymidylate synthase 0.1337 0.6988 0.5
Mycobacterium tuberculosis Probable thymidylate synthase ThyA (ts) (TSASE) 0.0434 0.1842 0.1373
Loa Loa (eye worm) hypothetical protein 0.1118 0.5741 0.5741
Mycobacterium ulcerans hydroxymethylglutaryl-coenzyme a (HMG-CoA) reductase 0.1118 0.5741 0.4779
Echinococcus granulosus sterol regulatory element binding protein 0.046 0.199 0.199
Trichomonas vaginalis conserved hypothetical protein 0.046 0.199 0.8446
Plasmodium falciparum bifunctional dihydrofolate reductase-thymidylate synthase 0.1337 0.6988 0.5
Echinococcus multilocularis thymidylate synthase 0.0434 0.1842 0.1842
Echinococcus multilocularis sterol regulatory element binding protein 0.046 0.199 0.199
Leishmania major dihydrofolate reductase-thymidylate synthase 0.1337 0.6988 1
Mycobacterium tuberculosis Dihydrofolate reductase DfrA (DHFR) (tetrahydrofolate dehydrogenase) 0.1866 1 1
Entamoeba histolytica serine/threonine protein kinase, putative 0.0111 0 0.5
Onchocerca volvulus 0.0434 0.1842 1
Trypanosoma cruzi dihydrofolate reductase-thymidylate synthase 0.1337 0.6988 1
Brugia malayi CHE-14 protein 0.046 0.199 0.199
Trypanosoma cruzi 3-hydroxy-3-methylglutaryl-CoA reductase, putative 0.1118 0.5741 0.8215
Brugia malayi hypothetical protein 0.0207 0.0544 0.0544
Plasmodium vivax bifunctional dihydrofolate reductase-thymidylate synthase, putative 0.1337 0.6988 0.5
Echinococcus multilocularis protein dispatched 1 0.046 0.199 0.199
Echinococcus multilocularis hydroxymethylglutaryl coenzyme A reductase 0.1118 0.5741 0.5741
Giardia lamblia 3-hydroxy-3-methylglutaryl-coenzyme A reductase 0.0525 0.2357 1
Brugia malayi Hydroxymethylglutaryl-coenzyme A reductase family protein 0.1118 0.5741 0.5741
Schistosoma mansoni hypothetical protein 0.02 0.0503 0.0503
Schistosoma mansoni bifunctional dihydrofolate reductase-thymidylate synthase 0.0434 0.1842 0.1842
Echinococcus granulosus dihydrofolate reductase 0.1866 1 1
Echinococcus granulosus Protein patched homolog 1 0.046 0.199 0.199
Echinococcus granulosus geminin 0.02 0.0503 0.0503
Echinococcus granulosus thymidylate synthase 0.0434 0.1842 0.1842
Echinococcus granulosus hydroxymethylglutaryl coenzyme A reductase 0.1118 0.5741 0.5741
Trichomonas vaginalis 3-hydroxy-3-methylglutaryl-coenzyme A reductase, putative 0.0525 0.2357 1
Schistosoma mansoni hypothetical protein 0.02 0.0503 0.0503
Schistosoma mansoni hydroxymethylglutaryl-CoA reductase (NADPH) 0.1118 0.5741 0.5741
Loa Loa (eye worm) hypothetical protein 0.046 0.199 0.199
Trichomonas vaginalis 3-hydroxy-3-methylglutaryl-coenzyme A reductase, putative 0.0525 0.2357 1
Trypanosoma brucei dihydrofolate reductase-thymidylate synthase 0.1337 0.6988 1
Brugia malayi Dihydrofolate reductase 0.1866 1 1
Trichomonas vaginalis 3-hydroxy-3-methylglutaryl-coenzyme A reductase, putative 0.0525 0.2357 1
Loa Loa (eye worm) abnormal chemotaxis protein 14 0.046 0.199 0.199
Trichomonas vaginalis conserved hypothetical protein 0.0207 0.0544 0.2308
Leishmania major 3-hydroxy-3-methylglutaryl-CoA reductase 0.1118 0.5741 0.8215
Echinococcus multilocularis protein patched 0.046 0.199 0.199
Trypanosoma cruzi dihydrofolate reductase-thymidylate synthase, putative 0.0207 0.0544 0.0779
Schistosoma mansoni dihydrofolate reductase 0.1866 1 1
Schistosoma mansoni niemann-pick C1 (NPC1) 0.046 0.199 0.199

Activities

Activity type Activity value Assay description Source Reference
MIC (functional) NA 0 uM In vitro minimum inhibitory concentration for the inhibition of human rhinovirus-14 (HRV-14) replication by binding to viral capsid; NA= inactive at the 10 micromol. ChEMBL. 2158559
MIC (functional) = 5.18 uM In vitro anti-rhinovirus activity of the compound was measured as mean MIC for five serotypes, HRV-1A, -2, -22, -41, and -50 ChEMBL. 2913305
MIC (functional) = 35 uM In vitro anti-rhinovirus activity was measured as maximum testable levels - highest concentration of compound which causes no apparent effect on the cell monolayers ChEMBL. 2913305

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

2 literature references were collected for this gene.

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