Detailed information for compound 1582242

Basic information

Technical information
  • TDR Targets ID: 1582242
  • Name: (5R)-4,5-dimethyl-3,5-di(phenyl)-1,2,4-oxadia zole
  • MW: 252.311 | Formula: C16H16N2O
  • H donors: 0 H acceptors: 0 LogP: 3.35 Rotable bonds: 2
    Rule of 5 violations (Lipinski): 1
  • SMILES: CN1C(=NO[C@]1(C)c1ccccc1)c1ccccc1
  • InChi: 1S/C16H16N2O/c1-16(14-11-7-4-8-12-14)18(2)15(17-19-16)13-9-5-3-6-10-13/h3-12H,1-2H3/t16-/m1/s1
  • InChiKey: TXEAQKHSZUDTDA-MRXNPFEDSA-N  

Network

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Synonyms

  • 4,5-dimethyl-3,5-diphenyl-4,5-dihydro-1,2,4-oxadiazole
  • MLS001179537
  • SMR000475963
  • ZINC04146943
  • AE-842/32631023

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Homo sapiens ataxin 2 Starlite/ChEMBL No references
Homo sapiens ubiquitin specific peptidase 1 Starlite/ChEMBL No references
Homo sapiens geminin, DNA replication inhibitor 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 %

Obtained from network model

Ranking Plot


Putative Targets List


Species Potential target Raw Global Species
Toxoplasma gondii IMP dehydrogenas 0.0162 0.7578 1
Loa Loa (eye worm) IMP dehydrogenase 1 0.0162 0.7578 1
Wolbachia endosymbiont of Brugia malayi IMP dehydrogenase 0.0162 0.7578 0.5
Mycobacterium ulcerans inosine 5-monophosphate dehydrogenase 0.0153 0.7024 0.8869
Schistosoma mansoni hypothetical protein 0.0205 1 1
Trypanosoma cruzi inosine-5'-monophosphate dehydrogenase, putative 0.0162 0.7578 1
Leishmania major guanosine monophosphate reductase 0.0162 0.7578 1
Trypanosoma brucei inosine-5'-monophosphate dehydrogenase 0.0162 0.7578 1
Onchocerca volvulus Putative GMP reductase 0.0068 0.2128 0.5
Trypanosoma cruzi GMP reductase 0.0162 0.7578 1
Trypanosoma cruzi inosine-5'-monophosphate dehydrogenase, putative 0.0162 0.7578 1
Leishmania major inosine-5-monophosphate dehydrogenase 0.0162 0.7578 1
Brugia malayi inosine-5'-monophosphate dehydrogenase family protein 0.0162 0.7578 1
Trypanosoma cruzi GMP reductase 0.0162 0.7578 1
Mycobacterium leprae Probable inosine-5'-monophosphate dehydrogenase GuaB3 (IMP dehydrogenase 2) (inosinic acid dehydrogenase) (inosinate dehydrogena 0.0085 0.3149 0.0954
Trypanosoma brucei GMP reductase 0.0162 0.7578 1
Brugia malayi GMP reductase 0.0068 0.2128 0.2808
Loa Loa (eye worm) GMP reductase 0.0068 0.2128 0.2808
Mycobacterium ulcerans inosine 5'-monophosphate dehydrogenase 0.0162 0.7578 1
Trypanosoma cruzi inosine-5'-monophosphate dehydrogenase, putative 0.0162 0.7578 1
Mycobacterium leprae Probable inosine-5'-monophosphate dehydrogenase GuaB2 (IMP dehydrogenase) (IMPDH) (IMPD) 0.0162 0.7578 1
Plasmodium falciparum inosine-5'-monophosphate dehydrogenase 0.0153 0.7024 1
Plasmodium vivax inosine-5'-monophosphate dehydrogenase, putative 0.0153 0.7024 1
Brugia malayi inosine-5'-monophosphate dehydrogenase 0.0068 0.2128 0.2808
Echinococcus multilocularis geminin 0.0205 1 1
Brugia malayi inosine-5'-monophosphate dehydrogenase 0.0068 0.2128 0.2808
Mycobacterium tuberculosis Probable inosine-5'-monophosphate dehydrogenase GuaB2 (imp dehydrogenase) (inosinic acid dehydrogenase) (inosinate dehydrogenase 0.0162 0.7578 1
Schistosoma mansoni hypothetical protein 0.0205 1 1

Activities

Activity type Activity value Assay description Source Reference
Potency (functional) 0.7079 uM PubChem BioAssay. qHTS for Inhibitors of ATXN expression. (Class of assay: confirmatory) ChEMBL. No reference
Potency (functional) 5.0119 uM PubChem BioAssay. Inhibitors of USP1/UAF1: Primary Screen. (Class of assay: confirmatory) ChEMBL. No reference
Potency (functional) 16.3601 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) 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

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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