Detailed information for compound 1673786

Basic information

Technical information
  • TDR Targets ID: 1673786
  • Name: 2-[3,5-dibromo-4-[4-methoxy-2-(3-methylbenzoy l)-5-propan-2-ylphenoxy]phenyl]acetic acid
  • MW: 576.274 | Formula: C26H24Br2O5
  • H donors: 1 H acceptors: 3 LogP: 7.1 Rotable bonds: 8
    Rule of 5 violations (Lipinski): 2
  • SMILES: COc1cc(c(cc1C(C)C)Oc1c(Br)cc(cc1Br)CC(=O)O)C(=O)c1cccc(c1)C
  • InChi: 1S/C26H24Br2O5/c1-14(2)18-12-23(33-26-20(27)9-16(10-21(26)28)11-24(29)30)19(13-22(18)32-4)25(31)17-7-5-6-15(3)8-17/h5-10,12-14H,11H2,1-4H3,(H,29,30)
  • InChiKey: TZASJPUDKFUECT-UHFFFAOYSA-N  


Substructure search Similarity search

Network

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Synonyms

  • 2-[3,5-dibromo-4-[5-isopropyl-4-methoxy-2-(3-methylbenzoyl)phenoxy]phenyl]acetic acid
  • 2-[3,5-dibromo-4-[5-isopropyl-4-methoxy-2-[(3-methylphenyl)-oxomethyl]phenoxy]phenyl]acetic acid
  • 2-[3,5-dibromo-4-[4-methoxy-2-(3-methylphenyl)carbonyl-5-propan-2-yl-phenoxy]phenyl]ethanoic acid

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Rattus norvegicus Glucocorticoid receptor Starlite/ChEMBL References
Homo sapiens nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor) Starlite/ChEMBL 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
No druggable targets predicted by sequence similarity
Obtained from network model

Ranking Plot

Putative Targets List

Species Potential target Raw Global Species
Brugia malayi Nuclear hormone receptor family member nhr-19 0.0018 1 1
Schistosoma mansoni retinoid-x-receptor (RXR) 0.0018 1 1
Brugia malayi Nuclear hormone receptor family member nhr-25 0.0018 1 1
Echinococcus multilocularis nuclear receptor 2DBD gamma 0.0018 1 1
Schistosoma mansoni RAR-like nuclear receptor 0.0018 1 1
Loa Loa (eye worm) nuclear hormone receptor family member nhr-40 0.0018 1 1
Loa Loa (eye worm) hypothetical protein 0.0018 1 1
Brugia malayi Nuclear hormone receptor family member nhr-31 0.0018 1 1
Loa Loa (eye worm) nuclear hormone receptor family member nhr-14 0.0018 1 1
Echinococcus multilocularis ecdysone induced protein 78C 0.0018 1 1
Loa Loa (eye worm) hypothetical protein 0.0018 1 1
Brugia malayi Ligand-binding domain of nuclear hormone receptor family protein 0.0018 1 1
Schistosoma mansoni retinoic acid receptor RXR 0.0018 1 1
Schistosoma mansoni nuclear hormone receptor nor-1/nor-2 0.0018 1 1
Echinococcus multilocularis hepatocyte nuclear factor 4 alpha 0.0018 1 1
Brugia malayi steroid hormone receptor 0.0018 1 1
Onchocerca volvulus Protein ultraspiracle homolog 0.0018 1 0.5
Schistosoma mansoni thyroid hormone receptor 0.0018 1 1
Brugia malayi photoreceptor-specific nuclear receptor 0.0018 1 1
Brugia malayi Nuclear hormone receptor family member nhr-1 0.0018 1 1
Echinococcus granulosus FTZ F1 alpha 0.0018 1 1
Onchocerca volvulus Bile acid receptor homolog 0.0018 1 0.5
Brugia malayi Nuclear hormone receptor family member nhr-19 0.0018 1 1
Schistosoma mansoni coup transcription factor 0.0018 1 1
Brugia malayi Nuclear hormone receptor family member nhr-49 0.0018 1 1
Loa Loa (eye worm) hypothetical protein 0.0018 1 1
Echinococcus multilocularis COUP TF:Svp nuclear hormone receptor 0.0018 1 1
Echinococcus granulosus hepatocyte nuclear factor 4 alpha 0.0018 1 1
Echinococcus multilocularis Nuclear hormone receptor family member nhr 41 0.0018 1 1
Echinococcus multilocularis FTZ F1 nuclear receptor protein 0.0018 1 1
Loa Loa (eye worm) nuclear Hormone Receptor family member 0.0018 1 1
Onchocerca volvulus Steroid hormone receptor family member cnr14 homolog 0.0018 1 0.5
Loa Loa (eye worm) hypothetical protein 0.0018 1 1
Echinococcus granulosus Nuclear hormone receptor family member nhr 41 0.0018 1 1
Loa Loa (eye worm) nuclear hormone receptor family member nhr-31 0.0018 1 1
Schistosoma mansoni photoreceptor-specific nuclear receptor related 0.0018 1 1
Brugia malayi Nuclear hormone receptor family member nhr-25 0.0018 1 1
Brugia malayi Steroid receptor seven-up type 2 0.0018 1 1
Loa Loa (eye worm) hypothetical protein 0.0018 1 1
Brugia malayi Nuclear hormone receptor family member nhr-3 0.0018 1 1
Brugia malayi nuclear hormone receptor 0.0018 1 1
Schistosoma mansoni FTZ-F1 nuclear receptor-like protein 0.0018 1 1
Echinococcus granulosus ecdysone induced protein 78C 0.0018 1 1
Loa Loa (eye worm) nuclear hormone receptor family member nhr-1 0.0018 1 1
Loa Loa (eye worm) hypothetical protein 0.0018 1 1
Loa Loa (eye worm) hypothetical protein 0.0018 1 1
Loa Loa (eye worm) steroid hormone receptor 0.0018 1 1
Echinococcus granulosus nuclear receptor 2DBD gamma 0.0018 1 1
Echinococcus granulosus nuclear receptor 2DBD gamma 0.0018 1 1
Loa Loa (eye worm) hypothetical protein 0.0018 1 1
Brugia malayi Nuclear hormone receptor family member nhr-14 0.0018 1 1
Echinococcus multilocularis FTZ F1 alpha 0.0018 1 1
Echinococcus multilocularis thyroid hormone receptor alpha 0.0018 1 1
Schistosoma mansoni Tr4/Tr2 (homologue) 0.0018 1 1
Brugia malayi Nuclear hormone receptor family member nhr-40 0.0018 1 1
Schistosoma mansoni thyroid hormone receptor 0.0018 1 1
Echinococcus multilocularis nuclear receptor 2DBD gamma 0.0018 1 1
Brugia malayi nuclear receptor NHR-88 0.0018 1 1
Brugia malayi Ligand-binding domain of nuclear hormone receptor family protein 0.0018 1 1
Onchocerca volvulus 0.0018 1 0.5
Echinococcus granulosus FTZ F1 nuclear receptor protein 0.0018 1 1
Echinococcus granulosus retinoic acid receptor rxr beta a 0.0018 1 1
Brugia malayi Nuclear hormone receptor family member nhr-41 0.0018 1 1
Echinococcus granulosus COUP TF:Svp nuclear hormone receptor 0.0018 1 1
Brugia malayi Nuclear hormone receptor-like 1 0.0018 1 1
Schistosoma mansoni nuclear receptor 2DBD-gamma 0.0018 1 1
Schistosoma mansoni nuclear hormone receptor 0.0018 1 1
Loa Loa (eye worm) nuclear hormone receptor family member nhr-41 0.0018 1 1
Loa Loa (eye worm) nuclear hormone receptor family member nhr-49 0.0018 1 1
Schistosoma mansoni steroid hormone receptor ad4bp 0.0018 1 1

Activities

Activity type Activity value Assay description Source Reference
IC50 (binding) = 19 nM Displacement of [3H]dexamethasone from human glucocorticoid receptor expressed in baculovirus infected Sf9 cells after 16-18 hrs by beta counting ChEMBL. 22917520
IC50 (binding) = 20 nM Displacement of [3H]dexamethasone from human glucocorticoid receptor expressed in baculovirus infected Sf9 cells after overnight incubation by scintillation counting ChEMBL. 22917520
IC50 (functional) = 400 nM Antagonist activity at human glucocorticoid receptor expressed in CHOK1 cells assessed as inhibition of dexamethasone-induced alkaline phosphatase expression after 46 hrs by reporter gene assay ChEMBL. 22917520
IC50 (functional) = 410 nM Antagonist activity at human glucocorticoid receptor expressed in GRAF cells assessed as inhibition of dexamethasone-induced alkaline phosphatase expression after 48 hrs by reporter gene assay ChEMBL. 22917520
IC50 (functional) = 2.49 uM Antagonist activity at glucocorticoid receptor in rat hepatocytes assessed as inhibition of dexamethasone-induced trypsine aminotransferase expression incubated for 30 mins prior to dexamethasone-induction measured after 4 hrs by reporter gene assay ChEMBL. 22917520
IC50 (functional) = 2.5 uM Antagonist activity at glucocorticoid receptor in rat H4IIE cells assessed as inhibition of dexamethasone-induced trypsine aminotransferase expression after 24 hrs by reporter gene assay ChEMBL. 22917520

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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