Detailed information for compound 919106

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 464.489 | Formula: C25H25FN4O4
  • H donors: 2 H acceptors: 4 LogP: 4.24 Rotable bonds: 7
    Rule of 5 violations (Lipinski): 1
  • SMILES: NC(=O)NC(=O)C([C@@H]1c2ccc(nc2Oc2c1cccc2F)c1ccc(nc1)OC(C)C)(C)C
  • InChi: 1S/C25H25FN4O4/c1-13(2)33-19-11-8-14(12-28-19)18-10-9-16-20(25(3,4)23(31)30-24(27)32)15-6-5-7-17(26)21(15)34-22(16)29-18/h5-13,20H,1-4H3,(H3,27,30,31,32)/t20-/m0/s1
  • InChiKey: HQFHTXSVKRXPKT-FQEVSTJZSA-N  


Substructure search Similarity search

Network

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Synonyms

No synonyms found for this compound

Targets

Known targets for this compound

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

Activities

Activity type Activity value Assay description Source Reference
Activity (binding) = 54 % Agonist activity at glucocorticoid receptor in human HeLa cells assessed as NP-1 transactivation by luciferase reporter gene assay relative to dexamethasone ChEMBL. 24980053
Activity (binding) = 79 % Agonist activity at glucocorticoid receptor in human A549 cells assessed as E-selectin transrepression by luciferase reporter gene assay relative to dexamethasone ChEMBL. 24980053
Activity (binding) = 82 % Agonist activity at glucocorticoid receptor in human A549 cells assessed as AP-1 transrepression by luciferase reporter gene assay relative to dexamethasone ChEMBL. 24980053
Activity (binding) = 101 % Agonist activity at glucocorticoid receptor in human whole blood assessed as inhibition of LPS-induced TNF production incubated for 20 hrs prior to LPS challenge measured after 5 hrs by ELISA relative to dexamethasone ChEMBL. 24980053
EC50 (binding) = 3.8 nM Agonist activity at glucocorticoid receptor in human A549 cells assessed as E-selectin transrepression by luciferase reporter gene assay ChEMBL. 24980053
EC50 (binding) = 6.7 nM Agonist activity at glucocorticoid receptor in human A549 cells assessed as AP-1 transrepression by luciferase reporter gene assay ChEMBL. 24980053
EC50 (binding) = 59.2 nM Agonist activity at glucocorticoid receptor in human HeLa cells assessed as NP-1 transactivation by luciferase reporter gene assay ChEMBL. 24980053
EC50 (binding) = 355 nM Agonist activity at glucocorticoid receptor in human whole blood assessed as inhibition of LPS-induced TNF production incubated for 20 hrs prior to LPS challenge measured after 5 hrs by ELISA ChEMBL. 24980053
Ki (binding) = 0.7 nM Binding affinity to glucocorticoid receptor (unknown origin) by fluorescence polarization assay ChEMBL. 24980053
Ki (binding) = 312.5 nM Binding affinity to progesterone receptor (unknown origin) by fluorescence polarization assay ChEMBL. 24980053
Stabilty (ADMET) = 86 % Metabolic stability in mouse liver microsomes assessed as compound remaining ChEMBL. 24980053
T1/2 (ADMET) = 191 min Half life in human liver microsomes ChEMBL. 24980053

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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