Detailed information for compound 132546

Basic information

Technical information
  • TDR Targets ID: 132546
  • Name: 7-[3-[4-[hydroxy(diphenyl)methyl]piperidin-1- yl]propoxy]-4-oxochromene-2-carboxylic acid
  • MW: 513.581 | Formula: C31H31NO6
  • H donors: 2 H acceptors: 4 LogP: 2.44 Rotable bonds: 9
    Rule of 5 violations (Lipinski): 2
  • SMILES: OC(=O)c1cc(=O)c2c(o1)cc(cc2)OCCCN1CCC(CC1)C(c1ccccc1)(c1ccccc1)O
  • InChi: 1S/C31H31NO6/c33-27-21-29(30(34)35)38-28-20-25(12-13-26(27)28)37-19-7-16-32-17-14-24(15-18-32)31(36,22-8-3-1-4-9-22)23-10-5-2-6-11-23/h1-6,8-13,20-21,24,36H,7,14-19H2,(H,34,35)
  • InChiKey: QBCZMKJBVLPNFM-UHFFFAOYSA-N  

Network

Hover on a compound node to display the structore

Synonyms

  • 7-[3-[4-[hydroxy(diphenyl)methyl]-1-piperidyl]propoxy]-4-oxo-chromene-2-carboxylic acid
  • 7-[3-[4-[hydroxy(diphenyl)methyl]-1-piperidinyl]propoxy]-4-oxo-1-benzopyran-2-carboxylic acid
  • 7-[3-[4-[hydroxy(diphenyl)methyl]piperidin-1-yl]propoxy]-4-oxo-chromene-2-carboxylic acid
  • 7-[3-[4-[hydroxy(diphenyl)methyl]piperidino]propoxy]-4-keto-chromene-2-carboxylic acid
  • 7-[3-[4-[hydroxy-di(phenyl)methyl]piperidin-1-yl]propoxy]-4-oxochromene-2-carboxylic acid
  • 7-[3-[4-[hydroxy-di(phenyl)methyl]-1-piperidyl]propoxy]-4-oxo-chromene-2-carboxylic acid
  • 7-[3-[4-[hydroxy-di(phenyl)methyl]-1-piperidinyl]propoxy]-4-oxo-2-chromenecarboxylic acid
  • 7-[3-[4-[hydroxy-di(phenyl)methyl]-1-piperidyl]propoxy]-4-keto-chromene-2-carboxylic acid
  • 7-[3-[4-[hydroxy-di(phenyl)methyl]piperidin-1-yl]propoxy]-4-oxo-chromene-2-carboxylic acid

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 immunophilin 0.0105 1 1
Loa Loa (eye worm) hypothetical protein 0.0091 0.8068 0.8068
Onchocerca volvulus 0.003 0 0.5
Giardia lamblia 70 kDa peptidylprolyl isomerase, putative 0.0105 1 0.5
Trypanosoma brucei FK506-binding protein (FKBP)-type peptidyl-prolyl isomerase, putative 0.0105 1 0.5
Loa Loa (eye worm) FKBP-type peptidyl-prolyl cis-trans isomerase-12 0.0105 1 1
Echinococcus multilocularis peptidyl prolyl cis trans isomerase FKBP4 0.0091 0.8068 0.8068
Trypanosoma cruzi peptidyl-prolyl cis-trans isomerase, putative 0.0105 1 0.5
Leishmania major fk506-binding protein 1-like protein 0.0105 1 0.5
Brugia malayi FKBP-type peptidyl-prolyl cis-trans isomerase-59, BmFKBP59 0.0105 1 1
Plasmodium falciparum peptidyl-prolyl cis-trans isomerase FKBP35 0.0105 1 0.5
Entamoeba histolytica peptidyl-prolyl cis-trans isomerase, FKBP-type, putative 0.0105 1 0.5
Trichomonas vaginalis fk506-binding protein, putative 0.0105 1 0.5
Trypanosoma brucei peptidyl-prolyl cis-trans isomerase, putative 0.0105 1 0.5
Trypanosoma cruzi FK506-binding protein (FKBP)-type peptidyl-prolyl isomerase, putative 0.0105 1 0.5
Onchocerca volvulus Cell death protein 3 homolog 0.003 0 0.5
Echinococcus granulosus peptidyl prolyl cis trans isomerase FKBP4 0.0105 1 1
Mycobacterium ulcerans FK-506 binding protein, peptidyl-prolyl cis-trans isomerase 0.0105 1 0.5
Echinococcus multilocularis peptidyl prolyl cis trans isomerase FKBP4 0.0105 1 1
Treponema pallidum peptidyl-prolyl cis-trans isomerase, FKBP-type, 22 kDa (fklB) 0.0105 1 0.5
Echinococcus granulosus peptidyl prolyl cis trans isomerase FKBP4 0.0091 0.8068 0.8068
Giardia lamblia FKBP-type peptidyl-prolyl cis-trans isomerase 0.0105 1 0.5
Trichomonas vaginalis peptidylprolyl isomerase, putative 0.0105 1 0.5
Entamoeba histolytica peptidyl-prolyl cis-trans isomerase, FKBP-type , putative 0.0105 1 0.5
Trypanosoma cruzi peptidyl-prolyl cis-trans isomerase, putative 0.0105 1 0.5
Trypanosoma cruzi FK506-binding protein (FKBP)-type peptidyl-prolyl isomerase, putative 0.0105 1 0.5
Schistosoma mansoni immunophilin 0.0105 1 1
Schistosoma mansoni immunophilin FK506 binding protein FKBP12 0.0105 1 1
Loa Loa (eye worm) FKBP5 protein 0.0105 1 1
Leishmania major peptidylprolyl isomerase-like protein 0.0105 1 0.5
Trichomonas vaginalis peptidylprolyl isomerase, putative 0.0105 1 0.5
Echinococcus granulosus peptidyl prolyl cis trans isomerase FKBP1A 0.0105 1 1
Schistosoma mansoni immunophilin 0.0091 0.8068 0.8068
Plasmodium vivax 70 kDa peptidylprolyl isomerase, putative 0.0105 1 0.5
Trichomonas vaginalis immunophilin, putative 0.0105 1 0.5
Echinococcus multilocularis fk506 binding protein 0.0105 1 1

Activities

Activity type Activity value Assay description Source Reference
IC50 (functional) = 22.8 uM Compound was evaluated for inhibition of contraction in guinea pig ileum induced by leukotriene D4 (LTD4). ChEMBL. 7608912
Kb (functional) = 5.25 nM Compound was evaluated for antihistaminic activity against isolated guinea pig ileum. ChEMBL. 7608912

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.

If you have references for this compound, please enter them in a user comment (below) or Contact us.