Detailed information for compound 1270168

Basic information

Technical information
  • TDR Targets ID: 1270168
  • Name: N-[(3R,4S)-1-methyl-4-[4-(3-methylsulfonylphe nyl)phenyl]pyrrolidin-3-yl]propane-2-sulfonam ide
  • MW: 436.588 | Formula: C21H28N2O4S2
  • H donors: 1 H acceptors: 4 LogP: 2.62 Rotable bonds: 6
    Rule of 5 violations (Lipinski): 1
  • SMILES: CN1C[C@@H]([C@H](C1)c1ccc(cc1)c1cccc(c1)S(=O)(=O)C)NS(=O)(=O)C(C)C
  • InChi: 1S/C21H28N2O4S2/c1-15(2)29(26,27)22-21-14-23(3)13-20(21)17-10-8-16(9-11-17)18-6-5-7-19(12-18)28(4,24)25/h5-12,15,20-22H,13-14H2,1-4H3/t20-,21+/m1/s1
  • InChiKey: VERZXIJVGYAQGS-RTWAWAEBSA-N  

Network

Hover on a compound node to display the structore

Synonyms

  • N-[(3R,4S)-1-methyl-4-[4-(3-methylsulfonylphenyl)phenyl]-3-pyrrolidinyl]propane-2-sulfonamide
  • N-[(3R,4S)-4-[4-(3-mesylphenyl)phenyl]-1-methyl-pyrrolidin-3-yl]propane-2-sulfonamide

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Homo sapiens glutamate receptor, ionotropic, AMPA 2 Starlite/ChEMBL References

Predicted pathogen targets for this compound

By orthology
Species Potential target Known druggable target/s Ortholog Group
Echinococcus granulosus glutamate receptor 4 Get druggable targets OG5_128645 All targets in OG5_128645
Loa Loa (eye worm) hypothetical protein Get druggable targets OG5_128645 All targets in OG5_128645
Loa Loa (eye worm) glutamate receptor 1 Get druggable targets OG5_128645 All targets in OG5_128645
Echinococcus granulosus glutamate receptor 2 Get druggable targets OG5_128645 All targets in OG5_128645
Echinococcus granulosus glutamate receptor 2 Get druggable targets OG5_128645 All targets in OG5_128645
Brugia malayi Glutamate receptor 2 precursor Get druggable targets OG5_128645 All targets in OG5_128645
Echinococcus multilocularis glutamate receptor subunit protein glur Get druggable targets OG5_128645 All targets in OG5_128645
Echinococcus multilocularis glutamate receptor 2 Get druggable targets OG5_128645 All targets in OG5_128645
Echinococcus multilocularis glutamate receptor 2 Get druggable targets OG5_128645 All targets in OG5_128645
Echinococcus multilocularis glutamate receptor, ionotrophic, AMPA 3 Get druggable targets OG5_128645 All targets in OG5_128645
Loa Loa (eye worm) hypothetical protein Get druggable targets OG5_128645 All targets in OG5_128645
Loa Loa (eye worm) hypothetical protein Get druggable targets OG5_128645 All targets in OG5_128645
Brugia malayi Glutamate receptor 1 precursor Get druggable targets OG5_128645 All targets in OG5_128645
Echinococcus granulosus glutamate receptor ionotrophic AMPA 3 Get druggable targets OG5_128645 All targets in OG5_128645
Echinococcus multilocularis glutamate receptor 4 Get druggable targets OG5_128645 All targets in OG5_128645
Echinococcus multilocularis glutamate receptor 2 Get druggable targets OG5_128645 All targets in OG5_128645
Echinococcus granulosus glutamate receptor subunit protein glur Get druggable targets OG5_128645 All targets in OG5_128645
Echinococcus granulosus glutamate receptor 1 Get druggable targets OG5_128645 All targets in OG5_128645

By sequence similarity to non orthologous known druggable targets
Species Potential target Known druggable target Length Alignment span Identity
Echinococcus granulosus Glutamate receptor ionotropic kainate 2 glutamate receptor, ionotropic, AMPA 2 883 aa 810 aa 34.0 %

Obtained from network model

Ranking Plot


Putative Targets List


Species Potential target Raw Global Species
Loa Loa (eye worm) hypothetical protein 0.0051 0.0021 0.4062
Echinococcus granulosus Glutamate receptor ionotropic kainate 2 0.0036 0.0006 0.1012
Mycobacterium ulcerans AcrR family transcriptional regulator 0.9889 1 0.5
Echinococcus granulosus Glutamate receptor ionotropic kainate 2 0.0036 0.0006 0.1012
Loa Loa (eye worm) hypothetical protein 0.0051 0.0021 0.4062
Echinococcus multilocularis glutamate receptor 2 0.0076 0.0046 0.8025
Echinococcus granulosus glutamate receptor 2 0.0076 0.0046 0.8025
Echinococcus multilocularis glutamate receptor, ionotrophic, AMPA 3 0.0087 0.0058 1
Schistosoma mansoni glutamate receptor NMDA 0.0036 0.0006 1
Echinococcus granulosus Glutamate receptor ionotropic kainate 2 0.0036 0.0006 0.1012
Echinococcus granulosus glutamate receptor ionotrophic AMPA 3 0.0087 0.0058 1
Echinococcus multilocularis Glutamate receptor, ionotropic kainate 2 0.0036 0.0006 0.1012
Mycobacterium ulcerans transcriptional regulator 0.9889 1 0.5
Echinococcus granulosus glutamate receptor subunit protein glur 0.0062 0.0032 0.5626
Echinococcus multilocularis glutamate receptor 2 0.0087 0.0058 1
Echinococcus multilocularis glutamate receptor subunit protein glur 0.0062 0.0032 0.5626
Echinococcus multilocularis Glutamate receptor, ionotropic kainate 2 0.0036 0.0006 0.1012
Loa Loa (eye worm) glutamate receptor 1 0.0081 0.0052 1
Loa Loa (eye worm) hypothetical protein 0.0051 0.0021 0.4062
Echinococcus granulosus glutamate receptor 2 0.0087 0.0058 1
Mycobacterium ulcerans TetR family transcriptional regulator 0.9889 1 0.5
Echinococcus multilocularis Glutamate receptor, ionotropic kainate 2 0.0036 0.0006 0.1012
Echinococcus granulosus glutamate receptor 4 0.0051 0.0021 0.3651
Echinococcus multilocularis glutamate receptor 4 0.0051 0.0021 0.3651
Brugia malayi Glutamate receptor 2 precursor 0.0081 0.0052 0.5
Echinococcus multilocularis glutamate receptor 2 0.0081 0.0052 0.8988
Brugia malayi Glutamate receptor 1 precursor 0.0081 0.0052 0.5
Echinococcus granulosus glutamate receptor 1 0.0051 0.0021 0.3651
Mycobacterium tuberculosis Transcriptional regulatory repressor protein (TetR-family) EthR 0.9889 1 0.5

Activities

Activity type Activity value Assay description Source Reference
Activity (binding) = 75 % Positive modulation of human GluA2 flip receptor by FLIPR assay relative to cyclothiazide ChEMBL. 20971003
EC50 (binding) = 5 uM Positive modulation of human GluA2 flip receptor by FLIPR assay ChEMBL. 20971003
IC50 (binding) > 63 uM Displacement of [3H]-dofetilide from human hERG ChEMBL. 20971003

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.