Detailed information for compound 1934536

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 468.54 | Formula: C25H25FN2O4S
  • H donors: 1 H acceptors: 3 LogP: 3.38 Rotable bonds: 9
    Rule of 5 violations (Lipinski): 1
  • SMILES: COc1cccc(c1)CC(=O)N1Cc2c(C1)cc(cc2)S(=O)(=O)NCCc1cccc(c1)F
  • InChi: 1S/C25H25FN2O4S/c1-32-23-7-3-5-19(13-23)14-25(29)28-16-20-8-9-24(15-21(20)17-28)33(30,31)27-11-10-18-4-2-6-22(26)12-18/h2-9,12-13,15,27H,10-11,14,16-17H2,1H3
  • InChiKey: XEIUUMULWZILRT-UHFFFAOYSA-N  

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 mannosyl (beta-1,4-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase Starlite/ChEMBL References

Predicted pathogen targets for this compound

By orthology
Species Potential target Known druggable target/s Ortholog Group
Trichomonas vaginalis conserved hypothetical protein Get druggable targets OG5_130586 All targets in OG5_130586
Trichomonas vaginalis conserved hypothetical protein Get druggable targets OG5_130586 All targets in OG5_130586
Trichomonas vaginalis conserved hypothetical protein Get druggable targets OG5_130586 All targets in OG5_130586
Trichomonas vaginalis conserved hypothetical protein Get druggable targets OG5_130586 All targets in OG5_130586
Trichomonas vaginalis conserved hypothetical protein Get druggable targets OG5_130586 All targets in OG5_130586
Trichomonas vaginalis conserved hypothetical protein Get druggable targets OG5_130586 All targets in OG5_130586
Trichomonas vaginalis conserved hypothetical protein Get druggable targets OG5_130586 All targets in OG5_130586
Trichomonas vaginalis conserved hypothetical protein Get druggable targets OG5_130586 All targets in OG5_130586
Trichomonas vaginalis conserved hypothetical protein Get druggable targets OG5_130586 All targets in OG5_130586

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
Trichomonas vaginalis conserved hypothetical protein 0.0133 1 1
Trichomonas vaginalis conserved hypothetical protein 0.0133 1 1
Trichomonas vaginalis conserved hypothetical protein 0.0133 1 1
Trichomonas vaginalis conserved hypothetical protein 0.0133 1 1
Trichomonas vaginalis conserved hypothetical protein 0.0133 1 1
Trichomonas vaginalis conserved hypothetical protein 0.0133 1 1
Trichomonas vaginalis conserved hypothetical protein 0.0133 1 1

Activities

Activity type Activity value Assay description Source Reference
CL (ADMET) > 320 microL/min/mg Intrinsic clearance in human liver microsomes ChEMBL. 26258602
IC50 (binding) = 4.5 Inhibition of DGAT1 (unknown origin) assessed as effect on incorporation of [1-14C]decanoyl moiety into TG using [1-14C]decanoyl-CoA and 1,2-didecanoyl-sn-glycerol as substrates ChEMBL. 26258602
IC50 (binding) = 4.5 Inhibition of MGAT2 (unknown origin) assessed as effect on incorporation of [1-14C]decanoyl moiety into DAG using [1-14C]decanoyl-CoA and 1-decanoyl-rac-glycerol as substrates ChEMBL. 26258602
IC50 (binding) = 6.2 Inhibition of MGAT3 (unknown origin) assessed effect on incorporation of [1-14C]decanoyl moiety into triacylglycerol using [1-14C]decanoyl-CoA and 1,2-didecanoyl-sn-glycerol as substrates pre-incubated for 30 mins before substrate addition ChEMBL. 26258602
IC50 (binding) = 682 nM Inhibition of MGAT3 (unknown origin) assessed effect on incorporation of [1-14C]decanoyl moiety into triacylglycerol using [1-14C]decanoyl-CoA and 1,2-didecanoyl-sn-glycerol as substrates pre-incubated for 30 mins before substrate addition ChEMBL. 26258602
IC50 (binding) = 30 uM Inhibition of MGAT2 (unknown origin) assessed as effect on incorporation of [1-14C]decanoyl moiety into DAG using [1-14C]decanoyl-CoA and 1-decanoyl-rac-glycerol as substrates ChEMBL. 26258602
IC50 (binding) = 31 uM Inhibition of DGAT1 (unknown origin) assessed as effect on incorporation of [1-14C]decanoyl moiety into TG using [1-14C]decanoyl-CoA and 1,2-didecanoyl-sn-glycerol as substrates ChEMBL. 26258602
IC50 (binding) > 40 uM Inhibition of DGAT2 (unknown origin) using [1-14C]decanoyl-CoA and didecanoyl-sn-glycerol substrates incubated for 40 mins ChEMBL. 26258602
IC50 (binding) > 40 uM Inhibition of MGAT1 (unknown origin) assessed as effect on incorporation of [1-14C]decanoyl moiety into DAG using [1-14C]decanoyl-CoA and 2-oleoylglycerol as substrates ChEMBL. 26258602
Inhibition (ADMET) = 29 % Inhibition of CYP2C8 (unknown origin) at 3 uM ChEMBL. 26258602
Inhibition (ADMET) = 35 % Inhibition of CYP2C9 (unknown origin) at 3 uM ChEMBL. 26258602

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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