Detailed information for compound 29914

Basic information

Technical information
  • TDR Targets ID: 29914
  • Name: 2-[5-amino-2-(3-methylphenyl)-6-oxopyrimidin- 1-yl]-N-(4,4,4-trifluoro-3-oxo-1-phenylbutan- 2-yl)acetamide
  • MW: 458.433 | Formula: C23H21F3N4O3
  • H donors: 2 H acceptors: 3 LogP: 3.21 Rotable bonds: 9
    Rule of 5 violations (Lipinski): 1
  • SMILES: Cc1cccc(c1)c1ncc(c(=O)n1CC(=O)NC(C(=O)C(F)(F)F)Cc1ccccc1)N
  • InChi: 1S/C23H21F3N4O3/c1-14-6-5-9-16(10-14)21-28-12-17(27)22(33)30(21)13-19(31)29-18(20(32)23(24,25)26)11-15-7-3-2-4-8-15/h2-10,12,18H,11,13,27H2,1H3,(H,29,31)
  • InChiKey: XDTTYVCUSUPDCP-UHFFFAOYSA-N  


Substructure search Similarity search

Network

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Synonyms

  • 2-[5-amino-2-(m-tolyl)-6-oxo-pyrimidin-1-yl]-N-(1-benzyl-3,3,3-trifluoro-2-oxo-propyl)acetamide
  • 2-[5-amino-2-(m-tolyl)-6-oxo-1-pyrimidinyl]-N-(1-benzyl-3,3,3-trifluoro-2-oxopropyl)acetamide
  • 2-[5-azanyl-2-(3-methylphenyl)-6-oxo-pyrimidin-1-yl]-N-(4,4,4-trifluoro-3-oxo-1-phenyl-butan-2-yl)ethanamide
  • 2-[5-amino-6-keto-2-(m-tolyl)pyrimidin-1-yl]-N-(1-benzyl-3,3,3-trifluoro-2-keto-propyl)acetamide
  • 2-[5-amino-2-(3-methylphenyl)-6-oxo-pyrimidin-1-yl]-N-[3,3,3-trifluoro-2-oxo-1-(phenylmethyl)propyl]acetamide
  • 2-[5-amino-2-(3-methylphenyl)-6-oxo-1-pyrimidinyl]-N-[3,3,3-trifluoro-2-oxo-1-(phenylmethyl)propyl]acetamide
  • 2-[5-amino-6-keto-2-(3-methylphenyl)pyrimidin-1-yl]-N-[1-(benzyl)-3,3,3-trifluoro-2-keto-propyl]acetamide
  • 2-[5-amino-2-(3-methylphenyl)-6-oxo-pyrimidin-1-yl]-N-(4,4,4-trifluoro-3-oxo-1-phenyl-butan-2-yl)ethanamide

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Homo sapiens chymase 1, mast cell Starlite/ChEMBL References
Homo sapiens chymotrypsin C (caldecrin) 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
Species Potential target Known druggable target Length Alignment span Identity
Brugia malayi Trypsin family protein chymotrypsin C (caldecrin) 268 aa 236 aa 21.6 %
Brugia malayi Trypsin family protein chymase 1, mast cell 247 aa 295 aa 24.1 %
Obtained from network model

Ranking Plot

Putative Targets List

Species Potential target Raw Global Species
Echinococcus granulosus retinoic acid receptor rxr beta a 0.039 0.4643 1
Schistosoma mansoni retinoic acid receptor RXR 0.039 0.4643 1
Brugia malayi nuclear hormone receptor 0.0741 0.956 1
Loa Loa (eye worm) hypothetical protein 0.0713 0.9167 0.9589
Loa Loa (eye worm) nuclear receptor nhr-7B 0.0741 0.956 1
Echinococcus multilocularis retinoic acid receptor rxr beta a retinoic acid receptor rxr alpha a retinoic acid receptor rxr alpha 0.0359 0.4203 1

Activities

Activity type Activity value Assay description Source Reference
Ki (binding) = 50.6 nM In vitro inhibitory activity was determined against human heart chymase ChEMBL. 11312928
Ki (binding) = 50.6 nM In vitro inhibitory activity was determined against human heart chymase ChEMBL. 11312928
Ki (binding) = 455 nM In vitro inhibitory activity was determined against bovine pancreas chymotrypsin ChEMBL. 11312928
Ki (binding) = 455 nM In vitro inhibitory activity was determined against bovine pancreas chymotrypsin ChEMBL. 11312928
Selectivity (binding) = 8.99 The selectivity was determined for chymotrypsin to that of chymase ChEMBL. 11312928

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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