Detailed information for compound 19119

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 543.637 | Formula: C29H29N5O4S
  • H donors: 2 H acceptors: 5 LogP: 3 Rotable bonds: 8
    Rule of 5 violations (Lipinski): 2
  • SMILES: O=C([C@@H]1CC[C@@H]2N1C(=O)CN(C2)S(=O)(=O)C(c1ccccc1)c1ccccc1)NCc1ccc2c(c1)nc[nH]2
  • InChi: 1S/C29H29N5O4S/c35-27-18-33(39(37,38)28(21-7-3-1-4-8-21)22-9-5-2-6-10-22)17-23-12-14-26(34(23)27)29(36)30-16-20-11-13-24-25(15-20)32-19-31-24/h1-11,13,15,19,23,26,28H,12,14,16-18H2,(H,30,36)(H,31,32)/t23-,26-/m0/s1
  • InChiKey: NATAPHZBRGVFBE-OZXSUGGESA-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 coagulation factor X 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 multilocularis ryanodine receptor 44f 0.0152 0.3536 1
Trypanosoma cruzi inositol 1,4,5-trisphosphate receptor, putative 0.0179 0.4555 0.5
Schistosoma mansoni ryanodine receptor related 0.0213 0.5799 0.7496
Loa Loa (eye worm) hypothetical protein 0.0203 0.5445 0.9738
Trypanosoma brucei inositol 1,4,5-trisphosphate receptor 0.0179 0.4555 0.5
Loa Loa (eye worm) hypothetical protein 0.0207 0.5592 1
Loa Loa (eye worm) hypothetical protein 0.0173 0.4319 0.7724
Schistosoma mansoni inositol 145-trisphosphate receptor 0.0264 0.7737 1
Schistosoma mansoni inositol 145-trisphosphate receptor 0.0173 0.4319 0.5582
Leishmania major hypothetical protein, conserved 0.0122 0.241 0.5
Echinococcus granulosus ryanodine receptor 44f 0.0152 0.3536 1
Loa Loa (eye worm) hypothetical protein 0.0152 0.3536 0.6324

Activities

Activity type Activity value Assay description Source Reference
aPTT (functional) 0 s Activated partial thromboplastin time was determined after (iv) bolus dose of 0.75 mg/kg followed by an infusion of 50 microg/kg/min in rat arterial thrombosis model; Not determined ChEMBL. 11934583
Ki (binding) = 75 nM Inhibition of amidolytic activity of thrombin ChEMBL. 11934583
Ki (binding) = 75 nM Inhibition of amidolytic activity of thrombin ChEMBL. 11934583
MOT (functional) 0 min Mean occlusion time after (iv) bolus dose of 0.75 mg/kg followed by an infusion of 50 microg/kg/min was determined in rat arterial thrombosis model; Not determined ChEMBL. 11934583
Ratio (binding) = 11 Selectivity ratio, ratio of Ki against trypsin to Ki against thrombin ChEMBL. 11934583
TT (functional) 0 s Thrombin time was determined after (iv) bolus dose of 0.75 mg/kg followed by an infusion of 50 microg/kg/min in rat arterial thrombosis model; Not determined ChEMBL. 11934583

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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