Detailed information for compound 919400

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 453.839 | Formula: C17H16ClF4N3O3S
  • H donors: 2 H acceptors: 4 LogP: 3.08 Rotable bonds: 8
    Rule of 5 violations (Lipinski): 1
  • SMILES: O=C(C(c1ccc(c(c1)F)NS(=O)(=O)C)C)NCc1ccc(nc1Cl)C(F)(F)F
  • InChi: 1S/C17H16ClF4N3O3S/c1-9(10-3-5-13(12(19)7-10)25-29(2,27)28)16(26)23-8-11-4-6-14(17(20,21)22)24-15(11)18/h3-7,9,25H,8H2,1-2H3,(H,23,26)
  • InChiKey: ZXGJHWCNCLPEEQ-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 transient receptor potential cation channel, subfamily V, member 1 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
Leishmania major presenilin-like aspartic peptidase, putative,presenilin-like aspartic peptidase, clan AD, family A22A, putative 0.0428 0.0695 1
Echinococcus granulosus gamma secretase subunit aph 1 0.4542 1 1
Trichomonas vaginalis Clan AD, family A22, presenilin-like aspartic peptidase 0.0428 0.0695 1
Trypanosoma cruzi Aph-1 protein, putative 0.177 0.373 1
Echinococcus granulosus presenilin enhancer 2 0.0402 0.0636 0.0446
Echinococcus multilocularis presenilin enhancer 2 0.0402 0.0636 0.0446
Schistosoma mansoni subfamily A22A unassigned peptidase (A22 family) 0.0428 0.0695 0.0507
Brugia malayi Presenilin family protein 0.0428 0.0695 0.0634
Brugia malayi hypothetical protein 0.0209 0.0199 0.0134
Entamoeba histolytica presenilin 1 peptidase, putative 0.0428 0.0695 0.5
Trichomonas vaginalis Clan AD, family A22, presenilin-like aspartic peptidase 0.0428 0.0695 1
Brugia malayi gamma-secretase subunit pen-2 0.0402 0.0636 0.0574
Trypanosoma brucei presenilin-like aspartic peptidase, putative 0.0428 0.0695 0.1864
Echinococcus multilocularis presenilin 0.0428 0.0695 0.0507
Brugia malayi hypothetical protein 0.0209 0.0199 0.0134
Trypanosoma brucei Aph-1 protein, putative 0.177 0.373 1
Trichomonas vaginalis Clan AD, family A22, presenilin-like aspartic peptidase 0.0428 0.0695 1
Trypanosoma cruzi Aph-1 protein, putative 0.177 0.373 1
Echinococcus multilocularis gamma secretase subunit aph 1 0.4542 1 1
Echinococcus granulosus presenilin 0.0428 0.0695 0.0507
Loa Loa (eye worm) gamma-secretase subunit pen-2 0.0402 0.0636 0.0574
Toxoplasma gondii hypothetical protein 0.015 0.0066 1
Schistosoma mansoni gamma-secretase subunit aph-1 0.4542 1 1
Loa Loa (eye worm) hypothetical protein 0.0209 0.0199 0.0134
Loa Loa (eye worm) gamma-secretase subunit aph-1 0.4542 1 1

Activities

Activity type Activity value Assay description Source Reference
Ki (binding) = 0.2 nM Antagonist activity at human TRPV1 expressed in CHO cells assessed as inhibition of capsaicin-induced increase in intracellular Ca2+ level by FLIPR assay ChEMBL. 24948568

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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