Detailed information for compound 173686

Basic information

Technical information
  • TDR Targets ID: 173686
  • Name: benzyl N-[1-[3-(1,1-dioxo-3,4-dihydro-2H-benz o[e][1,2,4]thiadiazin-3-yl)-3-phenylbutyl]pip eridin-4-yl]-N-prop-2-enylcarbamate
  • MW: 588.76 | Formula: C33H40N4O4S
  • H donors: 2 H acceptors: 3 LogP: 6.09 Rotable bonds: 12
    Rule of 5 violations (Lipinski): 2
  • SMILES: C=CCN(C(=O)OCc1ccccc1)C1CCN(CC1)CCC(C1Nc2ccccc2S(=O)(=O)N1)(c1ccccc1)C
  • InChi: 1S/C33H40N4O4S/c1-3-21-37(32(38)41-25-26-12-6-4-7-13-26)28-18-22-36(23-19-28)24-20-33(2,27-14-8-5-9-15-27)31-34-29-16-10-11-17-30(29)42(39,40)35-31/h3-17,28,31,34-35H,1,18-25H2,2H3
  • InChiKey: MJDPZVNLAHDUND-UHFFFAOYSA-N  


Substructure search Similarity search

Network

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Synonyms

  • benzyl N-allyl-N-[1-[3-(1,1-dioxo-3,4-dihydro-2H-benzo[e][1,2,4]thiadiazin-3-yl)-3-phenyl-butyl]-4-piperidyl]carbamate
  • N-allyl-N-[1-[3-(1,1-dioxo-3,4-dihydro-2H-benzo[e][1,2,4]thiadiazin-3-yl)-3-phenylbutyl]-4-piperidinyl]carbamic acid benzyl ester
  • phenylmethyl N-[1-[3-(1,1-dioxo-3,4-dihydro-2H-benzo[e][1,2,4]thiadiazin-3-yl)-3-phenyl-butyl]piperidin-4-yl]-N-prop-2-enyl-carbamate
  • N-allyl-N-[1-[3-(1,1-diketo-3,4-dihydro-2H-benzo[e][1,2,4]thiadiazin-3-yl)-3-phenyl-butyl]-4-piperidyl]carbamic acid benzyl ester
  • phenylmethyl N-[1-[3-(1,1-dioxo-3,4-dihydro-2H-benzo[e][1,2,4]thiadiazin-3-yl)-3-phenylbutyl]piperidin-4-yl]-N-prop-2-enylcarbamate
  • phenylmethyl N-allyl-N-[1-[3-(1,1-dioxo-3,4-dihydro-2H-benzo[e][1,2,4]thiadiazin-3-yl)-3-phenyl-butyl]-4-piperidyl]carbamate
  • N-allyl-N-[1-[3-(1,1-dioxo-3,4-dihydro-2H-benzo[e][1,2,4]thiadiazin-3-yl)-3-phenylbutyl]-4-piperidinyl]carbamic acid phenylmethyl ester
  • AIDS-104789
  • AIDS-104769
  • AIDS104769
  • N-{1-[3-(1,1-Dioxo(2H,3H,4H-benzo[e]1,2,4-thiadiazin-3-yl))-3-phenylbutyl](4-piperidyl)}(phenylmethoxy)-N-prop-2-enylcarboxamide
  • AIDS104789

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Homo sapiens chemokine (C-C motif) receptor 2 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
Trypanosoma cruzi fructose-1,6-bisphosphatase, cytosolic, putative 0.2417 1 1
Echinococcus granulosus sodium:glucose cotransporter 0.0603 0.1986 0.1986
Echinococcus granulosus solute carrier family 5 0.0603 0.1986 0.1986
Onchocerca volvulus 0.0154 0 0.5
Echinococcus multilocularis sodium:glucose cotransporter 2 0.0603 0.1986 0.1986
Trypanosoma brucei fructose-1,6-bisphosphatase 0.2417 1 1
Echinococcus granulosus fructose 16 bisphosphatase 1 0.2417 1 1
Toxoplasma gondii fructose-bisphospatase I 0.0899 0.3291 0.3291
Schistosoma mansoni inositol transporter 0.0603 0.1986 0.1986
Schistosoma mansoni fructose-16-bisphosphatase-related 0.2417 1 1
Toxoplasma gondii sedoheptulose-1,7-bisphosphatase 0.0899 0.3291 0.3291
Trypanosoma cruzi fructose-1,6-bisphosphatase, cytosolic, putative 0.2417 1 1
Schistosoma mansoni inositol transporter 0.0603 0.1986 0.1986
Echinococcus multilocularis solute carrier family 5 0.0603 0.1986 0.1986
Echinococcus multilocularis fructose 1,6 bisphosphatase 1 0.2417 1 1
Echinococcus multilocularis sodium:myo inositol cotransporter 0.0603 0.1986 0.1986
Leishmania major 0.2417 1 0.5
Toxoplasma gondii fructose-bisphospatase II 0.2417 1 1
Echinococcus granulosus sodium:glucose cotransporter 2 0.0603 0.1986 0.1986
Loa Loa (eye worm) fructose-1,6-bisphosphatase 0.2417 1 1
Echinococcus granulosus sodium:myo inositol cotransporter 0.0603 0.1986 0.1986

Activities

Activity type Activity value Assay description Source Reference
IC50 (binding) = 18 nM Binding affinity against C-C chemokine receptor type 5 stably expressed in Chinese hamster ovary (CHO) cells using [125I]-MIP-1 alpha as the radioligand ChEMBL. 11720852
IC50 (binding) = 18 nM Binding affinity against C-C chemokine receptor type 5 stably expressed in Chinese hamster ovary (CHO) cells using [125I]-MIP-1 alpha as the radioligand ChEMBL. 11720852
IC50 (binding) = 55 nM Binding affinity against C-C chemokine receptor type 5 stably expressed in Chinese hamster ovary (CHO) cells using [125I]-MIP-1 alpha as the radioligand ChEMBL. 11720852
IC50 (binding) = 55 nM Binding affinity against C-C chemokine receptor type 5 stably expressed in Chinese hamster ovary (CHO) cells using [125I]-MIP-1 alpha as the radioligand ChEMBL. 11720852

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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