Detailed information for compound 29070

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 812.76 | Formula: C36H39F3N2O14S
  • H donors: 6 H acceptors: 10 LogP: 3 Rotable bonds: 16
    Rule of 5 violations (Lipinski): 3
  • SMILES: CSCCC(C(=O)OCC(=O)[C@@]1(O)C[C@H](OC2OC(C)C(C(C2)NC(=O)C(F)(F)F)O)c2c(C1)c(O)c1c(c2O)C(=O)c2c(C1=O)cccc2OC)NC(=O)C
  • InChi: 1S/C36H39F3N2O14S/c1-14-28(44)19(41-34(50)36(37,38)39)10-23(54-14)55-21-12-35(51,22(43)13-53-33(49)18(8-9-56-4)40-15(2)42)11-17-25(21)32(48)27-26(30(17)46)29(45)16-6-5-7-20(52-3)24(16)31(27)47/h5-7,14,18-19,21,23,28,44,46,48,51H,8-13H2,1-4H3,(H,40,42)(H,41,50)/t14?,18?,19?,21-,23?,28?,35-/m0/s1
  • InChiKey: OCYPQURUDMVASQ-WHDIUZRHSA-N  


Substructure search Similarity search

Network

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Synonyms

No synonyms found for this compound

Targets

Known targets for this compound

No curated genes were found associated with this compound

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
Trichomonas vaginalis protein farnesyltransferase alpha subunit, putative 0.0541 1 1
Echinococcus granulosus protein farnesyltransferase alpha subunit 0.0541 1 1
Loa Loa (eye worm) hypothetical protein 0.0541 1 1
Entamoeba histolytica protein farnesyltransferase alpha subunit, putative 0.0541 1 1
Trichomonas vaginalis protein farnesyltransferase alpha subunit/RAB geranylgeranyl transferase alpha subunit, putative 0.0401 0.4727 0.1427
Trichomonas vaginalis protein farnesyltransferase alpha subunit/RAB geranylgeranyl transferase alpha subunit, putative 0.0541 1 1
Schistosoma mansoni protein farnesyltransferase alpha subunit 0.0541 1 1
Trichomonas vaginalis protein farnesyltransferase alpha subunit, putative 0.0541 1 1
Toxoplasma gondii hypothetical protein 0.0401 0.4727 1
Trypanosoma brucei protein farnesyltransferase beta subunit 0.0377 0.3849 0.5
Leishmania major farnesyltransferase beta subunit 0.0377 0.3849 0.5
Plasmodium vivax farnesyltransferase beta subunit, putative 0.0377 0.3849 0.3849
Echinococcus multilocularis protein farnesyltransferase alpha subunit 0.0541 1 1
Loa Loa (eye worm) prenyltransferase alpha subunit repeat containing protein 0.0541 1 1
Giardia lamblia Rab geranylgeranyltransferase 0.0541 1 1
Trypanosoma cruzi protein farnesyltransferase, putative 0.0377 0.3849 0.5
Plasmodium vivax prenyltransferase alpha subunit, putative 0.0541 1 1
Plasmodium falciparum protein farnesyltransferase subunit alpha 0.0541 1 1
Trypanosoma cruzi protein farnesyltransferase, putative 0.0377 0.3849 0.5

Activities

Activity type Activity value Assay description Source Reference
ID50 (functional) = 0.83 uM Compound was evaluated in vitro for antitumor activity in CCRF-CEM culture of human leukemic lymphocytes ChEMBL. 3806576
ID50 (functional) = 0.83 uM Compound was evaluated in vitro for antitumor activity in CCRF-CEM culture of human leukemic lymphocytes ChEMBL. 3806576
ILS (functional) = 136 % Compound was evaluated in vivo for antileukemic activity in B6D2F1 male mice ChEMBL. 3806576
ILS (functional) = 136 % Compound was evaluated in vivo for antileukemic activity in B6D2F1 male mice ChEMBL. 3806576
T1/2 (ADMET) = 38 min Half-life time of the compound ChEMBL. 3806576

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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