Detailed information for compound 405383

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 1302.46 | Formula: C61H88FN17O14
  • H donors: 16 H acceptors: 14 LogP: -3.95 Rotable bonds: 30
    Rule of 5 violations (Lipinski): 4
  • SMILES: NCCCC[C@@H]1NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](CCCN=C(N)N)NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@@H](CC(=O)NCC(NC(=O)[C@H]2N(C1=O)CCC2)C(=O)N)NC(=O)[C@H](Cc1c[nH]c2c1cccc2)NC(=O)[C@H](NC(=O)[C@H](NC(=O)C)CC)Cc1ccc(cc1)F
  • InChi: 1S/C61H88FN17O14/c1-5-38(70-33(4)80)52(85)75-44(27-34-17-19-36(62)20-18-34)56(89)76-45(28-35-30-68-39-13-7-6-12-37(35)39)57(90)77-46-29-49(81)69-31-47(51(64)84)78-59(92)48-16-11-25-79(48)60(93)42(14-8-9-23-63)73-55(88)43(26-32(2)3)74-53(86)40(15-10-24-67-61(65)66)71-54(87)41(72-58(46)91)21-22-50(82)83/h6-7,12-13,17-20,30,32,38,40-48,68H,5,8-11,14-16,21-29,31,63H2,1-4H3,(H2,64,84)(H,69,81)(H,70,80)(H,71,87)(H,72,91)(H,73,88)(H,74,86)(H,75,85)(H,76,89)(H,77,90)(H,78,92)(H,82,83)(H4,65,66,67)/t38-,40+,41-,42+,43-,44-,45-,46-,47?,48-/m0/s1
  • InChiKey: DXBYLEFXVLWFIB-ZUQRYCASSA-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
Trypanosoma cruzi malonyl-CoA decarboxylase, mitochondrial precursor, putative 0.0525 0.2945 0.5
Echinococcus multilocularis equilibrative nucleoside transporter 3 0.0187 0 0.5
Trichomonas vaginalis equilibrative nucleoside transporter, putative 0.0187 0 0.5
Leishmania major malonyl-coa decarboxylase-like protein 0.0525 0.2945 0.5
Giardia lamblia Hypothetical protein 0.0187 0 0.5
Echinococcus granulosus equilibrative nucleoside transporter 3 0.0187 0 0.5
Echinococcus multilocularis equilibrative nucleoside transporter protein 0.0187 0 0.5
Trichomonas vaginalis equilibrative nucleoside transporter, putative 0.0187 0 0.5
Trypanosoma brucei malonyl-CoA decarboxylase, mitochondrial precursor, putative 0.0525 0.2945 0.5
Brugia malayi GnHR receptor homolog 0.0569 0.3322 0.3322
Trichomonas vaginalis equilibrative nucleoside transporter, putative 0.0187 0 0.5
Loa Loa (eye worm) hypothetical protein 0.1337 1 1
Wolbachia endosymbiont of Brugia malayi malonyl-CoA decarboxylase 0.1337 1 0.5
Trichomonas vaginalis equilibrative nucleoside transporter, putative 0.0187 0 0.5
Onchocerca volvulus Equilibrative nucleoside transporter, putative homolog 0.0187 0 0.5
Onchocerca volvulus Equilibrative nucleoside transporter, putative homolog 0.0187 0 0.5
Trypanosoma cruzi malonyl-CoA decarboxylase, mitochondrial precursor, putative 0.0525 0.2945 0.5
Entamoeba histolytica nucleoside transporter, putative 0.0187 0 0.5
Echinococcus granulosus equilibrative nucleoside transporter 0.0187 0 0.5

Activities

Activity type Activity value Assay description Source Reference
Activity (functional) 0 Evaluated for the ovulation effects in the rat by administering the drug at the doses (1.0 ug); 2/10 ChEMBL. 10715147
Activity (functional) 0 Evaluated for the ovulation effects in the rat by administering the drug at the doses (2.5 ug); 0/10 ChEMBL. 10715147
Ki (binding) = 0.36 nM Competitive radioligand binding assay, in human HEK-293 cells stably transfected with the rat Gonadotropin-releasing hormone receptor ChEMBL. 10715147

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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