Detailed information for compound 182533

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 741.833 | Formula: C39H47N7O8
  • H donors: 6 H acceptors: 7 LogP: 3.56 Rotable bonds: 23
    Rule of 5 violations (Lipinski): 3
  • SMILES: COC(=O)NC(C(=O)NN(C[C@@H]([C@@H](NC(=O)[C@@H](NC(=O)c1ccc2c(n1)cccc2)CC(=O)N)Cc1ccccc1)O)Cc1ccc(cc1)OC)C(C)C
  • InChi: 1S/C39H47N7O8/c1-24(2)35(44-39(52)54-4)38(51)45-46(22-26-14-17-28(53-3)18-15-26)23-33(47)31(20-25-10-6-5-7-11-25)42-37(50)32(21-34(40)48)43-36(49)30-19-16-27-12-8-9-13-29(27)41-30/h5-19,24,31-33,35,47H,20-23H2,1-4H3,(H2,40,48)(H,42,50)(H,43,49)(H,44,52)(H,45,51)/t31-,32-,33-,35?/m0/s1
  • InChiKey: FRIPPNBCKDHEHW-OKCSSABNSA-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
Human immunodeficiency virus 1 Human immunodeficiency virus type 1 protease Starlite/ChEMBL References

Predicted pathogen targets for this compound

By orthology
Species Potential target Known druggable target/s Ortholog Group
Schistosoma mansoni intracisternal A-particle retropepsin (A02 family) Get druggable targets OG5_131408 All targets in OG5_131408
By sequence similarity to non orthologous known druggable targets
Species Potential target Known druggable target Length Alignment span Identity
Trypanosoma brucei variant surface glycoprotein (VSG), putative Human immunodeficiency virus type 1 protease   99 aa 80 aa 27.5 %
Giardia lamblia DNA-directed RNA polymerase subunit D Human immunodeficiency virus type 1 protease   99 aa 90 aa 27.8 %
Candida albicans dethiobiotin synthetase Human immunodeficiency virus type 1 protease   99 aa 90 aa 22.2 %
Entamoeba histolytica retroviral aspartyl protease domain-containing protein Human immunodeficiency virus type 1 protease   99 aa 103 aa 31.1 %
Echinococcus multilocularis Chromobox protein 3 Human immunodeficiency virus type 1 protease   99 aa 95 aa 28.4 %
Mycobacterium leprae Hypothetical protein Human immunodeficiency virus type 1 protease   99 aa 86 aa 27.9 %
Entamoeba histolytica retroviral aspartyl protease domain-containing protein Human immunodeficiency virus type 1 protease   99 aa 103 aa 31.1 %
Candida albicans dethiobiotin synthetase Human immunodeficiency virus type 1 protease   99 aa 90 aa 22.2 %
Obtained from network model

Ranking Plot

Putative Targets List

Species Potential target Raw Global Species
Mycobacterium leprae POSSIBLE LYSOPHOSPHOLIPASE 0.0504 0.2486 1
Trichomonas vaginalis Clan SC, family S33, methylesterase-like serine peptidase 0.0504 0.2486 0.5
Trichomonas vaginalis valacyclovir hydrolase, putative 0.0504 0.2486 0.5
Mycobacterium tuberculosis 4,9-DHSA hydrolase 0.1282 0.8197 1
Trypanosoma cruzi monoglyceride lipase, putative 0.0504 0.2486 1
Plasmodium falciparum lysophospholipase, putative 0.0504 0.2486 1
Mycobacterium ulcerans hypothetical protein 0.0504 0.2486 0.2977
Echinococcus multilocularis fatty acid amide hydrolase 1 0.1373 0.8867 1
Trypanosoma brucei monoglyceride lipase, putative 0.0504 0.2486 1
Trichomonas vaginalis conserved hypothetical protein 0.0504 0.2486 0.5
Plasmodium falciparum esterase, putative 0.0504 0.2486 1
Schistosoma mansoni family A2 unassigned peptidase (A02 family) 0.0278 0.0823 0.0823
Trichomonas vaginalis Clan SC, family S33, methylesterase-like serine peptidase 0.0504 0.2486 0.5
Plasmodium falciparum lysophospholipase, putative 0.0504 0.2486 1
Loa Loa (eye worm) hypothetical protein 0.1373 0.8867 1
Echinococcus granulosus fatty acid amide hydrolase 1 0.1373 0.8867 1
Schistosoma mansoni fatty-acid amide hydrolase 0.1373 0.8867 0.8867
Echinococcus multilocularis fatty acid amide hydrolase 1 0.1373 0.8867 1
Plasmodium falciparum lysophospholipase, putative 0.0504 0.2486 1
Trichomonas vaginalis Clan SC, family S33, methylesterase-like serine peptidase 0.0504 0.2486 0.5
Mycobacterium ulcerans 2-hydroxy-6-oxo-6-phenylhexa-2,4-dienoate hydrolase BphD 0.1303 0.835 1
Trichomonas vaginalis conserved hypothetical protein 0.0504 0.2486 0.5
Mycobacterium ulcerans lysophospholipase 0.0504 0.2486 0.2977
Trichomonas vaginalis Clan SC, family S33, methylesterase-like serine peptidase 0.0504 0.2486 0.5
Treponema pallidum aspartyl/glutamyl-tRNA amidotransferase subunit A 0.0166 0 0.5
Trichomonas vaginalis Clan SC, family S33, methylesterase-like serine peptidase 0.0504 0.2486 0.5
Mycobacterium tuberculosis Possible lysophospholipase 0.0504 0.2486 0.3032
Echinococcus granulosus fatty acid amide hydrolase 1 0.1373 0.8867 1
Wolbachia endosymbiont of Brugia malayi aspartyl/glutamyl-tRNA amidotransferase subunit A 0.0166 0 0.5
Leishmania major monoglyceride lipase, putative 0.0504 0.2486 1
Entamoeba histolytica hydrolase, alpha/beta fold family domain containing protein 0.0504 0.2486 0.5
Entamoeba histolytica hydrolase, alpha/beta fold family domain containing protein 0.0504 0.2486 0.5
Trypanosoma brucei monoglyceride lipase, putative 0.0504 0.2486 1
Chlamydia trachomatis glutamyl-tRNA(Gln) amidotransferase subunit A 0.0166 0 0.5
Schistosoma mansoni amidase 0.1373 0.8867 0.8867
Brugia malayi amidase 0.1373 0.8867 1
Plasmodium vivax PST-A protein 0.0504 0.2486 1

Activities

Activity type Activity value Assay description Source Reference
ED50 (binding) = 0.118 uM In vivo antiviral activity (IC50) against HIV-1 protease. ChEMBL. 8759643
ED50 (binding) = 0.118 uM In vivo antiviral activity (IC50) against HIV-1 protease. ChEMBL. 8759643
ED90 (binding) = 1 uM In vivo for antiviral activity (ED90) against HIV-1 protease. ChEMBL. 8759643
ED90 (binding) = 1 uM In vivo for antiviral activity (ED90) against HIV-1 protease. ChEMBL. 8759643
IC50 (binding) = 31 nM In vivo antiviral activity (IC50) against HIV-1 protease. ChEMBL. 8759643
IC50 (binding) = 31 nM In vivo antiviral activity (IC50) against HIV-1 protease. ChEMBL. 8759643

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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