Detailed information for compound 1637275

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 646.773 | Formula: C43H38N2O4
  • H donors: 0 H acceptors: 4 LogP: 6.19 Rotable bonds: 10
    Rule of 5 violations (Lipinski): 2
  • SMILES: O=C(N1C/C(=C\c2ccccc2)/C(=O)/C(=C/c2ccccc2)/C1)CCCC(=O)N1C/C(=C\c2ccccc2)/C(=O)/C(=C/c2ccccc2)/C1
  • InChi: 1S/C43H38N2O4/c46-40(44-28-36(24-32-14-5-1-6-15-32)42(48)37(29-44)25-33-16-7-2-8-17-33)22-13-23-41(47)45-30-38(26-34-18-9-3-10-19-34)43(49)39(31-45)27-35-20-11-4-12-21-35/h1-12,14-21,24-27H,13,22-23,28-31H2/b36-24+,37-25+,38-26+,39-27+
  • InChiKey: HVHDWYASTVLPEV-ZQRNLMMQSA-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 3-methylcrotonyl-CoA carboxylase, putative 0.0173 0.2839 0.5074
Mycobacterium tuberculosis Probable acetyl-/propionyl-coenzyme A carboxylase alpha chain (alpha subunit) AccA2: biotin carboxylase + biotin carboxyl carrie 0.0173 0.2839 1
Trypanosoma cruzi 3-methylcrotonyl-CoA carboxylase, putative 0.0173 0.2839 0.5074
Schistosoma mansoni pyruvate carboxylase 0.0173 0.2839 0.2839
Trypanosoma brucei acetyl-CoA carboxylase 0.0455 1 1
Mycobacterium ulcerans bifunctional protein acetyl-/propionyl-coenzyme a carboxylase (alpha chain) AccA3 0.0173 0.2839 1
Trypanosoma brucei 3-methylcrotonyl-CoA carboxylase alpha subunit, putative 0.0173 0.2839 0.2839
Trypanosoma brucei unspecified product 0.0114 0.1329 0.1329
Leishmania major carboxylase, putative 0.0173 0.2839 0.2839
Entamoeba histolytica acetyl-coA carboxylase, putative 0.0078 0.0405 0.5
Wolbachia endosymbiont of Brugia malayi Acetyl/propionyl-CoA carboxylase, alpha subunit 0.0173 0.2839 1
Trypanosoma brucei 3-methylcrotonyl-CoA carboxylase alpha subunit, putative 0.0173 0.2839 0.2839
Echinococcus granulosus propionyl coenzyme A carboxylase alpha chain 0.0173 0.2839 0.2839
Plasmodium falciparum biotin carboxylase subunit of acetyl CoA carboxylase, putative 0.0329 0.6803 0.5
Toxoplasma gondii acetyl-coA carboxylase ACC2 0.0455 1 1
Echinococcus multilocularis propionyl coenzyme A carboxylase alpha chain 0.0173 0.2839 0.2839
Schistosoma mansoni acetyl-CoA carboxylase 0.0455 1 1
Leishmania major methylcrotonoyl-coa carboxylase biotinylated subunitprotein-like protein 0.0173 0.2839 0.2839
Trypanosoma cruzi acetyl-CoA carboxylase 0.0281 0.5594 1
Toxoplasma gondii pyruvate carboxylase 0.0173 0.2839 0.2839
Mycobacterium tuberculosis Probable pyruvate carboxylase Pca (pyruvic carboxylase) 0.0173 0.2839 1
Loa Loa (eye worm) carboxyl transferase domain-containing protein 0.0439 0.9595 0.5
Mycobacterium leprae Probable bifunctional protein acetyl-/propionyl-coenzyme A carboxylase, alpha chain AccA3 (BccP) 0.0173 0.2839 1
Schistosoma mansoni methylcrotonyl-CoA carboxylase 0.0173 0.2839 0.2839
Giardia lamblia Acetyl-CoA carboxylase/pyruvate carboxylase fusion protein, putative 0.0078 0.0405 0.5
Plasmodium vivax biotin carboxylase subunit of acetyl CoA carboxylase, putative 0.0329 0.6803 0.5
Echinococcus multilocularis acetyl coenzyme A carboxylase 1 0.0455 1 1
Leishmania major acetyl-CoA carboxylase, putative 0.0455 1 1
Mycobacterium ulcerans acetyl-/propionyl-coenzyme a carboxylase alpha chain AccA1 0.0173 0.2839 1
Toxoplasma gondii acetyl-CoA carboxylase ACC1 0.0455 1 1
Mycobacterium ulcerans acetyl-/propionyl-coenzyme a carboxylase alpha chain, AccA2 0.0173 0.2839 1
Schistosoma mansoni methylcrotonyl-CoA carboxylase 0.0173 0.2839 0.2839
Brugia malayi Carboxyl transferase domain containing protein 0.0439 0.9595 0.5
Chlamydia trachomatis biotin carboxylase 0.0157 0.2433 1
Mycobacterium ulcerans pyruvate carboxylase 0.0173 0.2839 1

Activities

Activity type Activity value Assay description Source Reference
CC50 (functional) = 0.071 uM Cytotoxicity against human HSC2 cells after 48 hrs ChEMBL. 22409967
Ratio (binding) = 50.2 Inhibition of human MDR1-mediated multidrug resistant in mouse L5178Y cells at 4 uM treated 10 mins before rhodamine 123 challenge measured after 20 mins relative to control ChEMBL. 22409967
Ratio (binding) = 73.4 Inhibition of human MDR1-mediated multidrug resistant in mouse L5178Y cells at 40 uM treated 10 mins before rhodamine 123 challenge measured after 20 mins relative to control ChEMBL. 22409967

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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