Detailed information for compound 73384

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 454.479 | Formula: C22H26N6O5
  • H donors: 5 H acceptors: 7 LogP: 0.76 Rotable bonds: 8
    Rule of 5 violations (Lipinski): 1
  • SMILES: OC(=O)CCC(C(=O)O)NC(=O)c1ccc(cc1)C1CC2N(C1)c1c(N)nc(nc1CC2)N
  • InChi: 1S/C22H26N6O5/c23-19-18-15(26-22(24)27-19)6-5-14-9-13(10-28(14)18)11-1-3-12(4-2-11)20(31)25-16(21(32)33)7-8-17(29)30/h1-4,13-14,16H,5-10H2,(H,25,31)(H,29,30)(H,32,33)(H4,23,24,26,27)
  • InChiKey: LCGIJUUGFUFBDH-UHFFFAOYSA-N  

Network

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Synonyms

No synonyms found for this compound

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Lactobacillus casei Dihydrofolate reductase Starlite/ChEMBL References

Predicted pathogen targets for this compound

By orthology
Species Potential target Known druggable target/s Ortholog Group
Mycobacterium leprae DIHYDROFOLATE REDUCTASE DFRA (DHFR) (TETRAHYDROFOLATE DEHYDROGENASE) Get druggable targets OG5_128410 All targets in OG5_128410
Mycobacterium ulcerans dihydrofolate reductase DfrA Get druggable targets OG5_128410 All targets in OG5_128410
Schistosoma mansoni dihydrofolate reductase Get druggable targets OG5_128410 All targets in OG5_128410
Schistosoma japonicum ko:K00287 dihydrofolate reductase [EC1.5.1.3], putative Get druggable targets OG5_128410 All targets in OG5_128410
Candida albicans hypothetical protein Get druggable targets OG5_128410 All targets in OG5_128410
Loa Loa (eye worm) dihydrofolate reductase Get druggable targets OG5_128410 All targets in OG5_128410
Candida albicans dihydrofolate reductase Get druggable targets OG5_128410 All targets in OG5_128410
Brugia malayi dihydrofolate reductase family protein Get druggable targets OG5_128410 All targets in OG5_128410
Candida albicans dihydrofolate reductase Get druggable targets OG5_128410 All targets in OG5_128410
Chlamydia trachomatis dihydrofolate reductase Get druggable targets OG5_128410 All targets in OG5_128410
Mycobacterium tuberculosis Dihydrofolate reductase DfrA (DHFR) (tetrahydrofolate dehydrogenase) Get druggable targets OG5_128410 All targets in OG5_128410
Echinococcus granulosus dihydrofolate reductase Get druggable targets OG5_128410 All targets in OG5_128410
Echinococcus multilocularis dihydrofolate reductase Get druggable targets OG5_128410 All targets in OG5_128410
Brugia malayi Dihydrofolate reductase Get druggable targets OG5_128410 All targets in OG5_128410

By sequence similarity to non orthologous known druggable targets
Species Potential target Known druggable target Length Alignment span Identity
Plasmodium yoelii thymidylate synthase, putative Dihydrofolate reductase   163 aa 139 aa 21.6 %
Babesia bovis dihydrofolate reductase/thymidilate synthase Dihydrofolate reductase   163 aa 133 aa 27.1 %
Toxoplasma gondii bifunctional dihydrofolate reductase-thymidylate synthase Dihydrofolate reductase   163 aa 138 aa 29.7 %
Onchocerca volvulus Putative dihydrofolate reductase Dihydrofolate reductase   163 aa 173 aa 27.2 %

Obtained from network model

Ranking Plot


Putative Targets List


Species Potential target Raw Global Species
Echinococcus multilocularis dihydrofolate reductase 0.0208 1 1
Chlamydia trachomatis dihydrofolate reductase 0.0208 1 0.5
Onchocerca volvulus 0.0014 0 0.5
Loa Loa (eye worm) hypothetical protein 0.0049 0.1789 0.1789
Echinococcus granulosus dihydrofolate reductase 0.0208 1 1
Brugia malayi hypothetical protein 0.0049 0.1789 0.1789
Loa Loa (eye worm) dihydrofolate reductase 0.0208 1 1
Schistosoma mansoni dihydrofolate reductase 0.0208 1 1
Brugia malayi hypothetical protein 0.0049 0.1789 0.1789
Onchocerca volvulus 0.0014 0 0.5
Onchocerca volvulus 0.0014 0 0.5
Brugia malayi Dihydrofolate reductase 0.0208 1 1
Toxoplasma gondii bifunctional dihydrofolate reductase-thymidylate synthase 0.0079 0.3378 0.5
Trypanosoma brucei dihydrofolate reductase-thymidylate synthase 0.0079 0.3378 0.5
Onchocerca volvulus 0.0014 0 0.5
Mycobacterium ulcerans dihydrofolate reductase DfrA 0.0208 1 0.5
Onchocerca volvulus 0.0014 0 0.5
Trypanosoma cruzi dihydrofolate reductase-thymidylate synthase 0.0079 0.3378 0.5
Mycobacterium tuberculosis Dihydrofolate reductase DfrA (DHFR) (tetrahydrofolate dehydrogenase) 0.0208 1 0.5
Onchocerca volvulus 0.0014 0 0.5
Plasmodium vivax bifunctional dihydrofolate reductase-thymidylate synthase, putative 0.0079 0.3378 0.5
Mycobacterium leprae DIHYDROFOLATE REDUCTASE DFRA (DHFR) (TETRAHYDROFOLATE DEHYDROGENASE) 0.0208 1 0.5
Echinococcus granulosus expressed conserved protein 0.0049 0.1789 0.1789
Loa Loa (eye worm) hypothetical protein 0.0049 0.1789 0.1789
Onchocerca volvulus Putative nachr subunit 0.0014 0 0.5
Leishmania major dihydrofolate reductase-thymidylate synthase 0.0079 0.3378 0.5
Plasmodium falciparum bifunctional dihydrofolate reductase-thymidylate synthase 0.0079 0.3378 0.5
Echinococcus multilocularis expressed conserved protein 0.0049 0.1789 0.1789

Activities

Activity type Activity value Assay description Source Reference
IC50 (functional) = 0.00000025 M Compound was evaluated for growth inhibition in L1210 murine leukemia cells ChEMBL. 3091834
IC50 (functional) = 0.00000025 M Compound was evaluated for growth inhibition in L1210 murine leukemia cells ChEMBL. 3091834
IC50 (binding) = 0.0000015 M Compound was evaluated for the inhibition of dihydrofolate reductase (DHFR)derived from Lactobacillus casei ChEMBL. 3091834
IC50 (binding) = 0.0000015 M Compound was evaluated for the inhibition of dihydrofolate reductase (DHFR)derived from Lactobacillus casei ChEMBL. 3091834
IC50 (binding) > 0.0005 M Compound was evaluated for the inhibition of thymidylate synthase (TS) derived from Lactobacillus casei ChEMBL. 3091834
IC50 (binding) > 0.0005 M Compound was evaluated for the inhibition of thymidylate synthase (TS) derived from Lactobacillus casei ChEMBL. 3091834
IC50 (functional) = 1 ng ml-1 Compound was evaluated for growth inhibition in Lactobacillus casei ATCC 7469 ChEMBL. 3091834
IC50 (functional) = 2 ng ml-1 Compound was evaluated for growth inhibition in Streptococcus faecium ATCC 8043 ChEMBL. 3091834
IC50 (functional) = 530 ng ml-1 Compound was evaluated for growth inhibition in Streptococcus faecium MTX-resistant ChEMBL. 3091834
IC50 (functional) > 10000 ng ml-1 Compound was evaluated for growth inhibition in Lactobacillus casei MTX-resistant ChEMBL. 3091834
Ki (functional) > 0.00000001 M Compound was evaluated for inhibitory activity against DHFR in L1210 cells ChEMBL. 3091834
Ki (functional) > 0.00000001 M Compound was evaluated for inhibitory activity against DHFR in L1210 cells ChEMBL. 3091834

Phenotypes

Whole-cell/tissue/organism interactions

Species name Source Reference Is orphan
Mus musculus ChEMBL23 3091834

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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