Detailed information for compound 1705070

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 380.43 | Formula: C18H19F3N4S
  • H donors: 1 H acceptors: 1 LogP: 3.81 Rotable bonds: 5
    Rule of 5 violations (Lipinski): 1
  • SMILES: Cc1ccnc(c1)NC(=S)N1CCN(CC1)c1ccc(cc1)C(F)(F)F
  • InChi: 1S/C18H19F3N4S/c1-13-6-7-22-16(12-13)23-17(26)25-10-8-24(9-11-25)15-4-2-14(3-5-15)18(19,20)21/h2-7,12H,8-11H2,1H3,(H,22,23,26)
  • InChiKey: CDHYMMSTDFXWEP-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
Bacillus subtilis 4'-phosphopantetheinyl transferase ffp Starlite/ChEMBL No references

Predicted pathogen targets for this compound

By orthology
Species Potential target Known druggable target/s Ortholog Group
Brugia malayi aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase Get druggable targets OG5_129301 All targets in OG5_129301
Schistosoma japonicum ko:K00142 aminoadipate-semialdehyde dehydrogenase [EC1.2.1.31], putative Get druggable targets OG5_129301 All targets in OG5_129301
Onchocerca volvulus Get druggable targets OG5_129301 All targets in OG5_129301
Echinococcus multilocularis L aminoadipate semialdehyde Get druggable targets OG5_129301 All targets in OG5_129301
Cryptosporidium hominis proteinx0005 Get druggable targets OG5_129301 All targets in OG5_129301
Loa Loa (eye worm) hypothetical protein Get druggable targets OG5_129301 All targets in OG5_129301
Schistosoma japonicum expressed protein Get druggable targets OG5_129301 All targets in OG5_129301
Echinococcus granulosus L aminoadipate semialdehyde Get druggable targets OG5_129301 All targets in OG5_129301
Cryptosporidium parvum phosphopantetheinyl transferase Get druggable targets OG5_129301 All targets in OG5_129301
Schistosoma mansoni aminoadipate-semialdehyde dehydrogenase Get druggable targets OG5_129301 All targets in OG5_129301

By sequence similarity to non orthologous known druggable targets
Species Potential target Known druggable target Length Alignment span Identity
Candida albicans aminoadipate-semialdehyde dehydrogenase small subunit 4'-phosphopantetheinyl transferase ffp   224 aa 183 aa 27.3 %
Onchocerca volvulus 4'-phosphopantetheinyl transferase ffp   224 aa 186 aa 26.3 %
Entamoeba histolytica hypothetical protein 4'-phosphopantetheinyl transferase ffp   224 aa 198 aa 28.3 %
Candida albicans aminoadipate-semialdehyde dehydrogenase small subunit 4'-phosphopantetheinyl transferase ffp   224 aa 183 aa 27.3 %
Trichomonas vaginalis conserved hypothetical protein 4'-phosphopantetheinyl transferase ffp   224 aa 197 aa 22.3 %

Obtained from network model

Ranking Plot


Putative Targets List


Species Potential target Raw Global Species
Mycobacterium tuberculosis Probable thymidylate synthase ThyA (ts) (TSASE) 0.0329 0.0345 0.0345
Plasmodium falciparum bifunctional dihydrofolate reductase-thymidylate synthase 0.2383 0.4454 0.5
Leishmania major dihydrofolate reductase-thymidylate synthase 0.2383 0.4454 0.5
Mycobacterium ulcerans dihydrofolate reductase DfrA 0.5154 1 1
Trypanosoma brucei dihydrofolate reductase-thymidylate synthase 0.2383 0.4454 0.5
Mycobacterium tuberculosis Dihydrofolate reductase DfrA (DHFR) (tetrahydrofolate dehydrogenase) 0.5154 1 1
Echinococcus granulosus dihydrofolate reductase 0.5154 1 1
Plasmodium vivax bifunctional dihydrofolate reductase-thymidylate synthase, putative 0.2383 0.4454 0.5
Brugia malayi thymidylate synthase 0.0329 0.0345 0.0345
Mycobacterium leprae DIHYDROFOLATE REDUCTASE DFRA (DHFR) (TETRAHYDROFOLATE DEHYDROGENASE) 0.5154 1 1
Toxoplasma gondii bifunctional dihydrofolate reductase-thymidylate synthase 0.2383 0.4454 0.5
Trypanosoma cruzi dihydrofolate reductase-thymidylate synthase 0.2383 0.4454 1
Echinococcus multilocularis dihydrofolate reductase 0.5154 1 1
Schistosoma mansoni dihydrofolate reductase 0.5154 1 1
Trichomonas vaginalis conserved hypothetical protein 0.0157 0 0.5
Brugia malayi Dihydrofolate reductase 0.5154 1 1
Onchocerca volvulus 0.0329 0.0345 0.5
Chlamydia trachomatis dihydrofolate reductase 0.5154 1 0.5
Loa Loa (eye worm) dihydrofolate reductase 0.5154 1 1

Activities

Activity type Activity value Assay description Source Reference
Potency (functional) 2.5119 uM PubChem BioAssay. Gel-Based Assay for Inhibitos of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase): Chemistry Optimization Follow up. (Class of assay: confirmatory) ChEMBL. No reference

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

No literature references available for this target.

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