Detailed information for compound 225031

Basic information

Technical information
  • TDR Targets ID: 225031
  • Name: tert-butyl N-[5-[(2-methoxy-6-methylphenyl)ca rbamoyl]-4-methyl-1,3-thiazol-2-yl]carbamate
  • MW: 377.458 | Formula: C18H23N3O4S
  • H donors: 2 H acceptors: 3 LogP: 3.76 Rotable bonds: 8
    Rule of 5 violations (Lipinski): 1
  • SMILES: COc1cccc(c1NC(=O)c1sc(nc1C)NC(=O)OC(C)(C)C)C
  • InChi: 1S/C18H23N3O4S/c1-10-8-7-9-12(24-6)13(10)20-15(22)14-11(2)19-16(26-14)21-17(23)25-18(3,4)5/h7-9H,1-6H3,(H,20,22)(H,19,21,23)
  • InChiKey: FUWPWSPNEHBSEJ-UHFFFAOYSA-N  

Network

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Synonyms

  • tert-butyl N-[5-[(2-methoxy-6-methyl-phenyl)carbamoyl]-4-methyl-thiazol-2-yl]carbamate
  • N-[5-[(2-methoxy-6-methylanilino)-oxomethyl]-4-methyl-2-thiazolyl]carbamic acid tert-butyl ester
  • tert-butyl N-[5-[(2-methoxy-6-methyl-phenyl)carbamoyl]-4-methyl-1,3-thiazol-2-yl]carbamate
  • N-[5-[(2-methoxy-6-methyl-phenyl)carbamoyl]-4-methyl-thiazol-2-yl]carbamic acid tert-butyl ester
  • N-[5-[[(2-methoxy-6-methylphenyl)amino]-oxomethyl]-4-methyl-2-thiazolyl]carbamic acid tert-butyl ester

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Plasmodium falciparum bifunctional dihydrofolate reductase-thymidylate synthase Curated by TDR Targets References

Predicted pathogen targets for this compound

By orthology
Species Potential target Known druggable target/s Ortholog Group
Theileria parva dihydrofolate reductase-thymidylate synthase, putative Get druggable targets OG5_127385 All targets in OG5_127385
Schistosoma mansoni bifunctional dihydrofolate reductase-thymidylate synthase Get druggable targets OG5_127385 All targets in OG5_127385
Leishmania infantum dihydrofolate reductase-thymidylate synthase Get druggable targets OG5_127385 All targets in OG5_127385
Plasmodium falciparum bifunctional dihydrofolate reductase-thymidylate synthase Get druggable targets OG5_127385 All targets in OG5_127385
Echinococcus granulosus thymidylate synthase Get druggable targets OG5_127385 All targets in OG5_127385
Schistosoma japonicum ko:K00560 thymidylate synthase [EC2.1.1.45], putative Get druggable targets OG5_127385 All targets in OG5_127385
Plasmodium vivax bifunctional dihydrofolate reductase-thymidylate synthase, putative Get druggable targets OG5_127385 All targets in OG5_127385
Cryptosporidium parvum dihydrofolate reductase-thymidylate synthase Get druggable targets OG5_127385 All targets in OG5_127385
Leishmania donovani dihydrofolate reductase-thymidylate synthase Get druggable targets OG5_127385 All targets in OG5_127385
Candida albicans Thymidylate synthase capable of functional substitution for S. cerevisiae CDC21 (YOR074C) Get druggable targets OG5_127385 All targets in OG5_127385
Loa Loa (eye worm) thymidylate synthase Get druggable targets OG5_127385 All targets in OG5_127385
Brugia malayi thymidylate synthase Get druggable targets OG5_127385 All targets in OG5_127385
Mycobacterium leprae PROBABLE THYMIDYLATE SYNTHASE THYA (TS) (TSASE) Get druggable targets OG5_127385 All targets in OG5_127385
Trypanosoma brucei dihydrofolate reductase-thymidylate synthase Get druggable targets OG5_127385 All targets in OG5_127385
Echinococcus multilocularis thymidylate synthase Get druggable targets OG5_127385 All targets in OG5_127385
Trypanosoma cruzi dihydrofolate reductase-thymidylate synthase Get druggable targets OG5_127385 All targets in OG5_127385
Mycobacterium ulcerans thymidylate synthase Get druggable targets OG5_127385 All targets in OG5_127385
Plasmodium yoelii thymidylate synthase, putative Get druggable targets OG5_127385 All targets in OG5_127385
Plasmodium berghei bifunctional dihydrofolate reductase-thymidylate synthase, putative Get druggable targets OG5_127385 All targets in OG5_127385
Schistosoma japonicum hypothetical protein Get druggable targets OG5_127385 All targets in OG5_127385
Trypanosoma brucei gambiense dihydrofolate reductase-thymidylate synthase Get druggable targets OG5_127385 All targets in OG5_127385
Neospora caninum Bifunctional dihydrofolate reductase-thymidylate synthase, related Get druggable targets OG5_127385 All targets in OG5_127385
Cryptosporidium hominis chain A, crystal structure of Dhfr Get druggable targets OG5_127385 All targets in OG5_127385
Leishmania major dihydrofolate reductase-thymidylate synthase Get druggable targets OG5_127385 All targets in OG5_127385
Toxoplasma gondii bifunctional dihydrofolate reductase-thymidylate synthase Get druggable targets OG5_127385 All targets in OG5_127385
Mycobacterium tuberculosis Probable thymidylate synthase ThyA (ts) (TSASE) Get druggable targets OG5_127385 All targets in OG5_127385
Leishmania mexicana dihydrofolate reductase-thymidylate synthase Get druggable targets OG5_127385 All targets in OG5_127385
Plasmodium knowlesi bifunctional dihydrofolate reductase-thymidylate synthase, putative Get druggable targets OG5_127385 All targets in OG5_127385
Candida albicans Thymidylate synthase capable of functional substitution for S. cerevisiae CDC21 (YOR074C) Get druggable targets OG5_127385 All targets in OG5_127385
Leishmania braziliensis dihydrofolate reductase-thymidylate synthase Get druggable targets OG5_127385 All targets in OG5_127385
Onchocerca volvulus Get druggable targets OG5_127385 All targets in OG5_127385
Babesia bovis dihydrofolate reductase/thymidilate synthase Get druggable targets OG5_127385 All targets in OG5_127385

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
Plasmodium vivax adenosine deaminase, putative 0.347 1 1
Leishmania major AMP deaminase, putative,amp deaminase-like protein 0.2386 0.6754 0.6702
Mycobacterium tuberculosis Probable adenosine deaminase Add (adenosine aminohydrolase) 0.347 1 1
Trypanosoma cruzi adenosine monophosphate deaminase, putative 0.2386 0.6754 1
Leishmania major hypothetical protein, conserved 0.1472 0.4018 0.3922
Brugia malayi adenosine monophosphate deaminase 0.2386 0.6754 0.6754
Trypanosoma cruzi AMP deaminase, putative 0.2386 0.6754 1
Schistosoma mansoni adenosine deaminase 0.347 1 1
Trypanosoma cruzi AMP deaminase, putative 0.2386 0.6754 1
Treponema pallidum adenosine deaminase 0.347 1 0.5
Schistosoma mansoni adenosine deaminase-related 0.347 1 1
Trypanosoma cruzi AMP deaminase, putative 0.2386 0.6754 1
Entamoeba histolytica adenosine deaminase, putative 0.347 1 1
Leishmania major AMP deaminase, putative,adenosine monophosphate deaminase-like protein 0.2386 0.6754 0.6702
Loa Loa (eye worm) AMP deaminase 0.2386 0.6754 0.6754
Schistosoma mansoni AMP deaminase 0.2386 0.6754 0.6754
Entamoeba histolytica adenosine deaminase, putative 0.347 1 1
Trypanosoma cruzi adenosine monophosphate deaminase-like protein, putative 0.2386 0.6754 1
Plasmodium falciparum adenosine deaminase 0.347 1 1
Loa Loa (eye worm) hypothetical protein 0.347 1 1
Trypanosoma cruzi AMP deaminase, putative 0.2386 0.6754 1
Leishmania major adenosine monophosphate deaminase, putative,AMP deaminase, putative 0.2386 0.6754 0.6702
Trypanosoma brucei adenosine monophosphate deaminase, putative 0.2386 0.6754 1
Trypanosoma cruzi AMP deaminase, putative 0.2386 0.6754 1
Trypanosoma brucei AMP deaminase, putative 0.2386 0.6754 1
Loa Loa (eye worm) hypothetical protein 0.1998 0.5594 0.5594
Loa Loa (eye worm) hypothetical protein 0.0914 0.2348 0.2348
Echinococcus multilocularis adenosine deaminase 0.347 1 1
Onchocerca volvulus 0.1472 0.4018 0.4018
Loa Loa (eye worm) hypothetical protein 0.1998 0.5594 0.5594
Trichomonas vaginalis adenosine deaminase, putative 0.347 1 0.5
Trypanosoma brucei AMP deaminase, putative 0.2386 0.6754 1
Trypanosoma brucei AMP deaminase, putative 0.2386 0.6754 1
Onchocerca volvulus Adenosine deaminase homolog 0.347 1 1
Echinococcus granulosus AMP deaminase 2 0.2386 0.6754 0.6754
Trichomonas vaginalis adenosine deaminase, putative 0.347 1 0.5
Plasmodium falciparum AMP deaminase, putative 0.2386 0.6754 0.6702
Toxoplasma gondii AMP deaminase 0.2386 0.6754 0.6702
Plasmodium vivax adenosine/AMP deaminase, putative 0.2386 0.6754 0.6702
Leishmania major adenine aminohydrolase 0.347 1 1
Onchocerca volvulus AMP deaminase 2 homolog 0.2386 0.6754 0.6754
Echinococcus multilocularis AMP deaminase 2 0.2386 0.6754 0.6754
Loa Loa (eye worm) hypothetical protein 0.1998 0.5594 0.5594
Mycobacterium ulcerans adenosine deaminase 0.347 1 1
Trypanosoma cruzi AMP deaminase 2, putative 0.1472 0.4018 0.5851
Toxoplasma gondii Adenosine/AMP deaminase domain-containing protein 0.347 1 1
Loa Loa (eye worm) hypothetical protein 0.1998 0.5594 0.5594
Mycobacterium leprae Probable adenosine deaminase Add (ADENOSINE AMINOHYDROLASE) 0.347 1 1
Leishmania major AMP deaminase, putative 0.2386 0.6754 0.6702
Loa Loa (eye worm) hypothetical protein 0.1472 0.4018 0.4018
Toxoplasma gondii Adenosine/AMP deaminase domain-containing protein 0.347 1 1
Echinococcus granulosus adenosine deaminase 0.347 1 1

Activities

Activity type Activity value Assay description Source Reference
IC50 (binding) = 24.3 uM In vitro inhibition of murine Lck kinase. ChEMBL. 14592495
IC50 (binding) = 24.3 uM Inhibition of murine Lck in presence of ATP ChEMBL. 17154512
IC50 (binding) = 24.3 uM In vitro inhibition of murine Lck kinase. ChEMBL. 14592495
IC50 (binding) = 24.3 uM Inhibition of murine Lck in presence of ATP ChEMBL. 17154512

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

2 literature references were collected for this gene.

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