Detailed information for compound 1482521

Basic information

Technical information
  • TDR Targets ID: 1482521
  • Name: N-cyclohexyl-2-methyl-1-propanoyl-2,3-dihydro indole-5-sulfonamide
  • MW: 350.476 | Formula: C18H26N2O3S
  • H donors: 1 H acceptors: 3 LogP: 2.99 Rotable bonds: 5
    Rule of 5 violations (Lipinski): 1
  • SMILES: CCC(=O)N1C(C)Cc2c1ccc(c2)S(=O)(=O)NC1CCCCC1
  • InChi: 1S/C18H26N2O3S/c1-3-18(21)20-13(2)11-14-12-16(9-10-17(14)20)24(22,23)19-15-7-5-4-6-8-15/h9-10,12-13,15,19H,3-8,11H2,1-2H3
  • InChiKey: KCDAIXUFWANNMC-UHFFFAOYSA-N  


Substructure search Similarity search

Network

Hover on a compound node to display the structore

Synonyms

  • N-cyclohexyl-2-methyl-1-propanoyl-indoline-5-sulfonamide
  • N-cyclohexyl-2-methyl-1-(1-oxopropyl)-5-indolinesulfonamide
  • N-cyclohexyl-2-methyl-1-propionyl-indoline-5-sulfonamide
  • EU-0092423

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Homo sapiens GNAS complex locus Starlite/ChEMBL No references
Homo sapiens nuclear factor, erythroid 2-like 2 Starlite/ChEMBL No references

Predicted pathogen targets for this compound

By orthology
Species Potential target Known druggable target/s Ortholog Group
Schistosoma mansoni Guanine nucleotide-binding protein G(s) subunit alpha (Adenylate cyclase-stimulating G alpha protein) Get druggable targets OG5_131088 All targets in OG5_131088
Brugia malayi GTP-binding regulatory protein Gs alpha-S chain, putative Get druggable targets OG5_131088 All targets in OG5_131088
Schistosoma mansoni Guanine nucleotide-binding protein G(s) subunit alpha (Adenylate cyclase-stimulating G alpha protein) Get druggable targets OG5_131088 All targets in OG5_131088
Echinococcus granulosus guanine nucleotide binding protein Gs subunit Get druggable targets OG5_131088 All targets in OG5_131088
Echinococcus granulosus guanine nucleotide binding protein Gs subunit Get druggable targets OG5_131088 All targets in OG5_131088
Echinococcus multilocularis guanine nucleotide binding protein G(s) subunit Get druggable targets OG5_131088 All targets in OG5_131088
Schistosoma mansoni Guanine nucleotide-binding protein G(s) subunit alpha (Adenylate cyclase-stimulating G alpha protein) Get druggable targets OG5_131088 All targets in OG5_131088
Echinococcus multilocularis guanine nucleotide binding protein G(s) subunit Get druggable targets OG5_131088 All targets in OG5_131088
Schistosoma japonicum ko:K04632 guanine nucleotide binding protein (G protein), alpha stimulating, putative Get druggable targets OG5_131088 All targets in OG5_131088
Loa Loa (eye worm) GTP-binding regulatory protein Gs alpha-S chain Get druggable targets OG5_131088 All targets in OG5_131088
By sequence similarity to non orthologous known druggable targets
Species Potential target Known druggable target Length Alignment span Identity
Schistosoma mansoni GTP-binding protein alpha subunit gna GNAS complex locus 394 aa 450 aa 28.7 %
Obtained from network model

Ranking Plot

Putative Targets List

Species Potential target Raw Global Species
Echinococcus granulosus lysine specific histone demethylase 1A 0.0363 0.1138 0.1315
Schistosoma mansoni Protoporphyrinogen oxidase chloroplast/mitochondrial precursor 0.2755 1 1
Mycobacterium tuberculosis Probable protoporphyrinogen oxidase HemY (protoporphyrinogen-IX oxidase) (protoporphyrinogenase) (PPO) 0.2393 0.8657 1
Mycobacterium ulcerans protoporphyrinogen oxidase 0.2755 1 1
Loa Loa (eye worm) hypothetical protein 0.0363 0.1138 1
Toxoplasma gondii histone lysine-specific demethylase LSD1/BHC110/KDMA1A 0.0363 0.1138 0.5
Loa Loa (eye worm) hypothetical protein 0.0363 0.1138 1
Echinococcus granulosus lysine specific histone demethylase 1A 0.0363 0.1138 0.1315
Loa Loa (eye worm) hypothetical protein 0.0363 0.1138 1
Loa Loa (eye worm) hypothetical protein 0.0363 0.1138 1
Leishmania major UDP-galactopyranose mutase 0.0363 0.1138 0.5
Toxoplasma gondii histone lysine-specific demethylase 0.0363 0.1138 0.5
Echinococcus granulosus protoporphyrinogen oxidase 0.2393 0.8657 1
Echinococcus multilocularis protoporphyrinogen oxidase 0.2755 1 1
Onchocerca volvulus 0.0363 0.1138 0.5
Trypanosoma cruzi UDP-galactopyranose mutase 0.0363 0.1138 0.5
Plasmodium falciparum protoporphyrinogen oxidase 0.0363 0.1138 0.5
Brugia malayi amine oxidase, flavin-containing family protein 0.0363 0.1138 1
Plasmodium falciparum lysine-specific histone demethylase 1, putative 0.0363 0.1138 0.5
Plasmodium vivax protoporphyrinogen oxidase, putative 0.0363 0.1138 0.5
Mycobacterium leprae PROBABLE PROTOPORPHYRINOGEN OXIDASE HEMY (PROTOPORPHYRINOGEN-IX OXIDASE) (PROTOPORPHYRINOGENASE) (PPO) 0.2755 1 0.5
Plasmodium vivax lysine-specific histone demethylase 1, putative 0.0363 0.1138 0.5
Schistosoma mansoni Lysine-specific histone demethylase 1 0.0363 0.1138 0.1138
Plasmodium falciparum conserved Plasmodium protein, unknown function 0.0363 0.1138 0.5
Plasmodium vivax hypothetical protein, conserved 0.0363 0.1138 0.5
Brugia malayi hypothetical protein 0.0363 0.1138 1
Echinococcus multilocularis lysine specific histone demethylase 1A 0.0363 0.1138 0.1138
Brugia malayi SWIRM domain containing protein 0.0363 0.1138 1
Plasmodium vivax hypothetical protein, conserved 0.0363 0.1138 0.5
Loa Loa (eye worm) hypothetical protein 0.0363 0.1138 1
Trypanosoma cruzi UDP-galactopyranose mutase 0.0363 0.1138 0.5
Echinococcus multilocularis 0.0363 0.1138 0.1138
Schistosoma mansoni amine oxidase 0.0363 0.1138 0.1138
Schistosoma mansoni amine oxidase 0.0363 0.1138 0.1138
Loa Loa (eye worm) hypothetical protein 0.0363 0.1138 1

Activities

Activity type Activity value Assay description Source Reference
Potency (functional) 10 uM PubChem BioAssay. qHTS for Agonist of gsp, the Etiologic Mutation Responsible for Fibrous Dysplasia/McCune-Albright Syndrome: qHTS. (Class of assay: confirmatory) ChEMBL. No reference
Potency (functional) 10.4179 uM PUBCHEM_BIOASSAY: Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 96 hour incubation. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID488745, AID488752, AID488774, AID504848, AID504850] ChEMBL. No reference
Potency (functional) 16.3601 uM PUBCHEM_BIOASSAY: Nrf2 qHTS screen for inhibitors. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID493153, AID493163, AID504648] ChEMBL. No reference
Potency (functional) 50.1187 uM PubChem BioAssay. qHTS for Small Molecule Inhibitors of the ERG Ets/DNA interaction. (Class of assay: confirmatory) ChEMBL. No reference

Phenotypes

Whole-cell/tissue/organism interactions

Species name Source Reference Is orphan
Plasmodium falciparum ChEMBL23

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.

If you have references for this compound, please enter them in a user comment (below) or Contact us.