Detailed information for compound 1529812

Basic information

Technical information
  • TDR Targets ID: 1529812
  • Name: 6-[(10aS)-1,3-dioxo-10,10a-dihydro-5H-imidazo [3,4-b]isoquinolin-2-yl]-N-(3-methylphenyl)he xanamide
  • MW: 405.489 | Formula: C24H27N3O3
  • H donors: 1 H acceptors: 3 LogP: 3.13 Rotable bonds: 8
    Rule of 5 violations (Lipinski): 1
  • SMILES: O=C(Nc1cccc(c1)C)CCCCCN1C(=O)[C@H]2N(C1=O)Cc1c(C2)cccc1
  • InChi: 1S/C24H27N3O3/c1-17-8-7-11-20(14-17)25-22(28)12-3-2-6-13-26-23(29)21-15-18-9-4-5-10-19(18)16-27(21)24(26)30/h4-5,7-11,14,21H,2-3,6,12-13,15-16H2,1H3,(H,25,28)/t21-/m0/s1
  • InChiKey: QDQFRZYNEOPYPG-NRFANRHFSA-N  


Substructure search Similarity search

Network

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Synonyms

  • 6-[(10aS)-1,3-diketo-10,10a-dihydro-5H-imidazo[3,4-b]isoquinolin-2-yl]-N-(3-methylphenyl)hexanamide
  • ZINC05427058

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Homo sapiens ATPase family, AAA domain containing 5 Starlite/ChEMBL No references
Homo sapiens GNAS complex locus Starlite/ChEMBL No references

Predicted pathogen targets for this compound

By orthology
Species Potential target Known druggable target/s Ortholog Group
Loa Loa (eye worm) GTP-binding regulatory protein Gs alpha-S chain 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
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
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
Echinococcus multilocularis guanine nucleotide binding protein G(s) 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
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 atpase aaa+ type core atpase aaa type core Get druggable targets OG5_139225 All targets in OG5_139225
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
Schistosoma mansoni divalent metal transporter DMT1B 0.058 0.5809 1
Loa Loa (eye worm) GTP-binding regulatory protein Gs alpha-S chain 0.0055 0.0311 0.0536
Plasmodium falciparum transporter, putative 0.058 0.5809 0.5
Echinococcus multilocularis divalent metal transporter DMT1B 0.058 0.5809 0.5809
Brugia malayi NRAMP-like transporter K11G12.4 0.058 0.5809 1
Echinococcus multilocularis guanine nucleotide binding protein G(s) subunit 0.0055 0.0311 0.0311
Schistosoma mansoni divalent metal transporter DMT1B 0.058 0.5809 1
Schistosoma mansoni Guanine nucleotide-binding protein G(s) subunit alpha (Adenylate cyclase-stimulating G alpha protein) 0.0055 0.0311 0.0536
Echinococcus multilocularis guanine nucleotide binding protein G(s) subunit 0.0055 0.0311 0.0311
Schistosoma mansoni Guanine nucleotide-binding protein G(s) subunit alpha (Adenylate cyclase-stimulating G alpha protein) 0.0055 0.0311 0.0536
Mycobacterium ulcerans divalent cation-transport integral membrane protein 0.0221 0.2053 0.0165
Mycobacterium tuberculosis Divalent cation-transport integral membrane protein MntH (BRAMP) (MRAMP) 0.0358 0.3488 1
Toxoplasma gondii divalent metal transporter, putative 0.058 0.5809 0.5
Echinococcus granulosus divalent metal transporter DMT1B 0.058 0.5809 1
Mycobacterium ulcerans divalent cation-transport integral membrane protein 0.0221 0.2053 0.0165
Loa Loa (eye worm) hypothetical protein 0.058 0.5809 1
Mycobacterium leprae possible membrane transport protein 0.0221 0.2053 0.042
Loa Loa (eye worm) hypothetical protein 0.058 0.5809 1
Onchocerca volvulus Protein Malvolio homolog 0.058 0.5809 1
Brugia malayi GTP-binding regulatory protein Gs alpha-S chain, putative 0.0055 0.0311 0.0536
Plasmodium vivax metal transporter, putative 0.058 0.5809 0.5
Echinococcus granulosus guanine nucleotide binding protein Gs subunit 0.0055 0.0311 0.0536
Mycobacterium ulcerans manganese transport protein MntH 0.058 0.5809 1
Echinococcus granulosus guanine nucleotide binding protein Gs subunit 0.0055 0.0311 0.0536
Schistosoma mansoni Guanine nucleotide-binding protein G(s) subunit alpha (Adenylate cyclase-stimulating G alpha protein) 0.0055 0.0311 0.0536
Mycobacterium leprae DIVALENT CATION-TRANSPORT INTEGRAL MEMBRANE PROTEIN MNTH (BRAMP) (MRAMP) 0.0358 0.3488 1

Activities

Activity type Activity value Assay description Source Reference
Potency (functional) 8.9125 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) 12.99 uM PUBCHEM_BIOASSAY: qHTS screen for small molecules that inhibit ELG1-dependent DNA repair in human embryonic kidney (HEK293T) cells expressing luciferase-tagged ELG1. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID493107, AID493125] ChEMBL. No reference
Potency (functional) 18.526 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) 18.526 uM PUBCHEM_BIOASSAY: Primary qHTS for delayed death inhibitors of the malarial parasite plastid, 48 hour incubation. (Class of assay: confirmatory) [Related pubchem assays (depositor defined):AID488752, AID488774, AID504848, AID504850] 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.

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