Detailed information for compound 343379

Basic information

Technical information
  • TDR Targets ID: 343379
  • Name: 2-(2,4-dichlorophenoxy)-N-[2-[2-dimethylamino ethyl(methyl)amino]-4-methylquinolin-6-yl]ace tamide
  • MW: 461.384 | Formula: C23H26Cl2N4O2
  • H donors: 1 H acceptors: 2 LogP: 5.18 Rotable bonds: 9
    Rule of 5 violations (Lipinski): 1
  • SMILES: CN(CCN(c1cc(C)c2c(n1)ccc(c2)NC(=O)COc1ccc(cc1Cl)Cl)C)C
  • InChi: 1S/C23H26Cl2N4O2/c1-15-11-22(29(4)10-9-28(2)3)27-20-7-6-17(13-18(15)20)26-23(30)14-31-21-8-5-16(24)12-19(21)25/h5-8,11-13H,9-10,14H2,1-4H3,(H,26,30)
  • InChiKey: FWSBSBDRADXORX-UHFFFAOYSA-N  


Substructure search Similarity search

Network

Hover on a compound node to display the structore

Synonyms

  • 2-(2,4-dichlorophenoxy)-N-[2-[2-dimethylaminoethyl(methyl)amino]-4-methyl-6-quinolyl]acetamide
  • 2-(2,4-dichlorophenoxy)-N-[2-[2-dimethylaminoethyl(methyl)amino]-4-methyl-quinolin-6-yl]ethanamide
  • 2-(2,4-dichlorophenoxy)-N-[2-(2-dimethylaminoethyl-methylamino)-4-methylquinolin-6-yl]acetamide
  • 2-(2,4-dichlorophenoxy)-N-[2-(2-dimethylaminoethyl-methyl-amino)-4-methyl-6-quinolyl]acetamide
  • 2-(2,4-dichlorophenoxy)-N-[2-(2-dimethylaminoethyl-methylamino)-4-methyl-6-quinolyl]acetamide
  • 2-(2,4-dichlorophenoxy)-N-[2-(2-dimethylaminoethyl-methyl-amino)-4-methyl-quinolin-6-yl]ethanamide

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Homo sapiens melanin-concentrating hormone receptor 1 Starlite/ChEMBL References
Homo sapiens melanin-concentrating hormone receptor 2 Starlite/ChEMBL References

Predicted pathogen targets for this compound

By orthology
No druggable targets predicted by orthology data
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
Echinococcus multilocularis Pyruvate dehydrogenase (lipoamide) kinase 0.0254 0.3276 0.5
Leishmania major developmentally regulated phosphoprotein-like protein 0.0254 0.3276 0.5
Schistosoma mansoni pyruvate dehydrogenase 0.0254 0.3276 1
Toxoplasma gondii ATPase/histidine kinase/DNA gyrase B/HSP90 domain-containing protein 0.0103 0 0.5
Trypanosoma cruzi developmentally regulated phosphoprotein, putative 0.0254 0.3276 0.5
Echinococcus granulosus Pyruvate dehydrogenase lipoamide kinase 0.0254 0.3276 0.5
Echinococcus multilocularis Pyruvate dehydrogenase (lipoamide) kinase 0.0254 0.3276 0.5
Trypanosoma brucei developmentally regulated phosphoprotein 0.0254 0.3276 0.5
Loa Loa (eye worm) hypothetical protein 0.0254 0.3276 0.5

Activities

Activity type Activity value Assay description Source Reference
IC50 (binding) = 4.5 nM Displacement of 15 pM [125I]-MCH from human MCH2R expressed in CHO-K1 in whole-cell binding assay ChEMBL. 16134937
IC50 (binding) = 4.5 nM Displacement of 15 pM [125I]-MCH from human MCH2R expressed in CHO-K1 in whole-cell binding assay ChEMBL. 16134937
IC50 (binding) = 5.9 nM Displacement of 15 pM [125I]-MCH from human MCH1R expressed in CHO-K1 in whole-cell binding assay ChEMBL. 16134937
IC50 (binding) = 5.9 nM Displacement of 15 pM [125I]-MCH from human MCH1R expressed in CHO-K1 in whole-cell binding assay ChEMBL. 16134937
IC50 (binding) = 9.4 nM Displacement of 150p M [125I]-MCH from human MCH1R expressed in CHO-K1 cells ChEMBL. 16134937
IC50 (binding) = 9.4 nM Displacement of 150p M [125I]-MCH from human MCH1R expressed in CHO-K1 cells ChEMBL. 16134937
IC50 (functional) = 66 nM Inhibitory concentration against 10 nM MCH-induced IP3 accumulation in CHO-K1 cells expressing human MCH1R after incubation with [3H]-myo-inositol ChEMBL. 16134937
IC50 (functional) = 66 nM Inhibitory concentration against 10 nM MCH-induced IP3 accumulation in CHO-K1 cells expressing human MCH1R after incubation with [3H]-myo-inositol ChEMBL. 16134937
KB (functional) = 5 nM Binding constant against melanin concentrating hormone receptor 1 expressed in CHO-K1 cell membranes as 1 nM [35S]-GTP-gammaS, accumulation ChEMBL. 16134937
Kb (functional) = 5 nM Binding constant against melanin concentrating hormone receptor 1 expressed in CHO-K1 cell membranes as 1 nM [35S]-GTP-gammaS, accumulation ChEMBL. 16134937
Solubility = 80 uM Solubility was determined by addition of 10 mM DMSO solution of test compound to PBS (pH 7) until opalescence ChEMBL. 16134937

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

1 literature reference was collected for this gene.

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