Detailed information for compound 209284

Basic information

Technical information
  • TDR Targets ID: 209284
  • Name: 3-(3,4-difluorophenyl)-2-(6-methylpyridin-2-y l)-5,6-dihydro-4H-pyrrolo[2,1-e]pyrazole
  • MW: 311.329 | Formula: C18H15F2N3
  • H donors: 0 H acceptors: 2 LogP: 3.45 Rotable bonds: 2
    Rule of 5 violations (Lipinski): 1
  • SMILES: Cc1cccc(n1)c1nn2c(c1c1ccc(c(c1)F)F)CCC2
  • InChi: 1S/C18H15F2N3/c1-11-4-2-5-15(21-11)18-17(16-6-3-9-23(16)22-18)12-7-8-13(19)14(20)10-12/h2,4-5,7-8,10H,3,6,9H2,1H3
  • InChiKey: JQLXLCYSWMVCLC-UHFFFAOYSA-N  

Network

Hover on a compound node to display the structore

Synonyms

  • 3-(3,4-difluorophenyl)-2-(6-methyl-2-pyridyl)-5,6-dihydro-4H-pyrrolo[2,1-e]pyrazole

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Homo sapiens activin A receptor, type IB Starlite/ChEMBL References
Homo sapiens thyroid hormone receptor, beta Starlite/ChEMBL References

Predicted pathogen targets for this compound

By orthology
Species Potential target Known druggable target/s Ortholog Group
Echinococcus granulosus TGF beta receptor type 1 Get druggable targets OG5_129709 All targets in OG5_129709
Schistosoma mansoni hypothetical protein Get druggable targets OG5_134830 All targets in OG5_134830
Echinococcus granulosus TGF-beta receptor type-1 Get druggable targets OG5_129709 All targets in OG5_129709
Echinococcus multilocularis thyroid hormone receptor alpha Get druggable targets OG5_134830 All targets in OG5_134830
Schistosoma japonicum ko:K04674 transforming growth factor, beta receptor I, putative Get druggable targets OG5_129709 All targets in OG5_129709
Schistosoma japonicum expressed protein Get druggable targets OG5_134830 All targets in OG5_134830
Echinococcus multilocularis Mitotic checkpoint protein PRCC, C terminal Get druggable targets OG5_134830 All targets in OG5_134830
Echinococcus multilocularis TGF beta receptor type 1 Get druggable targets OG5_129709 All targets in OG5_129709
Schistosoma japonicum Thyroid hormone receptor alpha, putative Get druggable targets OG5_134830 All targets in OG5_134830
Brugia malayi bone morphogenetic protein type 1 receptor Get druggable targets OG5_129709 All targets in OG5_129709
Schistosoma mansoni thyroid hormone receptor Get druggable targets OG5_134830 All targets in OG5_134830
Schistosoma japonicum ko:K08362 nuclear receptor, subfamily 1, group A, member 2, putative Get druggable targets OG5_134830 All targets in OG5_134830
Echinococcus granulosus Mitotic checkpoint protein PRCC C terminal Get druggable targets OG5_134830 All targets in OG5_134830
Loa Loa (eye worm) TKL/STKR/TYPE1 protein kinase Get druggable targets OG5_129709 All targets in OG5_129709
Schistosoma japonicum Thyroid hormone receptor alpha, putative Get druggable targets OG5_134830 All targets in OG5_134830
Schistosoma mansoni thyroid hormone receptor Get druggable targets OG5_134830 All targets in OG5_134830
Schistosoma mansoni protein kinase Get druggable targets OG5_129709 All targets in OG5_129709

By sequence similarity to non orthologous known druggable targets
Species Potential target Known druggable target Length Alignment span Identity
Brugia malayi photoreceptor-specific nuclear receptor thyroid hormone receptor, beta 461 aa 414 aa 24.6 %

Obtained from network model

Ranking Plot


Putative Targets List


Species Potential target Raw Global Species
Schistosoma mansoni thyroid hormone receptor 0.0164 0.7683 0.741
Echinococcus granulosus Mitotic checkpoint protein PRCC C terminal 0.0152 0.6646 0.6241
Echinococcus granulosus TGF-beta receptor type-1 0.0191 1 1
Schistosoma mansoni thyroid hormone receptor 0.0164 0.7683 0.741
Echinococcus multilocularis thyroid hormone receptor alpha 0.0164 0.7683 0.7404
Schistosoma mansoni hypothetical protein 0.0152 0.6646 0.6251
Schistosoma mansoni protein kinase 0.0191 1 1
Echinococcus multilocularis Mitotic checkpoint protein PRCC, C terminal 0.0152 0.6646 0.6241
Loa Loa (eye worm) TKL/STKR/TYPE1 protein kinase 0.0191 0.9976 1
Brugia malayi bone morphogenetic protein type 1 receptor 0.0191 0.9976 1
Echinococcus multilocularis TGF beta receptor type 1 0.0191 1 1

Activities

Activity type Activity value Assay description Source Reference
IC50 (binding) = 343 nM Inhibition of TGFR1 ChEMBL. 19640613
IC50 (binding) = 0.343 uM Inhibitory activity against TGF-beta type I receptor ChEMBL. 15177480
IC50 (binding) = 0.343 uM Inhibitory activity against TGF-beta type I receptor ChEMBL. 15177480
IC50 (functional) = 1.04 uM Inhibitory activity tested in NIH 3T3 cells ChEMBL. 15177480
IC50 (functional) = 1.04 uM Inhibitory activity tested in NIH 3T3 cells ChEMBL. 15177480
IC50 (functional) = 1.51 uM Inhibitory activity against TGF-beta dependentluciferase production in mink lung cells p3TP Lux ChEMBL. 15177480
IC50 (binding) > 20 uM Inhibitory activity against Mitogen-activated protein kinase p38 ChEMBL. 15177480
IC50 (binding) > 20 uM Inhibitory activity against Mitogen-activated protein kinase p38 ChEMBL. 15177480

Phenotypes

Whole-cell/tissue/organism interactions

Species name Source Reference Is orphan
Mus musculus ChEMBL23 15177480

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.

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